If You Have Type II Diabetes, What Target for Lowering Your HbA1c Should You Have?
 

There is a debate among experts what target level of Hemoglobin A1C should be your goal.(1)  Hemoglobin A1C, which stands for glycated hemoglobin, is believed to reflect your average blood sugar readings over a 3 month period.  The American College of Physicians just released new guidelines recommending that the new goal for HbA1C  should be between 7 and 8 but the American Diabetes Association disagrees, feeling that the goal should be to lower HbA1C below 7.(2) The American College of Physicians (ACP) made this recommendation based on some studies showing that when you aggressively try to lower blood sugar levels with using more and more medications at a certain point, you end up with too many side effects.  These negative effects include the blood sugar dropping too low–hypoglycemia–but also increased risk of heart disease. But elevated levels of glycated hemoglobin means that you increase the risk of the vascular complications of diabetes such as heart disease, strokeheart failurekidney failureblindnesserectile dysfunctionneuropathy, poor wound healing, gangrene, and gastroparesis (slowed emptying of the stomach).

 

The ACP based their recommendations on several clinical trials, including the ACCORD Trial, which was ended early due to a 22% increase in all-cause mortality, a 35% increase in cardiovascular-related deaths, and a 3-fold increase in risk for severe hypoglycemia in those who received intensive therapy.(3) What this tells me is not that it is a bad idea to lower your HbA1C below 6.5 but that when you do it by using an increased amount of drugs, you increase the potential side effects, which is not surprising. This is especially the case with using insulin and sulfonureas, as opposed to the newer categories of drugs, like GLP-1 analogues & SGLT-2 inhibitors. Each of these older drugs have more potential side effects, including increased heart disease, and when you combine multiple drugs, you are compounding this effect. This is quite a bit different than using diet, exercise, and lifestyle changes to lower HbA1C levels, which is the approach that we take at Weitz Sports Chiropractic and Nutrition.

 

Another trial that the ACP based their recommendations on is the ADVANCE trial which did achieve HbA1C levels of 6.5 and did not see an increase in the risk of death but it did result in a lower risk of kidney problems.(4) The risk associated with this trial was increased incidence of severe hypoglycemic events, meaning that at times the blood sugar dropped too much, which risks falling into a diabetic coma and dying. Once again, if you can accomplish this with diet and lifestyle changes, the risk of hypoglycemia is less, provided that the program is not too severe in limiting all carbohydrate foods.

 

Type II Diabetes is a disease directly related to diet and lifestyle and if you don’t significantly change your diet and lifestyle, it will only get worse. Medication only manages your downhill ride. The only way to change direction is to eat a low carbohydrate healthy diet such as Paleo or Keto or low glycemic Mediterranean, exercise regularly, and lose weight (if overweight). However, if you use a very carb approach, like keto, be very careful not to let your blood sugar drop too low and it would be best to work with a practitioner, like myself rather than doing it on your own. Make an appointment today to see Dr. Weitz for a nutritional consultation and hire him be your health coach till you reach your health goals. But expect this journey to take a number of months and perhaps a few years, but the benefits are worth it.

 
References:
2.  Qaseem A, Wilt TJ, Kansagara D, et al. Hemoglobin A1c Targets for Glycemic Control With Pharmacologic Therapy for Nonpregnant Adults With Type 2 Diabetes Mellitus: A Guidance Statement Update From the American College of Physicians. Ann Intern Med. 2018;168:569-576.
3. Gerstein HC, Miller ME, Byington RP, et al.  Action to Control Cardiovascular Risk in Diabetes Study Group Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med. 2008; 358:2545-59
4. Patel A, MacMahon S, Chalmers J, et al. ADVANCE Collaborative Group Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes. N Engl J Med. 2008; 358: 2560-72.
Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Improving Posture for Anti-Aging with Dr. Steven Weiniger: Rational Wellness Podcast 055
Loading
/

Improving your posture is an anti-aging strategy with Dr. Steven Weiniger, who is interviewed by Dr. Ben Weitz. 

[If you enjoy this podcast, please give us a rating and review on Itunes, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

3:49  Dr. Weiniger talks about some of the negative consequences of poor or weak posture, including neck and back pain.

8:32  The key to posture is taking a picture of yourself and drawing lines and measuring how you stack up. Then make some changes and next year take another picture and see if you have changed. 

9:22  The invention of the smart phone on top of the computer now has led to about 90% of people in the US having weak, folded posture being bent over with rounded shoulders and forwards head.  This is an epidemic in our society that is getting worse. 

10:22  I pointed out that the more time people spend on social media, the more lonely they get, which increases their risk of chronic diseases and early death. 

13:00  We talked about Dr. Weiniger’s PostureZone app that allows you to take a picture and measure where their head, torso and pelvis is in space over where they are standing. Those are the four posture zones and the Posturezone app lets you measure the degrees of deviation from vertical of the poor posture zone.  This app both lets people become aware of their posture and allows professionals to measure posture and generate reports showing changes over time before and after treatment. 

23:20 Dr. Weiniger explained how we go about constructing an exercise program to improve posture with his strong posture protocols. He also mentioned that chiropractic manipulation is very important in helping to improve posture, as is proper nutrition.

 



Dr. Steven Weiniger is a Doctor of Chiropractic with a specialty in posture analysis and correction. Dr. Weiniger is an author, speaker, and internationally recognized posture expert  https://www.bodyzone.com/posture-expert/  Dr. Weiniger has written Stand Taller Live Longer: An Anti-Aging Strategy available through Barnes and Noble  https://www.barnesandnoble.com/w/stand-taller-live-longer-steven-weiniger/1009154991?ean=9780979713606  and Posture Principles-–5 Principles of Posture. 

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as sports chiropractic work by calling his Santa Monica office 310-395-3111.


 

Podcast Transcripts

Dr. Weitz:            This is Dr. Ben Weitz, with the Rational Wellness Podcast, bringing you the cutting edge information on health and nutrition from the latest scientific research and by interviewing the top experts in the field. Please subscribe to Rational Wellness podcast on iTunes and YouTube, and sign up for my free ebook on my website by going to drweitz.com. Let’s get started on your road to better health.

                           Hey Rational Wellness podcasters, thank you so much for joining me again today. We’re going to talk about posture again and it’s such an important topic because it affects so many factors in our overall health. And as a chiropractor, I constantly see patients every day who come into the office and they say, “Doc, why does my back hurt? Why does my neck hurt? I didn’t lift anything, I didn’t do anything.” And so, in so many of these cases, posture is the unthought of, underlying cause and as somebody who’s into functional medicine, I always believe in trying to get to the root cause of problems. And the same thing for chiropractic, we can’t just correct your neck and back pain with a drug that’s gonna relieve the pain, we’ve gotta try to get to the underlying cause. And I personally have found that poor, bad, inefficient posture is a major factor, in not only the cause of their pain but also in your inability to heal properly from the pain. And the fact that, the pain is likely to come back.

                            By the way, all of you who enjoy the Rational Wellness podcast, please go to iTunes, or wherever you get your podcast and leave us a rating and a review. That will allow more people to find the Rational Wellness podcast. And so, our special guest for today is Dr. Steven Weiniger. Steve is a posture expert, he’s the author of Stand Taller, Live Longer, a tremendous book, the creator of the CPEP training program for professionals, helping people check their own posture with his PostureZone app that you can get on your phone, and he’s the chief posture evangelist of May. And May is posture month, and he’s the head of the posture month organization. Anyways, Steve, thanks so much for joining me today.

Dr. Weiniger:      Ben, thanks. Thanks for having me, I appreciate it. And the chief posture evangelist label came when we decided to do a public health initiative for a CPEP, Certified Posture Expert Professionals, and the label …

Dr. Weitz:           Hallelujah!

Dr. Weiniger:      Because basically, I’m going around and I’m talking to media. It was just a really cool thing that came out on CBS yesterday. We’ve been with them talking about posturing. I feel like I’m evangelizing. I’m cured. I’ve not been doing evangelical work, but it’s true because people … It’s something everyone knows about, but people don’t stop and really look at. And my job becomes making people talk about it and that’s why we’ve expanded posture month to not just CPEPS, but to anyone that’s worked with posture to be able to take a picture or to offer the public a picture of their posture to create awareness of what their posture looks like, because it affects your health in a tremendous way.

Dr. Weitz:           Cool. Can you tell us, what are some of the negative consequences of somebody having poor posture or inefficient posture?

Dr. Weiniger:     Well, there’s two sides to it. One is the health consequences and the other is the personal consequences. Beginning with the health that is one that’s most important even though it may not be the one that’s the most emphasized. It effects back pain and neck pain tremendously. A recent study found that 89 percent of primary care physicians, considered posture to be one of the primary causes of back and neck pain, which is not surprising because your body is not aligned, it puts more mechanical stress on your joints. Especially if you’re living on that all the time. But there’s other issues as well, because when your body is folded, it can affect how well you can breathe. It affects how different organs’ work and things like this don’t occur quickly, but especially if you want to get to the root core of the problems, if someone’s living with their body folded and they can’t take a deep breath … There’s been a lot of research that shows that breathing is really important for your health. If you don’t breathe, bad things happen.

Dr. Weitz:          And it’s important to breathe that way as I’ve learned, because I was always a mouth breather and recently, in the last six months, learned how to breathe through my nose with a help of a breathing professional. It makes a huge difference.

Dr. Weiniger:    And there are breathing professionals that work with posture as well, because it’s not just a reflex thing, when your head goes forward of your torso, it changes the muscle relationship in the front of your neck going to the mandible, the jaw bone. That effects the opening for the air coming down into the lungs. It’s easier to breathe with the chest than it is to breathe with the abdomen or the diaphragm. And once you’ve developed that habit, it becomes like any habit. It’s easier to move that way. Try this. Press your fingers like this. Look at which fingers are on top, the left one or the right one?

Dr. Weitz:         Which one’s on top?

Dr. Weiniger:    Yeah, when you’re looking at your thumb, which thumb is on top?

Dr. Weitz:         Oh, the right one.

Dr. Weiniger:    Okay, cross it the other way. Put the left one on top. If I asked you to cross your hands, things like this, a thousand times, how often would you do it this way?                                               Most people … If you worked with it your good. Most people I would do this, would find that …

Dr. Weitz:         Well, you see I play golf. So, actually this is my normal golf grip.

Dr. Weiniger:    In that case you’re not using it. But most people that do that, find that …

Dr. Weitz:         My wife is always reminding me that I’m not normal.

Dr. Weiniger:    No, you’re better than normal. You pay attention to your body. That’s the point. Once your body learns to move in a pattern, you keep on moving that way without thinking about it. And that stresses some muscles, stresses other ligaments and your body literally folds into that pattern. You think your moving one way, but a camera proves that you’re not moving that way and that’s why taking a picture so that you can see how you’re standing when you think you’re standing tall is one of the first ques to building posture awareness.

Dr. Weitz:         So, since you brought that up, how do people become aware that they have bad posture. Is it simply because they have neck pain and they go to a chiropractor and that chiropractor tells them they have bad posture?

Dr. Weiniger:    I really don’t like the phrase bad posture. Because no one’s posture … Unless someone’s body is perfect, their posture is not gonna be perfect. Your posture is bad if you’re having some symptoms from it and that’s for certain. But even if you might have symptoms …

Dr. Weitz:         How about if we call it inefficient posture? ‘Cause isn’t the key to posture, resisting gravity, and we can’t resist efficiently if we have a certain posture?

Dr. Weiniger:    Inefficient is a good way to look at it, especially from a sports point of view. The way that we talk about it would be what is weak posture. Because if your posture is inefficient your body is gonna be weak and it’s not about as being as strong as the strongest person in the world, or as tall as the tallest person in the world because that’s probably not most of our genetics. It’s about being as tall as your body should be, as strong as your body should be for what you’re doing. If you’re working your body inefficiently, your body is gonna get better movement inefficiently and that makes problems. So, the key to posture is just taking a picture of yourself and measuring. Not making a pathology of it, not making it bad, not making it a problem, but it make it just, when I’m trying to stand tall, this is what I look like. And looking at it, and then coming back next year and comparing it again and measuring your body as something your aware of. If you see your body folding from your one to two to three, if you look more and more like an old person, you’re gonna start feeling like an old person and having pains like an old person before you should be.

Dr. Weitz:         So Let’s say we call good posture optimal posture. Right?

Dr. Weiniger:    How about strong posture?

Dr. Weitz:         Okay, so, let’s say we call it strong posture. Can you say approximately what percentage of the population has weak posture?

Dr. Weiniger:    In our world …

Dr. Weitz:         Yes.

Dr. Weiniger:    There’s been this great invention that I don’t know that it was made by chiropractors, but if you wanted to invent something to have a device that you could put in front of people and then have them spend half their day hunched over with this over rounded forward typing on something, you’d have a hard time advising that business model, but it’s been great for chiropractors because we end up seeing and helping so many people walking around in pain. In our society, I’d say 90 percent are walking around with posture problems. One thing that I’ve noticed is when I travel, I’ll see families with kids, and sometimes the little girl looks like mom and the boy looks like dad, and usually when I used to see people like this, the kids had good upright erect posture and the parents were a bit more slumped forward in general. Now, the kids look worse than the parents. This is an epidemic going on in our society, and it’s getting worse.

Dr. Weitz:         So, this is negative health consequence of cellphones, on top of so many other health consequences. I was just listening to another podcast on my way in here and they were talking about how loneliness is a parameter that increases your risk of early death and chronic diseases.  The more people spend on social media, the more lonely they get. So you spend all this time interacting with other people, but not in a real way so, you end up decreasing your health as a result of that.

Dr. Weiniger:    And that’s a … I completely agree with that perspective. One of the things of that is, people spend a lot of time trying to curate the perfect image on social media so that they look really good. And when they then compare themselves to other people that look better, it becomes a competition of how well can I artificially make myself look good and if they compare themselves to other people. And it’s like a world full of barbies of people shaped in ways that no human being is shaped. Whereas if you and I are sitting together and we’re being comfortable and we’re opening up to each other, that’s a different kind of friendship than occurs online.

Dr. Weitz:        Yeah. That creates this unrealistic body image that people have when they see these people on Instagram and Facebook and Twitter and stuff, having these ridiculous looking bodies and they feel all worse about their own because they know nobody can look like that and those are not real images, unfortunately.

Dr. Weiniger:   And one thing that I’ve become more aware of personally is the old custom of breaking bread with people, we don’t talk about that, but when you sit down and you eat with somebody, it’s a more intimate thing where … People don’t show videos of themselves eating, they show videos of the meal because I can curate it, I can make it look right. I can put the glass to the left of it. I can arrange the silverware so it looks like the food they get are perfection. Whereas a video of somebody chomping away at something, that doesn’t look so good because that’s a more openness of how people truly are. And when you sit down and have a meal with someone, if you like them, that’s when you come away and you say, “We can have breakfast together. We can have dinner together.” The saying a long time ago was people breaking bread.

Dr. Weitz:        Yeah, interesting. So, how’s … Tell me about your app that lets people be able to take a picture and get a better since of how good or how strong or weak their posture is.

Dr. Weiniger:   Posturezone app is a free app that’s on iPhone, iPad, and Android. And it’s a way for everybody to take a picture of themselves and measure where their head, where their torso, and where their pelvis is in space over where they’re standing. Those are the four posture zones. And it’s not about trying to pathologies something with this is normal and this is not normal. I mean, if somebody is five foot five for male, and the normal population is 5’7 to six feet, does that mean that person that is 5 foot five is abnormal? Of course not. It means that’s the way that person is and there’s a population demographic. Normal means different things. You don’t want to confuse a normal population demographic with normal for that individual.

If someone’s 5’5, if they’re standing tall, they can have strong posture. If someone’s six feet and they’re slumped over down to five foot ten, they’ve got horrible posture. So it’s not about being tall, it’s about standing taller. So that’s the direction of that is aligning your head over your torso, over your pelvis, over where you’re standing. The more those four posture zones are vertically aligned, in a line, the taller the whole system is. The taller the person is. The more the person is flexing forward, the shorter they are, and what the Posturezone app does lets you measure the degrees of deviation from vertical of the poor posture zone.

Dr. Weitz:         Do you have it on your phone right now? Can you show us real quick how that works?

Dr. Weiniger:    Sure. I can show you on my phone. If this …

Dr. Weitz:         So this is an app. It starts out as a free app and then there’s advanced features that you can purchase on … You can put it on your phone, your iPad.

Dr. Weiniger:    You can put it on your phone, iPad. It’s 29 dollars for the pro version, which is for professionals. If you’re a professional watching this, you want the pro version ’cause it will let you take a comparison picture of somebody and compare it in a report over time. If you’re a regular user, the app will let you take pictures over time and compare them. You can just flip back and forth and look at your pictures and you can see the number, but you can’t create a report and you can’t keep things in tables to work with people. [inaudible 00:15:52] designed to give the consumer or the health enthusiast the ability to check their own posture and posture of friends, but if you’re doing it professionally, it cost 29 bucks, but it’s a one time thing. It’s not an all the time thing. The reporting is again, of the angles of deviation. It’s not saying this is normal, this is not normal. That’s like a fear based marketing thing that I don’t care for.

Dr. Weitz:         Hey … You ever done a study to validate this? Maybe with patients after whiplash?

Dr. Weiniger:    Working on it.

Dr. Weitz:         Okay.

Dr. Weiniger:    There’s a couple that are working on things that are working on exactly and there’s been other studies that have been done that point to the lack of validation of some other things that a lot of people talk about and that the most promising way of recepting posture is the head, torso, and pelvis over the gravity line, which is exactly what we do. Dolphins did a really nice study of that and that was the only thing that correlated with back pain. There are things like high shoulder or a high hip, really didn’t correlate though, it’s just … Over mechanical, as you put inefficiently, the more everything expands out, the more efficient mechanical advantage there’s gonna be but less energy is spilling, the less strain there is on muscles and joints.

Dr. Weitz:         Okay. Go ahead.

Dr. Weiniger:    So if you wanted to take a look at it, this is … My office is a mess, but if you … Don’t look at …

Dr. Weitz:         You gotta hold it … Right there, good. Okay.

Dr. Weiniger:    So basically … Oh, I’ve got a great idea. Don’t go away.

Dr. Weitz:         Okay, you gonna bring somebody in to help demonstrate it?

Dr. Weiniger:    I’m gonna bring Harry in.

Dr. Weitz:         Okay. Hi Harry.

Dr. Weiniger:    Harry is my posture [inaudible 00:17:38]. Okay we’re gonna see if we can do this. So basically, you want to take a picture and notice when I rotate this back and forth, the line turns green.

Dr. Weitz:         Okay.

Dr. Weiniger:    In the middle. When the lines green, it’s level. Since my screen is not level, this is gonna be a weird picture, but if I put Harry between those two lines, I can bracket him between those two lines and I’ve got a grid in the background that if I were smart, I’d have it setup where I could show you that grid, but that’s not today. That’s not gonna happen today.

Dr. Weitz:         That’s okay.

Dr. Weiniger:    Professionals will need the grid and if I took a picture of Harry, and this is not gonna be nearly level ’cause I’m not that coordinated, but if I can take a picture of Harry. Did we get it? I got it. Good, this is far from perfect, but I can then take … You don’t need to see this, but I need to set it up for side view or front view, I can take a side view. I can then move the brackets to bracket the head over the torso over the pelvis over where the feet are standing. And this is not well placed cause I can’t do this sideways very well, but I can then check that and it will measure the degrees of deviation the head over the feet, the torso over the feet, and the pelvis over the feet.

So just measuring how the body is balancing and what the body is going to be vertical. And this is what the free version does. If I wanted to add other lines, and let’s say that I’m a pitcher or a golfer, you can add another line. I can call that a golf line. And then I’d be able to make a line between my shoulder and my front foot for example if I wanted to add that measurement to see how my body aligns. When I think my shoulder’s right over my foot, if it’s really two degrees off, and I start working on it and then it’s one degree off, it’s going in that direction. It’s a way of bench marking the accuracy of your perception and of the way your body is to the truth of where your body is.

Dr. Weitz:                            Cool.

Dr. Weiniger:                     And you can then if you want to save it and I’ll just put it into a case, and hopefully this is nobody that I don’t want to show you.  Within that case, I can look at an image and compare Harry today to Harry yesterday. Or in the pro version, I can generate a report to compare that to prior images. No. Sorry, I can add that to prior images and move backwards. There we go. Where I can do a checkoff. You can see that and get a report and then I can generate that report … And the report disappeared. I can’t do this backwards very well. There it is. I can generate that report and that report that has those images as well as the deviations of where the body is in space. And the cool part for consumers, if you’re looking for a professional near you, on the bottom there’s a locator for CPEP so they can find somebody that’s in their area and now you know where I live, but where there’s a CPEP near them. And that is someone that if they want to work with a posture professional that can take a picture of their posture and help them to do exercises to strengthen their posture.

                    And that’s the idea behind posture month. People have to become aware of their posture ACE, A is awareness. Next part is C, control. Do exercise to strengthen your posture and professionals work with people from a clinical point of view, especially, really strong posture exercises to strengthen how people move. Other things like yoga, Pilates, are also what I call controlled motion exercises and they can help posture, but the external posture exercise have the advantage of being able to be very, very targeted to help someone’s weaknesses and strengthen their weaknesses especially when there’s been a problem that needs any kind of rehab.

Dr. Weitz:                            You know, another thought about using this and I just started to incorporate this app, is insurers, third party payers, want to see objective measurements of the improvement that we achieve with our treatments and we know our patients feel better, but simply having a patient who says, “I’m in pain.” And then saying, “Now I feel better.” That’s not very objective, of course, we use these zero to ten pain scales that the patients fill out and that’s a little bit of objectivity, but it’d be nice to have something like this that we can include in a report to either an insurer or on a personal injury case to show some objective improvement. So, I think this is pretty cool for that idea.

Dr. Weiniger:                     I’ve personally had adjusters that we’ve worked with and they said, “You know what, when you showed me the picture of what the person looked like the first time they came in and what they looked like a few weeks later after that, it makes it very real. People unlike online texts, that’s not real. A picture of you in eye when you see somebody talking that’s much more real.

Dr. Weitz:                          Yeah.

Dr. Weiniger:                     And then you have someone standing against an objective, that’s more real.

Dr. Weitz:                          Okay, so once somebody identifies that they have poor posture or once a practitioner whose maybe has gone through your program identifies somebody with postural issues, how do you go about correcting those?

Dr. Weiniger:                     The first thing you do is you take a picture so you benchmark where you’re starting from because it’s not necessarily correcting, it’s strengthening. My best review of this is almost certainly gonna be different because we have different genetics and we treat our bodies differently along the way. And your body is not gonna be balancing the exact same as somebody else’s, but having an awareness of how you’re balancing at the beginning. To strengthen balance you want to strengthen each of what are called the three elements of balance. How your body is aligning, how your body is balancing, and how your body is moving. And basically those words balance, alignment, motion or BAM, are what we talk about in my book Stand Tall and Live Longer and the posture exercises are what CPEPs and other professionals teach their patients and teach people and it’s often trainers and massage therapists that teach people how to do postural exercises.

For posture month, there’s a number of balance exercises we’re putting out every day and for each week, we’re going to be focusing people on one exercise. So week one, we’re focusing people on an alignment exercise, it’s really easy. Go to the wall, walk til your back’s against the wall. Remember when you were in school they told you that you should be able to line up your shoulders, your feet with shoulders, your feet, your butt, your shoulders and your head against the wall and be straight. Did they have that when you were in school?

Dr. Weitz:                         Well I remember doing that after the air raid drills.

Dr. Weiniger:                   Okay, same thing.

Dr. Weitz:                         Like that will really protect you if a nuclear bomb strikes near your school.

Dr. Weiniger:                   In my school, they had us hiding under the desk.

Dr. Weitz:                        Oh, okay. Like that’s gonna help you.

Dr. Weiniger:                   What does help you is connecting your perception of your body with how it really is. Going to the wall, stepping one foot away from the wall with your feet parallel, leaning your butt against the wall and your shoulders against the wall, and then really lock in. Look straight ahead. Keep your head level. And try to keep your head level, that’s the must. And move it back towards the wall. If your head can’t touch the wall, and keep it level then that’s saying that you’ve got some distortion where your head, torso, and pelvis aren’t lining up ’cause if you take your feet away, you should be able to align head, torso and pelvis unless there’s something holding something forward. The strong posture exercise all use what’s called the must versus try killing. The must in this exercise, keep your head level. If someone says, “Yeah, I can touch the wall.” But the head’s not level, they’re not doing the must. And if you can’t touch the wall, the exercise is quite simple, go as far back as you can, but keep it level. Keep your head level as you pull it back.

It’s similar to the turtleneck that some people teach from an exercise point of view, but it’s more effective because if you take your feet away from the wall, you’re reducing some of the impact of the solace on the upper lumbar and lower thoracic spine and it makes easier to isolate the real cause for that particular posture distortion.  And so practicing keeping your head level, pushing it back and doing that with your breaths. So, doing it for what we call five slow breaths. Breathing in, letting your head come forward, breathing out, pushing it back to the wall. And you’ll notice by the third or fourth, you can get a little bit more play if you’re doing it right when you’re stretching the tight link of the chain. Doing that twice a day for a couple of days, you may find that you start to find it easier to keep your head level, which is what we’re trying to do, to open the body up, which opens up the second week of posture month, which is the first balance exercise.

And the first balance exercise is holding your best strong posture and balancing by lifting one leg up so your thigh’s parallel to the ground and holding it for five slow breaths, and then repeating it on the other side. And doing that just three times a day, just dialing in to standing tall and you can’t see me now, but I’m lifting leg up because if I lift my leg up, and my body is going like this and I’m twisting, I’m not strengthening the muscles of my posture. You want to first do alignment so you have an awareness of what standing tall feels like and then hold that feeling, lock that awareness in, and then challenge it by lifting one leg up. And as you know from a rehab exercise point of view, the way you strengthen something is by challenging it. That’s the second week. Do that a couple times a day, second week.

The third week of posture month, we’re coming out with the first motion exercise, sitting on a ball and just like you would sit at work, sitting really tall and trying to only move your pelvis. So instead having to focus the head, torso posture zone, we’re moving the focus back to the torso, pelvis posture zone. The key is moving the ball making three circles to the right, three circles to the left, but there’s two musts here. One must is don’t move your knees. The second must is don’t move your torso. So you’re sitting tall, you’re not moving your knees or torso, the only thing left to move is your pelvis. It sounds really easy, but it’s way harder than it looks, especially when you try to make a circle to the right, many people that have any kind of an issue will quickly notice that their circle isn’t round, but there’s a lack spot in their motion where they’re not able to control something actively in that arc. And what they’ll also find that if they make three circles to the right and three circles to the left, the inaccuracies of motion, the kinks, the things that are locked, that they didn’t know that were not moving, are not the same on both sides.  And it’s been not able to be recruited and used when you’re really focusing on it when you’re not focusing on it, when you’re doing a bunch of other things at the same time, you’re not gonna be using it and that’s why there’s this prior protocols that become so powerful that isolate and strengthen the weak link in each individual’s movement connect chain.

Dr. Weitz:                          What do you say to patients who say, “You know, why do I need to do these dorky exercises? I’m already going to the gym and I’m doing squats and deadlifts. I’m doing one of these other exercise programs where I’m lifting all these free weights. Why do I need to sit on a ball?”

Dr. Weiniger:                     Because exercise is good, but exercising effectively is far more important. If someone … I remember going to the gym and seeing guys that were bench pressing 250 pounds and they were doing it by lifting their head up, rolling their shoulders in, and bouncing it off their chest. And just saying, “I’m benching 250.” And especially, those guys, if you try to go over to them and say, “Try doing this with tight form.” Their response is, “I can’t lift as much, and the only thing that’s important is how much I can lift.”

Dr. Weitz:                          Of course.

Dr. Weiniger:                     And that’s not good. If actually, you’re a chiropractor and you want to take care of patients, it’s great for business, but it’s lousy for people’s bodies. All motion begins with your posture. All motion ends with your posture, and that’s why the awareness part becomes so important. If in your awareness, you think standing tall is standing like this, when you exercise all of your exercises is gonna be like that. If you’re a golfer, if you golf, golf begins with the address position where you’re getting set up, standing tall and then you’re … That’s what every pro that I’ve ever spoken to tells you to do. It’s when you think you’re standing tall in an address position, you really adapted in some subtle way like those silly ball things that we just talked about that you said, then you’re going to be taking those in asymmetries into whatever that larger motion is.  The only way you can strengthen the subtltees is to focus on only them. When you’re doing big macro motions, you can’t be aware of the small subtltees. Your body thinks in whole motions, not individual muscles. Start focusing on the subtltees and such incredible power, both from a pain point of view as well as from a performance point of view, as well as how other people see it.  Because the other part we need to talk about is when your training well, people look at you better.

