¶ Introduction & Adair's Background
Hey everybody,
it's Dr Eric Balcavage. We're back for another edition of the thyroid Answers podcast. We have a guest today. Her name is Adair Anderson. She's a registered and licensed diet dietitian, nutritionist. She'll tell us
what that means in a second here. But we're going to talk about gut physiology, and we're going to talk about a test called the gut Zoomer test, which is a test I use pretty frequently, and there not only probably uses this test in her practice pretty frequently, but also is kind of an advisor with vibrant labs who's one of the is the company who actually produces the test. So Adair, welcome to the thyroid Answers
podcast. How are you today? I'm doing all so I guess the place to start is just to give every have everybody get a little bit of background about you. Who are you? What you do, and how did you get into working with vibrant labs and being here today to talk about the gut Zoomer test. Yeah,
great question. So, you know, I'm a dietitian nutritionist. Got the private practice, but also wanted to get involved on the lab side of things, and one of the women that I've looked up to in terms of educating people on evidence based stuff. Dr Marybeth Augustine worked at vibrant, and there was an opening for position on the clinical team, and I jumped at the opportunity to learn more about lab testing.
So been with vibrant for over four years now, and did such a good job on the clinical team, they've taught me and brought me over to the marketing teams, and I'm the Product Marketing Educator, where anytime we launch a new test, I get to explain that test to not only everyone internally vibrant but also all of our clients, all of the healthcare providers who order vibrant testing. So it's my job to learn the ins and outs of all the tests.
So let's talk a little bit about gi testing, maybe why it's important. From a medical standpoint, we typically think about the the GI track. Is there a problem in the GI tract? The testing that is typically done in a in a gastroenterology practice is a bit different than functional based testing. So can you touch base? Hey, what's the standard difference between a gas what a gastroenterologist is going to look at versus what some of these functional tests look at?
Yeah, so most gastroenterologists are going to be trying to diagnose something. So they're looking for elevated calprotectin to diagnose ulcerative colitis, Crohn's disease, that there's actually a change the mucosa, and it's like actively bleeding, you know, if there's like occult blood, for example, you can also do a oocyte and parasite test in Omp to look for actual parasite in the stool, although that is often falsely negative because they're stealthy and you can't
always find them. In contrast, a functional stool test is going to look at pretty much everything within the gut microbiome, well, specifically within the colon. It's stool test stools in the colon. And so in terms of vibrance, guts humor, we're looking at 150 commensal microbes, 76 pathogens, along with gut metabolites, digestive markers, gut antibodies. It's a really comprehensive look at exactly what is going on within that, the whole gastrointestinal
tract, tube. So are you digesting? Are you absorbing? Do you have a good balance of flora? Does your is your gut barrier intact? Do you have enough Secretory IgA? Do you have enough akermansia to help balance the mucin layer, the mucus layer, that is part of that barrier. Do you have leaky gut or not? Like you have intestinal hyper permeability, for example? So it gives you a deeper insight into, you know, what's really going on, and getting into the root cause of
what could be causing the eventual disease. But also in a preventative sense, gives you insight before that happens, you can prevent that ulcerative colitis or Crohn's disease from actually manifesting.
Yeah, and I'll add to that a little bit to even maybe from my perspective, just simplify it for the for the listeners a little bit more. When you're seeing a gastroenterologist, as Adair was saying, they're looking for a disease, a pathology, that they can cut out or medicate and say, Okay, you have X disease. And there's things called the Rome guidelines that they utilize for how they evaluate, assess and treat if you have no active pathology. That makes sense
based on the guidelines to cut out or medicate you. You will typically get diagnosed with irritable bowel syndrome or something along those lines. Your bowel is irritable. We can see some ear we can see some redness, maybe on a pathology based evaluation, but there's no pathology. There's no disease, although we would say if there's redness, inflammation, irredeem like there is something but the disease has not developed quite yet, right? So when we do a functional gi test, I should
finish that. If you go to a gastroenterologist and they do a
¶ Standard vs Functional GI Testing
pathology based testing, and it's all normal, you'll get diagnosed irritable bowel syndrome. You'll probably be provided maybe some symptomatic support, and then you'll be told to come back next year, and we'll do another assessment, and we'll keep looking at these pathology based tests until we find the pathology. And then once we have the pathology, we'll either cut it out or medicate you, and then we'll
manage the condition into perpetuity. What we're doing with functional medicine, or what we should be doing at functional medicine is exactly what Adair said. Why wait for the pathology to develop if we can measure the functionality of the GI tract, is there inflammation? What inflammation markers are elevated, and what can we learn from those markers? Is there decreased digestive capacity. And what might we start thinking about as to why the digestive capacity is is
reduced? Is there already permeability starting to develop, damage the intestinal lining, the starting develop and what can we do to intervene and then, if what's going on with the bacteria in the gut, and how might that be related to your signs, your symptoms, and what we might see on an exam, and not just on a gut zoom or a test or a GI test, but how does that reflect into like a good, comprehensive metabolic panel, and especially because the People on here are people
typically struggling with thyroid related issues? I've talked I talk about this all the time, how gut based issues are such a big problem for people who have thyroid and immune regulating, regulated disorders reduced t4 to t3, conversion. People say we just woke up one day and forgot how to do it. Your cells and tissues did not forget how to do it. It's usually an adaptive response. An adaptive response to some type of inflammatory process going on, and we can dig into that fun
stuff later. But the important part here is, when you go to a a gastroenterologist with your with your GI based symptoms, they are doing a different assessment than what we're doing with these tests, I often do the tasks. And if I see something that I think needs a physical evaluation, a medical evaluation, I'll say, hey, take these results my notes to your to the gastro. I think we need to get an evaluation done here, just to be on the safe side. And they'll often say, I don't even
know what these things are. I don't run these tests. They'll do a pathology based test and say there's nothing going on. I don't know why you're here, but these we don't want something to occur, and that they're not running these tests on a regular basis, therefore they really don't have a knowledge base about what all these things mean. And so that's part of the discussion today, is, why would we do this test, and what do these things mean? You okay with all of
that? Sounds great.
So functional gi test. There's lots of them on the market, and I I've been in I've been in practice 30 years, so I've seen lots and lots of functional gi tests. But the gut Zoomer is the test I run exclusively at this point, when I when I want to initially evaluate what's going on with gut and gut physiology. What sets the gut Zoomer test apart from all the other functional based gi tests that are on the market? Because sometimes people don't know they get they say,
Well, I had a GI test done. I had this one done, or that one done, or this one done. But what? What's your stance on why this test is maybe the best test to run on somebody well, for looking at the functionality of the GI track,
yeah. So the reason the gut Zoomer is sort of a step above the others is because we use the most evidence based gold standard methodology for identifying what is on the test, all of the markers, for example, for identifying commensal bacteria and pathogenic bacteria, we use real
time polymerase chain reaction, or RT, PCR. And in addition to that, we also do bead beating and somatic and thermal processes to get rid of any biofilms, to really get to the nucleic acids in order to identify those specific microbes. And we also use not only 16 s, but 20 3s and also
proprietary Sections and. Um, if you only use 16 s, and you give a company 20 different microbes, just running 16 s, you might end up seeing 80 different microbes, whereas when you're using 16 plus 23 plus proprietary mechanisms, you could accurately identify those microorganisms, certainly with pathogens like we they're known things like with E coli, we know exactly what to look for, and so you only need a couple of probes for pathogens.
But for commensals, there's so many of them, we have proprietary ways of identifying exactly that organism, so we know it's very accurate and precise. In fact, our gut pathogen study showed 100% oh gosh, I can never remember sensitivity or specificity. We got 100% specificity and a 95.9% sensitivity, meaning no false no false positives. If you have it, you have it. If Scott Zoomer says you have this pathogen, you absolutely have it. There's a small chance we've missed it.
But if you if it says you have it, you have it on the test. And then terms of the other methodologies we're using, LC MSMS, liquid chromatography, tnms spectrometry, which is a
gold standard for identifying small molecules. We are using that for all of our, you know, bile acids, short chain fatty acids, fecal fats, meat fiber, vegetable fiber, and then we're doing our proprietary chemiluminescence microarray for all of our gut antibodies, so tissue transglutaminase, staminating, glad and protein, anti Gliadin, anti actin, anti LPs, and also anti Saccharomyces cerevisiae antibody or ASCA. And I can totally dive into that, but at the top, that's like a, I
think it's still, look, yeah, that's a little too we don't need to go that deep. I think for some of this, because it's a lot of people are going, I don't even know what those things mean. So we'll try, and we'll kind of skip and we'll kind of scale it back a little bit. But there are
some tests that are available on the market. I'm not going to mention names, but people go and get these tests on their direct to consumer tests, and they and when I have an initial conversation with somebody, they're like, Oh, I had my GI I
¶ GUT Zoomer Advantages & Technology
had a functional gi test, and I'll get a test, and it's just a bunch of bacteria on there, and they're like, this is my gut test. And here's and maybe it's got some genetics, and here's the recommendations I was given. My challenge with those tests is, A, I'm not sure how accurate the information is. B, it's just the biome potentially, right? It doesn't tell me what's how well are you producing pancreatic enzymes to help break down and
kill the bacteria and the food that's coming in? It doesn't tell me anything about FAT, FAT, FAT malabsorption or lack of absorption of fats, right? It doesn't give me an idea of the intestinal lining. Is that starting to become problematic? There's a lot of things that aren't on those tasks, that are from my perspective, are critical to helping our clients.
Just looking at the bacterial balance, looking at the bacteria there, I don't know if it provides me with as much information that biome can change pretty rapidly, many times. And so it is sometimes I think the argument as to I hear from people in in the allopathic world, like the biome changes all the time. This is, it's a ridiculous test, but the biome stuff that we see on the gut Zoomer, we get information from
it, for sure. But I'm not looking at only the gut biome. I look at the gut biome and say, Okay, why is this the biome that this person is developing, and all of those other functional tests are important. So do you see a challenge with some of these direct to consumer tests that are just providing bacteria and then providing recommendations based on just the bacteria that's there?
Oh, absolutely, yeah, if you're just looking at the bacteria, like, as you said, it can change rapidly based on what you eat. For example, if you take a vacation to a tropical place and they're eating lots of pineapples and guavas, like the fruit loving bacteria will grow in numbers because you are feeding them, and then as soon as you go back home and start eating your meat potatoes, like those bacteria that were thriving on fruit will die because you're no longer
feeding them fruit like it can change very rapidly. And so when you want to look at what's going on in your microbiome and how that's impacting digestion, absorption and inflammation in the gut, you really want to start top to bottom and look at anything that could be going so starting again, thinking about the gut Zoomer from the top of the GI tract, from your mouth to your anus, like first you want to make sure, are you digesting your food, right? The gut Zoomer is going to look at pancreatic
elastase. It's going to look at bile acids. It's going to look at fecal fat. So are you digesting your food, and are you able to break it down in terms of fat? Fat breakdown through, through vial after that you want to see, are there a lot of good bacteria populating your gut? So for example, is it easier to build a house in Manhattan or the middle of Montana, where is
there more real estate? Right? Probably in Montana, there's more land available to build, maybe money aside, right, not thinking about that piece of it, but the fact that Manhattan is already populated, every square inch is covered in some type of concrete harder to build there. So we want a microbiome that has
lots of good microbes, commensals. We call them. We want lots of commensals, because that way, if a pathogen comes in, it's not going to find real estate, it's not going to find a place to build to live, whereas if you have low commensals, if it's like a barren wasteland, like there's nothing there,
anything can grow there. An example is that my friend went on a camping trip and use a little too much iodine to clean his water and end up wiping out, wiping out, like all of the microbes, and then got a cluster of difficile infection, because there's nothing to compete and prevent that from happening, and C diff is awful, so don't recommend doing that.
Well, we'll touch base on that. It will get we'll get back there. I do want to touch on one other thing you said regarding the testing, and it was regarding the biofilm breakdown, and I think this is really important. And years ago, when a really one of the more popular test, functional tests, came out, kind of new on the market, more markers than maybe was out there on previous testing, and I ran a test on somebody, and then I provided a an enzyme, a systemic enzyme,
and then there was a problem with the collection. We collected a kit about a week and a half later, and we get the new test results back, and the bacterial balance, there's a lot of difference. There lots of difference there. And so I, I'm like, What is going on here? And, you know, this is maybe more than a decade ago. And so I was like, What the heck. And then I I spoke with somebody. I reached out to a biologist, and
I said, Hey, what do you think would create this? Because I had reached out to the company, and they're like, I, you know, they gave me a bunch of comments, but none of them seemed to land appropriately. And he he said, Well, you provide a systemic enzyme. You probably broke down the biofilm. You should be doing that before every test anyway, right? I'm like, no, like, I wasn't at the time. Nobody was mentioning, Hey, we should do
this. And so it became the thing that I started doing. I don't do a lot of the other testing companies do what you guys do to try and break down biofilm prior to collection?
Yeah, I can't speak to what other companies are doing. I just know that we make sure to do these thermal, mechanical and enzymatic processes so the bead beating, literally beating, like with beads and a bead beater, like, moves around, knocks them around, so it breaks down that biofilm. It breaks down biofilm is sort of like the microbes building a home for themselves. It's like this little raft where anyone can go and live, and then they have this community. It's
sort of like a commune. But you want to, like, break that down and pull it apart. So we can actually get and identify what's in that, what's stuck inside the biofilm. Otherwise it could be
¶ Direct-to-Consumer Test Limitations
things could be hiding in there, like geese, for example. So bead beating mechanically breaks it down, you know, literally pulls it apart, sort of like chewing your food. Mechanically breaks down your food, and then enzymatically, anytime you add an enzyme, it's going to also break down those those compounds. And then third thermal processes is heating it as well. So when you heat something, it can also break it down, like it can soften vegetables when you cook them,
right? They're not crunchy now they're soft and mushy, like that's what we're doing to the biofilm. So it makes it a lot easier for it to disintegrate into a liquidy substance, so that when we do the polymerase chain reaction, when we're putting all the enzymes in there to make amplification happen, they can actually bind to the target, because it's not getting stuck.