Dr. Weitz:                         Are people actually making themselves worse by exercising in poor posture, and reinforcing that posture?

Dr. Weiniger:                    I’ll go back to what you said at the beginning. When a patient comes into you and they say, “Doc, why am I hurting? I’ve been going to the gym, I’m doing all this stuff, but this happened. What happened?” Because what you think you’re doing may not be what you’re really doing and everything that you do always begins with the posture. That’s why if you want to exercise effectively, you want to begin with effective posture.  And there’s been number of studies that have demonstrated that training bodies to move towards greater symmetry with greater accuracy makes a big difference in back pain. In fact, if you recall, last years guidelines both care of both acute and chronic lower back pain from the American College of Physicians said that surgery a lot of times is not good, opioids, not good, and they said things like Advil are not as highly recommended as they used to be and there should be alternatives like spinal manipulation, which chiropractors have been saying thank you very much, but also motor control exercises. That’s exercise really looking at the starting piece of motion. That’s precisely what the strength type exercise I designed to do.

Dr. Weitz:                          Okay, so do you tell somebody … Let’s say somebody comes in, and their posture is pretty bad. Do you tell them to stop all their other exercise until they can correct their posture or do you tell them maybe while they do their exercises, try as much as you can to get into a better posture?

Dr. Weiniger:                     And the better posture is what they’re learning to feel when they’re doing the strength posture exercises. Especially, if they’re working with a CPEP. But because if they’re coming in clinically, you want to be not creating more pain, not creating more tissue damage. So, you may possibly pull back from some of the exercise, and you may increase other exercises depending upon the person’s clinical story, the person’s exercise and their functional ability. That’s why we have the must versus try protocol becomes so powerful because we let you tailor it to their functional ability. The exercise is a test of what they can do functionally, which is then teaching them how to do in a way to strengthen the weak in their mechanic chain. So, in general, if you’re exercising, you want to work out quickly how to get the most benefit out of your exercising. That’s what a professional can help you do.

Dr. Weitz:                          Now, you talk about strengthening and balance, but what about stretching? So Let’s say you have this sort of rounded shoulder, forward head posture that you see in a lot of people and certainly strengthening the romboids and the middle and lower trapezius and some of the intrinsic neck muscles are important, but don’t you need to stretch out some of these shortened muscles in the front as well?

Dr. Weiniger:                     Absolutely, and that comes back to the point at the beginning. It’s not one thing, it’s everything. It’s like which tire on the car is most important? The left front, or the back rear? You’re going 60 miles an hour on the highway, you don’t want any of them to blow out. And if one blows out, the whole system doesn’t work the way its supposed to. In terms of correction, very very commonly someone’s gonna have a short pectoralis, more likely a short pectoralis minor, coracobrachialis, which the muscle underneath that is another really, really common shortness that’s missed because if you think about it, if there’re different layers of muscles, which there are, if the superficial muscles are tight, then other parts are gonna move differently. If the short muscles are tight, the muscles closer to the center of action of rotation of each joint, then nothing around that is gonna be able to move and you can stretch the superficial mussels out all day long, but you’ve gotta also get the deep ones. That’s why the pattern can be really different for different people.

And it’s what you just did, it’s not just open up what’s on front, it’s simultaneously strengthening what’s in back, but it’s not just the front and the back because when we did this, we also unfold the torso pelvis a little bit. We lean towards the back. So, if there’s an imbalance between torso and pelvis, that’s gonna keep on pushing it forward and you can try to open this up, but you’re gonna have to do something else to compensate. Posture is a whole body phenomenon. It’s not just your head, it’s not just your back, it’s literally how you balance your body. And that’s why the balance exercises are so key to strengthening posture.

Dr. Weitz:                            And what’s the role of chiropractic in this?

Dr. Weiniger:                     Tremendous. Chiropractic’s main goal of focus began with spinal manipulation, which is working on the segments of the spine, the vertebrae of the spine to restore motion and to allow more normal neurologic function because the spine houses the spinal column and that connects the brain to the muscles and then the nerves. And if those are not moving well, if there’s not accurate information coming to the brain, it means the way that you think you’re moving is even less likely how you’re moving. From a biomechanics perspective, if there’s a locked link in the chain, so my hands should be moving like this, and my fingers are not moving, it’s gonna move like that. That’s gonna put more stress on one joint, more exercise on one joint, and less on others. The same thing happens in the spine where one spinal segment is working more, breaking down more, getting more exercise at one level, and less at others and that imbalance then drives how everything else is moved. So the combination of chiropractic spinal manipulation with strong posture exercise is like this.

Dr. Weitz:                            Right. For those in the audience who aren’t really familiar with what chiropractic does is, one of the core factors treatments of chiropractic that really no other professional really does effectively is the manipulation or adjustment and it sounds like your understanding is similar to mine, is we’re trying to find those particular joints in the body, whether they be spinal, or extra spinal, in the shoulders or elbows or knees or wherever, and making sure all those joints are moving freely in all those different directions that they’re supposed to move in. For example, your spinal joints are supposed to bend forwards and backwards and side to side and rotate and we’ve gotta make sure they’re doing all those motions so that you actually can attain the type of posture and maintain that type of posture.

Dr. Weiniger:                     Exactly, and I talked about the spine, because you said where chiropractic began, but from a perspective of postural rehab perspective, we also want to be … A good chiropractor to me addresses all of the links in the kinetic chain because if you’ve got a problem with your big toe. I drop a cinder block on your big toe, your posture when you walk is gonna go to heck ’cause it’s gonna hurt and you’re gonna adapt to it. So a good chiropractor should be able to address all the links in what we call the kinetic chain. It’s the body how to move symmetry, how to move with greater symmetry. In other words, a chiropractor unlocks motion, stimulates neurology to function more accurately, but if you don’t retrain the body to move more accurately, it’s gonna keep ongoing back to the old patterns. The chiropractor unlocks and restores motion, strong posture exerciser retrains that motion. They both fit together.

Dr. Weitz:                          One more question. Is there a role for nutrition in promoting posture?

Dr. Weiniger:                     Oh, absolutely. If your body doesn’t have the materials that you need from a biochemical basis to function, it’s gonna function adaptively. Everything from enough water, which is something that is one of the underrated issues with a lot of people with lower back pain, to enough calcium, to other things like functional medicine that you can use to stimulate or to decrease how different things are functioning to address it. Our bodies are not just biomechanical, it’s not just nutritional, it’s both working together.  As well as, biopsychosocial or attitudinal or mind or emotional, however you want to phrase it. Your head space, your attitude, will affect your posture and effect your health, and effect your biochemistry. They’re all together as mind, body, and spirit, which is kind of how chiropractic began once upon a time and it’s cool seeing more things go in that direction now.

Dr. Weitz:                          There you go. That’s kind of a evangelical saying from the posture evangelist. With a prayer here.

Dr. Weiniger:                     It’s funny because as you’ve noticed, I’ve got … I wear a number of different hats, and I’ve been at different boards and I didn’t want it to sound stuffy. I wanted to make it more of a fun thing to engage people and that was literally put out there as a kidding around and some people started banting it around and it became kind of what it is, but it’s true. Posture can make a big difference in your life. The posture month. Be aware of your posture, take control, engineer for a strong posture environment and next year recheck and see how you’re doing. And all the time, do basic posture exercises. You have a problem, see someone that can help. And the Posturezone app lets you check it and will help you find somebody.

Dr. Weitz:                          Cool. And so for listeners who want to get a hold of you, what’s the best way for them to contact you or get ahold of your book and learn about your programs?

Dr. Weiniger:                     From a public point of view, Stand Taller Live Longer, is the website for the book because that’s the name of the book. From the public point of view, Bodyzone.com, is where public information is. In the professional point of view, Posture Practice is where we teach people how to be CPEPs to strengthen people’s posture and from everyone’s point of view, download the Posturezone app. And all of those sites have ways to contact us that they can get a hold of me.

Dr. Weitz:                          Sounds great. Thanks, Steve. Keep spreading the word.

Dr. Weiniger:                     I appreciate it. I very much enjoyed it. Thank you.

Dr. Weitz:                          Okay, I did too. Talk to you soon.

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Heavy Metal Detox with Dr. Christopher Shade: Rational Wellness Podcast 054
Loading
/

Dr. Christopher Shade discusses how to test for and remove heavy metals from the body with Dr. Ben Weitz.

[If you enjoy this podcast, please give us a rating and review on Itunes, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

2:25  Dr. Shade talked about how he got interested in studying mercury and developed a way to separate different forms of mercury as part of getting his PhD. 

3:35  Dr. Shade explained that he tried heavy metal chelaters like DMSA and DMPS and these made him much sicker, which led him to design better supplements for detoxification.   

5:45  I asked Dr. Shade to explain why his tests for heavy metals are more accurate than other tests on the market?  I then asked how serum testing can be that accurate, since it only reflects recent exposure and not metals that have been stored in the tissues for months and years?  This is why we do oral chelation challenge and collect urine for six hours to detect metals that have been stored in the tissues and are now being released through the urine.  Dr. Shade challenged that view and explained that chelaters like DMSA do not go into the cells and cause metals to dump into the urine.  What they actually do is pull metals from the lymph and the red blood cells and bind it out into a form that’s easily filtered out through the kidneys.  And serum reflects the body burden. And urine also is somewhat reflective of body burden and urine has a baseline level of metals, in contradiction to the assumption that there is no baseline of metals until the chelation challenge. Also, after the serum levels rise due to a recent exposure, such as eating some fish, it takes 45 to 60 days for the serum levels to go back to the previous level in a healthy person and up to 300 days in an unhealthy person.   

10:51  Dr. Shade described how organic methylmercury from fish is represented very well in the blood, while inorganic mercury from dental amalgams doesn’t represent itself very well in the serum.  But inorganic mercury is seen much better in the urine, provided that the kidneys are functioning properly and the kidneys can become damaged by mercury.  Quicksilver Scientific offers the Mercury Tri-Test, which separates out the inorganic from the organic mercury and measures mercury in blood, hair, and urine.  Hair is only reflective of organic (from fish) mercury and you can have a mouth full of almagams and it will not show up in the hair.  Quicksilver also offers the blood metals panel.  Here is a link to Quicksilver’s website with more information on their testing, including why urine challenge testing with oral chelators is problematic: https://www.quicksilverscientific.com/testing/clinical-metals-testing 

20:19  I asked if Dr. Shade ever measures antibodies to metals and he said that he is interested in looking at that and thinks that it may show patients who become symptomatic with metal exposure. 

22:18  Dr. Shade said that undiagnosed Lyme Disease may become symptomatic when treating the metals because raising the glutathione levels reboots the immune system. If you then send them out for more Lyme Testing they may then test positive when they were negative before. So you need to focus on controlling the infection with antimicrobials before you can effectively complete your metal detox program. 

22:58  Dr. Shade explains his approach to removing toxic metals from the body.  You can use the same approach for mercury, cadmium and arsenic, while the approach for lead is a little different.  Mercury is detoxified well by glutathione, but you also need glutathione S-transferase and transmembrane transporters and also magnesium.  So if we want to build a system of detoxification, we need to build glutathione levels. We need to turn up the activity of the transferase, and we need to turn up and support the activity of the the transport proteins.  And when it gets down to the GI tract, we need to grab it before it gets reabsorbed.

25:40  Liposomal glutathione is better absorbed and someone with mold toxicity or Lyme disease are sick and will have a tough time making glutathione from NAC. Taking liposomal glutathione is better than taking NAC in a diseased person.  Dr. Shade mentioned a study showing that 600 mg liposomal glutathione produced a 30% increase in glutathione levels in six hours while 600 mg IV glutathione only produced a 15% increase in six hours. 

30:15  Dr. Shade explains what a liposomal formula is and how it works.  You are creating a fat soluble bubble with phosphatidylcholine and tucking the glutathione in it, so it gets absorbed like a fat would and it passively absorbs into the upper GI tract.  Dr. Shade also explained that by making his liposomal products small enough, some of them will pass through the oral mucosa and directly into the capillaries, so you should hold the liposomal products directly in your mouth for 30 seconds before swallowing. He explained that all of his products are between 20 and 80 nanometers since below 100 they get much better absorbed but you also don’t want them to be too small or you have problems with nano particles toxicity. 

33:15  Once you get glutathione into the cells, then you need to up-regulate the transferase and get those membrane transporters working by invoking NRF2 by using Lipoic acid and polyphenols. You can also use sulfurophanes from crucifers and garlic oil.  The best polyphenols to use are green tea extract, pine bark extract, red wine extract, grape seed extract and haritaki. 

34:55  Dr. Shade explains that to get the transporter proteins working well, you need to stimulate the liver-gall bladder system and promote the flow of bile. The transport of toxins into the bile tree is synonymous with and linked intimately with bile transport. The two transporters that move bile from the hepatocyte into the bile tree are the bile salt export pump and MRP2, the multidrug resistance pump number 2. The MRP2 is the is also the toxin transport and thus it moves both toxins and bile salts.  These transporter proteins get up-regulated and down-regulated together, so cholestasis is toxostasis.  Thus, if you move bile, you move toxins.  If you don’t move the toxins from the liver into the bile, they get dumped into the brain and you get inflammation in the brain, the kidneys, you get lower back pain, skin rashes.  He likes to use herbal bitters to get bile and toxins flowing and also phosphatidylcholine to help solubilize the bile to keep it flowing. Then, when the toxins are moving through the GI tract, you want to use binders like thiol-functionalized silica, charcoal, clay, zeolites, and chitosan, so these toxins don’t get reabsorbed.

39:28  Dr. Shade explains why modified citrus pectin is not a good binder for toxins like heavy metals, though it helps to remove toxins by reducing inflammation.

           

                             



Dr. Christopher Shade is a PhD researcher and a recognized expert on mercury and liposomal delivery systems. He has lectured and trained doctors in the U.S. and internationally on the subject of mercury, heavy metals, and the human detoxification system. He founded Quicksilver Scientific and Quicksilver is an industry leader in blood metals testing and the development and production of superior liposomal delivery systems. Quicksilver Scientific is the only company to offer advanced mercury speciation testing (the Mercury Tri-Test), which comprehensively assesses for the body burden of mercury. Here is more information about the metals testing: https://www.quicksilverscientific.com/testing/clinical-metals-testing  Quicksilver Scientific is dedicated to producing superior nutraceutical products tailored at supporting the human detoxification system for the optimization of health. https://www.quicksilverscientific.com/home

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as chiropractic work by calling his Santa Monica office 310-395-3111.


 

Podcast Transcripts

 

Dr. Weitz:          This is Dr. Ben Weitz with the Rational Wellness Podcast, bringing you the cutting edge information on health and nutrition. From the latest scientific research, and by interviewing the top experts in the field.  Please subscribe to the Rational Wellness Podcast on iTunes and YouTube, and sign up for my free ebook on my website by going to drweitz.com.        Let’s get started on your road to better health.  Hey Rational Wellness Podcasters. Thank you so much for joining us again today. For those of you who enjoy this podcast, please give us a ratings and review on iTunes.

                          Our topic for today is heavy metal toxins. This is a very important topic. We recently had Dr. Joe Pizzorno on talking about toxins, and now we’re going to focus in on heavy metals, mercury, lead, all the other heavy metals. And these are incredible important, can have all kinds of effects for our health, can play a role in various chronic diseases. And I’m very excited that I’ll be speaking with Dr. Christopher Shade, who is a PHD researcher and the founder and CEO of Quicksilver Scientific, a heavy metal testing and nutritional supplement company. Quicksilver Scientific is known especially for its detoxification products and its unique supplement delivery systems, and it’s patented mercury speciation test. Christopher, thank you for joining me today.

Dr. Shade:         Thanks, Ben, it’s a pleasure to be here.

Dr. Weitz:          Good, good, good. So can you tell me a little bit about your background and how you became interested in mercury and heavy metal testing?

Dr. Shade:         Oh, sure thing. I’ve a very circuitous background to get here. Grew up a scientist in an academic family. Got a little disillusion with reductionist science, went out into the woods, I was an organic farmer for a long time, sort of a Thoreau summer starting farms and stuff. And then one thing or another led me back into getting a graduate degree around pollution in the environment. I was looking at agricultural pollution and I got a masters in that.

Dr. Shade:         Then when I went to do my PHD, I didn’t really find the research that was going on there that interesting, but I found this guy who was specializing in global cycling of mercury as a toxin in the environment. And I ended up working with him. And they needed new analytical developed, new systems for separating different forms of mercury, which is really crucial to understanding their movement through the environment and movement through the body. And so I developed that, patented that, and graduated and started a company around that testing, originally doing environmental testing and then switching over into health and wellness. Because I wanted to get back to this human focused look at toxins in the environment and health in the environment, and cycle it back into looking at personal health.

                         And I brought this testing in, showed it to people like Hal Huggins and Dietrich Klinghardt, original pioneers in mercury toxicity. And they really liked that, but you know you bring up a problem, you gotta bring up a solution. And at the time, everybody was working with chemical chelators for getting rid of mercury and other heavy metals. And I thought I would do testing in conjunction with people using chelators, and so I tried all those chelators on myself and I got myself really into a hole. I really blew out my adrenals, I blew out my neurological balance, my immune system.  And while I was in the middle of just being in this dark night of my biochemical soul, I was watching these functional medicine meeting lectures here in Boulder County.  I was watching Bob Roundtree and Nigel Plummer from Pharmax, and they were talking about GI health and the GI system calling the shots in so much stuff. And I realized that a lot of amalgam toxicity was having so many metals in the GI tract.  And I was trying to push things through the kidney, but I should clear out liver GI functioning first.

                          And that led me to make my first detox supplement, which was kind of a chelator for the GI tract. It was like taking a clay or an activated charcoal and making it specific for metals. And as I did that and cleared everything out of my GI tract, I just opened up all my problems, I just cleared everything away. And introduced that product, which is now known as IMD, or Intestinal Metals Detox.  I introduced that to Huggins and Klinghardt and it filled a big void in everybody’s tool chest and it led me to research why it worked, and that led me to understand all the processes of the glutathione system and how the body’s naturally supposed to get rid of these metals. And that metal toxicity is not a deficiency of chelators, it is a deficiency of your own chemo defense system. And then when we optimize that, we can get rid of all these metals and at the same time make us resilient or resistant to other toxic insults. And so my whole life work became developing systems for optimizing all of that in people.

Dr. Weitz:            Cool. So can you explain about your heavy metal testing and why it ends up being more accurate than so many other testing?  And I keep coming back to whenever I look at serum testing I always think, you know, that’s only going to give us current levels of metals and so that’s why we’ve tended to do the oral challenge and then collect urine for six hours afterwards, with the idea that we’re going to liberate some of these metals, mercury, that’s been stored in the body, sometimes for months, years, maybe decades at a time. So how can you get a sense from testing of stored metals as well as what’s circulating and has come into the body recently?

Dr. Shade:           Right. But this is all … What did you just say to me? You said, “Well I think that this is only what’s circulating.”  Why do you think that? Did you do the primary research? Did you figure out why you think that?  Or are you just parroting what the guys who did chelation testing told you? Answer the question.

Dr. Weitz:            I have always been told that certain testing is only-

Dr. Shade:           Exactly.  Always been told is the problem there.

Dr. Weitz:            Including by the way some of the companies that do certain testing will tell you that as well.

Dr. Shade:           This is just what became the dogma of what’s going on. And the reality is that 20, 30 years ago we didn’t have really good testing to look at baseline levels. Like in urine, if you extended your discussion you’d say, but in urine there’s no metals in urine so I challenge it. That’s not true at all. There’s always a baseline of metals that are going on in the urine. And they are a filtrate of what’s happening in the whole blood, which is the plasma and the red blood cell. And the plasma and the red blood cell are in a steady state with what’s in the tissues.

                           Now for that whole argument that you brought up to be correct, that would mean that the chelators would go into all the cells and take a representative amount out into the serum and then make it go into the urine. But if you look at DMPS and DMSA, all the data around that says that they don’t do that. All the data around it says that they never cross the blood brain barrier, they don’t go into the cells. What they do is take what’s in the lymph and the red blood cells and bind it out into a form that’s easily filtered out through the kidneys.

                           And in a very famous paper that was done in Sweden in the mid-’90s, they were trying to look at DMPS and if it really reflects long term body burden, or if it’s just amplifying what you can already find in the body.  And they took acutely exposed workers who work with mercury directly, they took dentists with a long term burden, and then they took people with amalgams and people without amalgams.  And they looked at inorganic mercury in the plasma, and inorganic mercury in the urine before and after taking DMPS, 300 milligrams IV.  And what they found was that the mercury in the urine is linearly correlated with mercury in the plasma, and mercury in the urine after the challenge was linearly correlated with mercury in the urine before the challenge, and with mercury in the plasma before the challenge.

                          You’ve got these compartments and there’s a back and forth between them all. It’s not that the mercury comes in and goes into the tissues and sticks there and then leaves the blood. What happens, like if we went out for dinner tonight and we eat swordfish, a high mercury meal, we’re going to absorb that mercury in there and it’s going to peak between 12 and 18 hours after we eat. And it’s going to be much higher than our baseline is. So from our baseline let’s call it, let’s just give it a number. Say I’m at 5. I’m going to eat this meal, my peak is going to go up through maybe even 10 or 15, and then over 2 to 3 days it’s going back to this next baseline. And let’s call that 6.  And from the time to get from 6 back to 5, the original baseline, how long is that? It’s 60 days, 45 to 60 days in a healthy individual. As many as 300 days in an unhealthy individual. It’s not 2 to 3 days. The 2 to 3 days story was about a bolus that goes in, it goes up and peaks and comes back to a new baseline, and then it comes back.  But where people were kind of throwing their hands up with what’s urine mean, what’s blood mean? What’s going on here?  Methylmercury represents itself very well in the blood and will give you high levels.  Inorganic mercury from dental amalgam doesn’t represent itself very well.  It works on a lower scale.

                       Now why is that? It’s because of the distribution between the blood and the tissues. There’s always more in the tissues, which the prevailing wisdom is right about. There’s more in the tissues than the blood. But there’s a ratio between the two. And maybe it’s 10 fold more in the tissues for methylmercury and 30 to 50 fold more for inorganic mercury. And so dental amalgams and blood levels didn’t seem to correlate very well. But fish and blood levels did correlate well. But dental amalgams correlated pretty well with urine, and fish didn’t so well. That’s because methylmercury you find a lot in the blood, inorganic mercury, small amount in the blood. In the urine it’s all inorganic mercury. And so it’s reflective of the inorganic mercury levels in the serum, if the kidneys are transporting correctly.  And this comes down when we talk about detox we’re going to talk about pathways in the liver, you have the same pathways in the kidney. And when they get damaged, and they’re easily damaged, then that urinary representation of the blood blows out and you have low urine, high blood. Alright, but if it is working, then urinary mercury’s an inorganic mercury exposure.  Hair, you have Naturopaths going through all these soups to explain what hair meant compared to blood or intake. Hair is only fish. You can have a mouth made out of dental amalgam, if you eat no fish you have no mercury in your hair.

                     So there was all this improper, imprecise understanding of the pools of mercury, the compartments, and the interactions between them all. And so we just said, we’ll take the chelator, boom, a bunch comes out through the urine and we can compare people that way. And you can, but it’s not a very sophisticated way to go. And humans always do this, in order to justify that, they create this whole story that the mercury’s never in the blood except for like the last two days, and it’s all in the cells and the challenge pulls it all out of the cells and gives you this long term mercury number. But I pulled five or six different papers out of the literature where they examine that, and none of it worked.

                    Get this, one paper on DMSA, they took a grouping of people who had worked in the Chlor-Alkali factory, you sit there with a pool of mercury and stir it, and it’s an electrolysis cell, to split sodium chloride into sodium and chlorine. It’s the highest exposure you can ever get. So they all worked there and then they stopped working there for either one year or three years, but that’s the highest level of burden you can take into your body there is.  And then they took the general population and they measured urine before and after DSMA chelation.  Before DMSA chelation the guys who worked with the pools of mercury before were higher than the mainstream. But after chelation, the differences leveled out totally. There was no statistical difference between the two and there’s a reason for that. Because DMSA is really no good on inorganic mercury, which is what you get for that vapor form. But it’s pretty good on methylmercury. So this is a measure of how much fish these two groups ate. And it’s the same, because they were just a cross section of the population for methylmercury exposure, but one of them had significant inorganic mercury exposure.  So there’s all these papers showing the failure of the challenges to show long term burden. The exception being EDTA challenge and bone lead versus blood.  EDTA challenge is better correlated with bone lead than blood is, but blood’s still not bad.  You just have to take these scales, you’re looking for these huge, big scales, you’ve focused them down, and key for us for mercury, you separate methyl and inorganic mercury.  Give them their own reference ranges in the blood. Then once you have that inorganic mercury separated away from the fish-based methylmercury, that’s supposed to correlate perfectly with urine. And when it doesn’t, then you see it building up in the blood and you know where the damage is. It’s to transporters in the proximal tubules. It’s not even related to glomerular filtration. And you know when you treat them you have to focus on that. So there’s the whole story.

Dr. Weitz:      Yeah, so to sort of highlight a couple of points that you’re making is number one, the oral chelators like DMSA, they’re not effective at removing mercury and heavy metals from the tissues like we think they are.

Dr. Shade:     No, they remove from the blood plasma, maybe a little bit of soft tissue, lymph, and then the metals redistribute from the cells into the blood. And that’s when it’s important to have things that up regulate the chemistry that dumps out of the cells into the blood. Like lipoic acid. If you go to the Cutler theory, Cutler thought that DMSA was clearing the body and lipoic acid was clearing the brain. And he would start with DMSA and then he would move to DMSA and lipoic acid. DMSA clears from the blood and then lipoic acid gets the cells that dump into the blood. And then the DMSA can take it.

Dr. Weitz:      Interesting. So the first point is the oral chelators are not effective at removing the metals from the tissues. And two, the serum testing is actually effective for measuring mercury that’s in the body for up to 300 days.

Dr. Shade:     Yeah. And as long as you have the right testing. If you go to Labcorp, they’re not measuring low levels, and they’re not separating the two forms of mercury. So once you separate the two forms and you can measure really, really low, then everything’s good.  For instance, if say we’re measuring you and you have a lot of dental amalgams, but you never eat fish. Your total mercury in the blood might be say 0.5 parts per billion. Now the limit of detection for Quest is 1 part per billion. And some labs it’s 0.5. And so you’ll like less than the detection limit, less than 1. And they’ll say you have no mercury. But all of it is inorganic mercury. If you look at our reference ranges once you separate methyl and inorganic mercury, 0.5 parts per billion if inorganic mercury is the 95th percentile. It’s a very, very high amount.  And if your urine to blood ratio is good and your kidneys are working well and if you measured your urine, your urine would actually be fairly high. And so it was just, oh, we’ll measure serum. It only shows a little bit of one story. We’re measuring urine, only shows a little bit of story. You gotta put all this stuff together with the right technology. And there’s a beautiful story about the disposition of the metals and your excretion ability all in that one test.

Dr. Weitz:            So your company offers this tri-metals test that measures mercury through serum, urine, and hair.

Dr. Shade:           Yeah, that’s called the Mercury Tri-Test. Those three, blood, hair, urine.

Dr. Weitz:            And then there’s another test that measures multiple metals, and that’s a serum test.

Dr. Shade:           Yeah, that’s our blood metals panel, where you’re looking at nutrient metals and toxic metals. So the nutrients, you’ve got classic calcium, magnesium, copper, zinc. Most are really important because they have to be in a certain ratio. When you have high copper and low zinc, you’re synergistically toxic with all your other metals and it’s a marker of a serious dysfunction. So is calcium:magnesium.  Then you’ve got co factor detoxification metals like selenium, molybdenum, which is crucial for sulfur cycling, and you’re taking a lot of sulfur compounds when you’re detoxing. And lithium, which is a big one for B vitamin cycling.  And then in your toxics you’ve got the major four, arsenic, cadmium, lead and you have mercury but just as total mercury. If you’re just looking at somebody who’s a big fish eater and you want to know is it high, is it low, it’s sort of a good first cut.  A lot of people think, well if it’s high there then I’ll go do the Tri-Test. But if you have a patient who has dental amalgams but doesn’t eat fish, you’re not going to see anything in the total mercury blood. You need to go to the test that separates the two and looks at inorganic separate from methyl. It’s like they’re two totally different metals.

Dr. Weitz:            So ideally, if you have somebody that you suspect has serious metal issues, you really need to do both tests.

Dr. Shade:           You do both and you have a map of everything then. Both functional excretion capacity, sourcing, and your whole metals map, nutrient and toxic all together.

Dr. Weitz:            You ever measure the antibodies to metals?

Dr. Shade:           No, but every time I hang out with-

Dr. Weitz:            Dr. Vojdani?

Dr. Shade:           Yeah.

Dr. Weitz:            He spoke at our meeting last month so I got to hang out with him, it was great.

Dr. Shade:           Yeah. And so hopefully I hired guys to be in charge of a clinical research program here, and we’re starting to really crank out a lot of stuff. And so that’s on our list is to reach out to Dr. Vojdani and get a bunch of patients. Because he had said to me, “Well I think when you see the levels are high you’re going to see antibody response.” My take is very different.  When you see an antibody response, that’s going to mean that a certain level of metals is infinitely worse than maybe a higher level with no antibodies. So the antibody and the levels together will correlate with symptomology. And we’ll see, because you’re going to find a lot of people who are super symptomatic at low levels, and it’s this diffused whole immune dysregulation and neurological dysregulation. And the amount of mercury is really hard to justify that that’s doing it alone. But if they’re allergic to that mercury, then that can give those symptoms.

Dr. Weitz:            Yeah, boy, those can be some of the toughest patients, some of these chronic patients, and you’ve been doing mercury protocols and years later they’re still sick. Those are the toughest patients.

Dr. Shade:           Yeah, they’re very difficult. It’s very multifactorial, why did the immune system turn on it. There’s usually layers and layers of stuff going on.

Dr. Weitz:            Yeah, in one of the discussions you were having with somebody else, you were talking about how when you’re trying to get rid of metals or mercury, at a certain point sometimes that will increase some of the infections and you’ll have to stop and fight that off, like SIBO will recur.

Dr. Shade:           One of the things that we see a lot is that with Lyme, undiagnosed Lyme, when we start treating the metals we bring the glutathione levels up, it reboots the immune system and it starts reacting to the Lyme and they feel horrible. And then you send them out for more lyme testing and then they show positive on their Western blots, and then they have to take a side road and get some antimicrobial therapy before they can come back and just do the metals. Although there’s still detoxification support for that. So in the complex cases I would say there’s a sort of pendulum between microbial focusing and toxin focusing.

Dr. Weitz:          So can you talk about your strategy for helping to remove metals, and how much does it change depending upon the metal?

Dr. Shade:         Oh, good, good question. And I’ve gone to a more broadly focused detoxification strategy, but let’s just look at mercury now. And mercury, cadmium and arsenic are playing by basically the same rules, and lead plays by a different set of rules. And then cadmium a little bit straddles the fence between the two. So mercury is the classic glutathione dependent detoxification. So if we’re in a cell, say there’s a cell here and we got a protein and there’s a mercury stuck to it, we gotta get the mercury off of the protein because mercury’s blocking the function of the protein. So you’re going to have glutathione floating around in the cell. But it doesn’t just go and grab the mercury on its own. You need glutathione S-transferase. Glutathione S-transferase is part of the phase two detoxification proteins called transferases, where they link something you make, like glutathione, onto something you want to get rid of, like mercury. And so that transferase would be me, and it changes the bond structure on the mercury so it can come off the protein and go with the mercury. 

Dr. Shade:         So then we got a mercury glutathione complex in the cell, we gotta get it out.  Now it doesn’t just passably diffuse out.  There is a series of transmembrane transporters that depend on magnesium and ATP, meaning you need to energy to turn them over and you need magnesium.  And they actively push that complex out of the cell.  Okay, so the cell’s free, but it’s out in the body. And it’s in the extracellular environment and then that’ll join in to the blood flow and then how do we get it out from there? In the liver you got another transmembrane transporter that’s feeling around for these things, grabs it, pulls it into the hepatocyte, and another one that’s another one in these family of transporters that dumps it into the bioflow. And then from the bioflow goes down to the GI tract and out to fecal excretion. That’s when everything’s working well.  So if we want to build a system of detoxification, we need to build glutathione levels. We need to turn up the activity of the transferase, and we need to turn up and support the activity of the the transport proteins. And when it gets down to the GI tract, we need to grab it before it gets reabsorbed.  So we like to bring in liposomal glutathione for building glutathione.

Dr. Weitz:        Now how much is glutathione actually absorbed? Those of us in a Functional Medicine world have it in our heads, we’ve been told glutathione’s not absorbed, you gotta take NAC, that’s the only way to do it. If you end up in the emergency room with acetominophen toxicity, they’re going to give you IV NAC, so NAC’s the way to go. But now that we have these better forms of glutathione, like liposomal, how much is actually absorbed?

Dr. Shade:       Right, and so in … These total amounts absorbed in kind of vary and we’re doing a lot of research to show how much goes in and how these different approaches compare. But first, why would we do … Let’s just assume we get the liposome in and then we’ll come back to how well liposomes are absorbed, and what’s required for a liposome to be absorbed, because all liposomes aren’t the same. It’s like all cars are not the same, all wines are not the same. There’s a vast range of quality.

                       But first just assume that it gets in there. Why would you use that instead of NAC?  Now in the cases of really compromised individuals who are very sick, people with lyme disease, mold toxicity, things where there’s actually blockages of the enzymes that are synthesizing glutathione.  For instance, there was a paper done using ready liposomal glutathione in cell cultures and they took immune cells from HIV patients, which are notoriously poor at making glutathione, and they’re getting all these infections because of the low glutathione. And that’s one thing that people miss about glutathione is it’s an essential factor for proper immune response, it’s not just about detoxification.  So they found in these cells, they were challenging them with the tuberculosis culture, they culture the white blood cells, the put tuberculosis in, and for the cells to be able to handle the tuberculosis, they needed to raise the reduced glutathione levels. And then the cells could deal with this. And they tried two ways to do it.  One was NAC, and the other one was liposomal glutathione into the cell cultures. And they needed 5,000 times more NAC to raise the glutathione levels up the way that the liposomal glutathione did. 5,000 times. Because those enzymes are epigenetically being blocked by disease states. So when you’re sick, just pouring NAC in, it’s hard to get the levels up. You’re healthy, that’s a good way to go. If you have snips for poor glutathione production, then you want to think about both as differing strategies.

                      Then liposomes, what gets in, what doesn’t. We’re actually in the middle of a study right now where we’re measuring all the different liposomes on the market and the factors that go in to getting these into absorption. And we just got a study back from our Japanese partners, we’ve got a bunch of Japanese doctors who use our stuff, they wanted data on glutathione, I didn’t have it yet, so they went and got Doctors’ Data, blood glutathione test. They took 10 people, measured baseline, gave 5 of them IV and 5 of them liposomes, 500 milligrams each. And then they measured them six hours later. To see not right away, if you do an IV you spike up, but often you spike right back down. So they said six hours later, what’s the effect on this system?  IV six hours later there was a 15% jump above baseline. Liposome, a 30% jump. Anything that gets you a 30% jump is awesome. But the fact that we just beat the IV, because the IV has no mechanism for really interacting with cells. Glutathione’s not really good at getting in the cells. But the liposome showed its ability to raise the levels for an extended period of time. It was a beautiful piece of work. But in all the other data that we’ve got on liposomes, the membranes have to be right and the size has to be right.

Dr. Weitz:       And by the way, liposomal basically means putting it in a fat soluble form, right? Essentially combining it with phosphatidylcholine.

Dr. Shade:      Well what you’re doing is using phosphorylcholine to make a little bubble that’s sort of watery on the outside, fatty on the inside. And you’re making like a little cell and you’re tucking the glutathione in there. And so it absorbs like a fat would. It passably diffuses across the upper GI. So that’s why they say it’s like it’s like fat soluble, because it absorbs like a fat.  But if you make them small enough, they pass right through the oral mucosa into the capillaries in the oral mucosa. In fact in the blood uptake studies that we did with vitamin B12, we had a very significant bump in the blood levels in two minutes after holding it in the mouth. That’s why with our liposomes you take them orally, you swish them around your mouth, you let them hold in there 30 to 60 seconds and you swallow. The uptake begins there. Even if … You get to the stomach acid and the bile salts, you’re starting to beat on those liposomes. So the faster you start that journey, the better.  And that journey only begins that far up in the GI tract when they’re really small. We call them nano liposomes because they’re below 100 nanometers. And all of our products are between 20 and 80 nanometers. This is not a threat, don’t worry about nano tech. Because when you’re absorbing fats in your diet, you make something called a chylomicron. It’s triglycerides surrounded by phosphatidylcholine with a couple of apolipoproteins that you use as delivery vehicles to bring the fatty acids to the cells to use them. And those range down to 70 nanometers in size. So those are lipidnanoparticles, and you have a whole enzyme system for dealing with phospholipid based nano particles to take them apart, use the phospholipids in your cells, in your membranes. You can use them as fatty acids for energy, you can make acetylcholine.  So this delivery system is really good but it only worked when we got it below 100 nanometers. And all this other stuff on the market is selling you the dream of the liposome but they’re 2, 3, 400 nanometers, and I just don’t see any evidence that they’re working. So we’re really spending a lot of money and a lot of time working out exactly what works and what doesn’t work. Alright, so that’s the glutathione story.

Dr. Weitz:     What about the idea of spraying some in your nose, because Dr. Vojdani was talking about how there’s a route of entry from the nose for bacteria directly into the brain.

Dr. Shade:     No, that’s a great idea but it’s not a dietary supplement, then it’s a compound pharmacy product. Because a dietary supplement has to go through the GI tract.  Don’t think I don’t have a couple of nasal applicators here in my office. I did that, but I can’t do it on the market. So there’s the story there.

So back to our detox story, we got glutathione in, and now we need to up-regulate the transferase and get all those transporters working. So now we want to invoke NRF2, which is the little switch, the protein inside the cytoplasm that when you activate it, it goes into the nucleus and turns on all the chemo protective genes. It’s like the light switch for all the protection genes. So you want an NRF2 up regulator. So the things that do that, lipoic acid is probably my favorite. There’s a number of compounds from crucifers, like sulforaphane is very well known but there’s some drawbacks with those. There’s things from garlic that work very well. And don’t get deodorized garlic because it’s actually the stink of the garlic that works, it’s garlic oil that does it.  Then polyphenols, I love polyphenols.

Dr. Weitz:     Resveratrol.

Dr. Shade:    Well resveratrol’s not a great NRF2. It’s more in the SIRT 1 activation, so mitochondrial up regulation. But it is a polyphenol. And then people say curcumin, and that’s not the best either. The good ones are green tea extract, pine bark extract, red wine extract, grape seed extract. The Ayrevedic polyphenols from haritaki is one I use a lot. So all of those are really good NRF2 up-regulators.

                     And with that comes glutathione S-transferase. There’s also a bump to glutathione synthesis in there. So that’s working, and there’s also a bump to the transport proteins. But to really get the transport system working well, I like to work from the GI–gallbladder–intestinal axis here. Why am I talking about that? Because the biggest transport system that’s happening here is from the hepatocyte into the bile ducts. And that transport of toxins into the bile tree is synonymous with and linked intimately with bile transport.  There are two transporters that move bile from the hepatocyte into the bile tree. And it’s the bile salt export pump and MRP2, the multidrug resistance pump number 2. The MRP2 is the toxin transport, it moves toxins and it moves bile salts, and obviously the bile salt pump moves bile salts. These guys get up-regulated and down-regulated in unison. So cholestasis is toxostasis. If you move bile, you can’t move -toxins.

                   So what happens to the toxins that are in the liver when you can’t move them into the bile? There’s another door out of the liver back into the blood. It’s a pressure release valve. When you wind up a bunch of toxins in the hepatocyte, and the hepatocyte can’t deal, it can’t move them out fast enough, it dumps them back into the blood.  Where do they go from there? Brain, neuroinflamation. Kidneys. Lower back pain. Skin, rashes and things coming out through the skin. These are all the classic detox reactions, and they’re all caused from a failure to continue to move bile. So we’re taking our cues here from the early 1900s and the prohibition time when bitters was the medicine for everybody because it was the only way to drink, but it also cured half of what ails you, because stuck liver was what was going on. And when you open up liver, bitters activate those transporters, and when you open that up and you dump bile, you dump toxins and you start feeling better. So we use a lot of bitters.  We use a lot of phosphatidylcholine just on its own, not even in liposomes, because PC is always being donated from the hepatocyte cell membranes into the bile flow because it helps fluidize the bile flow. People talk about thick bile, PC is what’s solubilizes it. And it actually forms little mixed micelles with the bile salts so that the bile salts, which are a detergent, don’t dissolve the bile tree.  And the reason you have pressure release valves from the hepatocyte is when bile salts build up in there, they dissolve the hepatocyte. And so you’re dumping those back into the blood and then bringing them up when you can use them. So when you’re always moving out, you’re always moving toxins out of the system.

                 But what else are you doing? You’re cleaning the upper GI tract. Everybody’s talking about SIBO and SIFO, like it’s a new infection. Do you really believe that you have an infection in the small intestine that has to be treated? Why do you have an infection? It’s not like a creature came in and is living there in a classical infection sense. It’s crawling it’s way … It’s just bacteria in your lower GI tract crawling their way into the upper GI tract. Because the upper GI tract is supposed to be washed by bile. The antimicrobial detergent that washes the upper GI tract and acutely brings glutathione along with PC into the upper GI tract as part of the metabolism in the upper GI.  Upper GI is doing mostly chemical reactions. Detoxing things in food, and pulling things out of blood and dumping them into that GI tract, and then the microbes start growing further on down. And in fact, in people with congenital intrahepatic cholestasis, meaning you’re not able to move bile salts from the hepatocyte into the bile tree, those people are statistically higher cases of SIBO, and when you treat them, it keeps coming back.

                 So this bile flow, this keeping things moving out, is a crucial part of keeping the transport chain open, keeping the liver open, and then coming in with binders to bind these toxins in the GI tract so you don’t absorb them. And that’s binders like our IMD, which is thiol-functionalized silica for metal, or charcoal. Clays and zeolites, Chitosan, those are all grabbing different parts of the toxin pool and we blend those all together-

Dr. Weitz:            What about pectins, like modified citrus pectin?

Dr. Shade:           Now modified citrus pectin, I don’t buy into that at all. So remember my … No, I buy into it’s use therapeutically, I don’t buy into the idea that it can bind toxins. Because remember my PHD is in mercury chemistry. I designed the whole analytical system we use to model out what molecules bound mercury as it moved from the sky to the rain to the bacteria to the plankton to the fish to the people. We know this stuff really, really well. And there ain’t nothing in modified citrus pectin that’s going to be a good toxin binder.  But remember this, inflammation blocks detoxification. When inflammation is down, detoxification gets blocked because detoxification’s part of the antioxidant system and inflammation is pro oxidant. So they just go like this. And modified citrus pectin is a very nice immune modulator, especially in the GI tract, and it turns down inflammation in the GI tract. When you turn down inflammation in the GI tract, you release a stuck immune system and allow it to detox more. And I believe that that’s why modified citrus pectin has a therapeutic value in detoxification. And it probably does bind a lot of other toxins that are made, maybe it binds an endotoxin, maybe it binds some of the other dysbiotic toxins, maybe it gets a little bit of mold toxin. It does have a therapeutic thing but arguing for it mechanistically as a mercury binder is not a good path for the argument.

Dr. Weitz:            It’s interesting because it’s in a lot of products that are designed for removing heavy metals.

Dr. Shade:           Yeah. And again, I think therapeutically it works but not in the way that they’re describing. And my whole goal, my whole path here has been one of shedding light on the path, and the light is on the light of the mechanism that things are working. I am big into empirical medicine and knowing what’s worked and what hasn’t. But until you reduce that to mechanism, you can’t take the next step of effectively bringing together the best players for a different problem, and designing a higher order of natural medicine.

Dr. Weitz:            Right. Just a word on the SIBO. You know part of the theory about one of the reasons for SIBO, apart from decreased bile secretion, is that you get decreased motility and you get a blockage of the migrating motor complex which causes these peristaltic waves to happen in between eating that helps to clear out the small intestine.

Dr. Shade:           Flush, clean, flush, clean, flush, clean. You’re right. And so it has two sides to it. How do they get blocked, are they poisoned, is it a microbe, is it a toxin? But somehow they get locked down.

Dr. Weitz:            Well there’s that whole cytolethal toxin theory of Dr. Pimentel’s, and they even have a blood test for it.

Dr. Shade:           And what are those called?

Dr. Weitz:            It’s a cytolethal-

Dr. Shade:           distending toxin?

Dr. Weitz:            It’s an endotoxin secreted by a campylobacter jejune or some form of food poisoning that secretes a toxin that then damages the nervous system of the small intestine.

Dr. Shade:           Yeah. And when you go into the body and you look at what really amplifies toxins-

Dr. Weitz:            It secretes a cytolethal distending toxin.

Dr. Shade:           Cytolethal distending toxin.

Dr. Weitz:            Yeah, Dr. Pimentel has a test for it, I think it’s called the IBS check test.

Dr. Shade:           Okay, cool, I’m going to look more into that. Because things like endotoxin amplifies all the toxicity through the body because it’s pro inflammatory. And there’s papers looking at the damage of mercury alone and mercury plus endotoxin and it’s synergistically higher. And I was talking about those transporters that are moving the bile salts and the toxins. Well what blocks them the best? Endotoxin. And it actually causes the transporters to be pulled out of their membrane and internalized into a little vesicle in the hepatocyte. And you really want to damp the inflammation, get those transporters back in there to drain everything out.  And it was great, we put a paper, Carrie Decker and I wrote a paper in Townsend Letter about all these pathways and nutraceuticals work on these things. And one of the interesting things about milk thistle is that it actually preserved the transporter’s ability to stay in the membrane during the stress of high toxicity.

                           But another thing that blocks that is excess estrogen. And something that opens it up is progesterone. So there’s estrogen progesterone balance, estrogen dominance actually locks up your gallbladder. And in the brain estrogen dominant winds up the glutamate system which gives you anxiety, it makes you sympathetic dominant. But the gallbladder’s also para sympathetically innervated, so it’s working against you on so many different levels. So stress, estrogen dominance, leaky gut and endotoxin, all this is blocking your ability to detoxify.

Dr. Weitz:            And Dr. Vojdani at Cyrex Labs has a test, it measures anticytolethal distending toxin and also vinculin. That’s the part of the small intestine that gets damaged and they have a test for that.

Dr. Shade:           See me writing all this down. Distending toxin, I like that. Alright.  See, this goes back to understanding mechanism. The more we understand mechanism, the more we can reach out to other people that are working in different fields and say let’s bring this together and really let’s lock this down. And it’s an amazing time in the whole history of natural medicine where you go into PubMed and you see that there’s research being done all over the world on all the different natural compounds and the genes they hit, the proteins the express, interactions between the two. We’re getting all of the mechanism of all these transporters all down. This is a brilliant time where we can design the most powerful natural medicine systems.

Dr. Weitz:            That’s great. This has been an awesome discussion, Dr. Shade. So for listeners and practitioners who are interested in getting some of this testing done, or getting a hold of your products, are the testing and products available to laypersons or should they just go through functional medicine practitioners like myself? How does it work?

Dr. Shade:           Yeah, so Quicksilver Scientific is dominantly a professional company. We’re offering the testing to the practitioners, they pass it through. You guys buy the supplemental through wholesale, you pass them through. You use our protocols or individual products. But there’s such a world of hyper informed self medicators out there, and they’re dying for this stuff and I gotta give it to them because that’s me, too. And so we do sell direct to consumer all but some. Like there’s some real pro-grade stuff, like the EDTA, that’s practitioner only. But most of the other stuff is available. Even the testing, but but that’s state by state, about half the states allow direct access testing where you can buy a kit from us, go to to a clinic, get the blood draw done and send it back.  But it’s always good to go through a practitioner, because they’re going to bring a wealth of experience of all the other things that they’ve seen. And they’re going to button up the whole protocol and they’re going to put the little extra things you need in there. There’s “Oh no, did you think about doing this and this?”  So both are available, but we’d like people to work with practitioners.

Dr. Weitz:            That’s great. And for those who want get more information, where should they go?  

Dr. Shade:           Quicksilverscientific.com. And we have a whole new website being launched in about two weeks. Right now Quicksilver Scientific, if you’re buying as an individual, it will move you over to Quicksilver Life, our second website, which is a retail website. But they’ll all be merged together as Quicksilver Scientific in about two to three weeks. And there’s different things, it’ll be one site with different things available to you depending upon your journey in there, there’ll be more stuff available to the practitioner.

Dr. Weitz:            That’s great. Thank you, Dr. Shade.

Dr. Shade:           Great, thank you so much, it’s been great hanging out here with you, Ben.

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Low Dose Immunotherapy with Dr. Karima Hirani: Rational Wellness Podcast 045
Loading
/

Dr. Karima Hirani speaks about Low Dose Immunotherapy and Low Dose Allergy therapy with Dr. Ben Weitz .

[If you enjoy this podcast, please give us a positive review on Apple Podcasts, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

3:33 We discussed Low Dose Allergy therapy (LDA), Low Dose Immunotherapy (LDI) and the differences between them. Low Dose Allergy therapy has been around for 50 years, having been called Enzyme Potentiated Desensitization in England. This was eventually brought to the US by Dr. William Shrader, who is one of the head people at the American Academy of Environmental Medicine. LDA is a form of Low Dose Immunotherapy using a proprietary formula of a broad-based mixtures of allergens (antigens) made immunologically active by the enzyme glucuronidase. It is used for allergies, but allergies can present as autism and using LDA you can see improvements in speech and language.

6:00  Besides LDA, her other top LDIs are yeast, Lyme, and strep for PANDAs.  Rather than the traditional method of subcutaneous injections of the FDA, they are using it as sublingual drops, thanks to Dr. Ty Vincent.  And they are using further serial dilutions of the FDA tincture that comes from the compounding pharmacy that makes it, since it is too potent. It ends up being diluted a quadrillion times, so it is really a homeopathic formula.  The same T regulatory cells that are found under the skin are also present under the tongue.  This is a way to train the immune system to build tolerance.

10:08  Dr. Hirani often finds Lyme Disease in her patients with autism and Lyme Disease is really a condition of immune dysfunction. The Lyme LDI seems to turn off the autoimmune component of the chronic Lyme disease.

12:15  Dr. Hirani explains that PANDAS found in kids is the pediatric autoimmune neuropsychiatric diseases after strep infection.  She gets amazing results with LDI to create immune tolerance and this alleviates many of the symptoms. This also turns off such infections that create chronic illness. She will also often give such patients high dose vitamin D to help the immune system. 

15:25  Dr. Hirani noted that if she gives a dose that is too strong and it can trigger a herx reaction. If she has an autistic kid and she gives too strong a dosage of strep LDI, it can trigger a strep infection and these kids will have strong reactions, so she may prescribe an antibiotic and she will use a rescue formula of supplements.

20:04  Dr. Hirani explains that in the last few years many more patients are testing positive for Lyme infections with the Western Blot and they will also often have a low CD 57, which is a marker of immune dysfunction.  She will also often test her patients for Lyme, Epstein-Barr, cytomegalovirus, Human Herpes virus 6, herpes 1 and 2, mycoplasma, measles, mumps, strep, and varicella IgM titers. The measles, mumps, and varicella titers can result from the vaccines and these things can trigger an autoimmune disease in these kids, as these infections turn off and on.  

 



Dr. Karima Hirani is available to see new patients by calling her office in Culver City at (310) 559-6634. You can get additional information about Dr. Hirani by going to her website http://www.drhirani.com/

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as chiropractic work by calling the office 310-395-3111.


 

Podcast Transcripts

Dr. Weitz:           This is Dr. Ben Weitz with the Rational Wellness Podcast, bringing you the cutting-edge information on health and nutrition from the latest scientific research and Bible interviewing top experts in the field. Please subscribe to the Rational Wellness Podcast on iTunes and YouTube, and sign up for my free e-book on my website by going to drweitz.com. Let’s get started on your road to better health.  Hey, Rational Wellness podcasters. Thank you for joining me again today. We have a very exciting show. We’re going to be interviewing one of my friends for a long time Dr. Karima Hirani. She has a thriving practice in Culver City. She is a medical doctor who specializes in functional and integrative care. Doctor, let me give you a little bit of introduction into her background and then we’re going to highlight a couple of therapies that she’s using in her practice, which are low dose allergy and low dose immunotherapy. We’ll also going to try to cover neurotherapy if we have enough time.

                                So Dr. Karima Hirani is board certified in family medicine, as well as in integrative and holistic medicine, as well as in clinical homeopathy. She holds a Master’s Degree in Nutrition from UCLA.  She specializes in autism, ADD, and PANDAS in children. She also treat adults with chronic illness.  She is an expert in specific types of treatment that she uses for her chronic patients, including low dose allergy therapy, low dose immunotherapy, and neurotherapy.  Low dose allergy therapy and low dose immunotherapy are essentially ways to help individuals overcome allergies and food sensitivities to foods, chemicals, molds, toxins. This therapy can be used for whole range of chronic illnesses, including autoimmune diseases and chronic fatigue and Lyme disease, et cetera. So this is a type of therapy that helps to balance the immune system when the body is not able to tolerate certain bacteria, fungi, viruses that live within us that others can tolerate or maybe that your own body could have tolerated at a different point in time. This is certainly the case with Lyme disease and many other chronic diseases that many of us in the functional medicine world find coming into our offices very frequently.

                                Dr. Hirani, thank you for joining me today.

Dr. Hirani:           Thank you for having me. It’s a pleasure.

Dr. Weitz:           Boy, we’ve known each other for a long time. How many years have we known each other?

Dr. Hirani:           A long time, maybe 15, 20 years.

Dr. Weitz:           Yes, yes. I remember going to all those Dr. Bland seminars and I would always get to talk to Dr. Hirani.

Dr. Hirani:           Yes.

Dr. Weitz:           So can you explain a little bit about the differences–What is low dose allergy therapy? What is low dose immunotherapy? What are the differences between those?

Dr. Hirani:           So low dose allergy therapy has been around essentially for about 50 years now. It was first discovered in England. It was called Enzyme Potentiated Desensitization. It was brought to United States several decades ago by Dr. William Shrader. He is one of the head people at the American Academy of Environmental Medicine. He and many other doctors have been using low dose allergy therapy for several decades. What they’re using it for is to treat allergies. As you know as a functional medicine doctor, one of the most important things that we look at is allergies in our patients. Sometimes allergies don’t present as the classical symptoms, where you have the runny nose, itchy eyes, teary eyes, et cetera, sneezing.  Allergies can present as chronic fatigue.  Allergies can present as autism. When we treat with LDA, we see amazing things happen, anything from improvement in speech and language.  To my adults patients, they are not tired as much anymore.  Their brain fog is better.  They lose weight, because when you have allergies or you have a chronic infection, it can cause inflammation and then it can lead to weight gain.  So we see a whole spectrum of improvement by just giving the patient the LDA.  Again, I have to really stress the fact that it’s not the typical allergy symptoms that you should be looking at. You should really be thinking of everyone as having potentially allergies and then to just give them a trial dose of the LDA. That’s usually one of the first treatments that I offer without even doing any functional medicine testing on my patient. I just give them the LDA dose and then we see what happens.

Dr. Weitz:           What percentage of patients do you see some sort of positive response?

Dr. Hirani:           I haven’t really like scientifically quantified it, but if I could just generalize, my top three most beneficial LDA-LDIs is LDA is one of them and then I have my other LDIs, which are really effective in my patients are yeast and Lyme and then Strep for PANDAS. These four seemed to be my most effective treatments.

Dr. Weitz:           Interesting. So my understanding of LDA is that this could best be described as a form of low dose immunotherapy and is a proprietary mixture of foods and other things that could create allergic reaction.  Is that sort of the way to understand it?

Dr. Hirani:           Absolutely, absolutely. Ty Vincent, thanks to Ty Vincent.  We’ve taken it one step further and that traditionally, most doctors were just injecting in the skin. They were just using the original dose that you get from the compounding pharmacy because this proprietary mixture comes from one compounding pharmacy in the United States. What Ty Vincent has been doing and he’s taught doctors like myself to do is to make further serial dilutions of the actual LDA because many, many patients are extremely sensitive. The original tincture that comes from the compounding pharmacy is too potent.  So that’s something that we’ve done.  We’ve been able to help even more patients than we could by LDA by making the serial dilutions.

Dr. Weitz:           Now it’s interesting because this is something that’s alluded billions even trillions of times, right?

Dr. Hirani:           Correct, yes, like quadrillion, quadrillion times.

Dr. Weitz:           Essentially, we’re talking about a homeopathic formulation. There’s really no real amount of the original compound sort of just the energy of it essentially, right?

Dr. Hirani:           It’s the energetic imprint that’s been left in the mixture and that’s what we’re giving the patients, and I do it and I think Ty Vincent does it also. We do it sublingually. We’ve moved away from the subcutaneous injection because it’s very painful.  It leaves behind big red bump and itchiness and swelling.  Patients don’t care for that.  So when we do it sublingually, we have the same T regulator cells that are subcutaneous that are under the skin.  There are also under the tongue.  So we’re basically training the immune system to build tolerance.  That’s what we’re doing.

Dr. Weitz:           In contrast with homeopathic medications, if a homeopath wants to give you a more potent formulation, he makes it more dilute. But with the low dose immunotherapy when you make it more dilute, it’s less potent, right?