Yeah, and so this isn't for the listener. This is really important because the or almost all the organisms, have this biofilm. It's their kind of protective coating. It's like me sitting in my office. Nobody knows I'm in here, right? They can, you know, they can hear me, maybe. But the the immune system, if there's bacterial overgrowth, the immune system sometimes can't see through those biofilms to get at the organism. So you could have all kinds of signs and symptoms.
But if. Doing a test and you haven't used some type of systemic enzyme or biofilm disruptor prior to testing, or the lab that's doing the testing isn't going through that process to mechanically break down or enzymatically break down that biofilm. You may not see what might be contributing some of the immune some of the immune based challenges that are going on, and maybe some of the signs and symptoms, right? Exactly. So
I want to talk about commensals and pathogens. Okay, because these terms may not be familiar to everybody, and the way I explain it is, commensal bacteria aren't necessarily good or bad, but they're like the neighbors. In my neighborhood, there's 114 homes here. Everybody who owns a home here
deserves to be here, okay? But if I've got one of my neighbors, likes to party a lot, likes to invite everybody over and their party until, you know, all hours of the morning every night, even though they are part of the neighborhood, it is going to potentially create a problem for me, right? And if I have another neighbor who loves to live in his their vacation home in Florida seven to eight months out of the year, and that means those seven to eight months out of the year, they're not taking
care of their property, it becomes disheveled. It doesn't look great. The grass is great, growing too high and it too can become a problem, right? So sometimes people think, I either have pathogens and that's a problem, that these commensal bacteria, which are bacteria that are supposed to be there, can't be a problem. So let's, let me have you just kind of break down. What do we consider a pathogen? What are commensals?
Are there good? Is it or am I wrong? Are commensals only good, or can they also be problematic?
Yeah, great. Thanks to break down a nuance apart here so pathogens are things you do not want you know, for example, clustered in difficile, like it causes illness in your body, it causes whatever diarrhea or gastrointestinal upset. These are things that don't provide any benefit, and they shouldn't be there, right? They're not supposed to be there. So pathogen, when you get it, you want to get rid of it most of the time, unless it's self
limiting. But that's another conversation. In terms of commensals, you can have a probiotic commensal which provides benefit to its host. So these are probiotics like akkermansia or plus or fecal bacteria and presni or roseberia that create short chain fatty acids or create vitamins like V 12 that help us as a host to give us benefit. And then, as you said, there's also just bacteria that live in existence,
like in the neighborhood. However, sometimes they can get turned to be a more pathogenic like strain, because of what else is going on in the environment. So for example, when someone is acting out poorly, like in a elementary classroom, like it leads more kids to also act out. And sort of it sort of changes the the mental, the mentality of those microbes to be more on the pathogenic, not pathogenic side, but like on the bad side, to be more, more problematic.
Problematic. That's a good word, problematic, and also sometimes when you have too much of a particular bacteria, for example, when you have too many lipopolysaccharide producing bacteria, to me, the gram negative bacteria from the Proteobacteria phyla that causes more inflammation in the gut. Because LPS is inflammatory, it can cause endotoxemia after eating. It's actually what causes sepsis if you get an infection like in an organ outside of your gastrointestinal
tract. So the balance of microbes is also really important,
yeah, and we call that the diversity, right? That. And we see that there's two indexes on the gut, Zoomer test and those two index give us some idea of like, how many different types of organisms, of these commensal organisms, we have, and how how balanced they are in between each other, right? Exactly. And we won't necessarily break them down, but that part's important. If we see that you have lots of commensals, but the diversity is not very good, then that that
¶ Biofilm Disruption Critical Process
can be one of the reasons why we have some signs and symptoms correct. So in a standard allopathic approach, they're typically not looking at the commensal bacteria at all correct, from my knowledge base, they're typically really just looking at pathogenic organisms only. And I think the reason, from my perspective, that they don't look at the commensals is because they don't really have a strategy to address commensals. So we don't, we don't address them. Mm.
Right, right, exactly.
So when we are looking at inflammation in the GI tract, well, let's, let's keep on the dysbiosis standpoint. A lot of times people are, I think, confused a little bit, like, how could I have bacterial imbalance, like, where is it coming from? And we probably need to talk about that a little bit like, what is the primary thing that leads to an imbalance? Let's just talk commensal bacteria. What's, what are some of the primary things that would lead somebody's
commensal bacteria? These are the bacteria that should be in the GI tract, most of them in the colon. But what would cause these bacteria to be dysregulated?
Oh, yeah, the number one cause is probably not eating enough fiber, rich foods, not enough plants.
So there's a whole community that would argue with you on that, right? You know that, right? So, but why would plant based foods? Because that that community would say plants have toxins. Toxins damage the GI lining, therefore plants are bad. You should not eat plants. But let's talk about why fibrous based plants could be beneficial to the gut and the GI tract.
Yeah, I'm solidly in camp fiber over here for sure. So come after me, if you want folks who believe the other side. But yeah. So what feeds our short chain fatty acid producing bacteria are prebiotics, fibers, polyphenols. These all come from plants. Our microbes will take these undigested carbohydrates and things and turn them into short chain fatty acids. Short chain fatty acids are essential for
the gut lining. They heal and seal the gut. They help produce new cells people, they actually there's a study that showed people who had higher short chain fatty acid levels had better COVID outcomes like short chain fatty acids are really important. It is like the number one source of fuel for your colonocytes. And you don't have enough of them, your colon cells are literally starving. And eating plants is what feeds these good microbes, feeds these 10 months old microbes,
yeah, and so I'm in agreement with you, but I'll take the other side of it as well too. Okay, so for the listener, like, if you are, if you already have a lot of gut based issues going on, you have a lot of signs and symptoms and
issues going on and a lot of inflammation in the GI tract. It is, it is, there is a truth to the fact that plants have some level of toxins in them, my belief is that primarily, when we eat healthy, properly raised crops, and we eat them in season, when they're when they're at when they're ripe, they have a lower level of toxicity. That's probably not problematic, but plants don't have much of a way to defend themselves. So having higher level of toxicity when they're
not ripe protects them. In nature, we have a tendency to pull our our crops way before they're ripe, we force ripen them in a factory somewhere, so they look beautiful and we can then we eat them. But that doesn't necessarily mean that the toxicity of the plant is is gone because we force ripened it. It may still have a higher level of toxicity, but even
those toxins in the plant have a benefit. In a healthy GI tract, they are like exercise for the immune system of the GI tract, if you're not constantly stimulating the immune system to some degree low level, the immune system gets weaker over time. So these plant based foods, healthy in season, appropriately ripened, can have a positive effect in beefing up the immune perspective, immune system, from my perspective, it's like lifting weights, you could argue, Eric, why would you
ever lift weights? If because weight lifting breaks your muscle tissue down, correct? It does. It creates, breaks it down, creates low grade inflammation, but that low grade inflammation then helps me build a bigger, stronger muscle tomorrow, so today, if I have to lift something heavy, I actually have the ability to do it. If I never did anything to strengthen my muscles, I wouldn't be able to do it, and I'd probably get injured. Is that fair?