Dr. Hirani:           Correct, yes.

Dr. Weitz:           I mean that makes rational sense to me. One of the problems I always had with homeopathy is to tell me you’re going to dilute it, another hundred thousand, million times and it gets more potent. It just totally is very difficult for my rational, scientific mind to wrap around.

Dr. Hirani:           The way that traditional homeopaths look at it is when you further dilute it, it’s working at a deeper level. To me it makes sense because when we have to further dilute these potions and we give them to patients who can tolerate them, these are patients that are probably really affected at a deeper level than somebody who can just handle the original mother tincture.  So to me, I see a correlation.

Dr. Weitz:           So when you’re treating a chronic condition like … I read some of your blog posts and watched your video that you did at the Autism conference. So you often find Lyme disease as an infection that affects patients with autism, right?

Dr. Hirani:           Yes, and my adult patients as well with chronic illness.

Dr. Weitz:           So essentially, when you look at Lyme disease, you’re not really looking at it as a disease that is like a typical acute infection. This is something that’s really creating a problem because it’s created, the body is reacting, the immune system is overreacting to it. It’s not that the bacteria is actually eating away your tissues or things like that, right?

Dr. Hirani:           Exactly. I think that there’s two processes going on. One is there is this infection that seems to turn on and off. When it’s off, the immune system thinks the infection is still there, so it’s mounting an attack against the patient. It’s this autoimmune phenomenon that is really making the patient really ill, so that the LDI, the line of the I that we give to the patient seems to turn off the autoimmune aspect of the illness.  Does it ever get rid of the illness?  We’re not quite certain, but we certainly seem to have amazing results just in curing all of these symptoms and getting rid of all of these symptoms from the fatigue to the joint pains to the brain fog.  I mean, you name it, we’ve seen improvements.  So the autoimmune concept, the reason why it makes a lot of sense to me and it may not make a lot of sense to a lot of doctors if they’re not treating PANDAS. Are you familiar with PANDAS?

Dr. Weitz:           Somewhat.

Dr. Hirani:           So if you understand PANDAS, for your audience, PANDAS stands for Pediatric Autoimmune Neuropsychiatric Disorders Associated with Strep.  So this is an autoimmune phenomenon that has occurred after a Strep infection.  These kids can have OCD. They can have ticks.  They can have aggression, ADHD, anxiety, bedwetting, whole host of symptoms that they can have.  So this is an autoimmune response to this infection.  When I first heard Dr. Ty Vincent speak and he was talking about the autoimmune concept of infection of these infections like Lyme and yeast and Epstein-Barr, it just like it rang bells in my head and it just made sense.  I just dived into it and I’ve had amazing results in my chronically ill patients.

Dr. Weitz:           Now this is a different way of thinking about infections and say the average person who thinks about a flesh-eating Staph bacteria, you have this bacteria, it’s eating away at you. Unless you get rid of it, you’re going to end up suffering dire consequences. In this sense, you’re thinking of an infection as the problem is not really the bacteria per se that’s damaging your tissues. It’s that your immune system is not tolerating it, right?

Dr. Hirani:           Exactly. It’s the autoimmune aspect of it. For example, I’ve had patients who come in with oral herpes or with genital herpes. We’ll give them their herpes LDI and we will turn off the infection. So we can literally turn off active infections by giving the LDI to them. So what does that tell you? It tells me that there’s a huge autoimmune component to these infections and that a lot of these infections are probably they’ve been living with us for eons.  Probably not causing us a lot of harm but for some reason in the last several decades, these infections are being threatened and so they’re coming alive. They’re creating all of this autoimmune havoc in the body and then creating all this chronic illness.

Dr. Weitz:           So do you ever use killing strategies at the same time? Do you ever prescribe antimicrobial herbs, so that you can knock down the bacteria at the same time that you’re getting your body to be more tolerant of it?

Dr. Hirani:           No, I don’t need to.

Dr. Weitz:           You don’t need to.

Dr. Hirani:           I don’t need to. It’s wonderful.  Patients come to me from other doctors with this laundry list of supplements and herbs that they’ve been on.  I don’t need to give them anything other than just high dose vitamin D, because the vitamin D seems to just really help the immune system and help the LDIs and the LDA work better. That’s really all I need. Now if I give a dose that’s too strong, say let me use PANDAS again, so I gave a Strep dose to a child and it was too strong for the child, it can trigger a Strep infection. In autistic kids, they can go bonkers. So in that case, I do sometimes need to prescribe the antibiotics and some rescue treatments to turn off the, we call it the herx reaction. So sometimes I do need to prescribe antibiotics, but it’s very rare or we have the parasite LDI. The parasite LDI is just a boon for my children, because they have classical symptoms of parasites from teeth grinding to foul-smelling gas to hair pulling, licking, chewing, mouthing.  So when I give them the parasite LDI, if it works, it’s miraculous. It turns all of the symptoms off and the parents are thrilled. When it’s too strong, it can actually worsen all of those behaviors, so in which case sometimes I have to prescribe a parasite medication for them and a bunch of oral supplemental rescue treatments for them.

Dr. Weitz:           So it’s interesting you bring up parasites. We know that there are some parasites where protozoans or even some worms that coexist in humans and actually maybe beneficial for us and there are others that can kill us. So how do you resolve knowing when you want to be tolerant, the difference between I want to be tolerant of something my wife does that’s really annoying to me as opposed to I don’t really want to just be tolerant of Charles Manson living in my house because it’s probably not going to be good to just be tolerant of it?

Dr. Hirani:           Well, basically if you’re walking into my office and you have symptoms, you’re not tolerant of these organisms that are living in you. Then if you got classical symptoms, in adults it tends to be just a foul-smelling gas.  I had one young woman.  She is still a patient of mine. She had this habit of picking at her skin.  She was picking away at her skin and she had all of this scarring and acne.  I treated her with the parasite LDI and all of that picking went away.  So if the patient presents to me with classical symptoms of parasites, you have to know what those symptoms are.  If you give them the LDI, you’re going to turn it off and you’re going to be so grateful.  The foul-smelling gas, I mean, how many patients have you seen that have problems with flatulence and foul-smelling?  You give them the right dose of the LDI and you just turn it off, I mean it’s miraculous, so.

Dr. Weitz:           I just read about some airplane. that had to have an emergency landing because some guy wouldn’t stop passing gas.

Dr. Hirani:           He needs the parasite LDI.

Dr. Weitz:           Once again, I just want to come back to the same thing. How do you know that it’s not a parasite that’s going to eat its way through your intestine and eat away at your liver and your brain? There are some parasites that are deadly and you don’t just want to be tolerant of them.

Dr. Hirani:           I get what you’re saying. What you need to understand is that LDI isn’t going to kill these infections. LDI is just helping your body become tolerant to them. If you already have a tolerance, then that LDI is not going to do anything. It’s not going to make it worst. For example, like Ty Vincent says, he doesn’t really have any symptoms of Lyme but he tried one of the Lyme LDIs and he noticed that his plantar fasciitis went away. So he obviously had a symptom that he didn’t associate with Lyme. Again, if you don’t have any symptoms and I give you the LDI and you don’t have a problem, it’s not going to make anything worse. It’s not going to turn off the parasites. Does that make sense to you?

Dr. Weitz:           Yes, it definitely makes sense. Treating somebody’s chronic conditions are so difficult.  So when you get a patient with autism, how do you know where to start? I know that you said you find Lyme. Do you test for Lyme? Do you just try a Lyme protocol or?

Dr. Hirani:           I’ve been doing this for a long time now so I can have it down to science. So I do do a whole battery of testing on these patients. Before I even get the results back, they all go home with the LDA, because like I said the LDA is one of my most effective treatments. When they come back for follow-up to do lab work review, I am now testing for Lyme through Medical Diagnostics Laboratories. A ton of these kids are coming up positive with the Western Blot whereas way back like maybe 10 years ago, nobody was turning up positive. All of a sudden, so many patients are turning up positive with Lyme. So this is very helpful to convince my parents. Before I was even doing the western blot or the MBL labs, I would just use the CD57 as a biomarker and everybody has a low CD57.

Dr. Weitz:           What is the CD57?

Dr. Hirani:           The CD57 is a white blood cell that gets rid of infection and also cancer cells. So in everyone that walks in my door, adult or child, the majority of the time I would say about 90% of the time, this biomarker is abnormal. It’s low and that’s a marker of immune dysfunction. Lyme disease, Epstein-Barr, CMV, even heavy metals have been shown to lower the CD57. So when I do this lab test and I show it to the parents or my adult patient, I tell them that, “Look, this could be a marker for Lyme and let me treat you with the Lyme LDI.” I do so and then lo and behold they’re better.   

Dr. Weitz:           So what percentage of the improvement do you see in kids with autism using your protocol with the Lyme LDI? Do you do other things or is that a protocol in of itself?

Dr. Hirani:           So almost every kid gets the Lyme LDI.  It may not be the second or the third, because sometimes they have active measles or mumps in their blood.  So I check for IgM titers in kids that have been vaccinated. So if they come and they have anything that’s IgM positive, like either the measles or the mumps, now nobody is testing for this. I’m probably one of few physicians that’s doing this testing.  I’m encouraging other doctors to measure this but if they’re not, shame on them.

Dr. Weitz:           Well, so is that a test offered by conventional labs? Where do you got to tested it?

Dr. Hirani:           Quest, LabCorp, they all do that. The LA County Department of Health doesn’t like that I’m measuring the IgM, because IgM means active infection. So they have to go through the process of calling me and finding out if this patient has active mumps or active measles. Usually, the child does not have any evidence of an active infection, but I know that it’s affecting their brain because these infections can cause an encephalitis. So when I see these IgM positive infections, sometimes even the varicella because these two vaccines, the MMR and the varicella were live viral vaccines. So sometimes these vaccines can trigger an autoimmune response and then the infection is turning on and off. So if I see these active infections and the titers are really high in the blood, I might first want to treat these infections. Or if the Strep titers are really high indicating PANDAS, I might want to treat with that first. So it really depends on what lab results show and then I go by all of that. So I usually go after, of course, the active infections first.

Dr. Weitz:           So what’s your complete panel? Which different things are you testing for when you get a typical kid with autism say?

Dr. Hirani:           So I test for Lyme. I test for Epstein-Barr. I test for cytomegalovirus. I test for Human Herpes virus 6. I test for herpes one and two. I test for mycoplasma and then I test for varicella. I think that’s about it and I check the IgG and the IgM titers, so.

Dr. Weitz:           IgG and IgM titers for which particular vaccines or organisms?

Dr. Hirani:           All of those that I just mentioned.

Dr. Weitz:           Oh okay.

Dr. Hirani:           IgG and IgM for all of those that I mentioned.

Dr. Weitz:           I mean, you also do the measles-mumps-rubella.

Dr. Hirani:           Exactly. The MMR, IgG, IgM exactly yes.

Dr. Weitz:           Okay, and the varicella, right?

Dr. Hirani:           The varicella, correct.

Dr. Weitz:           What about other vaccines like influenza?

Dr. Hirani:           So I don’t necessarily test titers for those if the parents tell me that my kid got the DTaP and then we lost him. We have the DTaP LDI. We have the hepatitis B LDI. I don’t use those quite as often as I use the MMR and the varicella. Now I do need to tell you that I don’t just treat the IgM. If the IgG, which indicates past infection and these IgG antibodies are super high in the blood, I will also treat those with LDI. I mean, we’ve seen just amazing things happen like I had two-year-old kid with active Epstein-Barr virus. We gave him the EBV LDI. Luckily, it was the right dose and he is talking now. So, I mean, when you treat these infections especially these active infections, it’s a big deal. Of course, infection is not the only thing we treat. We treat heavy metals, because these kids are loaded with heavy metals. So aluminum is huge in these kids.

                As being a proud … I don’t now if you came across a recent study that was published just at the end of last year. It came out of England where they autopsied the brains of I think 10 autistic kids who had died for unfortunate reasons. They found shockingly high amount of aluminum in their brain. So we know that these heavy metals are also playing a role in these kids.

Dr. Weitz:           Where are they getting these levels of aluminum?

Dr. Hirani:           That’s the big controversy. You may have heard of the chemtrails. Have you heard about the chemtrails?

Dr. Weitz:           No.

Dr. Hirani:           So I think that’s something you need to really look into, because you see those planes flying above when it’s a clear sky? You see those planes?

Dr. Weitz:           Okay, yes.

Dr. Hirani:           They’re spraying aluminum on us.

Dr. Weitz:           Really?

Dr. Hirani:           It’s been purported that it’s for climate control. However, a lot of people question the truth to that because-

Dr. Weitz:           How does it affect climate control?

Dr. Hirani:           Yes, exactly, I don’t know. Why are we trying to control the climate, I don’t know. Basically, every single country in the world has chemtrails. These are chemtrails you can see in every country in the world yet nobody seems to question it. Nobody seems to care about it. Nobody is talking about it. [inaudible 00:28:01] from Malibu collect her rainwater two days in a row. She sent it to a lab that tests for heavy metals. The rainwater had 50 times the acceptable amount of aluminum in-

Dr. Weitz:           Wow.

Dr. Hirani:           So, yes, it’s coming down on us. The aluminum is coming down. Obvious sources of aluminum are also aluminum foil, non-stick cookware. All of these things are sources of aluminum.

Dr. Weitz:           What about the aluminum that’s often found in vaccines?

Dr. Hirani:           They’re definitely an issue as well, absolutely yes. We have to consider that as a concern for these kids.

Dr. Weitz:           In fact, my understanding is the aluminum is often added to the vaccines as an adjuvant, meaning it’s something to actually create immune system reaction, because-

Dr. Hirani:           You know what? The aluminum hasn’t been found to be a great adjuvant. It’s not a great adjuvant-

Dr. Weitz:           Oh, really.

Dr. Hirani:           … but yet they use it. There’s a really great book that you might want to read. It’s by Mayer Eisenstein. He’s an MD, PhD. He’s a pediatrician, sorry, he’s an MD, JD; I apologize. He’s an attorney. He had to go back to law school to protect himself because he’s not anti-vaccine, but he’s very pro educating his parents about what’s in the vaccines. He’s published a book showing you the effectiveness of these adjuvants and aluminum is really not a very effective adjuvant.

Dr. Weitz:           Interesting. So then you will administer a low dose immunotherapy of aluminum to help these kids?

Dr. Hirani:           Yes. Again, we see amazing results. Even my Alzheimer’s patients, their cognition gets better, their thought processes in another language. The autistic kids their speech becomes amazing what we see with the aluminum.

Dr. Weitz:           Once again, one thing I’m having trouble wrap my head around is you’re now creating a tolerance to the aluminum. Don’t you want to remove the aluminum?

Dr. Hirani:           That’s something we don’t know for sure because we haven’t studied it. I personally think that by giving the aluminum LDI to the patient we’re actually helping the immune system remove these metals from the body, because these metals–it’s very hard to eliminate them especially if you have poor detoxification. I think that these LDIs are helping the body excrete them. I haven’t really done like a comparison study, some case studies on my patients to show like a before and after urinary porphyrins perhaps because that’s a lab test that we can use to determine if they have heavy metals. That’s something I definitely need to do and then I can really definitively say we did this LDIs and now the porphyrin levels have lowered so obviously it’s helping excrete these metals. So I personally think it’s doing that.

Dr. Weitz:           Do you ever combine it with a heavy metal detox protocol of some kind whether that be glutathione or NAC or chelators or something along those lines?

Dr. Hirani:           I combine it a lot. So I’m actually known as the chelating doctor. So I have a lot of experience chelating these kids from doing the transdermal, so topical to suppository to IV chelation, so I combine those a lot. Then I also have patients who don’t want to, parents who don’t want to do any kind of traditional chelation then we will just do the LDIs, and I have them on detox supplements as well, like glutathione, etc.

Dr. Weitz:           Interesting. Of those various forms of chelation, which one do you find to be the most effective?

Dr. Hirani:           As far as the traditional?

Dr. Weitz:           Yes, yes, but just stepping away from the LDI just for a second, even though I know that’s our main topic. We were talking about chelation. You mentioned suppositories and oral chelation, etc. Which do you find to be the most effective?

Dr. Hirani:           So the IV chelation is the most effective. The number two most effective is the suppositories. The number three most effective is the transdermal. I like to start with the transdermal actually on the younger kids because it’s so non-invasive. It’s just a cream that parents can apply at home. I send them home with the mineral supplement. I tell them that it’s going to pull out the good stuff as well, so you need to replenish with the mineral supplement. Then you need to look at for yeasty and parasite behaviors, because remember that parasites and yeasts, they actually hold on to your metals for you. So when you’re chelating, you’re also removing the metals from the yeast and you’re removing the metals from the parasites. So these bugs are going to get activated and these kids will present with symptoms of yeast and parasites, so we have to treat with either LDI and/or prescription medications like for yeast or for parasites.

Dr. Weitz:           Interesting. So one of the real benefits of using this low dose immunotherapy is not only is it especially effective, especially in the case of a skilled practitioner like yourself, but it has very low side effects. Isn’t that right?

Dr. Hirani:           Exactly, exactly. So with the LDI, parents are usually very eager to jump on it and I’m happy to prescribe it because it’s very safe. There’s always the risk of having a dose that’s too strong and I warn the parents about that. I tell them that “Look, if that happens, you just have to email me and I will send a protocol to do that’s a rescue treatment protocol with high-dose glutathione, high-dose CoQ10, high-dose vitamin D. If those three supplements are not working, then I’ll bring them into my office and we do rectal ozone and we do an auto-urine injection and we do a foot bath. I find that the ionic foot bath is very, very complimentary to detox and to treating especially herx reactions in patients. So I have a whole host of rescue treatments that I offer in the office for patients to do at home should the dose be too strong. I haven’t had too many problems with children herxing from the heavy metal LDIs, as I have with, I’ve had more herx reactions from the infection LDIs than I’ve had from the heavy metal LDIs.

Dr. Weitz:           For people watching this podcast who aren’t familiar with the herx reaction, can you explain what that is?

Dr. Hirani:           A herx reaction is a reaction that you get after you’ve taken a particular treatment. So for example, even Lyme patients who were doing antibiotics can have a herx reaction. So when we give an LDI dose that was too strong, the patient can have a herx reaction. The herx reaction is basically a worsening of your current symptoms or an emergence of new symptoms that you never had before, or a re-emergence of symptoms that you had before but they’ve come back again and now you’re really ill from these reactions, the symptoms that you had in the past but now they’ve come back again, or you never had them and now you have them. Or you have symptoms already and now the herx reaction is making your symptoms just worse than what they were before you took the LDI. So that is the risk that we are taking. We’ve tried to come up with methods to lower the risk especially with the muscle testing.

                I’ve identified 18 red flag symptoms that if the patients have any one of these 18 red flags, we automatically go 10C weaker on the dose that we find through the autonomic response testing to further minimize the risk of having a negative reaction. So it’s very important to have that discussion with parents because it is going to happen at some point with some particular LDI. We just have to reassure them that majority of the time, probably about 95 to 98% of the time, we’re able to reverse it.

Dr. Weitz:           When the patient does have adverse reaction to this low dose immunotherapy, you have to wait a certain period of time and then give them a lower dosage or less concentrated dosage.

Dr. Hirani:           Exactly. We tell the parents or we tell the patient that we need to wait now two months before we can retry this same LDI again, but we’re going to go 10C weaker or 20C weaker in terms of the dosing to really, because what I explain to them is if you herx from this reaction, that means you have a serious major issue with this particular bug or with this particular heavy metal and that we need to treat that again.

Dr. Weitz:           With respect to kids with autism, I’m sure it’s best if you can get to these kids early. What about the parent who has a kid who’s seven years old, 10 years old, 16 years old and none of the treatments have really been effective. Is this something that at that point can still be beneficial?

Dr. Hirani:           Oh, yes. Older kids, I have a 20-year-old kid and a 22-year-old kid that are just doing amazing. In fact, their dad is supposed to send me a video testimonial so I can post it on my YouTube channel, https://www.youtube.com/user/HiraniWellness. This kid, for example, his dad has left no stone unturned. His dad has tried everything out there for his kid. He has done chelation. He has done everything. He will tell you that nothing has helped his kid as much as the LDIs have helped his son. They can have a normal life now.

Dr. Weitz:           He just started this recently, right?

Dr. Hirani:           Two years ago, because I’ve been doing it. I just started it in 2015, so it will be three years now.

Dr. Weitz:           Wow, that’s great. That’s awesome, Dr. Hirani. What is your YouTube channel?

Dr. Hirani:           It’s just Dr. Hirani.

Dr. Weitz:           Okay good.

Dr. Hirani:           Dr. Karima Hirani.

Dr. Weitz:           Okay great. So I think that was a great amount information for our listeners to absorb and very, very helpful. Is there any final thoughts you would like to provide us?

Dr. Hirani:           Well, if your patients are out there struggling especially the adult patients with any kind of chronic illness, whether it’s IBS or chronic pain or brain fog, do give LDI and LDA a chance because it could be really life changing.

Dr. Weitz:           For practitioners who are listening to this who’d like to investigate LDA and LDI, where should they go to learn more information or attain some of these products?

Dr. Hirani:           They should contact the American Academy of Environmental Medicine. They should buy the LDA manual and they should attend one of the LDA courses at AAEM. Then they should also contact Ty Vincent and then buy his manual for LDI. When you buy his manual, he will also send you all of the LDIs and then in his annual he tells you how to make the further dilutions and how to use LDI. Nobody talks about the muscle testing. So if you’re new to muscle testing, I recommend you maybe check out Dr. Dietrich Klinghardt and take one of his courses on autonomic response testing. I’ve only taken level one. I don’t need to do all of the other levels because I don’t need to. The level one was good enough. So do think about using some sort of muscle testing to find the right dose. If you don’t and you’re just guessing like Ty Vincent and other doctors are, then you’re going to herx more patients than you want. So that’s my advice.

Dr. Weitz:           It’s my understanding that these are over the counteri and can be recommended by chiropractors and non-MDs as well. Isn’t that correct?

Dr. Hirani:           I’m really not sure about that because you have to check with Ty Vincent about that. With the LDA, I know you have to be an MD because you have to-

Dr. Weitz:           The LDA.

Dr. Hirani:           … order that from a compounding pharmacy. With the LDIs, it’s possible that you can get it from Ty Vincent. I don’t know if he is requiring you to be an MD. I don’t know because he never asked me for my medical license, so it’s possible.

Dr. Weitz:           Okay, excellent. So for viewers, listeners, and practitioners who would like to get a hold of you, what’s the best way for them to contact you?

Dr. Hirani:           Drhirani.com is my website. There’s a Ask Dr. Hirani a Question, so they can contact me there. So it’s D-R, Hirani, H-I-R-A-N-I dot com.

Dr. Weitz:           Great. Thank you so much, Dr. Hirani. I’d love to have you back at some point and talk about neurotherapy.

Dr. Hirani:           I would love to, I can’t wait, because these are two of my most amazing treatments on mother practice.

Dr. Weitz:           Awesome. Thank you and so nice to touch base with you again.

Dr. Hirani:           So much, Ben. It was a pleasure. Bye.

Dr. Weitz:           Bye.

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Lyme Disease with Dr. William Rawls: Rational Wellness Podcast 044
Loading
/

Dr. William Rawls talks about Lyme Disease and how to effectively treat it with Dr. Ben Weitz

[If you enjoy this podcast, please give us a positive review on Apple Podcasts, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

3:12  Dr. Rawls explains his journey from OBGYN to chronic Lyme disease patient. He was originally diagnosed with fibromyalgia.

5:58  Testing for Lyme Disease.  “When I see someone, and they have all the symptoms of Lyme Disease, I put them in the category of having Lyme Disease no matter what that testing might show.”

10:10  Dr. Rawls explained that we all have lots of microbes in us, but it is not until our immune system is disrupted that infections with Lyme Disease or Babesia or Mycoplasma cause you to become sick. Dr. Rawls explains that Lyme Disease is really a condition of immune dysfunction.

11:52  Dr. Rawls explains his seven different categories of immune system disruptors: 1. Poor diet, 2. Toxins, 3. Emotional stress, 4. Physical stress, 5. Oxidative stress, 6. Artificial radiation, 7. Microbiome dysbiosis/Leaky gut

15:43  I asked Dr. Rawls, “Do you think there’s an increase in the number of people that are contracting Lyme or is it more the case that our modern lifestyle is leading people to become sick from Lyme disease?” Dr. Rawls explained that while it is true that with global warming there are more ticks, he feels that it is more related to our modern lifestyle.

20:45  Dr. Rawls explains that antibiotics are not particularly effective for chronic infections and they are indiscriminate killers that damage our microbiome and our mitochondria.  Dr. Rawls finds herbal therapy to be more effective for chronic intracellular infections like Lyme Disease and Bartonella. Some of his favorite herbs include Andrographis, Cat’s claw, Japanese knotweed, Neem, and Mimosa pudica.

30:32  Dr. Rawls mentions that magnesium, esp. at higher dosages, tends to be problematic for patients with Lyme Disease by making symptoms worse. 

32:10 I asked Dr. Rawls if he uses detox protocols in his treatments and he said that rather than including a separate detox phase of the treatment, he regards the whole recovery from Lyme process as a form of detox. 

 

 



Dr. William Rawls is available for consultations and speaking and can be contacted at his website where you can find lots of information about Lyme Disease  https://rawlsmd.com/          You can get information about his herbal protocols at https://vitalplan.com/.

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as chiropractic work by calling the office 310-395-3111.


 

Podcast Transcripts

Dr Weitz:             This is Doctor Ben Weitz with the Rational Wellness Podcast bringing you the cutting edge information on health and nutrition from the latest scientific research, and by interviewing the top experts in the field.  Please, subscribe to the Rational Wellness Podcast on iTunes, and YouTube. Sign up for my free ebook on my website by going to drweitz.com. Let’s get started on your road to better health.  Hey, Rational Wellness podcasters, thank you so much for joining me again today, and we have such an important topic.

We are going to talk about Chronic Lyme Disease. Lyme disease is a very complicated, and confusing disease. It starts with an acute infection from a tick bite, but it can become chronic, and go on for years, and years.  The tick bite results in an infection with a corkscrew-like bacteria, typically known as Borrelia burgdorferi. Since it was first discovered, we’ve learned that there are a number of different variations, and species of Borrelia.  After this initial infection, it can create a chronic condition, and this chronic condition is really what we want to focus on, that’s really the condition that creates the most problems. It’s difficult to detect, it’s difficult to treat. Many of the patients who have Chronic Lyme Disease are not even aware that they were bitten by a tick bite. Or the exposure could’ve been years ago, and it’s not connected up to when they actually got sick.  The Centers for Disease Control estimates that there are approximately 300,000 new cases of Lyme disease per year in the US, and it seems to be increasing.

                                Our special guest today is Dr. William Rawls. He was a practicing OB-GYN for 15 years when he found himself dealing with Fibromyalgia and Lyme disease, likely from a tick bite years earlier. He discovered that antibiotics made him worse, and he found that herbs worked better, though his medical training had him very biased against the idea of using herbs. He dug into the literature about Lyme Disease, and he discovered through trial and error how to restore his health. He ended up dedicating himself to treating patients with Lyme Disease, and he wrote three books, including his latest, which is Unlocking Lyme, which is the most informative and well-written book on Lyme Disease that I have ever read. Doctor Rawls, thank you for joining us today.

Dr Rawls:             Thank you very much, it’s my pleasure.

Dr Weitz:             Can you explain what happened when you found yourself not feeling well? How did you figure out that you had Lyme Disease? How did you go about correcting yourself?

Dr Rawls:             Like most everyone with a Lyme Disease story, it was convoluted. My health gradually deteriorated, I didn’t have any memory of a tick bite, other than I got bitten by ticks almost continually when I was younger. I chose the profession of OB-GYN because it was a field of medicine that was wellness oriented, it wasn’t drug heavy, which just … it jived well with my personality.  The downside was the call. I went to a small town, and ended up taking call every second to third night. That went on for about 15 years.

Dr Weitz:             By the way, taking call means that you’re on call at a hospital if there’s an emergency.

Dr Rawls:             On call, yeah. If someone is in labor, or in the emergency room, you get called. Most of the time, virtually, every time I was on call, I was at least waking up, and a lot of times I was up all night long. That went on for 15 years. I got to the point that I couldn’t sleep when I wasn’t on call, and my body was just deteriorating.  At first, you go to your local physician, and other physicians in the community, and find that they really don’t know what’s going on. You end up with this diagnosis of fibromyalgia. I considered Lyme Disease, but I did the initial screening test and it was negative.  Because, I had all the symptoms of fibromyalgia, which are basically the same as Chronic Lyme, which are basically the same as the early stages of most Chronic Illnesses.

Dr Weitz:             What were those symptoms?