I think so. Yeah. So I think
there's a benefit to them, but I also understand why. Sometimes, when people already have a lot of inflammatory processes going on, they go, Oh, I switched my diet and I felt much better. Well, a that dietary switch probably
create a big change in your gut biome. And if you are more plant based, and that was and you already had inflammation and dysbiosis and other things creating disruption there, minimizing some of those plants and plant toxins might calm the inflammatory process at least temporarily, but I do agree that. Short chain fatty acids are critically important, and we'll talk that more about that in a sec.
Then there's also the digestive piece and the stress piece as well, because someone can be eating the perfect diet, but they're stressed all the time. And anyone who studies stress knows that when we're stressed, our blood flow is shunted away from our digestive organs, away from our fertility organs, into our arms and legs so we can run our fight, so we can literally flee or fight and survive the
situation. Because if you're about to be food for a bear, there's no reason to digest our food in terms of prioritization, the goal number one is get rid of get out of the danger zone. And so when that happens once or twice a month? Like, no big deal. But when it happens all day, every day, and I have lots of clients who are stuck in fight or flight,
yeah, absolutely. And I talk about, I always look at somebody's physiology from the perspective, is this a person in homeostasis or allostasis? And I talk from the lens of the cell danger response, and that's why, on this podcast, in my book, and all the things I talk about, I don't think thyroid physiology is broken. I don't think the immune system is out of control. I think everything is an
¶ Commensals vs Pathogens Deep Dive
adaptive response. And so many of our clients are under an excessive stress load, and somebody might say, but you know, I had the same stressors. Then this happened, and now I'm back to the same stress load. I can't handle it right, because you had an excessive stress load. You were managing it. You were in homeostasis. But then that extra stressor pushed you into cell stress response, and that shifted you into Allostatic regulation. You up regulate, start up regulating the
sympathetic nervous system. Brain gets more wired, more as you said, more energy, more blood flow goes to the brain and the muscles so we can run. What gets down regulated, gut physiology, sex hormone regulation, detoxification pathways, these sleep, like all of these things that make us feel wonderful, get down regulated, right? And we ramp up the the immune the defense mechanisms and the hormone that helps us regulate the shift from homeostasis to allostasis is
thyroid hormone. By decreasing the conversion of t4 to t3 in the cells that are perceiving stress and danger, we actually slow down mitochondrial function. We stiffen cell membranes from a protection standpoint, and that doesn't make us feel good, but that allows that lower t3 state actually activates the cell defense mechanisms inside the cells. So we often look at the low t3 and somebody's like, oh
my gosh, your body can't convert t4 to t3 anymore. That is such nonsense, in my opinion, that is the adaptive response and adding more thyroid hormone in that situation, especially t3 Yes, you can give a temporary hit of improvement, but actually can increase the oxidative stress in the inflammatory process that's going on, up regulate the sympathetic nervous system and down regulate the parasympathetics. So I fully agree that stress, right, real or perceived, right? Everybody
thinks it's just emotional. So it's what you think about, your work, your relationships, right, your partner like what you worry about, right on a daily basis. And so many of us, I think, are in chronic perceived stress, and we don't even realize it.
Totally agree. Would you say that for the top five things that cause the cell danger response, stress is one of those top five? Well,
I look at stress as the big category. So, right? So stress is stress, your cells don't really know the difference. So I look at definitely mindset, like, What's going on between the six inches of my ears? Because you know this too, right? I could get yelled at and I could be like, Oh man, that person's crazy. It doesn't bug me, right? Or I could get yelled at and I go, Oh my gosh. And now I get angry, and that changes my physiology, right? COVID, you mentioned
COVID. The COVID comes. Everybody goes inside, people, some people stressed, worried, my oh my gosh, my money. What am I gonna do job? Other people are going, This is awesome. I can work from home. I'm moving to the beach. I'm gonna start investing in these different things where they need me and that person under the same stress situation thrives, right? So it's it's really not the stuff as much is, is, can I
manage it, and how do I perceive it? That's so I always tell people the mindset is one of those top things that create stress. Number two, for me, is somebody's habits. What do they do, day in, day out, right? Those things that their habits Make, make or break them. Okay? Number three is sleep fitness. To me, prioritizing Sleep, sleep, good sleep. Habits, good sleep behaviors. Good sleep schedule is critical. Number
four, diet, what we eat feeds our microbes, right? We've got more microbes than we got genes, so if we don't feed us, well, we're not just feeding us for taste and wow, that makes me feel happy, but we have we're feeding the microbes. So what we feed them, determines what grows. And then my fifth, like foundational, what I call fitness factor, is physical
fitness. Because we, I'm sure you know this physical movement, physical exercise at the right amount, not excessive, but the right amount can have huge impact on our overall physiology, from neurotransmitters, hormones and gut physiology. So those are my foundational five. I've got 13 other ones I work through with clients from, hey, what's your relationship like? What's your what's going on with your finances, like those, all of those things create our body's perception of danger
totally. Yeah, you can go into new ones from all of those too, in terms of like diet, also circadian rhythm. Are you eating at the same time every day? Because your body will anticipate the food and will actually start getting digestive juices ready to go, which is why when you wake up for an early morning flight, you're not hungry, and when you eat, then you don't digest as well.
Yeah, absolutely. And so the key piece, I think, for a lot of people, when we're running these tasks, right, when we're running a gut test, is that the gut Zoomer tests, or whatever other tests they run, it tells a story, but it doesn't tell the story, right? Some people like, Okay, you got dysbiosis. I'm going to do my gut protocol for the next 30 days, 60 days, and they do, and somebody goes, I
feel better, I function better. And then two, three months off supplement support, they're like, having problems again. What we see on these functional gut tests is the result of your habits, your behaviors, your lifestyle and all those things. So yes, we often have to intervene and help this kind of reset itself. But we also, if we don't change the environment, the perceived environment, we don't we don't wind up changing
the terrain. And if we don't change the terrain, why would we expect 90 days after all my supplemental support that the problem isn't going to come back. Would you agree?
I totally got terrain theory never present. So
let's talk the we want to talk a little bit about the digestive capacity, and we can see problems many times on the gut Zoomer task with reduced digestive capacity. But if we had to give somebody some guidance, they get a gut zoom or test. They see decreased pancreatic enzymes on there. They see fat malabsorption on there. Like, what are things that somebody as a clinician or a client, if the clinician goes over the test, what are the things that might be they should
be thinking about, like, why? Like, I always say, Look, if you have decreased pancreatic enzymes, I can give you digestive enzyme temporarily, but we got to figure out why. So what are the things that you would suggest just generally, when you see reduced digestive capacity? What are the things you want to help inform your clients of like, Hey, here's things we need to consider, or that you're instructing a clinician who's coming for you. Of like, hey, how do I interpret
¶ Factors Affecting Gut Health
this thing? Yeah,
so number one, just overall stress level. Are you stuck in fight or flight on a more incremental segment, like before meals? Are you taking some deep, relaxing breaths to get in to rest and digest. And then are you actually being with your food and eating your food, enjoying your food, like when you go to a nice restaurant, you have a drink, you relax,
everything tastes amazing. You're really in the moment. But if you're just eating food to get to the next thing, or you're eating while doing something else, like working or studying, which is the worst, like, are you really there with the food? No, it's just going in the body's like, I don't what are we doing right now? Are we thinking? Are we working? Are we digesting and so making mealtime a time to just nourish your body and paying attention? Some people call this mindful eating.
So smelling the food, I don't know if your mouse ever started watering after you smell cookies out of the oven. Like that's your body getting a head start on digestion, so smelling the food, really tasting the food, noticing textures, eating more slowly, putting the fork down between bites, if you have a hard time eating slow, maybe eating with a non dominant hand, or using chopsticks, eating with other people, having
conversation, anything to slow down the eating. So it takes longer, I know in a lot of Mediterranean countries, they'll have like, meal time last two hours, and it's a social event. Everyone's happy and enjoying life like that's what a meal should be. It should be a time to nourish your body. So if that's not what your meal time looks like, that would be a great place to start. And then the other component is eating
about the same time every day, so you. Get into eating rhythm, that circadian rhythm and alignment with when your body anticipates food, so you have the best ability to digest, absorb and assimilate those nutrients and utilize them for repairing toward muscle tissue or restoring your your immune system, for example. Yeah,
I agree with those things. The other thing I would add to that is you gotta chew your food. When we think about what's going to start to cause acids and enzymes to be released. Chewing your food appropriately really sets the stage. That's where the food starts to break down. In the chewing process, we start to we have enzymes that start to break it down orally. Then from there, we start putting stuff into the stomach, and the stomach acid then gets stimulated, and that
should start to break it down. And the downstream impacts of digestion are really based on the acidity of the kind the stuff that's leaving the stomach to come into the small intestine. There's sensors there that tell the gallbladder, hey, you got to release some stuff. Pancreas, you got to release some stuff here. If you're just gulping, gulping down, throwing some water down on top of it. And that, I guess, would be the other thing I would say is, hey, don't be drinking if you're
thirsty. When you're eating, you're probably not chewing your food appropriately. So do you agree with those pieces as well? Absolutely.
Yeah. And for people who have hard time chewing, look at your teeth. Go to a dentist like get that fixed as well. If you have pain in your mouth, it's going to be hard to chew missing teeth, anything like that,
yeah. And I would say too. If you got oral issues and you're struggling with chronic hypothyroidism, thyroiditis, reduce conversion of t4, to t3 what goes on in the oral cavity can be be a huge driver of your immune inflammatory issues, and your reduced conversion of t4, to t3 other lab, there's another lab out there I like, and they do a panel that looks at some of The most common organisms that trigger immune conditions and oral bacteria. I can't tell you
how many patients who I've worked on my gut. I've done this, I've done that, I've done that, and we look at their oral fitness through a questionnaire. I'm like, Alright, there's some oral there. You're got some areas here. We should get checked out. And then if we do run a test and that, here you go, oral bacteria popped up. I don't have any tooth problems. I
don't have any pain. I don't guess what. You got antibodies to these oral bacteria, which means they are creating a reaction, and that also so the oral cavity becomes really critically important.
Yeah, I decline. What a cavitation. She addressed it, and all of a sudden she lost a bunch of weight and was able to, sort of like, totally excel in her physi physical, like, performance. Yeah,
I have a client 20 years ago. I think she had a wisdom tooth pulled out. And we worked on a lot of different things, and we then we ran that task, and I'm like, Yeah, positive for oral bacteria because I don't have any, I don't have any root canals. I don't have any cavities. I don't think else. I'm like, Well, go get a comb. Well, go get a cone beam X ray done. The first dentist, I think, just did a
regular x ray. The second dentist did a cone beam. And sure enough, in that pocket was a whole bunch of infection in there. And I'm like, That's why you can't get your immune systems stable. That's why your thyroid gland is under attack. That's why you can't convert t4 to t3 Well, what do we do? We do? You got to get cleaned out like this. And so it's been a process to do that. But things are oftentimes hidden, even
where we don't have signs or symptoms. I don't want to, I want to stay on this kind of theme so we're chewing and we need to have appropriate stomach acid. The gut Zoomer doesn't have a an assessment specifically for stomach acid production.
It does not but
we do have the next steps and for the for the listener, if you have a clinician who's looking at general blood chemistry labs and looking at your signs and symptoms, we can pretty much give you an get an idea that you have low stomach acid production, but it's not on on this test, because this is really more a functional test further down the GI tract, but there are markers of let's take pancreatic elastase one. Let's talk about what that is and why
might it. What should it? What should the range kind of look like, and if it is low, what are the common strategies and what are your thoughts when that when that value is low?
Yeah. So pancreatic elastase, one is an enzyme released by the pancreas. It does not get to grade it when it goes through your GI tract. So when we measure in the stool, it's a good representation of how much pancreatic juice your pancreas is releasing in response to a meal. So it's a stand in representation of how well your pancreas can release enzymes to help you digest break down and somatically break down your food in order to better absorb it. So when it's low,
that's indicating. To mean that something is not allowing the pancreas to release the amount of digestive juice it needs to break down your food. So why is that usually stress? Maybe something's going on with the immune system in the pancreas, or
I'll jump in there and give you some more. One of the things that's really important is there's this thing called a sphincter of ODI, which is where the pancreatic duct and the bile duct come together, and the sphincter opens up to allow the digestive capacity, these digestive pieces to come into the into the small bowel, if you have low stomach acid production, that may reduce the amount of release that's coming in. That's number one. Number two, that sphincter muscle is
¶ Interpreting GUT Zoomer Results
controlled by the amount of T available, t3 so if you have low t3 in the GI tract or and or circulation, that sphincter muscle may not open up as well as it should. And if you have estrogen, excessive estrogen, estrogen metabolites, estrogen dominance going on, estrogen will also cause that sphincter to be tighter, so it reduces the release of enzymes into the GI tract. The amount of circulating t3 also plays a role in how much pancreatic enzyme is going to be produced in the first place,
because you need t3 to support that. So there's lots of mechanisms there, and there's one other one that I I've consider, and that is, if somebody's in a cell stress response, and they've got glucose resistance, and they're struggling to produce appropriate levels of insulin to regulate it. There are there is research that what can happen is some of the pancreatic cells will become insulin producing cells, even though their primary function is to make pancreatic
enzymes. The pancreas will say, Look, we we can't deal with the glucose in the that's in the system. Now we need more insulin to deal with it. And so since food, more food coming in isn't a priority, let's hijack some of these cells and we'll make them insulin generating cells. And what goes down is the pancreatic enzyme output. So those are some of the things from my point of view.
Oh, I can tell you're the third expert, Dr Balcavage. Like I did not know that hormone like estrogen dominance, can slow down digestion, because that happens so often. And the guy has this marker called beta glucuronidase, which also could be contributing to estrogen access. If you're not making too much, you might just not be eliminating it.