Dr Rawls:             Fatigue, feeling like you have a flu every day, aches and pains all over, weird neurological symptoms, pins and needles, burning feet, blurry vision, it just went on, and on, and on. Basically, my whole body was collapsing.  It was later after I started taking my health in my own hands that I ultimately discovered that it was, and I did have a positive test for Borrelia, but have come to know Chronic Lyme quite a bit differently than I think most people do.

Dr Weitz:             What do you think is the best way to test for Lyme, or do you think it’s even worth testing for it?

Dr Rawls:             It’s always a loaded question. Our testing right now is fair at best. Something to know about the testing is, all the labs that are doing testing for these microbes that we found to be associated with Chronic Lyme, the standard of testing is for acute infection, in other words, when it’s a brand new infection, the microbe has just entered the body, and the reaction of the immune system is strong, and the microbe levels are high. But, most everybody being tested has chronic infection, where the immune system has these responses been attenuated, and the microbe levels are really, really low.  When you look at the rate of testing an acute infection, which may be a sensitivity, or ability to find the microbe, as high as 95%, it probably drops to around 20% or less with Chronic infection.  Often, the testing is marginally valuable. When I see someone, and they have all the symptoms of Lyme Disease, I put them in the category of having Lyme Disease no matter what that testing might show. But, then you have to come around to defining what exactly is Lyme Disease.

Dr Weitz:             What do you think about Doctor Vojdani’s lab, which does the antibody testing, do you think that’s a little more accurate?

Dr Rawls:             There are two ways to test. One is you can test directly for particles of the microbe, typically DNA from the microbe, or you can test for the reaction of the body to the microbe. But in either case, when you’re looking for a chronic infection, you’re talking about very low levels of microbe, and an immune response that’s been attenuated, pushed down by the microbes themselves.  The testing becomes less, and less valuable. I think we’re going to get better, and as we do, I think what we’re going to find is there are a whole lot more forms of Borrelia than just Borrelia burgdorferi, we already know that there are about 12+ worldwide.

Dr Weitz:             12, wow.

Dr Rawls:             Probably a lot more. Then, there are all the other microbes that are associated with Lyme beyond Borrelia. As we get better testing, what we’re going to find is an awful lot of people are carrying these microbes that aren’t sick. It’s a lot more widespread than most people realize.

Dr Weitz:             Why are there always associated other microbes like babesia, and mycoplasma, why does that exist?

Dr Rawls:             Because we all have them, quite frankly. That goes beyond that basic definition of what Lyme Disease is. When you look at humans, we are wonderful microbe collectors. We start at birth, we pick up the microbiome, the collection of microbes from our mother, and we add to that throughout life.  When you look at insects like ticks, and mosquitoes, and all the other insects, and all the other ways you can get microbes, we’re constantly picking up microbes throughout our lifetime.  A high percentage of people, mycoplasma, 75% of people with Lyme have mycoplasma. Well, if you look at any general population worldwide, somewhere between a third and three quarters of any population, healthy or otherwise, will have mycoplasma.  Same is true with all these other microbes, bartonella, babesia, all of these things. All of us pick these things up, it’s not until your immune system gets disrupted that these things start to become a problem, and that’s what happened in my case. I didn’t get ill until I trashed my immune system.

Dr Weitz:             Interesting. I guess that’s why you write that Lyme Disease is really not so much an infection as a disease of immune dysfunction.

Dr Rawls:             Yeah. When I look at fibromyalgia, and Lyme Disease, and all of the chronic autoimmune type diseases, I see a lot of commonality there. I think, ultimately, we’re going to see more and more associations between most chronic illnesses and these things that I call stealth microbes. The characteristics of all the microbes that are associated with Lyme and so many of these others things are that they live inside cells, and they infect white blood cells, and through doing that, they are able to manipulate the immune system.  They are doing a couple of things. They’re pushing the immune system away from being able to take care of inner-cellular microbes. Microbes that have infected cells, they suppress that part of the immune system. But they gear up other parts of the immune system that cause this systemic inflammation, and that helps break down tissues to have access for food sources. Because that’s basically what these microbes want, is they just want nutrients to survive.

Dr Weitz:             You write in your book about seven different categories of immune system disruptors, can you go into those for us?

Dr Rawls:             Sure, yeah. That was the initial part of my change in approach. When you look at conventional medicine, we do a great job of treating acute situations. Our whole system is based on acute illness. Most drugs treat things acutely.  It wasn’t until about 1960 that we started focusing on chronic illness, and trying to find drugs that treated chronic illness, but still, if you look at it, we treat chronic illness acutely, in most cases.  It appeared to be a fundamental flaw of through instead of treating the illness, why are we not looking at it and say “Why is the patient sick? What made this person sick?” For a few things, broken leg, heart attack, stroke, that cause is very evident, but when you look at chronic illnesses, it’s less so. It’s usually a combination of things that come together.  They’re pretty obvious, I think most people can pick these things up, if you sit in a group and ask people “What do you think causes illness?” The first thing most people talk about is food. We’re eating an abysmally bad diet for humans, 200,000 years we ate forage food, and now we’re eating all these processed grain products, and it’s just not good for us, it suppresses immune function in a variety of ways.

                                Toxins, we live in a pretty toxic environment. There’s subtle toxins throughout all of our food, and air, and water. Stress, living in the modern world causes stress, really uncomfortable. Just sedentary lifestyle. We’re built to move, and we now sit in front of computers all day, and it’s just not good for us.  One that’s a little harder to define is what the effect these computers, and cellphones, and all the things that are surrounding you right now have. But there’s no doubt that they do disrupt our energy flow, and our normal energy pathways.

                                Free radicals, when we metabolize food, we generate free radicals, but inflammation itself is free radicals. Then, the microbes, we all pick up microbes and some are worse than others. People that don’t pick up Borrelia and some of the things that come with Lyme Disease are less apt to get a chronic illness, but again, I think there are lots of people out there that have these microbes but aren’t ill, because they haven’t had those other factors come together to set the stage for the immune disruption that allows these microbes to flourish.

                                In other words, I had these things in my body for years, and years, and it wasn’t until that I ate bad food, didn’t sleep for years, and years, was under constant stress with a busy, busy practice, that’s when these things started to flourish, and started to compromise my health. It wasn’t one thing.  These things are distributed throughout all the tissues in the body, it’s not like a pneumonia where you have an infection in the lung, it’s throughout your entire body. Everything breaks down. That’s what Chronic Lyme is.

Dr Weitz:             Do you think there’s an increase in the number of people that are contracting Lyme or is it more the case that our modern lifestyle is leading people to become sick from Lyme disease?

Dr Rawls:             Yeah. That’s a difficult question to answer, absolutely. There is no doubt that with global warming, there are more ticks.

Dr Weitz:             Okay, that makes sense.

Dr Rawls:             When I was studying this, I pulled studies that they were looking at well-established tick populations in the arctic that were 10 or 20 years ago, and [crosstalk 00:16:23] the tropics. Everywhere there are warm-blooded animals, there are ticks, and other biting insects.  Maybe there are more ticks, maybe ranges of ticks are changing, but I would say submit that these things have been present for a very, very long time. Looking back, historically, you can pick a lot of people, it’s interesting, I was reading on Darwin recently, and he had all these chronic symptoms throughout his lifetime. He was a guy that was definitely in the forest, in the woods, exposed to a lot of different insects, he had all symptoms of Lyme Disease, it was really interesting.  These things have been going on, it’s just that we haven’t recognized it, and our testing … you know, you look back, there’s no reference point. The testing 20 years ago, or 30 years ago, was terrible, absolutely terrible. It’s getting better, but it’s fair at best. Without a reference point, and without good testing, how do you have any idea whether the incidents of this microbe is increasing?  Plus, people are becoming more aware. People are starting to put together these symptoms, they’re starting to get tested. A lot more people are becoming aware of Lyme Disease, a lot more people are being tested. That increases the incidents artificially, who’s to say that all those people back 40, or 50 years ago didn’t have this? Honestly, my grandfather was an outdoorsman, and he had all the symptoms of Lyme Disease. But, he didn’t he had Lyme Disease back then because nobody knew what Lyme Disease was.  I think that’s, somewhat, at least at this point, an unanswerable question.

Dr Weitz:             Do you think Lyme Disease can be transmitted by anything other than a tick bite? Do you think it can be transmitted by sexual contact, or saliva, or any other vectors?

Dr Rawls:             I think it’s possible, but what you find is microbe specialize. Let’s look at two corkscrew bacteria. One is Borrelia, causes Lyme Disease, the other one is Syphilis. There are a lot of similarities between those two illnesses, and they’re both very similar microbes.  Syphilis is primarily, when that microbe evolved, it found a niche that it could be easily transmitted sexually in human populations. It specialized in that. That isn’t to say that syphilis couldn’t be transmitted by a tick, but it specialized in being concentrated in sperm, and vaginal fluids, so it would be easily transferred between humans. Basically, all these microbes want to do is transfer from one host to another.

                                Borrelia on the other hand chose ticks, there’s very good evidence that it’s been doing that for not thousands of years, but absolutely millions of years. Possibly all the way back to the dinosaurs.  Yes, it is possible that it is transmitted sexually, and it is possible that it is carried in other microbes. It has been found in mosquitoes. I’ve seen too many families that have, whole families Lyme Disease to suggest that it isn’t spread sexually or in utero.  But, it doesn’t particularly specialize in that. You don’t typically find high concentrations of Borrelia in seminal fluid or vaginal fluid. I didn’t say it can’t, it’s just if you gave it a chance, it rather work with a tick. The tick, it has a really cozy relationship that it helps the tick in the tick helps it. It’s predominantly tick borne, no doubt.

Dr Weitz:             You’ve written that you didn’t find, and you don’t find with your patients antibiotics to be particularly helpful, and you’ve found herbal therapies to be much more effective, and other nutritional protocols. Can you talk about why antibiotics are not particularly effective for Lyme? What sorts of herbal protocols you find effective?

Dr Rawls:             Sure. Yeah, we could talk about this for an hour, but I’ll condense it here. Antibiotics like most drugs, are designed for acute infections. You have someone with pneumonia, they have an extra cellular microbe, that doesn’t live inside cells, it’s consolidated in one area of the body, it’s growing very rapidly, it’s turning over generations very rapidly. That’s what antibiotics are built for. You put that person in the hospital, and they’re going to turn the corner in a day or two, and be well in a couple of weeks. 

The problem with antibiotics is that they’re indiscriminate. When you’re going to hit the fastest growing microbes the most, but the longer you use them, the more you’re going to affect all of the microbes in the body. What tends to happen is you suppress your normal, friendly flora, and you grow out pathogens in the gut.  I always look at antibiotic therapy as being a race. Are you going to kill the offending microbes before you disrupt the entire microbiome and suppress immune system functions even more?

                                Other things with antibiotics is they actually, they destroy our mitochondria, mitochondria are ancient bacteria that we incorporated into our cells eons ago. They disrupt biofilms in the colon. When we talk about biofilms, everybody’s worried about biofilms. Your immune system deals with biofilms quite well, and actually, you want to protect some biofilms. You have a biofilm in your colon that is protective, and it’s very important. Antibiotics disrupt that biofilm.

                                There’s a whole list of reasons why when you apply these things to a chronic, intra-cellular infection, it just doesn’t work as well. Because when you look at these microbes, Borrelia, mycoplasma, bartonella, all of these things, they’re intracellular, they’re growing very slowly, they’re distributed throughout tissues in the whole body.  When you hit them with antibiotics, you end up hitting your normal flora harder than you hit these microbes. Typically, the solution that most people follow is “Well, we’re not going to get them in days or weeks like with pneumonia. You’re going to have to hit them for months, or years.” You lose the race almost every time. Not to say that there aren’t people that do recover with antibiotic therapy, but I’ve seen all too many people that had squandered their life savings on expensive, intravenous antibiotic therapy just to be much, much worse than when they started.

                                The advantage of herbal therapy is that you’re talking about a whole different thing. Plant medicine, you’re talking about a spectrum of substances that the plant is producing to protect itself. The plant has to figure out the friend versus foe problem also. Plants have to deal with these threatening kinds of microbes, but they have to protect their normal flora.  One of the interesting things that I’ve found about herbs is they typically don’t disrupt the gut. But they are more suppressive. I wouldn’t use herbs to treat an acute pneumonia, but for the stealth microbes you have the suppressive effect without disrupting your normal flora, and you’re enhancing immune, you’re rebalancing immune system function at the same time. You can literally use these things for months and years.  I’ve been taking herbs almost continually for 10 years, and things just keep getting better every year. It’s a gradual thing, you do have to create long-term, but herbs, because they suppress the stealth microbes, they don’t disrupt the normal flora, and they restore normal immune function, are just a really nice choice.  

Dr Weitz:             Now, can you talk about some of your favorite herbs for Lyme Disease?

Dr Rawls:             Fortunately, there are a lot of them. Early on I happen to read a book by a guy named Stephen Buhner, who wrote Healing Lyme, it was a well-known book. I used that core protocol starting out, but then I built out beyond that.  What you find is, virtually, all herbs has some anti-microbial and immune enhancing properties. His initial protocol, the top of the list, was Andrographis, which is a really nice herb, has some really nice antiviral properties too, especially for flu, it’s probably one of the best things out there for flu.  Cat’s claw, which is from the Amazon, another great herb that was used for syphilis, so we know it has some activity against Borrelia, which is really important.  Then, we have so many other, the Japanese knotweed, sarsaparilla, but the list goes on and on. Neem is a good antimicrobial, has some really nice properties. One I’m looking at now is mimosa pudica, which is an excellent herb. The list just goes on and on.

Dr Weitz:             Is that from the mimosa tree?

Dr Rawls:             Pardon?

Dr Weitz:             Is that from the mimosa tree? Right? There’s a tree.

Dr Rawls:             Right. No, this is a mimosa plant, the leaf looks like mimosa, but it’s a ground cover. But it’s the touch-me-not plant, if you touch it, it folds its leaves up. It’s a really cool plant. Turns out that it just has some fantastic medicinal properties, a wide range of properties. There are just unlimited number of things that we can use.

Dr Weitz:             Japanese knotweed resveratrol is interesting. We use that as part of an antiaging protocol for its polyphenol properties. I never knew that it had antimicrobial effects as well.

Dr Rawls:             Well, yeah, no doubt about it. There are other places you can get resveratrol, grapes, the muscadine grape we have in North Carolina has some really nice properties. But when you look at the whole herb, Japanese knotweed, or all of the other chemicals that come in grape seed, or in grapes in general, you’re not talking about just resveratrol.

Dr Weitz:             I agree.

Dr Rawls:             Resveratrol by itself does have antimicrobial properties that has some really nice antiaging properties, but the herbs also have a full spectrum of other components that are really important. But when you talk about anti-aging, those system disruptors that I talked about, those are the things that are causing us to age.  When you look at herbs, they’re counteracting all of those things. They’re loaded with antioxidants. They balance the immune system. They balance the microbiome and suppress the stealth microbes that I think are part of all of aging and illness, in a chronic illness.   All the herbs, if you’re looking at an anti-aging protocol, it matches what we would do for Chronic Lyme almost to the tee, it’s really interesting.

Dr Weitz:             One thing I find interesting is, I deal a lot with patients with SIBO, Small Intestinal Bacterial Overgrowth, and there’s a series of herbs, antimicrobials, that we typically use for those patients, and it includes berberine, oregano and thyme oil, garlic, and those don’t seem to be effective against Lyme, I guess, because I don’t see those in the list of herbs recommended for Lyme, typically.

Dr Rawls:             Berberine and your berberine containing herbs, goldenseal, coptis, so many others. Berberine is the predominant one that I find to be top of the list for SIBO. The others that you mentioned are also excellent. But they’re not absorbed systemically as well. That’s the thing about berberine, it gets absorbed into the urinary tract, you get it into your GI tract, so it’s good for urinary things, it’s good for GI things. It’s not as good for systemic infections. But it is just exceedingly good for so many things.  Really great for balancing the gut, I think it’s better than a probiotic for balancing the microbiome in the gut.

Dr Weitz:             Interesting. You write in your book that magnesium can make Lyme symptoms worse, I thought that was kind of an interesting … I often recommend magnesium, we find a lot of patients are low in magnesium. How can magnesium be a negative for Lyme?

Dr Rawls:             That one it’s hard to answer. I’ve heard it theorized, the microbe use magnesium, and therefore if fuels the infection. I’m not sure whether I buy that or not, I’m not sure whether it causes micro imbalances in our minerals in the body, but I have noted it personally, and noted it with other people.  When I took high doses of magnesium, after a while, after I used it, my symptoms just got worse and worse until I stop the magnesium. That is really common. I’m choosy, I think a lot of people can take magnesium, probably a lot of people need magnesium, but it’s still you have to be careful with.

Dr Weitz:             Interesting. Do you ever use IV vitamins?

Dr Rawls:             I don’t personally, and I haven’t in my practice, but for somebody who’s really ill, I think there can be some benefit to get you there a little bit faster, which I think is a fairly reasonable thing to do. But glutathione and vitamin C, especially, seem to be beneficial.

Dr Weitz:             Do you use detox protocols in your treatments? We had Melanie Gisler speak at one of our meetings about Lyme Disease. She likes to include detox into her protocols.

Dr Rawls:             Yeah, I just did a webinar pretty recently on detox, and really did a deep dive on what we’re doing. My conclusion was when you look at Lyme recovery, it is detox, the whole thing. This concept of just doing this protocol, and I’m done with that, and I’ll move on to other parts of recovery, nah, it’s an initiation.  But the whole recovery process is detoxing. When you look at detox, it’s really clean food, it’s lots and lots of vegetables. But if you look for one thing that detoxes the body better than anything on the face of the earth, it’s vegetables. Lots, and lots of fresh vegetables.

                                No matter what diet you choose, I think that the golden rule for any healthy diet is it needs to be at least half vegetables, or more. Eat more vegetables than anything else. Because the vegetables are binding the toxins, pulling them out of the body, and vegetables are going to be lower in toxins than a lot of other kinds of processed foods. That’s really important.  The vegetables help enhance liver function. Then you throw in the herbs on top of that, you know, we’re talking about berberine, berberine is a really nice bile-stimulant, you got to get your liver moving. You throw some andrographis in there, which is another bile-stimulant, and really enhances liver function, and protects the liver. Throw in some milk thistle too if you like.

                                So many of our herbs are doing the things that we want to do with detoxification. Then, cleaning up air. I’m spending a lot of time studying research that I can find on negative ions, and negative ion generators, and essential oils for just cleaning up the air, making our air better, filtering water.  I don’t see detox as a thing that’s done, I think detox is something you embrace for a lifetime. A detox protocol is a way to get initiated in that, but it becomes “This is how you live your life.” You live a clean life, and that’s what enhances immune function. That is not only what’s going to help you recover from chronic illness, but it’s also going to help you slow down the processes of aging in general.

Dr Weitz:             Cool. What do you think about ozone? That’s very popular in LA for Lyme protocols, is using some form of ozone.

Dr Rawls:             Yeah, I think if you have asked me five years ago, I would say “That’s crazy. Ozone is just really toxic.” But, I’ve since come around, there has been enough literature out there, and I have been to enough lectures and really studied it enough to recognize that I think it does have value. All of these microbes are very oxygen sensitive, basically, we’re infusing high reactivity oxygen species that are free radicals. They do have a pretty strong effect on the microbes.  Of the types, you can either inject ozone, or you can run someone’s blood to a hyperbaric chamber with ozone that pushes ozone into the blood, and then back in the body, and that circulates over and over. I think it does have an effect.  Are you going to eradicate all the microbes? No, because they’re so deep in the tissues, and they’re inner-cellular, you’re not. But I think it has value.  

Here’s the thing; I think it’s important to put in perspective. If I have someone that is doing all the things that they need to do to rebuild their immune system, they’ve cleaned up their diet, they’ve cleaned up their lifestyle, they’re living a clean lifestyle, they’re embracing the herbs, and they’re not quite getting there, or they want to get there a little faster. You know, their immune system is on the rebound. Then ozone can be beneficial. It might be what I call a heroic therapy that might get them there a little bit quicker.

                                Whereas, I’ve met all too many people that aren’t doing those things, and are going for ozone, and they might feel better for a week or two, or a month. But, then they’re right back where they started. Then, they’re doing it again, and again.  It’s expensive, and every time you use it, every time you use it, you’re going to do more damage to your blood vessels. There’s a certain amount of toxicity with it. You’ve got to be really frugal in that use.  The message with ozone is do all the things that you need to do first to rebuild your immune system, then if you want to get there quicker, or if it’s not quite getting all the way there, then I think ozone is a consideration. But, as a stand alone therapy, I don’t think that’s a good choice.

Dr Weitz:             Great. Great. This was really good information Doctor Rawls. Is there any final thoughts you’d like to tell our listeners and viewers?

Dr Rawls:             Let’s see. The big thing is, when you look at Chronic Lyme Disease, I think you’re fundamentally looking at a model of all chronic illness. More and more, as I searched the literature, I find that we’ve lost connections to our ancient past. The food we’re eating is abnormal, our world is full of toxins, our microbiome is less diverse, and it contains more pathogens than it ever has. Herbs are part of the missing link.

                                I’ve been thinking about it, it was very differently as of late. I’ve just rewrote our diet guide, and you study, and humans ate foraged food for 200,000 years. It wasn’t until about 10,000 years ago that we started adopting grains. Really, most intensely 100 years ago.  That foraged food was roots, and leaves, and stems, and bark off of trees, it was anything that might have some calories. Humans ate a lot of it. It was very bitter. When you look at the concept of digestion, bitter is really, that’s what initiates our digestion, because all the food was bitter for several hundred thousand years.  But all of that food was loaded with phytochemicals, these substances that we find in herbs. Those things are typically very bitter, they don’t taste good. We selectively bred all of those things out of our food now.  Our food tastes better, it’s higher in carbohydrate, it doesn’t have the bitterness typically, and we like it better. But it’s missing that spectrum of phytochemicals. The only way you can really get it back now is herbs, because herbs have been cultivated to actually enhance the presence of those things.  I’m starting to see herbs not as something you do therapeutically, but as a true deficiency, something that is really, really missing. When you look at paleo diets, and other things, people are eating a paleo diet because they’re not foraging food out in the woods, and they’re still missing those ancient phytochemicals that are so important for our health.  Whether you’re talking about treating Lyme disease, or antiaging, or virtually anything else, I see herbs as really an essential component of what people should be doing.

Dr Weitz:             That’s a great clinical pearl. How can viewers get a hold of you?

Dr Rawls:             We’ve got an informational website called rawlsmd.com, I got a lot of information about Lyme disease, connections to the book, and that sort of thing. Then, we also have a website called Vital Plan, that we do carry some products and things on that. Either way, they can find lots of other information, and yeah, it’s important.

Dr Weitz:             Are you available for consultations?

Dr Rawls:             I am. I do do consultations. I’m spending more of my time just writing, though, at this point, because I can reach so many more people writing, and doing webinars, and doing shows like this. We can connect, and I can get this information out there in a bigger way.

Dr Weitz:             That’s great. Thank you, Doctor Rawls.

Dr Rawls:             Thank you very much for having me, it was a real pleasure.

Dr Weitz:             Excellent, I enjoyed it too.

 

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Weight Loss with Dr. Philip Goglia: Rational Wellness Podcast 042
Loading
/

Dr. Philip Goglia speaks about how to help his clients lose weight with Dr. Ben Weitz. 

[If you enjoy this podcast, please give us a positive review on Itunes, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

1:48  Dr. Goglia explains how he increases compliance among his clients by asking clients who don’t follow their food program to “walk the pig.” He actually has a large plastic pig with wheels and a leash around it that he asks clients to bring home if they have not been following their meal plan. This increases his clients’ compliance with their weight loss program. 

3:56  Philip briefly explained his metabolic typing concept that allows him to determine the best nutrition program for each person.  Philip explained that this program is both proven by science and tested in practice by him and others since the 1980s. He says that when he was studying nutrition at Duke University they discovered three metabolic structures: clients who are efficient at digesting fats and proteins, clients who are efficient at eating carbohydrates, and duel metabolizers. This will also be indicated by their lipid profile that he tests in office. Once you are eating an appropriate macronutrient pattern for how your body works, you’ll find that you have more energy, you’ll lose weight, and you’ll be healthier.  And this food program will be sustainable over time. If not, you’re on the grapefruit and milk diet and you might lose 10 lbs but you’ll just gain it back later. Also, don’t be fooled by weight loss. If you start almost any new food program, because your calories were mismatched and all over the place and because your caloric heat patterns are stabilized, you’ll lose 10 lbs.  But does this program suit your chemical structure–that is the big question?  According to Dr. Goglia, if you are on the wrong food program for your metabolic type, your weight loss will stop. At this point, clients are inclined to think that they need to exercise more and eat less. But calories are a measure of heat energy and your metabolism is a measure of that heat. If you don’t create enough heat, you can’t burn fat. If you exercise more, you break down muscle tissue. If you exercise more, you need to eat more to support new muscular density. The more you eat, the more heat you generate and more bodyfat you lose. Think about taking up less space in the room. Weigh as much as you can, taking up less room in the room. Muscle is heavy and dense.

11:20  Dr. Goglia explained that you need to keep in mind that working out, going to the gym is not building you up. It breaks you down. It is when you rest and sleep and when you eat protein that you use to build muscle.

12:44  Philip discusses the proper diet and explains that 70% of the population is fat and protein efficient and have insulin resistance and will do better on a high protein, high fat, managed carbohydrate program. We have all these low carb programs today like Paleo, South Beach, Bullet Proof, and Ketogenic, but Dr. Atkins was very successful years ago with a low carb program and his program is really being rebranded without giving him credit. Dr. Atkins was the one who said you are not going to run a marathon at night and you don’t need a bunch of carbs with dinner. These carbs will just prevent your body from going into deep REM sleep, so you’ll wake up tired and craving carbs again. Your dinner should be your biggest protein meal to rebuild the muscle you have broken down.

15:16 I asked Dr. Goglia what his recommendations are for types of exercise for weight loss?  Philip explained that he will often recommend that they start by focusing on changing their diet and just continue with their current exercise regimen. Once they are eating properly, then we can strategically modify their exercise to help them accomplish their goals. 

 



Dr. Philip Goglia is available to see clients by contacting his office at 310.392.4080 or through his website http://www.pfcnutrition.com/

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure, as well as chiropractic work, by calling the office 310-395-3111.

 

Improve Your Thyroid Function With Proper Nutritional Supplementation 
Approximately .4% of people in the United States have hypothyroidism, an under-functioning thyroid gland, and an additional 4-8% of people in the US have a mild form of hypothyroidism known as subclinical hypothyroidism, meaning that they have an elevated Thyroid Stimulating Hormone but don’t have significant symptoms of low thyroid. The most common symptoms of hypothyroidism are fatigue, hair loss, dry skin, feeling cold, poor memory, brain fog, constipation, and weight gain. When screening for thyroid, the Thyroid Stimulating Hormone (TSH) is most commonly tested, however, we find it helpful to also run free T3, free T4, and the thyroid antibodies, TPO and TG. Over 90% of patients in the US with hypothyroid have autoimmune hypothyroid, referred to as Hashimoto’s Thyroiditis, so we find it helpful to run the thyroid antibodies to see what level of autoimmune disease is present. If autoimmune disease is present, it is important to try to discover some of the triggers and causes of of it and not just take thyroid hormone and forget about the cause of the problem.
 

Studies show that there are a group of nutrients that are important for the proper functioning of the thyroid gland, including iodine, selenium, zinc, iron, vitamin D, magnesium, and Coenzyme Q10. Some of these nutrients are important for the production of thyroid hormone as well as for the conversion of the inactive T4 thyroid hormone produced by the thyroid into the active T3 form mostly in the peripheral tissues, especially in the liver, gut, skeletal muscle, and the brain, but also in the thyroid gland itself. There are a number of triggers that can set off or exacerbate autoimmune disease, including the nutrient deficiencies just mentioned. There are other factors that are important for thyroid health and which can be triggers for thyroid autoimmune disease (Hashimoto’s), including adrenal status (esp. if cortisol levels are too low or too high), chronic infections, leaky or unhealthy  gut, heavy metals and other toxins, including flouride, chlorine, and bromide, estrogen fluctuations, PCOS, imbalances of the TH1/TH2 immune system, as well as a number of prescription drugs. Medications that can interfere with thyroid function and T4 to T3 conversion include the following:

               1.  antibiotics & antifungals (i.e. sulfonamides, rifampin, keoconazole),
               2.  anti-diabetics (Orinase, Diabinese),
               3.  diuretics (Lasix),
               4.  stimulants (amphetamines),
               5.  cholesterol lowering medications (Colestid, Atromid, LoCholest, Questran, etc.),
               6.  anti-arrhythmia medications (Cordarone, Inderal, Propanolol, Regitine, etc.),
               7.  hormone replacement (Premarin, anabolic steroids, growth hormone, etc.),
               8.  pain medication (morphine, Kadian, MS Contin, etc.),
               9.  antacids (aluminum hydroxides like Mylanta, etc.) and
               10. psychoactive medications (Lithium, Thorazine, etc.).
 