Yeah, and so, but it's, these are the things like, when I'm going through the tests, and it's, I think it's important when you're when, when somebody's running this test, right? We can't just read it. We have to interpret it, right, just like blood work. People like, oh, it's outside the optimal range, therefore you need this or it's inside the optimal range, so therefore it's good. Well, no, it's not. If you have hypothyroid signs and symptoms, your TSH is normal.
That's totally inappropriate for you, right? There's reasons why that TSH means be suppressed. Same thing when we look at these tasks, right? And we look at this gut Zoomer, and we see these things a lot of those patients, and I'm guessing you would do the same thing. There's decreased pancreatic enzyme output. Let's support with a pancreatic with a digestive enzyme right now. But that's not the long term strategy. The long term strategy is to get the pancreas to actually release
this stuff more appropriately. Absolutely,
it's short term symptom reduction mechanism. And then meanwhile we support in order to return you to homeostasis.
Exactly what about the bile physiology component of this in the fat malabsorption? Can you talk about that a little bit?
Yeah. So vibrance guts. Zoomer measures several bile acids, two primary, two secondary, and then it gives you the ratio as well. So we're looking to see, are you properly converting the primaries into secondaries? You know, are you able to reabsorb bile, because we utilize it multiple times. It
gets recycled. Is that happening? And then we also look at fecal fats to see and affirm like if there's fat, if there's elevated fat in your stool, if you have floaty stools and oily stools, it indicates you're not able to digest and absorb your fats, your fat soluble vitamins, your omega three fatty acids, the stuff that helps with proper like healthy skin and eyes and brain development. So it looks at all of those things as well. So
the when we if somebody has on a on the gut, zoom or test, they've got multiple markers of fat malabsorption. Hmm, but their bile acid percentages, the metabolites are normal. Do they do they still have a potential bile gallbladder, liver issue going on? Oh,
good question. So they could have just had a really high fat meal, and their body just couldn't handle it. Or you know, the percentages may be okay, but it's percentage. It's not actual amount. So it's not telling you if there's enough of it or not just showing you the ratios of primaries and secondaries.
Correct. That's what I would say, too, because I've had patients that I've gone through the test with them, they're like you said, I had a problem with bile and physiology and fat, but this the bile acid metabolites are, are normal, right? Those are percentages that doesn't tell us total
circulating. And my opinion, you correct me if I'm wrong, we're looking at the primary bile acids are what you're when you eat, your liver releases bile acids that are already ready from your gallbladder, and then those bile acids are being recycled five, six times through the meal. And most of those
primary bile acids are being cycled through the system. We're looking at the primary bile acids on there are ca and CDCA that are on that form, there's a very small percentage of primary bile acids that make it to the colon, about 5% of the bile acids. And then we're looking at the secondary bile acids. And to me, what this really gives us tonight, idea when we look at the bile acid metabolites is, how well are those bile acids
being resorbed? Am I getting too much moving down that track and getting into the colon, and then it gives us a little bit of a story about what's happening with the colonic bacteria and how they might be converting those and there's another little nuance that's important here, and I won't get too technical on it, but I write hormone plays a role in which bile acid
percentages we see on there. So when I see somebody based on their medication, I might see an alteration in the percentage of ca or CDCA, and that's being influenced by the amount of t3 that's getting to the liver, because that changes those a bit. So that's how I look at it. So when patients say, but my bile acids metabolites look good, I'm like, that's part of the picture. But the thing that I were more concerned about to
¶ Short-Chain Fatty Acids (SCFAs) Role
say, hey, is there fat malabsorption issues here, and bile issues and pancreatic enzyme issues, is we look at those fecal fats, right? Because if you're if you're eating fat, sometimes people say, Well, maybe I just eat too much fat. I don't know if that's necessarily the case, but a lot of people just don't have great bile flow. I mean, just and if we look on that test and we see low pancreatic enzyme output, then there's a good chance that we're going to have some fat
malabsorption, correct? Yeah,
and it takes bile to move bile, so sometimes, if you have sludgy bile, just giving a bolus of like pudka Toro Deoxycholic acid, that can get it flowing again.
Yeah, and let's talk about, we're going to talk about intestinal permeability here in a bit, but this right here we talk about where we're at with this fat malabsorption. We're talking about bile that, too plays a role, and when we can where we're going to talk about permeability and intestinal permeability, right? So the I don't know if you want to touch base on the role of bile acids in maintaining those tight junctions, or do you want me to take that?
Why don't you give it a stab? I
absolutely so bile acids, just so everybody knows bile acids, these things don't just break down fats. Bile acids are anti microbials. Direct anti microbes at top end of the GI tract. They start killing the bacteria that makes it past the oral cavity, makes it past stomach acid, it starts entering into small intestine. Bile acids are there. They start breaking down biofilms and doing that stuff. As those bile acids move down the GI tract and are absorbed through the intestinal
cells. That bile acids actually help maintain those intestinal tight junctions. We're going to talk about something else that's really important on this task, that helps us get an idea of intestinal tight junctions, but those that bile helps regulate healthy tight junctions. So if you don't have good bile flow, and you have fat malabsorption, more than likely you're going to start breaking down the intestinal barrier and leading to potentially what we call intestinal permeability, or
leaky gut. Those those bile acids at the end of the GI tract also activate some of the things on the inflammatory panel, the beta defenses and other things to help deal with the bacterial overgrowth and prevent it. So if you don't have good bile flow, you don't kill bacteria coming in from your food or your oral cavity at the top end of the GI tract, and you can't control the bacteria as well at the bottom end of the GI. Eye track. Did I miss anything? I think you got it all right, fantastic. So
let's talk short chain fatty acids. What are these things and why are they important?
Yeah, so short chain fatty acids are going to be the post biotics made by your commensal bacteria. So they're turning mostly carbohydrates into these short chain fatty
acids. You can also have putrefactive, not short chain fatty acids, but the proteolytic versions, where it's breaking down protein, like fermenting protein, and those are not as good, but the short chain fatty acids from carbohydrate sacral lytic fermentation that's going to create these byproducts that are very beneficial to the body, and helps heal and seal the gut, helps repair the gut barrier, helps signal to the immune system. Just in general, really good things.
Yeah, the short chain fatty acids really important for the people with immune dysregulation. You're about 70 we think the literature says maybe about 70% of the immune system surrounds the GI tract. And that's why we're all kind of look at the GI tract when we're saying, hey, there's immune inflammatory problems. We gotta have a healthy gut. Everything's gotta come in, in through the gut. Everything's gotta come out through the gut, and there's such a signaling
mechanism to the immune system. Interestingly, there's a direct lymph connection from gut to thyroid for everybody, just so you know, if problems in the gut can directly impact the thyroid from a lymph perspective, not just a blood perspective, but a lymph perspective, but the short chain fatty acids are a huge driver to Reg, to up regulate what are called the T regulatory cells. So if you have an immune inflammatory process that gets started, we want that to happen. We want the immune system to
defend us. But if you don't have healthy short chain fatty acids, the off switch may not be there to calm the whole process down. So once that thing gets turned on, if you don't have the right bacteria, you don't have the right diet, the right bacteria to produce these short chain fatty acids, you may initiate immune response, but it may be hard to turn that off. You okay with that? You saying that? Yep, that
all makes sense, perfect.
So what is if somebody has there's a lot of times when people say, I eat a lot of plant based foods, why would my short chain fatty acids be low? What? What's your take on that? Huh, good
question.
So my take when somebody tells me that I'm like, Look, there's couple pieces here. What you put into your body is going to have an input and an impact on the bacteria that grows. If what you're consuming, even though you eat a lot of plant based foods, if they are more processed based foods, or more alcohol or more more sugars or other things that actually prevent these bacteria that take these short chain the
fibers and convert them into short chain fatty acids. If those are down regulated, you could eat all the plant matter in the world, and you're not going to produce the appropriate
¶ Intestinal Permeability & Zonulin
short chain fatty acids. Are you okay with that?
Yeah, so when you said plant based, what I'm thinking of is Whole Foods, like I went to best year University School of holistic medicine. So when I hear plant based, I think of like carrots and apples and almonds and black beans and brown rice and quinoa. I don't think of like a vegan thing that's full across, like, the processed food. Like, yeah, totally. It's, it's, you have to eat real food. You have to eat food that's from nature. Like, you can recognize it. Your
grandma could, you could cook it in your own house. Like, that's, that's the food that fuels and feeds us. It's not the convenient stuff that lives on a shelf for 12 years. And
is it fair to say that the life perception of life based stressors could potentially change the bacterial balance. So therefore, even that whole food based diet is great, but it the bacteria are being altered by the stress response. So they're not there to really at a high enough level to produce these
things, absolutely, absolutely, and we know that stress reduces your Secretory IgA as well, which is part of that barrier. It's part of the defense. It's like the guards around the castle when you have low Secretory IgA, it's like they're sleepy and they don't really protect you anymore.
Yeah, so that's another that's another thing that's on here on this test, and I think it's an important marker. So let's talk about what Secretory IgA is. I think it's important that people know what it is, and then, if it's low, what should that be telling us? And if it's high, what should that be telling us?
So Secretory IgA. A is a type of immunoglobulin. So we're looking at the immune system, and there's a sweet spot in the middle where you want it to be. If it's too low, it means your immune system isn't able to fight against a pathogen. It isn't able to fight against the neighbor that's doing naughty things. But if it's too high, that means it's actively trying to fight against that pathogen. It's actively trying to fight against something that's causing
dysbiosis in the gut. So we want it optimally to be at that normal level and not on either side, although it's probably easier to treat the high side, because you identify what it's fighting against and then get rid of that or adjust the diet, lifestyle, all the things to balance it back. It's a little bit harder to bring it up if it's low, because that's usually indicating you've been under stress for a long time, and it takes a while to bounce back.
Yeah, I want to come back to that from a testing perspective, but I I see this as well. Like, I think the same way, like, if we see dysbiosis and inflammation, I'm hoping that the secretory IgA is elevated, right? Somebody be like, Well, why would you want it high? Listen, if somebody's breaking into your home, I want the cops. I want lots of them,
right? I want them coming. That tells me that your immune system is appropriately responding if you have a lot of inflammation and you have low Secretory IgA, I'm worried that you don't have an immune system that's capable of dealing with it, and we really need to help out. And not only does the secretory IgA influence your gut physiology, but all of your mucous membranes, so all systems, nasal passages, oral cavity, eyes,
pelvic area, right? Like everywhere where you have these mucus memories, these coatings, these protective coatings of that kind of as a barrier from outside to inside. The Secretory IgA system is the police force there, right? So if they're weak, you're more susceptible to chronic organisms getting into the system and becoming latent or active or acute or replicating infections. But more oftentimes, what we'll see is that these are people with chronic, latent infections.
They're not in a replicating mode where, like, oh my gosh, I got a fever, I got chills, I got all that. But they have chronic health, low grade health issues, because this the organisms are like, nobody's stopping us. Let's go. I would do the same thing, right? Well, there's no nobody to stop me from walking on the private beach. Great. I'm going to go on the private
beach. Why not? Right? So Secretory IgA is critically important from an assessment, when we assess that, because that really does tell us, like, the state of the immune system, right? It does, yeah, there's, we're going to come back to maybe rechecking this and maybe some strategies here. But Zonulin, there's a lot of discussion about Zonulin, fecal Zonulin versus Zonulin antibodies. Some people say fecal Zonulin is not a good marker of intestinal
permeability. They say you gotta run blood tests and antibody tests. Other literature says fecal Zonulin can be used what's vibrant stance. I would say they would believe that it has, that it's can be used as a potential marker of intestinal permeability. But why did they? Why do what's the, what's the general thought process regarding fecal Zonulin? Let's start with what is fecal Zonulin, and if it's elevated in
the stool, what does that mean? And how does that maybe differ from blood testing, if you're if you're good with that,
yeah. So I like to think of Zonulin as, like the key that unlocks the tight junctions. So when there's Zonulin present, it means the tight junctions have been told to open up. It's like Open sesame. There's actually a study by Dr Alessio Fasano that talks about this. It's called Open sesame. So Zonulin opens a tight junction. So when you see Zonulin in the gut, it means that sometime when that stool was formed, Zonulin was released, the tight junctions
opened. So there was recently been depending on how long it takes you between stools, it recently has been leakiness in your gut. The reason we would also do a blood based test is because we look at Zonulin antibodies, and Zonulin antibodies provides a snapshot, or, sorry, a report card of how
long and how often Zonulin has been elevated. So whereas, like Zonulin, just Zonulin, and a blood test will tell you if it's actively elevated, like a fasting blood sugar, like, what is it right now, a anti Zonulin is going to give you a report card. If it's IgA, it's like the last week. If it's Iggs, maybe the last couple of months, it'll tell you how often it has been
elevated over that time period. It's like hemoglobin a 1c it gives you a past perspective, yeah, and they can both be helpful in hand, but if you have elevated Donald in your stool, it means you had elevated Daniel in before you in creating that. All, yeah,
so I think, like, I see both sides of the argument, but it's on here when we start to see it elevated, like, if you don't have antibodies yet, that doesn't mean we don't have a problem, right, right? We got an issue we need to address. We gotta, we gotta reduce the inflammatory process. We gotta deal with the dysbiosis. We've got to support appropriate bile flow and short chain fatty acids so that we
have less breakdown of the barrier. If we don't do that, whether you have a positive antibody test or not, you're probably going to have one, right? Is that fair?