You can see Dr. Weitz for a comprehensive nutrition consultation and after going through a detailed history with him, he can prescribe recommended laboratory testing to try to help determine some of the underlying triggers for your autoimmune thyroid disorder. These could include functional stool analysis, other gastrointestinal testing, such as SIBO breath testing and/or testing for H. pylori, provocative urine or serum testing for heavy metals or other toxins, testing for chronic viral infections, nutrition testing, hormone testing, or organic acid urine testing.

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
The Microbiota, Autoimmune Disease, and Stool Analysis with Dr. David Brady: Rational Wellness Podcast 041
Loading
/

Dr. David Brady discusses the microbiota, autoimmune diseases, and stool analysis with Dr. Ben Weitz.

[If you enjoy this podcast, please give us a positive review on Itunes, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

4:53  I mentioned that I had just reread Dr. Brady’s 2013 excellent and important paper clearly laying out some of the connections between the microbiota and autoimmune diseases, Molecular Mimicry, the Hygiene Hypothesis, Stealth Infections and Other Examples of Disconnect between Medical Research and the Practice of Clinical Medicine in Autoimmune Diseasehttps://scirp.org/journal/PaperInformation.aspx?PaperID=27948  I consider this mandatory reading for anyone in Functional Medicine. 

7:10  Functional Medicine doctors might look to the gut and order stool testing for patients with autoimmune disease but this makes no sense to conventional medicine. But Dr. Brady pointed out that medical research is in line with the Functional Medicine approach, as there are many studies linking gut dysbiosis and specific gut pathogens with specific autoimmune diseases. Here is a slide that Dr. Brady provided me on this: 

10:10  The Importance of the Microbiota and the Microbiome.  Dr. Brady discusses the need to look at ourselves and our state of health in what is called the super organismal context, meaning it’s not just us and our cells, and our biochemistry, and our physiology. It’s also all of those other organisms that share our experience. The organisms that live on us, in us, through the gastrointestinal track. Research is really supporting the importance of the microbiota and the links with chronic diseases, like autoimmune conditions.

13:02  Discussion of Dysbiosis.  Dr. Brady explained that dysbiosis is a term that came from EE Metchnikoff and it refers to an imbalance of the bacteria in the gut. You don’t necessarily have a parasite or pathogen. You get an overgrowth of opportunistic organisms, which when overgrown become problematic, referred to as potentially pathogens. It’s aligned more with a state of illness or lack of optimal wellness of the host.

15:58  I asked why we might have a pathogenic bacteria that comes in through our gut and it becomes a permanent resident that we have trouble erradicating, but when we consume healthy probiotics they are only temporary residents?  Dr. Brady explained that this is not necessarily the case. Most pathogens fortunately pass through and don’t actually take up residence in our gut. And when you look at beneficial probiotics, like lactobacillus, bifidobacteria, they make up a small minority of the GI microbiota in its totality, which is mainly made up of anaerobic bacteria, not aerobic or facultative organisms. These beneficial organisms have an incredibly beneficial effect even though you are not really reseeding the gut, which a lot of practitioners make the mistake of thinking that they can if they just take enough billions of probiotics. They are more like pixie dust. They change cytokine expression. They are more like messengers than foot soldiers.

20:27  We discussed the link between digestive health and autoimmune diseases, including the hygiene hypothesis.  Dr. Brady pointed out that he laid out some of these arguments in his paper in the Open Journal of Rheumatology and Autoimmune Disorders noted above and also in a similar paper that he wrote in the Townsend Letter   http://www.townsendletter.com/June2012/autoimmune0612.html   Our modern methods of sanitation and hygiene have reduced our exposure to infectious diseases in order to reduce cholera, typhoid, dysentery and and similar serious infections that result from drinking contaminated water. But we have taken it too far by the overuse of antibiotic soaps and wipes and the frequent use of antibiotics and not letting your infants play in the dirt and put things in their mouths. This reduces our exposure to microbes in our environment and prevents us from developing the tolerance that we should have and our immune system may overreact to organisms that are not much of a threat. We’re left instead with an immune system that’s stuck in an overaggressive stance, and more likely to crossover with subtle differences between what it’s trying to actually attack, which would be a microbe, and a host tissue, like a joint, or like a thyroid gland.

23:30  Dr. Brady discussed how helminth therapy (worms) can help with immune system regulation.  

28:29  We discussed the best way to test the microbiota with proper stool testing, including using the GI Map test through Diagnostic Solutions that Dr. Brady is has helped to develop. Dr. Brady explained that GI Map uses a more sophisticated quantitative PCR, polymerase chain reaction, method of detecting both pathogenic and also opportunistic microbes that may have overgrown. Dr. Brady explained that this is a clinical test that can enable you to determine if a microbe that is found is clinically relevant and needs to be treated, including if it may result in autoimmune diseases. This should be distinguished from testing that uses next-gen sequencing like a uBiome test, which was not meant for making clinical decisions on patients at the point of clinical care.  

 



Dr. David Brady can be contacted at his website https://drdavidbrady.com/ You can check out the site for The Fibrofix book that he wrote at https://www.fibrofix.com/ You can get information on the GI Map stool test from Diagnostic Solutions at https://www.diagnosticsolutionslab.com/

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as chiropractic work by calling the office 310-395-3111.


 

Podcast Transcripts

Dr. Weitz:            This is Dr. Ben Weitz, with the Rational Wellness Podcast. Bringing you the cutting edge information on health and nutrition from the latest scientific research and by interviewing the top experts in the field. Please subscribe to the Rational Wellness Podcast at iTunes and YouTube and sign up for my free ebook on my website, by going to drweitz.com. Let’s get started on your road to better health.  Hey, Rational Wellness podcasters, thank you so much for joining me again today, and we’ve got a very interesting topic.

We are going to talk about the microbiota, autoimmune diseases and stool testing, with a very special guest, Dr. David Brady. The microbiota is a community of commensal or good bacteria, symbiotic, neutral and pathogenic bad bacteria. This microbiome has been found in every multi-cellular organism from plants to animals that has ever been studied. The microbiota includes, bacteria, archaea, protozoans, fungi and viruses. The microbiota is crucial for the health of the host, esp. for the immune system, hormone production, metabolism and a host of other important health processes.  The term, the microbiome is often used interchangeably with microbiota, even though technically microbiome refers to the genetic makeup of these microorganisms. The main place that the microbiota exists in humans is along the digestive tract. But these microorganisms also live in the vagina, along the urinary tract, the lungs, the mouth, the eye, on the skin, lining virtually every mucous membrane in the body. In fact, almost everywhere. Some would also argue that worms that have lived in the bodies of humans for thousands of years, are also important organisms that contribute to this community of microorganisms, and are important for the health of the host. Listen to episode 38 of this Rational Wellness Podcast where I interviewed Dr. William Parker about worm therapy.

                                Now, when it comes to autoimmune disease we’ve been seeing a huge increase in the rate of autoimmune diseases, especially in the US and other developed countries in the last 10 to 20 years. Now, autoimmune diseases are diseases in which our immune system, which is designed to kill outside pathogens starts focusing its attention inwards, and starts attacking our own tissues. This is believed to be partially related to the decline of bacterial diversity in the microbiota in the gut, and the breakdown of the gut lining, often referred to as leaky gut. There are now over 80 recognized autoimmune diseases including Hashimoto’s hypothyroidism, celiac disease, type I diabetes, inflammatory bowel disease, MS, psoriasis, lupus, rheumatoid arthritis. Properly analyzing our microbiota with accurate stool testing can potentially enable us to determine whether we have a healthy microbiota. It may enable us to intervene and potentially prevent or reverse autoimmune diseases through changes in diet, lifestyle and nutritional supplementation.

                                In order to help sort this out, I’m thrilled that we’re being joined today by Dr. David Brady, an internationally known speaker, Doctor of Chiropractic, Naturopathic physician. He’s also a Professor at the University of Bridgeport. He’s the Chief Medical Officer for both Designs for Health, and Diagnostic Solution Labs. Dr. Brady is a prolific writer, having published a number of scientific papers, contributed chapters to various text books, and he’s also written several books, including his latest, The Fibro Fix, published in 2016. Dr. Brady, thank you for joining me today.

Dr. Brady:            Hey, thank you for having me. It’s a pleasure to be on your podcast.

Dr. Weitz:            Excellent. So, before we get started with the questions, I just wanted to say, this morning while I was eating breakfast, I just reread your 2013 article from the Open Journal of Rheumatology and Autoimmune Diseases on “Molecular Mimicry, the Hygiene Hypothesis, Stealth Infections and Other Examples of Disconnect between Medical Research and the Practice of Clinical Medicine in Autoimmune Disease”. I feel like this is such an important paper. It so clearly lays out the link between the microbiota and autoimmune diseases. For me, this is one of those seminal papers in Functional Medicine, along with Dr. Fasano’s Scientific American paper on leaky gut, and some of Dr. Vojdani’s papers, that I strongly encourage every Functional Medicine practitioner and even laypersons interested in a functional approach to autoimmune diseases, to read this paper. And so, on behalf of the Functional Medicine community, Dr. Brady, I thank you for your contributions to our profession.

Dr. Brady:            Well, thanks for those nice comments. I’m sorry to ruin your breakfast, but I’m very happy to be included in that prestigious list of colleagues that you threw me into. I’m not sure I deserve that, but thank you anyway. It was just me trying to get some of these concepts out there into the conventional medical literature, which we’ve always held true for my whole career in Functional Medicine, which is over 25 years. These concepts are nothing new to us in Functional Medicine, that the ecology of the gut is of prime importance to the over health of the organism. That it’s really the place where the meter, the setpoint, the balance of the immune system in general starts, is with mucosal immunity in that really quite complex and potentially full of toxins and antigenic material in the GI lumen. It was really getting some of those overarching concepts out to colleagues that may not be familiar with the way we deal with autoimmunity and we deal with chronic disease even.

Dr. Weitz:            Yeah. I imagine that a lot of the conventional medical doctors, if somebody went to a Functional Medical practitioner and was concerned about autoimmune disease and ordered a stool test, they’d say, what are you doing? Are you out of your mind? What does that have to do with anything.

Dr. Brady:            Yeah. It’s amazing. Medical research is right in line with Functional Medicine. What they’re looking at right now in the fields of immunology, in the fields of autoimmune disease and rheumatology, and gastroenterology, and right on down the line is really in harmony with what we’ve understood in Functional Medicine for a longtime. They’re pushing the boundaries of the granularity at which we understand it and how all the dominoes fall and how all the underlining mechanisms, and making new associations between aberrant patterns, let’s say, in the GI health area or the microbiota, and specific chronic disease including autoimmune diseases, but really we’re kind of talking the same … We’re singing the same tune, but that’s not the case when you cross over into clinical medicine.

                As you said, if someone with an autoimmune disease goes to a rheumatologist, let’s say a classic rheumatology managed disorder like rheumatoid arthritis, they’re highly unlikely to have any attention paid to their GI microbiota, or their gastrointestinal environment, or the health of their GI mucosa. Getting a stool analysis, they don’t do that. That’s what the gastroenterologist does. The problem is, the gastroenterologist doesn’t do a stool analysis for those things. They don’t do any work-up in autoimmune disease. When they do, do a stool analysis, it’s a very limited stool analysis that’s really meant to look for pathogenic disorders that cause diarrhea or maybe fueling an inflammatory bowel disease in some cases. Even that is generally not done.

                                There’s really a disconnect right now between conventional medical research in the conventional Western paradigm, and the practice of medicine. They really don’t connect very well. I really do think that the current research and the threads of it and where it’s going really harmonizes more with the Functional Medicine approach than it does with the conventional medical approach.

Dr. Weitz:            Can you explain the important of the microbiota and why it plays an important role in our overall health, as well as with the link with autoimmune diseases?

Dr. Brady:            Yeah. From a 30,000 foot sort of overarching kind of concept, I will try to do that. For most of Western Medicine’s history, we’ve looked at the human condition from the standpoint of our own physiology, our own biochemistry, our own metabolites, and things like that. But, we really have just now begun to break out of that very reductionist, myopic way of looking at ourselves. We need to look at ourselves and our state of health in what is called the super organismal context, meaning it’s not just us and our cells, and our biochemistry, and our physiology. It’s also all of those other organisms that share our experience. The organisms that live on us, in us, through the gastrointestinal track. We know that they are roughly equivalent to us as far as number of organisms to number of cells in our body. We know that they house many more genes than we do, probably 100 times or more, more genetic material than we do. They genes talk to our genes. We have to deal with and process and react to their metabolites, the things that they express on their surface. It’s really a community. We think that we carry around these bugs, and maybe they’re carrying around us when you look at the numbers. When we look at our overall state of health or dis health, or illness we have to factor in all of those components, not just ourselves.

                                Finally, that’s beginning to happen. It’s with the microbiome project and the study of the microbiota in general. As you correctly pointed out and most practitioners don’t understand the nuance there. The microbiota are the actual organisms, their phylum, their genus, their species, that are on us, in us, around us. Where the microbiome is all of the genetic material of those organisms plus all of the metabolites that they’re producing. It’s really more, when we look at the microbiome, we’re looking at not what bugs are present, but what is their overall impact on our condition. They are slightly different, but usually they’re used interchangeably. It is true that we have a tremendous amount of organisms living on our skin, living in our lungs, any mucous membrane, but the most complex environment is the microbiota, the portion of the microbiota that has been most firmly linked to not only the association, but now the genesis of specific chronic diseases, and nothing more closely connected or the dots most conveniently connected than in autoimmune disease than the GI microbiota.  All those bugs that live in the gut are of prime importance and it’s probably along with specific immune modulating antibody drugs if you will, in onco therapy, that and the microbiota and the microbiome are the hottest areas of research in the Western Medical paradigm, by far.

Dr. Weitz:            You use the term dysbiosis is some of your writings. Can you explain what that means and what it’s importance is?

Dr. Brady:            Yeah. It’s actually quite an old term that has had a reemergence with this sort of burgeoning microbiota research and understanding of why these bugs are so important in the gut. But, it was originally termed I believe, by E. E. Metchnikoff, who is a Russian zoologist and physiologist who is known to have coined the term, orthobiosis and dysbiosis. Orthobiosis, ortho meaning normal, biosis the microbes that live in the gut. So, orthobiosis is a healthy beneficial balance of microbes in the gut, that would be aligned with a healthy state of the organism. Where dysbiosis is where there is some sort of aberrant pattern. Things are not quite in the right balance. It’s not necessarily a state where there’s pathogenic infection that would cause acute fulminating diarrhea or some specific acute disease state, but dysbiosis is when things are just not right. There’s overgrowth of opportunistic organisms of various classes. It’s aligned more with a state of illness or lack of optimal wellness of the host.

                                Of course Metchnikoff is the father of probiotic therapy in the modern western paradigm, after he observed mainly populations, which we would now call a blue zone, in Bulgaria who were living high up in the mountains. They were living to very advanced ages for the time, and they were living very healthfully into those advanced ages. He wanted to know what was different about them. They lived in a very nice environment up in the mountains. They never retired. They kept working. They were very active. They had a good social network. All the things that we understand now about the blue zones. But what he really found striking is that they tended to use the milk, or the dairy from cows that were free-range feeding on the local vegetation in the mountains. They were culturing it and making what we would now call like a yogurt or a cultured dairy product from it, a kiefer, a yogurt, cheeses, things like that. They were getting a high intake of these organisms that were used to ferment the dairy. Now we know that strain is lactobacillus bulgaricus. Right? Because of Bulgaria, from that community. So he was really the father of probiotic therapy and obviously a real hero of Functional Medicine.

Dr. Weitz:            Isn’t it interesting how when we consume bacteria from yogurt, or if we get some pathogenic bacteria that enters our GI tract, it ends up populating our microbiome, or microbiotic? But, when we take probiotic supplements, apparently they’re only temporary residents there. Do we know why that is? Why is it that if a bacteria, especially a pathogenic bacteria comes into our system through our gut, all of a sudden becomes a permanent resident, whereas we take these healthy probiotics and they only become temporary visitors.

Dr. Brady:            Well, I’m not sure that’s always accurate.

Dr. Weitz:            Oh, okay.

Dr. Brady:            I think it depends on the state of the GI environment in that host. Certainly we’re exposed to pathogens transiting our GI tract all the time in food mass and things like that. They probably don’t setup more than they do. It depends on the virulence of the specific pathogen. Some of the are really nasty critters and if we get almost any exposure to them, even a robust host would be very likely to fall ill. But, we’re getting exposure to lots of organisms that we would not want to set up and colonize our GI environment all the time, and they don’t.

                                Conversely, the beneficial organisms, some of them colonize, some of them don’t. They can colonize from a good quality probiotics, or cultured or fermentable foods, or not. I think in both cases, I think it’s really host-dependent than it even is what the actual source of the environmental seeding of the gut is. But, you mentioned the pathogens might be more likely to take hold than a beneficial organism. Why might that be the case? Well, pathogens are pathogens for a reason. They’re very virulent. They’re aggressive. They’re very robust, so they can cause significant disease, where things that we would consider commensal or beneficial organisms don’t have that dramatic effect on us. Quite frankly, they’re extremely outnumbered.

                                When you look at things like beneficial probiotics, like lactobacillus, bifidobacteria, they make up a small minority of the GI microbiota in its totality, which is mainly made up of anaerobic bacteria, not aerobic or facultative organisms. But, it’s interesting, those beneficial or commensal organisms, they are very powerful. They have tremendous clinical effects as we know from the research studies, and as we know from clinically utilizing them even though they don’t represent much of the population in the gut. They have effects that are far more powerful and reaching than their numbers suggest. That is sort of a pet peeve of mine. I think even in functional medicine, in nutritional medicine, and integrative medicine, I think practitioners still make the mistake of thinking of probiotics and probiotic therapy as a numbers game. That you’re going to fundamentally reseed the gut and change the numerical arrangement of the person’s gut, and we know that that doesn’t occur, from serial assessments with molecular stool analysis.

                                You can change it temporarily but you don’t change it long term, numerically. But that doesn’t mean that you don’t have profound clinical effects, because Stig Bengmark, one of the world’s experts in probiotics for instance, talks about probiotics as pixie dust. Right? It’s not a matter of how much. It’s a matter that you actually introduced the organism and the peptides associated with it, and the metabolites associated with it. It’s actually talking to the GI or what we would call the enteric nervous system, but also the enteric immune system. That it’s actually changing cytokine expression. It’s changing mucosal immunology by virtue as being a messenger more than a foot soldier, if that makes sense.

Dr. Weitz:            Sure. It’s about communication.

Dr. Brady:            Yeah, exactly.

Dr. Weitz:            You often speak about the links between digestive, or gastrointestinal health and autoimmune diseases, including what is known as the hygiene hypothesis. Dr. Parker, who I interviewed a few weeks ago, he uses an analogy of leaving your teenager home alone with nothing to do. He or she will often get into trouble. Can you explain what the hygiene hypothesis is and how this contributes to autoimmune diseases?

Dr. Brady:            Yeah. There’s a couple of major thematic things that you need to understand in the modern autoimmune epidemic. I do try to go through them one at a time in that paper that you mentioned in the open, Journal of Rheumatology and Autoimmune Disorders, and also in a similar paper that I had in the Townsend Letter. The hygiene hypothesis is pretty simple. It just basically says that, in the western industrialized countries, we’ve cleaned our environment up so much, and some would argue with that because they think, what about all the toxins. We’re talking more from an exposure to microbe standpoint. The way we’ve cleaned it up is basically with modern hygienic water treatment, water supplies to large populations. We’re no longer in a village taking water out of a stream, that another village a couple miles up was going to the bathroom in.

                                It’s not that kind of environment anymore. We don’t live in caves. We don’t live on dirt floors. We live in houses. We use antibiotics. These days, a lot of mothers unfortunately are scrubbing their young children with antibiotic triclosan laden soap every ten minutes because they’re germaphobic. They won’t let them crawl on the ground. They won’t let them put something in their mouth that was on the ground. Really that’s part of … Infants have that oral phase where they’re putting things in their mouth all the time, purposely to get exposure to their environment, to learn to have some level of tolerance to the microbes we share our planet with and learn how to react appropriately. To have the right setpoint of surveillance, where if we’re exposed to something that could really do us harm, like a pathogen that we would mount a robust reaction, appropriately. But that if it is other organisms that really aren’t that much of a threat, that we don’t freakout and overreact to them.

                                Part of that learning process, when the immune system is young and learning to size up their environment, is to have exposure to a larger diversity of different types of organisms. We’ve taken away that exposure to a large degree, and we’re left instead with an immune system that’s stuck in an overaggressive stance, and more likely to crossover with subtle differences between what it’s trying to actually attack, which would be a microbe, and a host tissue, like a joint, or like a thyroid gland.

                                It’s interesting you brought up helminth through worm therapy. One of the things we’ve eliminated most dramatically compared to our ancestors even 100 years or more ago, is helminths, or worms. Worms have been in our intestines for the whole time we’ve been on the planet essentially. We’ve radically changed the landscape when it comes to helminths in the last 100 years, certainly in the last 50 years, in particular in the western industrialized countries, where we really don’t have nearly as many worms or helminths in, let’s say, young childrens’ intestinal tracks. Those helminths, it’s very interesting. In order to survive and be symbiotic with us, they put out different chemical messengers that actually down-regulate our immune response. The body’s response to that is to up-regulate. It’s reaction to try to kind of find this homeostatic balance. We kind of meet in the middle, if you will.

                                But if you very suddenly in an evolutionary context take away the helminths that are suppressing the immune system, the body’s set point then is left to hobbit in too aggressive of a stance. With that theory there were certain researchers that talked about using maybe helminths as therapy. Of course, they observed populations in what we would consider underdeveloped countries where these helminth infections, round worms and things like that, are extremely common. It was probably most observed in Laos, in Vietnam, and stuff like that, and westerners were in there in different interventions as we know. They did observe that the children there had no allergies, no atopy, they didn’t have hay fever. They didn’t have dermatitis. They had none of that kind of stuff until they started treating them for the worms. When they started giving them anti-helminthic, antiparasitic medication, all of sudden those pediatric populations started developing those disorders like we see in western children. That provided further connect the dots kind of information.

                                Joel Weinstock, who is a famous medical physician and researcher, did most of this work seminally at the University of Iowa, but now I believe he’s at Tuft’s in Massachusetts for quite a longtime. He did work with trichuris, or pig whipworm, in treating inflammatory bowel disease, like ulcerative colitis and Crohn’s disease, to significant success in that there’s actually helminth-based drug therapy for inflammatory bowel disease in Europe. The drug is call OvaMed, there. It’s in, I think, phase three trials here in the US, but not approved to date.

Dr. Weitz:            Interesting. So, they’re actually using helminths? Is that what it is?

Dr. Brady:            Yes. A lot of integrative or functional medicine practitioners use helminth therapy sort of in an off label way. They’re not a drug, per se, but it’s called h.diminuta, which some people call it, rat tapeworm. It’s not a tapeworm. It’s a helminth, or roundworm, actually. It’s really a beetle derived, or an insect derived helminth that is then consumed by rodents when they eat the insects, and then it can inhabit their GI microbiota. But, it’s a benign helminth that if you give it to the human host, it will setup there. It will exert the beneficial immune modulatory effects of a helminth, but that if you stop giving it over a time, it goes away. It will not sustain over long periods of time in the human host unless you keep reseeding it.

                                That’s one of the reasons why Weinstock used trichomatous, because for the same reason that roundworm can affect positive changes associated with helminths, but you have to give it continuously. So, if you do give it as therapy, you don’t then have to go eradicate it with another therapeutic agent should you want to get rid of it in that subject.

Dr. Weitz:            Now, it’s my understanding that at the present time, helminths are not approved by the FDA, so how would one of your patients get a helminth?

Dr. Brady:            Well, there are some practitioners who use them.

Dr. Weitz:            Can they be legally administered?

Dr. Brady:            I don’t know, technically. It’s not approved as a drug. They’re not being used as a drug, per se, for specific disease process, but they can be accessed, I believe online. I have patients coming in that are using them, and they are getting them, but they’re not technically approved in the US, no.

Dr. Weitz:            Right. Okay. Interesting. I think the human hookworm is another one that’s being used for certain therapies. So, let’s see. What are some of the best ways to analyze the gastrointestinal system? I understand you’re involved with Diagnostics Solutions, GI-Maps is your stool test. So, a lot of us Functional Medicine practitioners have been using stool testing to try and analyze microbiota. My limited understanding of stool testing is, a number of years ago we started using the GI Effects stool test, which was a genetic based test. Genova bought it, and then at some point, I remember going to a seminar that was put on by Doctors Data, and some paper came out criticizing genetic-based stool testing, and saying that there were problems with it. As I understood it, one of the issues with it is if you’re detecting the genetic basis, of let’s say, a parasite, it could be a parasite that’s not really there. So, they were touting their culture-based stool testing.

                                Genova then seemed to have modified the GI Effects and started using culture again, for parasites instead of pcr genetic testing. A number of the practitioners that I know in the Functional Medicine community were not happy with that test anymore. They felt like it wasn’t picking up things that like, parasites and other pathogens that they had seen on the GI Effects and they were able to eradicate and help their patients. Now they felt like this test wasn’t finding some of those. It’s my impression that your GI-Maps test is stepping in to help out using a more sophisticated type of genetic testing to help us find what’s going on in the gut. Is that right?

Dr. Brady:            Yeah. Well, that’s a long story and I’m going to probably differ from getting involved in the internal squabbles and politics between the various commercial interests in companies, but I can say that I’ve been doing stool analysis in my clinical management of patients and research for 25 years plus. Once upon a time, the only thing we had was culture-based old school microbiology-based testing, because that’s all we had. It was really before PCR was readily accessible, certainly by clinicians.

Dr. Weitz:            And by the way, PCR is what?

Dr. Brady:          Polymerase chain reaction. It’s what’s used to amplify DNA to be able to do a lot of the molecular or DNA-based technologies that we see today that have transitioned from research to actually clinical tests. But basically, here’s the reality. Molecular is where it’s at. A lab that does a microbial or culture-based technology claiming that molecular is not the way to go and we should do culture-based methodology, is like someone driving by on Main Street in a modern US city, in a horse and buggy, yelling that we should not use cars. This is a better mode of transportation. That’s how absurd it is.  This is based on one study, with about 30 samples, funded by that lab and it was directly comparing to another lab who is a competitor of theirs who was using a test that was developed in-house with a quasi-molecular methodology, which was not a developed methodology by a major bioscience company, and had a valid third party validated. In many cases these platforms are FDA cleared for various uses. That’s not what this was. This was the first attempt in the Functional Medicine space, many years ago at a molecular stool technology, and the first attempt was at Metametrix Clinical Laboratories. They did it for all the right reasons. I applaud them for the first attempt. For whatever reasons they decided not to use one of the already developed and vetted out by very large bio companies technology, they decided to develop their own methodology, in-house. I don’t know what their exact reasons for that was. Sometimes that’s done for reasons of developing protected intellectual property rights and things like that.

                                We know when that test first came out, it was a big step forward. But it did suffer from some problems. One there were  longer than expected turnaround times, because the methodology was a little bit long and unwieldy. It wasn’t fully molecular either. Elements of it were molecular. Elements were not. And, it actually did not suffer from not finding things. It suffered if anything from oversensitivity. And what practitioners may remember is getting a lot of what’s called, basically that the organism type was detected, but taxonomy unavailable. A lot of that was theorized to be what we call, scattered DNA. A little bit of DNA of different kind of organisms that can be located in the food mass.  That doesn’t implicate all molecular technologies as suffering from those same problems. If you go to any major hospital pathology lab, at an academic medical center in the western world right now, they are running their samples using DNA molecular technology. When someone has a systemic infection, if they nick a bowel, and they have sepsis or something, and they’re coming in with some really weird infection, and they’re going into organ failure, and they need to know what it is, they need to know now and they need to know what’s going to kill it, what antibiotics will be effective, which antibiotics will it be resistant to, they do not do culture technology. They do molecular technology. That’s just how it works. You just need to apply it to stool testing in the proper way.

                                That’s what we set about doing with GI-Map. We developed this in the incubator at the molecular biology center at Georgia Tech University, which is the number one molecular biology center in the world.  Along with one other center in Massachusets who were the first to map the human genome.  Very advanced technology and talents. Basically, when we developed the GI-Map, we took a very different route. Many of us were actually involved in that first generation testing. We were sort of the ones who didn’t win out in the argument of look, we need to use a bulletproof technology that’s already been totally vetted, tested out, and in many cases cleared by FDA for certain applications. That’s what we did, but we applied it across a wide spectrum of clinically relevant organisms in a manner that a Functional Medical doctor would want to see.

                                In conventional Gastroenterology, when they do stool testing, even if they’re using molecular, they’re generally looking for a very short list of pathogens that may be causing diarrhea in a patient. The Functional Medicine doctor needs a much wider lens. We want to look not only across pathogens, and not only five or six pathogens, but a long list of pathogens in classes including bacterial, fungal, protozoal, helminth, viral. Right? The viral realm, but then we want to look at commensals. We want to look at beneficial organisms, and a whole range of those. We also want to look at opportunistic organisms. That’s really where the gold is, the opportunistic organisms that have the potential to overgrow if the environment is right, if the host is susceptible to it.

                                A lot of these opportunistic organisms when they overgrow to a certain level, can then create problems, and they are associated with the genesis … First of all they were just associated with different disorders, like various autoimmune diseases, but now we actually have the emergence of causal data and mechanisms by which we know how the higher presence of a certain bacterium, let’s say, in the gut, can actually ultimately translate to an immune attack against your joints, or against your thyroid, or against your nervous system. In the GI-Map, we’re using what’s call quantitative PCR. PCR, polymerase chain reaction, right? It’s a molecular technology. We’re hunting the DNA of these bugs, but we’re doing it with a quantitative platform. What that means is we get the actual numbers of the organisms, versus other molecular technologies, which are also good, but they’re not meant for the same application, which is caused next-gen sequencing, which many people may know of.

                                Examples of the two. Next-gen sequencing is a test like a uBiome test, where a lot of people get that done. It’s not a test that was ever meant for, nor was it developed for making clinical decisions on patients at the point of clinical care. It’s a research test meant for metadata collection and analysis to quantify signatures, not qualify, I should say, signatures of the microbiota. Meaning, what is a normal GI microbiota looks like on the West coast of the United States, or in Eastern Europe, or in Asia? Because it’s not going to be the same. It won’t be the same in people following different types of diet schemes. What those kind of tests do with next-gen sequencing is they look at a long, long list of organisms in the gut, many of which have no clinical significance that we’re aware of. They’re reporting them as a percentage of the total organisms. They’re never saying how many are there. They’re just saying what percentage of the total organisms does this genus of organism makeup, or they can look at it from the phylum level. They’re only looking at one little portion of the DNA.

It restricts them from getting down to the species level, and they certainly cannot get to the level of looking at the characteristics of the organism, like virulence factors for instance, which answers the question, is this form of lets say, H-pylori a problematic form, or a benign form? Because it was never meant to do that. They don’t look at pathogens. They don’t quantify anything. It’s a very valuable test for research. The reason uBiome, and companies like that are doing that test is to try to answer these questions, and find these major associations between overgrowth in one way, and a certain autoimmune disease, and what they were really doing is collecting massive amounts of data to then monetize it by selling it to pharma as a metadata set to develop drugs and things like that. That’s why you can do the test at such a small amount and actually you’re paying less than it probably costs them to run the test. Same with 23andMe. They made all their money by selling all their metadata to pharma. So, if you’re okay giving your data over, and your genetic information for that purpose, that’s fine.

                                The GI-Map though, uses quantitative PCR, because it’s a clinical test. We’re looking at a range of organisms in the classes of pathogens, commensals and opportunists that we know have clinical significance. If they overgrow they’re going to cause diarrhea, or they’re going to cause gastric upset, or they’re going cause disease, or they’re associated with autoimmunity. We carve out different sections for autoimmune triggers that we know have this organism has a certain expressed, let’s say peptide on its surface, which looks a lot like a host protein. Organisms like klebsiella, citrobacter, or proteus, prevotella, overgrowing in the gut beyond a certain point, puts the person at risk if they’re genetically susceptible to things like rheumatoid arthritis ankylosis spondylitis, or Yersinia overgrowth and Hashimoto’s or Grave’s disease. I can go on down the line with a whole bunch of other ones, but the test is quantifying using molecular technology across that broad range of organisms that have clinical significance so you can decide for instance, if a pathogen is coming back elevated, it’s beyond a certain cut point, which we know is clinically significant, it means you need to treat that.

                                You’re not going to get that from a uBiome.  It’s just not intended to do that.  And then parallel to that, we’re running all of the modern stool chemistry.  We’re calculating for inflammation, and even bowel cancer risk.  Zonulin for intestinal permeability or leaky gut. Things like elastase-1 for pancreatic excretin output. Steatitic for amount of fat in the stool. Beta glucuronidase for risk for estrogen dominance in females based on the function of their microbiota.  Things like total secretory IgA and antigliadin secretory IgA, are you reacting to gluten and gliadin containing grains at the level of the gut lining, that’s mucosal immunology. It’s not a test for Celiac disease per se, but it let’s someone know, hey, maybe my immune response is not super compatible with these field grass greens.

Dr. Weitz:            Let’s say you find a pathogen like Yersinia, which you’ve written about how that’s connected with autoimmune thyroid disease. Can you explain how the appearance of a pathogen in your gut can lead to an autoimmune disease that affects your thyroid?

Dr. Brady:            Yeah. There’s a couple of possible mechanisms, but probably the most direct line or understood one is a process called molecular mimicry. Let’s take Yersinia as an example since you brought it up. Yersinia on its surface has some proteins or peptides that … All microbes have surface characteristics, structurally. These help communicate with other like organisms. It helps them form a locus of infection, or a colony, and provides communication and other types of things. That is where the immune system learns that organism. So, a naive T-cell let’s say, will be educated to react to that peptide on the Yersinia because other parts of the immune system have looked at it and said, this isn’t me. I don’t know this structure, therefore it must be something foreign. It’s a potential threat. It’s an antigen. Let’s develop antibodies to bind to that antigen to cover all those surface peptides so it can’t communicate and bind and form a locus of infection. But, it’s also being tagged for other cellar elements of your immune response, to take it out basically, whether its phagocytosis of other types of processes. Basically it’s using the structure of that protein or peptide on that surface of that organism.

   Now, the reason why we can have an association between not just one microbe, but a long list of microbes and a certain autoimmune disease is because many of these surface proteins or peptides are conserved across various families of organisms. In rheumatoid arthritis, we have klebsiella, citrobacter, prevotella, we have proteus, we have a lot of different organisms, which we have a similar response to. It’s not a one organism, one disease type of scenario. That’s what freaks conventional medicine out, because it rocks the one cause, one disease paradigm. You have to think a little bit more complicated. But, those surface proteins on Yersinia, coming back to the question, have a structural similarity to TSH receptors on the thyroid. They’re not exactly the same, but they’re enough the same that if you also harbor a genetic propensity or an HLA pattern to overreact to that environmental antigen, that you will kind of freakout when you see that reaction. You’re going to then be susceptible to reacting to something else that looks a lot like it.

                                It’s a mistake in identity. It’s like the TSH receptor is a doppelganger to the protein on the Yersinia, and when you develop these antibodies to bind to that antigen to get to the gut to fight the infection, they see the TSH receptor on the thyroid and they go, close enough, and they lock into your thyroid and they tag your thyroid for destruction by the rest of your immune system and you get an erosive inflammatory response against the gland, which in the early stages creates an over secretion of the gland. So, inflamed glands generally over secrete their hormone. So with Hashimoto’s you get a hyperthyroid state, but when enough of the thyroid is destroyed and you don’t make enough thyroid hormone, you end up in the hypothyroid sort of bimodal presentation of Hashimoto’s. Most people don’t even get diagnosed until it’s in the hypo stage, where they have high antibodies, low hormones.

                                So, that’s an example of molecular mimicry, but there are other examples that we know, such as if you have bad oral hygiene and you have overgrowth of P. gingivalis, which is the most common organism that causes gum disease or periodontal disease. We know that that organism produces an enzyme, which actually will citrullinate host peptides, so it modifies arginine on host proteins and citrullinates them and makes them a hapten. They’re no longer your own structure. They look foreign to the immune system. The proteins that they citrullinate are things like collagen, vimentin, fibrinogen, all of the things that make up the schematics structures of joints and things like that. You’re really susceptible to develop autoimmune arthritides, basically like rheumatoid arthritis. That’s why in diagnostics when we do a rheumatoid panel, yeah, they do rheumatoid factor, but what’s the other test they do? Anti-cyclic citrullinated peptide.

                                What’s creating the citrullination of those peptides that has been understood for a while, we’re not finding out is the organism overgrowing in the mouth creating the enzyme, which is facilitating that protein modification. We’re going to learn a lot more about these type of phenomenon in the next 10 or 20 years, I’m sure. We’re probably just scratching the surface.

Dr. Weitz:            I just want to point out that one of the really exciting things is, you can have a patient who doesn’t have hypothyroidism, doesn’t yet have an autoimmune disease, and you can find some of these pathogens like Yersinia and some of these other pathogens in the gut, and or you could do auto antibody testing.

Dr. Brady:            Usually you do them in combination if you have a strong family history, you’re suspicious for some reason. If you come back with thyroid predictive auto antibodies in a serological test, then we look into the GI microbiota for sure, to find out if there is Yersinia, or is there other changes in the ecology that we need to address by either eradicating the bug that we know is associated and trying to change the landscape to the level of our ability to do so. But, also addressing things like hyperpermeability or leaky gut. We’ll have our eye on the zonulin and the calprotectin marker. We’ll look at anti-gliadin secretory IgA in the case of autoimmune thyroiditis, because we know agglutinate and antibody complexes have an affinity for the thyroid. That’s why people with let’s say, frank’s Celiac disease, where they have significant reaction to gluten and gliadin, they have about 20 times the rate of autoimmune thyroid conditions as non-Celiac’s.

Dr. Weitz:            Through this analysis and through a Functional Medicine approach you can truly prevent some of these autoimmune diseases before they’ve even developed. I just think that, that’s so amazing.

Dr. Brady:            Hypothetically, we don’t have the long term, longitudinal studies to prove that, but certainly there’s no harm in doing so, and there’s potential big upside. I can tell you that clinically we have seen patients who we did all of these things, taking what we call the straws off the camel’s back. We can’t change their genetic propensity for a certain autoimmune disease. We can’t change our HLA patterns and things like that. Right? At least now. At least yet, but what we can do is change their exposures within our ability to do so, within the ones that we understand. Right? Which is if I have someone that’s coming back with HLA B27, and they’ve got a family history of rheumatic arthritides and things like that, well, I’m for sure going to be doing a stool analysis on them looking for klebsiella, citrobacter, patellare, all of those.

                                If I find those things, I’m using things to eradicate that to the best of my ability and I’m usually using standardized botanicals, volatile oils, things that have a little bit more of a functional nudging affect and are going to take down those opportunists without bombing everything out. Without getting rid of all the normal organisms, I’m going to backfill with probiotics and the right pre-biotics. I’m going to use the right kind of blocking agents to block antigen antibody interaction and immune proliferation. Things like N-acetylglucosamine. Things like mycologist botanicals. We use these in gut therapy all the time, whether its okra, cat’s claw, aloe, there’s slippery elm.  There’s all these kind of botanicals that have historical use in gut function that we used to think just coated the gut and allowed it to heal. Actually they work in a much more complex fashion with glycobiology on blocking immune proliferation and docking of the antigen or the antigen with the antigen presenting cell to the T-cell. And we’re going to be doing things like glutamine, and other things to help the gut lining. Making sure the vitamin D levels are good, because that affects junction expression proteins that can treat leaky gut. We’re going to get them on a good whole fresh food diet. We’re going to get them off of dietary antigens.

                                Sometimes we’ll run a cellular response test looking for up regulation of innate immunity or inflammation due to certain foods, like an ALCAT test or something like that which is not a food allergy test. It’s innate immune response to food test. We’ll utilize those types of strategies and basically bring everything we can to the fort to change their lifestyle, change the landscape to where … Fasano talks about the triative autoimmune disease. Genetic susceptibility, an environmental antigen and leaky gut. We can’t change the genetic susceptibility, but we can change the exposure in many cases. We can certainly change the leaky gut. That’s where we go after, on those two legs of the stool, if you will.

Dr. Weitz:            So, leaky gut or hyperpermeability, you’ve mentioned that several times. That is where the mucosal membrane of the gut breaks down, creating spaces where toxins say, given off by bacteria like endotoxins and other toxins can enter our system and create problems.

Dr. Brady:            Right. Correct. Not only LPS, and things from the microbiota, but actual toxins themselves in the food mass, and toxins that are metabolites of the microbiota, but also foods themselves. If we’re allowing translation of complex peptides that are not broken down enough in the digestive process, of food that maybe perfectly benign if you had an intact gastrointestinal lining and adequate stomach acid and digestive enzymes, becomes antigenic and fuels the fire of the immune system if you’re not producing enough hydrochloric acid, or you’re taking a PPI, or histamine receptor, antacid type of medication, and or you’re not putting out enough digestive enzymes, and you have leaky gut. Sometimes it takes a bunch of things to gang up on you, but these things are not all that uncommon.

                                What the GI-Map tries to help the clinician do is answer a lot of those questions. Are there pathogens there? Are there overgrowth of opportunistic organisms? Are there not enough commensal organisms? But also, is the pancreas putting out enough enzymes? Do you have enough secretory IgA to have proper immune surveillance along the GI mucosa? Are you reacting to gliadin in a way that would be more excessive than what would be considered normal? Is there signs of inflammation, which causes damage to the GI mucosa like calprotectin being elevated? And, are you producing the glycoprotein that can actually directly cause leaky gut, which is zonulin? Trying to put all of those things together, all the clinically relevant markers that make sense for the clinician to need to know.

Dr. Weitz:            Do we know how accurate the zonulin measured in the stool is compared to serum zonulin versus zonulin antibodies?

Dr. Brady:            I don’t have a nearly as much familiarity with serum zonulin and zonulin antibodies. I know some laboratories do that. I know that there’s been some controversy over serum zonulin as a valid marker of intestinal permeability. But the best data and information out there is on fecal zonulin because that is where the rubber meets the road. It’s the enterocytes producing the zonulin, which is creating the hyperpermeability. I don’t think serum is the logical place to look for zonulin. I think the stool is the logical place to look for it.

Dr. Weitz:            Great. This has been an amazing podcast, Dr. Brady. Thank you so much for bringing our listeners some really interesting and clinically useful information.

Dr. Brady:            Sure.

Dr. Weitz:            Where can listers learn more about you, and your GI-Map testing?

Dr. Brady:            Sure. Well, if they just want to access some information about me and a lot of my articles, including the autoimmune articles we talked about and so forth, they can just hit my website at, drdavidbrady.com. Just D-R davidbrady.com. There’s a media tab with articles and things like that. A lot of full text stuff you can pull down. There’s a lot of interviews on different topics, in the media tab as well.  If they want more information on global pain and fatigue syndromes like fibromyalgia in my new book, The Fibro Fix, they can just go to fibrofix.com. F-I-B-R-O-F-I-X.com. And then finally, if they want information on the GI-Map test, from Diagnostic Solutions Labs, just go to diagnosticsolutionslab, so diagnosticsolutionslab.com. There’s a whole whitepaper, all supportive literature, lots of webinars, tutorials on interpreting the test, and there’s full clinical support when you order your first couple of tests and you need some assistance with that, as well. There’s instructions there on how to get test kits and so forth.

Dr. Weitz:            That’s basically for practitioners. For laypersons who’d like to get your stool tested see a functional medicine practitioner, like yourself Dr. Brady, like myself, Dr Weitz. If you want a listing for a functional medicine practitioners, you can go to the Institute of Functional Medicine website, and they have a listing of functional medicine practitioners. I think a good idea to see somebody like that who can really go through and interpret the data and help you to set up a program to improve your overall health.

Dr. Brady:            If there are practitioners out there who are not ordering clinicians with diagnostic ordering privileges, the GI-Map is also available for those practitioners through Evexia Diagnostics. So, E-V-E-X-I-A Diagnostics.com, formerly known as Doctor’s Choice. They have you work with physicians to get the test ordered.

Dr. Weitz:            Cool. That’s great. Thank you so much, Dr. Brady.

Dr. Brady:            You’re welcome. Thank you.

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Chronic Fatigue and Fibromyalgia with Dr. Kent Holtorf: Rational Wellness Podcast 040
Loading
/

Dr. Kent Holtorf speaks with Dr. Ben Weitz about how to help patients with Chronic Fatigue Syndrome and Fibroymalgia.  

[If you enjoy this podcast, please give us a positive review on Itunes, so more people will find The Rational Wellness Podcast] 

 

Podcast Highlights

1:49  Dr. Holtorf tells his story of dealing with Chronic Fatigue Syndrome that turned out to be caused by Lyme Disease. He was having thyroid and adrenal problems and needed support for them as well as HGH and testosterone.  He became a new person.

2:47  A few years later he was going through a stressful divorce and he crashed.  He found out he had Lyme Disease and he was being treated with round after round of high dose IV antibiotic therapy. He was even going into heart failure because his blood had become too thick. The antibiotics were not bringing about a long term cure, so he figured out that he had to treat the immune system to create balance.  He used ozone, umbilical cord stem cells, and peptides, all of which helped. The TH1 was suppressed and TH2 was increased and this has to be balanced to overcome these chronic infections.

5:30  We discussed worm therapy for immune system balance

6:07 We talked about a subtle form of hypothyroidism that is not picked up just by looking at TSH that is an important component in patients with Chronic Fatigue Syndrome and Fibromyalgia. Dr. Holtorf said that conventional thyroid testing–looking at TSH misses about 80% of cases of hypothyroidism and he likes to look at the Free T3/Reverse T3 ratio and Sex Hormone Binding Globulin and he is developing a new test, Active TSH. He also explained that the new T3/Reverse T3 assays are not as accurate since they crunch everyone together. He also uses a computer to measure achilles tendon reflex and if it is slow it indicates hypothyroidism.

13:12 We also discussed the role of adrenal dysfunction in chronic fatigue and fibromylagia. Dr. Holtorf will often use low dose timed release cortisol in these patients for three to six months. It’s usually not a primary adrenal problem, it’s a hypothalamic-pituitary-adrenal problem.

17:39 I asked Dr. Holtorf about his articles where he talks about the use of growth hormone for patients with chronic fatigue and fibromylagia. He said he tends to use growth hormone secreting peptides, since growth hormone is so regulated.

20:28 Dr. Holtorf talked about the role of chronic infections in fibromyalgia and chronic fatigue syndrome and he said that he especially sees Lyme Disease. There are often co-infections with Babesia and Bartonella. There may be other chronic infections like Epstein-Barre, HHV6, or CMV. The key to correcting these is to strengthen the immune system along with antibiotics or antimicrobials. He also often uses Low Dose Naltroxene (LDN), which is an opiate blocking drug, but it helps to balance the immune system. It’s also very inexpensive and very safe.

23:43 We discussed the fact that fibromyalgia and chronic fatigue syndrome patients often have coagulation problems. This is because the body responds to infection by increasing coagulation as part of the immune system activation.

 

 


Dr. Kent Holtorf can be contacted at his website https://www.holtorfmed.com/ and he is accepting new patients by calling 877-508-1177.

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and also specializing in Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure as well as chiropractic work by calling the office 310-395-3111.


 

Podcast Transcript

Dr. Weitz:                            Dr. Ben Weitz here, and I’m here with a very interesting guest, Dr. Kent Holtorf, and we’re going to talk about fibromyalgia and chronic fatigue problems. Dr. Kent Holtorf is a nationally recognized expert on fibromyalgia, chronic fatigue, and thyroid problems. He’s the medical director of the Holtorf Medical Group, and he has affiliate centers across the country. He’s also founder and director of the nonprofit National Academy of Hypothyroidism, which is dedicated to dissemination of new information to doctors and patients on the diagnosis and treatment of hypothyroidism. We’re going to speak to Dr. Holtorf today about fibromyalgia and chronic fatigue syndrome, two related and very difficult to treat conditions, often affecting women and affecting quite a number of people in the United States. Dr. Holtorf, thank you for joining us today.

Dr. Holtorf:                         Thank you so much. Pleasure. Thanks for having me.

Dr. Weitz:                            How did you get interested in treating chronic fatigue and fibromyalgia?

Dr. Holtorf:                         Well, basically, I was a very standardly-trained physician and going through medical school. I got so fatigued, I was like, “Something’s wrong.” Went to the doctors, who said, “Oh, you’re stressed out like the other students.” I’m like, “That’s not it.” “Oh, you’re depressed. Do they treat you bad?”  “That’s not it,” and just, basically, worried about functioning. Went on to residency and it got very bad. I’m like, “I don’t know if I can see patients.”

                                                Now, you’re kind of trained in medical school about alternative is quackery and all this, and I’m like, “I’m not getting help here. I’m going to some of these so-called alternative conferences,” and I realized, “Oh, my God, they are more evidence-based than what I was learning in residency.”  And basically, I treated myself with … thyroid was the big thing, a little adrenal support, cortisol, growth hormone, testosterone. “Oh, my God, I’m a new person,” and so I was able to function. And then I was doing anesthesia. Got out of that, because I’m like, “Okay, this is so boring.”  But the energy after that.

                                               And then, a number of years later when I was doing fine, I went through a stressful divorce, just crashed. We were treating Lyme disease at the time, and I’m like, “I know it’s Lyme.” This is just too bad, not just chronic fatigue syndrome, but a lot of chronic fatigue is Lyme. And then I went into heart failure, my blood was too thick. You could not pull it out. And what I found … I did four years at the highest dose IV antibiotics that I would never even give a patient. I’d stop for two weeks, it would come back. So, essentially, went all over the world looking at treatments, and I found that really, immune modulation is the cornerstone of successful treatment. Because all these patients just … they get a little better or worse with these antibiotic treatment, but you don’t treat the immune system. That’s the key, that’s what you need to do for long term improvement.

Dr. Weitz:                            So, what kind of treatment did you do to balance the immune system?

Dr. Holtorf:                         I did so many treatments. A lot of things work, but each thing works for different people. Ozone was very helpful, but we really found umbilical cord stem cells, great for immune modulation, lowering inflammation. And peptides, which is a new therapy that’s becoming again, a cornerstone of our therapy.  Really, what you see is what happens with chronic illness, especially chronic fatigue syndrome, chronic Lyme … there’s two sides to the immune system, Th1 and Th2. Th1 gets stuff inside your cells, Th2 gets stuff outside, because normally they’re balanced. With chronic Lyme and when Th1 gets suppressed, then your body increases Th2 and all this inflammation symptoms. But if you don’t increase this, modulate that immune system, then its long term success is very difficult.

Dr. Weitz:                            Yeah, yeah. Isn’t it also important to stimulate T regulatory cells as well?

Dr. Holtorf:                         Yeah, all that goes into it. The immune system is very complex. Th1 and Th2 is a way of looking at it. We’re practitioners, it makes sense, and what you really see … for instance, HIV. You look at who progresses in HIV directly correlates with how low the Th1 and how high the Th2 is.  So, it really shows with these chronic infections, we’re beating on people with these antibiotics, antivirals, and if you don’t address the immune system, you never get there.  Because the immune system is so low, you can get the antibiotics down, but the immune system has to basically, take over, because most people that have chronic Lyme or chronic infections, they basically, are able to suppress the infection, even though they have it. For instance, like getting chicken pox. You say, “Well I’m over the chicken pox, you’re really not. The body just basically, hasn’t suppressed it. It comes back out as shingles when your immune system’s low.  So it’s a good model for, “Hey, keep the immune system high, and you don’t get shingles again.” Same thing with Lyme, chronic fatigue syndrome, fibromyalgia.

Dr. Weitz:                            Yeah, it’s interesting. I interviewed Dr. William Parker last week and he was talking about using worms that you ingest and live in your intestines and the main effect is to help regulate the immune system.

Dr. Holtorf:                          Yeah, and those are great. As you said in your previous podcast, where they’re great with respect to autoimmune diseases of the gut. You find that third-world countries don’t get Crohn’s and Ulcerative Colitis because they have these worms. So, yeah, it modulates the immune system. Same thing, increased Th1 lowers that Th2 and we find … we haven’t used worms, but they seem like they fit right in with the model.

Dr. Weitz:                            Yeah. One of your articles on your webpage, you write that, “Central hypothyroidism and cellular resistance to thyroid hormone exists in the majority of patients with fibromyalgia and chronic fatigue syndrome.” What did you mean by this? How can this be tested for, and then how does it get treated?

Dr. Holtorf:                         When you look at studies that use TRH tests … so, most doctors, they basically look at TSH. The TSH, the basic hormone produced in the hypothalamus, tells the pituitary to excrete thyroid stimulating hormone, which then tells your thyroid to excrete T4, which then needs to go into the cell to convert to T3. So, all these things need to happen. Now, what do most doctors check? The TSH, which tells the level in the pituitary.

                                                So, when the pituitary level goes up, the TSH goes down, or the pituitary level goes down, TSH goes up. Now, what we’ve found with chronic inflammation, chronic infections, diabetes, dieting, obesity, what happens is that the pituitary’s different from every other tissue in the body. You have all this inflammation and this chronic illness going on, the pituitary levels go up, but the rest of the body goes down. So, what happens is, you get low TSH, which doctors will say … they’re taught that thyroid is very easy. If your TSH is high, your thyroid is low, if TSH is low, your thyroid is high. It’s normal, it’s normal.

                                                That is not the case with so many illnesses, especially with chronic fatigue syndrome and fibromyalgia. For instance, they did TRH testing in fibromyalgia patients. All of them were low, even though they had a TSH that was low normal, so it looked like they had a little bit high thyroid. So, it is totally inappropriate to use TSH in chronic fatigue syndrome and fibromyalgia. Also, we’re finding diabetes, and anyone with chronic dieting, any autoimmune disease, inflammation, all these things, the standard blood tests we’re using is missing about 80% of people with chronic illness.

Dr. Weitz:                            That’s kind of a controversial viewpoint, though, isn’t it?

Dr. Holtorf:                         Well, it is, because we’re just taught over and over that the TSH is what you look at, but I’ve published numerous reviews on this with hundreds of references from standard medical journals. It’s clear, it shows it, and when you show this data to people … “How come I don’t … why haven’t I heard this before?” I’m like, “It’s very complex. Doctors learn what they learn.”

                                                Basically, you look at the studies, most doctors are practicing twenty years behind what’s available in the medical literature. And they did a study and they found that it takes an average 17 years for a proven, new concept to be accepted into mainstream medicine.  And why is that? One, doctors don’t read medical journals. They don’t. They don’t have time, and if they do, they read the abstracts of the whole thing. Also, drug reps, basically, drive doctors prescribing, but the biggest reason was they found that if you give a doctor … Here’s a study, here’s five studies, ten studies, a hundred studies showing what you’re doing is wrong, they don’t want to read it. They say, “No, what I’m doing is fine.” They don’t have time. When you look at all these tests we’re doing for thyroid, you can’t just do the blood test. Doctors are like, I don’t have 15-20 minutes to spend with the patients and ask them all their symptoms. They have nine minutes, now.

                                                So, what do you get? You get an antidepressant. If your TSH is high, you get Synthroid, which doesn’t work very well, or if it’s normal, again, you’re just depressed or stressed. Go away, you’re done. So, that’s the really driving force. No one wants to take the time that it does to basically, treat thyroid appropriately.

Dr. Weitz:                            So what are the best tests to get an accurate measure of thyroid?

Dr. Holtorf:                         Now, we’re developing a new test called the Bioactive TSH. You find with, again, that pituitary dysfunction, your body secretes less active TSH, but that’s not available right now. That’s up and coming, hopefully.

Dr. Weitz:                            Active versus inactive TSH?

Dr. Holtorf:                         Yeah. And the standard test just picks up the amount of TSH, not the activity. So, you can see that if you have chronic illness, the TSH may be the same, but it’s less active. We’re working on that for 10 years, but we’re making some progress. You need to look at the Free T3, Free T4 levels. But one key is the Free T3/Reverse T3 ratio.  So, the body will take T4, which is inactive, secreted by the thyroid. It can either convert to T3, which is active, or Reverse T3.

                                            So Reverse T3 is the same thing, but backward. So it goes to the cell receptor, sticks there, but doesn’t do anything, so they say it’s inactive. But actually it’s blocking the active thyroid, so it’s a brake pedal for the thyroid. With stress or chronic illness, inflammation, chronic infection, you’ll make high Reverse T3. If you look at the Free T3/Reverse T3 ratio, it’s a very good marker. Now, with the little caveat, the new assays out are not that good. They kind of crunch everyone together. Before, five years ago, they were very telling. Now they’re a little … they’re telling, but not everyone’s exact cutoff. We need to look at that.

                                             Another marker is sex hormone binding globulin. People think of that in terms of testosterone, because it binds up testosterone, so people will say, “Well, we want to see what’s the free testosterone.” So, hormones can be bound up or free. The only ones that are active are the free. But sexual binding globulin goes up in the liver in response to two things. One is estrogen, one is thyroid. So, a woman comes in. Let’s say she’s menstruating normally, probably normal estrogen. If her sexual binding globulin is below 80, you know they’re low thyroid. And also, if you give thyroid and SHBG does not go up, you know they have thyroid resistance. So that’s a key test that so many doctors don’t know about, and they just don’t think about it.

Dr. Weitz:                           Interesting.

Dr. Holtorf:                         Symptoms are key, also. I mentioned body temperature, low body temperature, symptom assessments correlate very well. We have a computer that measures the relaxation phase of the muscle reflex. So, normal thyroid, the reflex will go “chu-chu”, but the lower the thyroid it goes “duhn-nyah.” The computer measures that.

                                            British Medical Journal, obviously, a major medical journal, showed that that test was better than blood tests for thyroid, correlated with symptoms better. Then we’ll also check everyone’s basal metabolic rate. And we’ll find that most people come in that have…

Dr. Weitz:                            How do you measure their BMR?

Dr. Holtorf:                         Basically, with a device that measures the oxygen output over 10 minutes. And it extrapolates for the whole day, so it tells you how many calories you burn. How much oxygen utilized equals how many calories you burn. Let’s say my metabolism is low, everyone’s like, “Yeah, right.” They’re metabolism is 25% lower. That correlates to about 500 calories a day, so they either have to eat 500 calories or less just to stay even, or exercise for about two hours. Or fix your metabolism. So we find that is a gold standard for basic metabolism, which equals the thyroid. The thyroid is the gas pedal for the metabolism.

Dr. Weitz:                            Right. So you’ve also written that most patients with fibromyalgia and chronic fatigue syndrome suffer from clinically significant andrenocortico dysfunction due to hypothalamic and pituitary dysfunction. And I see from some of your articles that you often treat both of these conditions with low-dose cortisol. How does this help, and maybe you could explain the mechanism.

Dr. Holtorf:                         The adrenals, as you know, basically, and a lot of people know, it’s a stress response. It helps your body to deal with stress. So many people say adrenal fatigue, I think that’s overused, you know that …

Dr. Weitz:                            Right. That seems to have been critiqued, right?

Dr. Holtorf:                         Yeah, and everyone’s like, “Okay, adrenal fatigue [inaudible 00:13:58].” But when-

Dr. Weitz:                            Do you like the four part adrenal-cortisol testing with the saliva?

Dr. Holtorf:                         I do. That way … because a lot of times you’ll see it. They’re not, in fact, when are they low or high? But it should be high in the morning and then come down and low at night. But, you’ll see people completely opposite. They don’t sleep, then they’re tired during the day. So, I think it is a good test.

                                               We’ll do a lot of blood tests, because we’ve been doing them a long time. We don’t need to do those things, but they’re certainly useful, because you get multiple times during the day. What happens with chronic infection, we talked about.  Pituitary dysfunction with the thyroid, same thing happens with the adrenals. The pituitary secretes ACTH, which tells the adrenals to go up.

                                               Now, what we find, it’s usually not a primary adrenal problem, it’s a hypothalamic-pituitary-adrenal problem. Normally, what they did, was do ACTH stimulation tests, which was considered the gold standard for adrenal dysfunction, and they found no difference in chronic fatigue syndrome or fibromyalgia. But the problem is, that only tests for primary. But when they did central testing they found that there’s again, hypothalamic-pituitary-adrenal dysfunction, which these tests showed up 90+ percent actually had HPA axis, hypothalamic-pituitary-adrenal dysfunction and responded very well to treatment. And they found that the ACTH stimulation test was no better than flipping a coin. So, again, that gold standard testing missed 80% of them, was no better than flipping a coin.

                                                And it’s very hard to do the central stimulation test. But if you look at the studies, for instance, the Journal of Infectious Disease in Brazil looked at chronic infections and how the adrenal levels correlated to serum levels. They found if they were lower than 12.6, they had about an 85% chance of being low adrenal, because when you’re sick, you should be higher, right?

                                                Let’s say, “What is normal adrenal function?” It depends on the person, it depends on the stress. If you’re in the ICU and have a normal adrenal level, you’re probably going to die. You need much more during times of stress, so with chronic infection you need more. So that’s just a quick and easy test to do for adrenal function, and say, “Hey, is this person low?” Look at all the symptoms. Giving low-dose cortisol, everyone’s like, “Oh, my gosh.” You know, especially if you’re an endocrinologist. It’s safer than actually doing the testing, the basic stimulation test. Much safer, does not suppress the adrenals, actually at low dose, it will improve adrenal function. And then, as you treat everything else, that will get better. Usually, we’ll treat for three to six months, or depends on the case. They’re often not on it longterm, and a lot adrenal support as well, and that often comes back.

Dr. Weitz:                             Yeah, I guess a lot of us have seen patients who are on prednisone for a long period of time for asthma, or some other condition, and they have all these side effects, and loss of bone, and all kinds of other things. That, I think- [crosstalk 00:17:01] worry comes from.

Dr. Holtorf:                          I also have written on this, about the low-dose, completely different. And I can’t remember the last time I gave prednisone, or any high-dose, because, yeah, you’re basically doing a disservice to the patients. Suppressing their adrenals, they’ve got to be on it, all the side effects, but again, optimal is optimal. Prednisolone is mega-doses, which, it’s going to have issues.

Dr. Weitz:                            Does it matter if you use cortisol or cortisone? Those are different, right?

Dr. Holtorf:                         Yeah, cortisol or hydrocortisone are the same thing. Those are interchangeable. We used to give time-released, compounded.

Dr. Weitz:                            You’ve also written about lower levels of growth hormone being correlated and being a contributing factor in fibromyalgia and chronic fatigue syndrome.

Dr. Holtorf:                         Again, the same thing. Growth hormone produces pituitary, usually at night, and it goes through your liver, increases IGF-1, things like growth factor, which has a lot of effects on healthy immune system, weight, all those things. Just like everything else, again, when you look at these chronic illnesses, everything that the pituitary controls, which is a lot of things, are dysfunctional.

                                           Studies by Bennett from the University of Oregon found that giving growth hormone, dramatic improvement in symptoms. And growth hormone is very controversial and very regulated because of athletes using for performance, which shows that it does work. We stopped over the years using straight growth hormone and more using secretagogues that stimulate your body’s own production, including peptides, we’re finding our key for that.

Dr. Weitz:                           Which peptides?

Dr. Holtorf:                         Ipamorelin, CJC. I’ve done a lot of lecturing on growth hormone secreting peptides, growth hormone secreting hormone. Now, you’ll get Sermorelin, or Semorelin, however people pronounce it, but either way. That is a growth hormone secreting hormone, and it does work, but it stops working in a couple months, so if you had a growth hormone secreting peptide to that, it works much better and longer. And it’s really, you can’t overdose, because your body will actually regulate it.

                                           It’s a nice way, very safe, much more cost-effective than growth hormone and you get the effects. It’s not great for bodybuilders, which we don’t see, but for the sick patient. Usually, the sicker the patient, the better the response to growth hormone, and healthy people, they might see some performance, endurance, but usually they don’t see dramatic effects. But, the sicker the patient, the more they respond, and very well-tolerated. I can’t remember the last I’ve had a side effect from growth hormone, or especially the secretagogues.

Dr. Weitz:                            What about some of the natural methods of elevating growth hormone levels, including certain amino acid supplements, and even heavy weight training has been shown to elevate growth hormone levels.

Dr. Holtorf:                         I think especially those you’ll see with healthy patients, the people that need it the most, those don’t work too well. Usually, they can’t do that stuff, especially heavy  weight training. They’re so fatigued. But healthy people can see benefit in those things, although, oftentimes, it’s highly variable and depends on the person. Those things can work, but usually with someone who’s very motivated to do those things.

Dr. Weitz:                            Okay. I see that you often see chronic infections as a factor in fibromyalgia and chronic fatigue syndrome. Which infections do you see most prevalently?

Dr. Holtorf:                         The big thing we’re seeing is Lyme, but there are so many other infections that go along with it. When someone has Lyme, they usually have multiple other infections, including co-infections. Babesia is a huge problem. It makes Lyme symptoms much worse and the treatment much harder. Bartonella, we’ll see much worsening symptoms, a lot of neurologic. People get diagnosed with schizophrenia and bipolar and they actually have Bartonella. But also when you see with Lyme, it suppresses the immune system, so you get all these … they’re not new infections but they’re reactivating infections. Such as Epstein-Barre, HHV6, CMV.

                                                The problem is when you test them. Normally, when you get an infection, we’re taught in medical school, your IgM antibody goes up first, and then after a while, IgG.  If it’s a new active infection, you should up IgG positive, whether HHV6, Epstein-Barre, but these are not new infections, they’re reactivating. So the body secretes  IgG.  The higher the IgG, the more like you have this active, chronic active infection. But a lot of people are told they don’t have these viruses. Not uncommonly, you need to treat the virus along with the Lyme or the other bacterial infection, because that’s suppressing the immune system. Antibiotics don’t touch it. But immune modulation, again, is key for all those, because they’re all coming out, because the immune system’s too low.  Whatever antibiotic or antiviral you need to get down the immune system. But if you get the immune system up, those start working. They work much better together.  We rarely give antibiotics or antivirals without the immune modulator.

Dr. Weitz:                             Do you use Immunoglobulin?

Dr. Holtorf:                          I love Gly BIG. And it, again, is another immune modulator.  It does the same thing; it increases Th1 and lowers Th2. It can also kill passively with the infections. But, the problem is, it’s expensive. So we’ll do, typically, the lower doses so people can afford it. It’s a great treatment. I wish it wasn’t so costly.

Dr. Weitz:                           What about LDN? Have you used that?

Dr. Holtorf:                         Yeah. LDN, I’m …

Dr. Weitz:                           Which is Low Dose Naltrexone.

Dr. Holtorf:                         Yeah, Low Dose Naltrexone, I’m on the advisory board for them, spoke at their conferences many times, and written a couple of chapters on LDN in chronic fatigue syndrome and fibromyalgia. Your listeners have probably heard of it before. It’s an opiate blocker, and they found that it’s usually used for people who go to the emergency room. They overdosed on opiates, pain pills, they give them that, it reverses it. But, what they found at a very low dose, it modulates the immune system. It kind of does that same Th1/Th2, so it’s a first-line treatment. Very safe, very little side effects. Some people get a little insomnia with it, but like anything, it doesn’t work for everyone, but it’s something to try because it’s very inexpensive, very cheap, very safe.

Dr. Weitz:                            I notice in your writings, you also talked about coagulation problems, fibrinogen, that kind of stuff, as being related to fibromyalgia and chronic fatigue.

Dr. Holtorf:                         And that’s another big issue that if you miss this, you may not get better. And what we found is, you get immune activation coagulation. A number of studies by Berg,  and others. The infection sets off the coagulation system, the body tries to wall off the infection by laying down fibrin and the blood gets very thick. I’ve mentioned that you could not draw my blood when I was very sick. You couldn’t take it out with a giant needle. And my D-dimer, which is a marker for this immune activation, was so high it was at about 50-fold increased risk for cardiovascular event in the next year. I said, “Oh, gee, I’ve got to get that down.”

                                               So the body lays down this fibrin, covers up the infection, which is good in the short-term, but now the body can’t get at it. And oxygen that normally takes two seconds to get in the cells, now takes up to two minutes. The cells are starved for oxygen, hormones can’t get through, waste products can’t get out, so until you clean up that fibrin, which may be a little bit of blood thinner, like Heparin. Coumadin and those other new ones don’t work. Or some fibrolytic enzymes can also help. And once you clean that up, it’s interesting. You’ll have people doing, let’s say, that it didn’t work. You give them a little, clean that up, do the same treatment again, and they’re like, “Oh, my gosh, it works.”

                                           That’s one of the keys that I think are missed frequently in providers that are treating Lyme, and it can make all the difference in treatment.

Dr. Weitz:                           Yeah, I found a combination of those enzymes along with high-dose fish oil also very helpful.

Dr. Holtorf:                         I agree. Again, multifactorial treatments usually are the key.

Dr. Weitz:                           Good, good, good. I think that’s all the questions I had for you. Anything else that you want to say about fib … By the way, fibromyalgia and chronic fatigue, for the most part, they can be treated as one condition?

Dr. Holtorf:                         Yeah, they’re essentially the same. You look at the … also the diagnoses are crazy, like, fibromyalgia, 11-18 tender points. There’s nothing special about those tender points. Look, you ask the patient if they’re significantly fatigued, if they have brain fog, sleep disorders, may or may not have muscle pain. They have it. You look at the blood test. People will say, the standard is, “Oh, there’s no blood test to detect it.”

                                            We can pick out chronic fatigue syndrome, fibromyalgia, on a blood test, on a panel, and how severe it is, about 80% of the time. So when people say, “Oh, there’s no  blood test that’s …”, we can pick how this person’s going to be essentially, probably bedbound, this person’s probably not too bad. And the blood test tells you. So it’s  not … everyone’s “Oh, it’s mental, it’s made up.”

Dr. Weitz:                            Right.

Dr. Holtorf:                         Well.

Dr. Weitz:                            And so the blood panel basically includes thyroid and cortisol and all these other factors we’ve been talking about?

Dr. Holtorf:                         Right. It’s usually a large blood panel because we like to get all the information, because they’re so many symptoms that are dysfunctional. We talked about a couple of  them. You got the pituitary-hypothalamic pituitary, all the hormones, mitochondrial dysfunctions, so the cells can’t make energy. You have the coagulation defects, you have the gastrointestinal system, what else? So many things you got, you got toxins, that are wrong with this condition, so when you look at studies, people say, “Oh, it’s because of sleep” or “it’s because of mitochondrial dysfunction or hormones or thyroid.” Who’s right? Well, they’re all right and it depends. You’ve got to find in the patient which things are affecting them the most.

Dr. Weitz:                            Great, great. You’ve provided us some really useful information, Dr. Holtorf. Thank you.

Dr. Holtorf:                         Great.

Dr. Weitz:                            For listeners and viewers who would like to get ahold of you, what’s the best way for them to get in contact with you?

Dr. Holtorf:                         Have them call the office, so we are in El Segundo by Los Angeles. We have centers also in Foster City, by San Francisco, Philadelphia and Atlanta. But you can call our 800 number, which, I’m not sure what it is. Our L.A. number is (310) 375-2705, or go to our website, holtorfmed.com or our nonprofit National Academy of Hypothyroidism, where all these studies that say, “Oh, they say my thyroid’s normal” and you’ll see hundreds of references showing that’s not true. And that’s N-A, like national academy, nahypothyroidism.org.

Dr. Weitz:                            That’s great. Thank you, thank you.

 

Weitz Sports Chiropractic and Nutrition
Weitz Sports Chiropractic and Nutrition
Brain Health with Dr. Steven Masley: Rational Wellness Podcast 039
Loading
/

Dr. Steven Masley explains how to improve your brain health with Dr. Ben Weitz. 

[If you enjoy this podcast, please give us a positive review on Itunes, so more people will find The Rational Wellness Podcast]

 

Podcast Details

1:30 I asked Dr. Masley how he came to write a book about the brain? Dr. Masley just published The Better Brain Solutionhttps://www.barnesandnoble.com/w/the-better-brain-solution-steven-masley-md/1126646685#/    Dr. Masley explained that in his clinic he looks at 100 markers of aging. He looks at arterial plaque growth, cholesterol, lipids, sugar, etc. He also looks at brain function, brain processing speed, memory, attention span, reactivity, and executive brain function. He also looks at food intake, nutrient intake, fitness, stress management, and toxic exposure. He has an easy to follow five step plan that improves brain processing speed by 25-30%.

2:45 I answered that that is great because cognitive problems, neurodegenerative conditions like Alzheimer’s Disease, are really on the rise and are now the leading cause of death in women, exceeding even cardiac and breast cancer. Dr. Masley said that he agreed and the number one most expensive disease is memory loss at $215 million per year and that is supposed to double in the next 12-15 years. It’s because the number one cause of memory loss is elevated blood sugar. I mentioned that some practitioners are now calling Alzheimer’s Disease Type III Diabetes due to this relationship between blood sugar and insulin resistance.

3:58 I asked Dr. Masley to explain what does blood sugar have to do with the brain? Dr. Masley said that it has to do with insulin resistance. Insulin is the hormone that helps us to store energy. When we eat carbs, whether it’s a healthy carb like broccoli or blueberries or whether it’s a refined carb, which causes a much bigger blood sugar surge like sugar or flour, the insulin rises in order to push the sugar into the cell. That’s a normal function, just like muscle cells. We push glucose in, and we build glycogen. When we go for our next workout, that glycogen in that muscle cell is ready to burn as energy. The challenge is if we don’t have a healthy lifestyle …if we don’t work out enough; if we eat too many refined carbs … our cells become full. They no longer respond to insulin. In fact, they become insulin-resistant. Once they’re full of energy, they say, “No, we’re not listening any more. We can’t store any more energy.”

Dr. Masley continued to explain that when brain cells become full of glucose, they shut down and stop working. Insulin resistance makes brain cells unable to process and use energy, so if we do a PET scan on the brain of someone who’s super fit and healthy, it would likely light up like a Christmas tree. When we do a PET scan and we look at energy burn on brain cells in patients with insulin resistance, it’s pretty quiet.  The brain is unable to process glucose’s energy. It’s dysfunctional. They have brain fog. They’re forgetful. They walk into a room; they don’t know why they’re there. They read a passage in a book, and they have to keep rereading paragraphs and they can’t remember people’s names.  Their brain’s not functioning, and if that’s not just a day or so, but it’s ongoing, that insulin resistance state, the brain cells being unable to use energy, they become dysfunctional. Then they die, and if they die, then every time a brain cell dies, the brain shrinks a little bit. If you have millions of brain cells dying, your brain is shrinking a lot, so insulin resistance, this abnormal blood sugar regulation, literally makes us unable to use our brain, shuts our brain down, kills off our brain cells, and it’s shrinking our brain. Nobody should want a shrunken brain. That’s what’s happening with this whole process, and it’s just … Who would’ve thought, at a time when blood sugar levels are high, that our brain cells would be starving? That’s normal physiology. That’s how our body works.

6:41  I interjected that an easy answer is to just have 10 Diet Cokes a day. We see what that does to brain shrinkage. Dr. Masley answered, Yeah, just shrink your brain like a grape to a raisin as quickly as humanly possible. That would be an effective way to finish yourself off.

7:03 I asked what is the best way to test for cognitive decline in your office? Dr. Masley answered that while there are many labs we could look at, like thyroid and blood sugar and sodium and mercury and B12, but he does cognitive testing on the computer.  These tests measure how your brain functions, looking at memory, both word memory and visual memory, as well as at brain processing speed and the ability to focus.  By doing such computer cognitive testing on a computer he can detect that someone’s having gradual cognitive decline 20 years before they have real memory loss, which gives you plenty of time to try to prevent it.

8:04 I asked which test he likes the best? Dr. Masley said that he uses CNS Vital Signs, Central Nervous System Vital Signs.

8:19 I said that in your book, The Better Brain Solution, you mention you write about 12 foods that will promote brain health. Which are these brain-healthy foods?

Dr. Masley said that he organizes these foods into groups. One group would be those with plant pigments, things like green, leafy vegetables; blueberries and cherries, those anthocyanins; dark chocolate. Those pigments literally protect our brain from oxidation and inflammation. They block it. One cup of green leafies a day, and your brain is literally 11 years younger than someone who doesn’t eat green, leafy vegetables. These plant foods are really pretty powerful, and we need more of them. Even coffee is beneficial, whether it’s decaf or not. It’s the pigment in coffe that protects our brain, rather than the caffeine.  Now with coffee, one or two cups of coffee has a benefit, maybe three. Four or more is actually harmful.  We call that a J-shaped curve. A little bit is good; excess is not better. That also applies to alcohol. Red wine in moderation also improves brain function and decreases cognitive decline, one or two servings with dinner.  Hard liquor and beer had no benefit, and if you drink more than two, three servings a day, no! It’s not good. All these are plant pigments, so those are all plant pigments that are good.

Another category is smart fats.  Our brain is mostly fat by weight. It’s 40 percent fish oil by weight, and 60 percent fat. We need healthy fats in our diet, and the idea of a low-fat diet to me is crazy. It’s now a closed case. They did the largest study probably ever with the low-fat diet versus a Mediterranean diet where they added more extra virgin olive oil or they add extra nuts, and by adding nuts or olive oil, brain function improved and cognitive decline slowed down. Those on the low-fat diet, their brains just kept shrinking, and they had increased dementia. Yes, we need healthy fats, like cooking with avocado oil and eating avocados and wild salmon and all the seafood that’s so good for us. Extra-virgin olive oil, nuts, dark chocolate, those are all great fats for our brain that we want more of.

Dr. Masley continued, that we need spices and herbs, because they’re anti-inflammatory. His favorite spices are Italian herbs, especially rosemary, and curry spices like tumeric. Those are very anti-inflammatory and they block oxidation,  He would also include a probiotic in the foods that have been shown to protect their brain.

11:29 I said that in your book, when you were talking about the healthy fats, I noticed that there was one healthy fat that’s really embraced by the functional medicine community today, and that’s coconut oil. It’s frequently mentioned as a fat that you should purposely take to promote brain health, but I get the impression that you’re not entirely convinced that coconut oil is a healthy fat.  Dr. Masley explained that he thinks of MCT oil (medium-chain triglycerides) from coconut oil as more of a supplement, which has been used in clinical studies and shown for people with mild cognitive impairment to improve their brain function.  But coconut oil only has 20 percent medium-chain triglycerides and it’s mostly other forms of fat.  Dr. Masley said that he uses coconut milk in his recipes in his Better Brain Solution book. But he doesn’t feel that we have the data for coconut that we do for MCT oil.

Also, there is one cardiac concern about coconut oil in people who have known cardiovascular disease, when we give them coconut oil versus olive oil, they showed endothelial dysfunction. Their arteries literally constricted, and they showed increased oxidation. Dr. Masley doesn’t recommend people with known heart disease or people who are being treated with cholesterol meds add coconut oil, because it can increase cholesterol 50 to 70 points.  For athletes, coconut oil is a great fuel source. If I’m on a two-, three-hour bike ride, I’m probably going to use coconut milk in my shake before I go to get those MCTs. I think of it as a healthy food source. I think it’s probably good for the brain but not proven. It’s great for athletes, but I’m still waiting to see. We don’t have the proof like for olive oil or for nuts or for seafood, which clearly have been shown to have brain help. We don’t have that yet for coconut oil, so I’m glad you asked.

14:01 I asked Dr. Masley if the worry is because of the saturated fat content, and what he thinks about the role of saturated fat in heart disease? Dr. Masley explained that he doesn’t think know that saturated fat is harmful and the bigger question: Is it clean? Does it have pesticides? If you’re eating meat and butter, is it organic? Is it from from a feed lot where they used Round-Up and all these chemicals? He’s much more concerned about, “Is it a clean fat?” than, “Is it saturated fat?”

There’s a caveat to that, which is that the 20% of people who have the APOE-4 genotype.  They tend to have more oxidation, more inflammation, have a higher risk for heart disease, for memory loss, and Alzheimer’s disease.  They tend to have very high cholesterol, so for them, saturated fat tends to increase their cholesterol even more, and there’s actually studies that show in the APOE-4 folks, that more saturated fat increases beta amyloid production.  Those with APOE-4 genotpye should keep saturated fat intake moderate, like no more than one or two servings per day.

16:12  I asked what is the best oil to use for cooking?  Depending upon which chart you look at, there’s a lot of controversy which temperature different oils burn at and which is the best oil to use depending upon what temperature you are cooking at.   Is it okay to use coconut oil at high heats? Dr. Masley said that if you use extra virgin olive oil, the smoke point’s 400, so he never goes above 375.  Coconut oil has an even lower smoke point–350, so it’s not a good oil for high heat cooking, but most people think that it is.  If the smoke point’s 350, he will only use low or medium-low heat. Rather than coconut oil, Dr. Masley prefers to use avocado oil, because it tolerates up to 520 degrees. If you use use coconut oil or coconut milk in a curry or a recipe like that, you should wait til you drop the heat to add it.  For high heat, the best oils are pecan or avocado.

18:07 I asked what constitutes high heat?  Dr. Masley answered that high heat is more than 475 degrees. Medium-high, like when we saute vegetables and protein is about 450-475, so you could use almond or macadamia nut oil. Or you could use pecan or avocado oil. Another alternative would be ghee, clarified butter, which tolerates up to 475 degrees. Regular butter only has a smoke point of 350 degrees and it starts to be damaged and turns brown as with medium to medium-high heat. When you purify it and you cook it at low heat and the foam comes up and you scoop off all those bubbles and you’re just getting it down to an oil that is very stable. Ghee is basically clarified butter and can be heated up to about 475. Also most people who are dairy intolerant can tolerate ghee because almost all of the proteins are gone. 

19:48 I then asked what are the most important supplements for brain health? Dr. Masley talked about the benefits of vitamin D, mixed folates, extra B12 in the methylcobalamin form rather than cyanacobalamin, chromium, and magnesium, which you could get in a two pill multivitamin/mineral. Dr. Masley also recommends fish oil, a probiotic, and curcumin, which comes from the spice turmeric. Rather than test patients for MTHFR, Dr. Masley prefers to just give all of his patients the active form of B vitamins, since it is so safe. 

24:55 I asked Dr. Masley to explain how exercise is important for brain health. Dr. Masley explained that his clinic data demonstrates that the number one factor that improves brain processing speed … literally to make your brain quicker, sharper, more productive … is fitness. It’s not about how many minutes spent per week.  All the relationship is with how aerobically fit you are and your muscle mass and strength. Independently, aerobic fitness clearly helps brain processing speed and even increases the size of your brain and helps improve insulin resistance, which is the number one cause for memory loss. Strength training does, too. Independent to aerobic activity, adding more strength training, adding more strength, muscle mass, improves insulin resistance. It helps enlarge the brain. You get brain derived neurotropic factor BDNF that goes up.  80-year olds have been shown to increase the size of their brain when they add strength training, so we really want both aerobic work and we want strength training on a regular basis. 

26:44 I asked about the dosage–How long do people need to exercise for? How much should be strength versus cardiovascular training, and how many times a week should they exercise?  Dr. Masley answered that he does  fitness testing in his office, so all his patients are required to come in and do push-ups and sit-ups and sit and reach and VO2 Max Stress testing. They show up in gym attire, and that’s what my patients expect. Other doctors’ offices, they get a blood pressure. With Dr. Masley, they’re doing push-ups and running up a hill. He goes through their nutrient intake and harasses them over their food.  Dr. Masley explained that when he measures fitness, he compares his patients to their age group and he’d like them to be in the top third for someone 10 years younger than their age. Dr. Masley feels that 20 minutes of intense interval training three days per week can give you the same benefit 30 minutes of moderate activity five days per week.  An ideal routine would be do intervals three times a week, strength training twice a week and then add yoga once a week and then do a moderate, long thing on the weekend, like a 23-mile bike ride or like a two-hour bike.

28:57 I asked Dr. Masley about the software program Heart Math, which he talks about in his book?  Dr. Masley explained that with Heart Math the patient is hooked up to a monitor to measure their heart rate variability and they are asked to do a meditation exercise and see how calm and relaxed they can get in two minutes. Most patients are so stressed out that they are not very good at relaxing. Heart Math tells patients whether they are calm, semi-calm, or agitated. Dr. Masley works with them with different verbal cues to get them to practice relaxing, such as “Think of going to the beach.” It’s a really fabulous feedback tool to help people get calm.

32:17 I asked Dr. Masley about the role of toxins such as tobacco, mercury, pesticides, etc. in affecting brain health.  Dr. Masley answered that the brain’s the most sensitive part of your whole body to toxins. If you have elevated pesticide levels, you’re 350 percent more likely to get Alzheimer’s, so we really do need to worry about pesticides. Tobacco drops brain processing speed and overall cognitive function. Alcohol at more than one or two glasses of wine is also a toxin. BPA lined cans are also a problem and two cans per week increases your risk of diabetes and insulin resistance by 20%. Dr. Masley also said that people should stop cooking with plastic and putting plastic containers in the microwave. He also talked about the danger of eating deli meats, hot dogs, and bacon with nitrosamines, which have been shown to be neurotoxic and to kill brain cells. We can actually kill off and make rodents have Alzheimer’s just from eating the amount of bacon people would get from going to the restaurant every day. 

 

Dr. Steven Masley can be contacted through his web site https://drmasley.com/ where you can get a free Better Brain Shopping Guide or by calling his office 844-300-2973.  I highly recommend his book, The Better Brain Solution, which is available from Amazon and Barnes and Noble, https://www.barnesandnoble.com/w/the-better-brain-solution-steven-masley-md/1126646685#/

Dr. Ben Weitz is available for nutrition consultations specializing in Functional Gastrointestinal Disorders like IBS/SIBO and Reflux and Cardiometabolic Risk Factors like elevated lipids, high blood sugar, and high blood pressure by calling the office 310-395-3111.