Yeah, I mean, and lots of things can trigger Zonulin release. So there's evidence in the literature showing gluten exposure can cause it, showing LPS bacteria can cause it, alcohol causes leaky gut. Don't
tell everybody that, no, no, but there's, there are so many things that do it. That's why we promote like, whole food, anti inflammatory, low process style diet, right? Not necessarily restricted diet. My opinion is restrictive diets are short term, temporary options, but long term, yeah, we want to be whole food based. Mediterranean style diet is probably a good, great place to be, if you had to think. But whole food based, low processed food based diet is, is really,
my opinion, the gold standard. And I think it's 8020 I try to explain 8020 80% good habit, 20% bad behavior. If you do that consistently with all what if I talk about all the fitness factors, you're probably going to be fine. If you have 20% good habit and 80% bad behaviors, you're in trouble. You're going to have problems. So fecal Zonulin, if that's elevated, that tells us we're running the risk to develop more intestinal
permeability. And let's talk about what that might mean for activating the peripheral immune system or inflammatory system,
yeah. So usually your tight junctions, or your the cells in your gut are really close together to provide provides a barrier. So things in the gut lumen, the stool, doesn't get into the bloodstream when the junctions are leaky. That means things in the gut lumen get towards the lamina propria, where there's immune cells, and the immune cells get activated more often, and when the immune cells are activated more often, that means you're going to have more inflammation.
Yeah, and the other thing, yeah, go ahead and it's systemic
in it, and it will manifest wherever you're most genetically susceptible. So could be joints. Arthritis could be hashimotoitis. Could be, you know, dementia could be just brain fog could be fatigue,
yeah, those inflammatory molecules are going to set the stage for problems. Right, tissue damage we get up regulation of the immune system when those tight junctions become more permeable. Poorly digested food matter. When we eat food, we break it down, especially the proteins from the big structure to a smaller stock structure we call a peptide. From the peptide into what we call amino acids. And the amino acids are really what's meant to be absorbed across the GI
barrier. But if we get higher levels of peptides crossing the barrier, that can start to trigger more immune type reactions, if we have LPs, you talked about, that's the coding of gram negative bacteria. You have gram negative bacteria, it's supposed to be in the GI tract, but the gram negative bacteria, if particulate of gram negative bacteria, or the bacteria itself, crosses that barrier, the immune system is going to become activated. We call those pimps, pathogen
associated molecular peptides. If there's damage to the intestinal tissue, and part of that enters into the bloodstream. We call that damps, damage associated molecular peptides, and those things activate the immune system. The damps say, Hey, it's me the gut that's damaged. The immune system goes, Oh, we gotta go to the gut. If there's tamps, they go, those bind to the immune cells and say, Hey, this is the thing we're looking for. Go find it and kill it. From a thyroid
perspective, I want to make sure everybody hears this piece. We think that a lot of times thyroiditis, you'll see it written up because it's gluten, and you eat gluten and it causes cross reactivity or molecular mimicry. But what we would often not talk about, I talk about it a bunch, is that the thyroid cells themselves have pattern recognition receptors. That
means not on immune cells. Immune cells, these PAMPs and damps, these danger particles attached to the immune system, to immune cells to activate the immune system, to tell it what's the problem and where the damage is, so they can help. But the thyroid gland has pattern recognition receptors, and this is why I said I said I don't think thyroiditis is a mistake.
I think it's a, it's a it's an adaptive response, because if those camps or damps bind to the thyroid cells themselves, the thyroid cell now becomes an immune like cell and initiates the release of inflammatory cytokines, inviting more lymph. Sites into the thyroid gland and creating more damage. It's not broken physiology, because it can that process can turn back off. But if you think about it from my perspective, if the cell that's under stress and danger is trying to down regulate its
metabolism, it can do it locally. If there's lots of cells and tissues in a systemic inflammatory or danger perspective, how does the body slow down the metabolism? You slow down the production of the primary hormone that drives metabolism and that occurs at the thyroid gland. And this is why I say thyroid physio, thyroid gland hypothyroidism, and is oftentimes recoverable, but we have to address the
things that are creating this immune activation. And you're right, those immune inflammatory chemicals, those damps, those PAMPs, they can create other tissues to be damaged in time. But a lot of times, I don't think of it as just like, okay, the immune system is going to damage the tissue. I think it has something to do with alterations of the local proteins, structures because of some of these things, damage
being done. And then the immune cells kind of scooping up a debris field and going, oh, there's an organism here, or a piece of something and a piece of tissue. I knew what the tissue was. I don't know what these two things are combined. And now, because that leaky gut and that LPS being out, now the immune system says, Well, I'm going to react to what, what was connected to that piece of material. Yeah, totally. So we're going to wrap this up, because I'm sure you've got
other things to do than listen to my boring voice, right? But there's, there's one more thing I want to cover on the test, and that is fecal anti Gliadin. Mm, hmm, okay. Now a lot of people are who've already been in the functional medicine space, are gluten free, dairy free, and they get a test done like this, and it is positive, and they're like, I am not eating wheat. How can that be? How would you explain that to somebody, why their fecal anti Gliadin might be elevated despite not
consuming it? Because that in some people's mind, until I explain it to them, they think the test can't be valid because I don't need it. Oh,
totally. This happens all the time. So one, there's a lot of cross contamination. If anyone eats out, you have no idea what's happening in the kitchen. Most fried things, there's cross contamination. French fries, they're probably also frying corn. Dogs covered in wheat. You're getting gluten exposure there. Like it just happens all the time. Vegetables, they'll fry those too that'll be covered
in gluten. So you really have to ask, Do you have a dedicated gluten free fryer if you're going to eat anything that's been fried out, period, full stop. Also, just things can happen in a kitchen, like, if it's not your kitchen, you would, you don't know. You really don't know. Other times there's just lack of understanding of what is gluten,
what's not gluten. And then we also, you know, I've had a client who, I had a client who lived just down the road from a wheat field and was inhaling gluten antigen all the time.
How to Move? Is it possible that somebody with poor digestion and permeability and eating other grain like foods could have their immune system that has become reactive or responsive to Gliadin or any of the Wheat peptides see a piece of UN poorly digested plant protein, let's say Corn Protein. And say, You know what that looks close enough in this chaotic situation, I think that's wheat.
It's a good question. I suppose it's possible.
This is where they talk about molecular mimicry or cross reactivity. So I don't know if the gut Zoomers test is more specific that it factors that piece out.
I know that our blood test is because we manufacture the exact peptides and proteins on our amino chip, on the silicone semiconductor wafer, and so I know it's specific to that thing. And I know antibodies are very specific to this thing they're attacking. But yes, absolutely, molecular mimicry can happen. It does happen. That's how we get Lyme arthritis, for example. That's how we get rheumatic fever. I think it is where you get a anyway. So, yeah,
possible. Oftentimes, when someone is reactive to the non gluten wheat peptides on vibrant wheat Zoomer, they also have reactivity to other grains like corn, rice, etc,
and the antibodies on this test. Test their Secretory IgA
antibodies. There are not. It's just looking at the level of Secretory IgA.
No. So the Glee, anti Gliadin, which antibodies are being tested? A Gliadin, right? Is it IGA antibody testing or IgG? It would be IGA.
It's gotta be IgA, because that's what's made on the mucosal surface, right?
So, because that leads to the next question, right? Which is, I eat gluten, I'm within the reference range, therefore I'm not reactive to it. And I always tell people, Look, it all depends on where you're at and it depends on what that Secretory IgA level is. Oh, yeah, so if you're 100 but your Secretory IgA is 300 and reduce and suppressed, then we're not really seeing your full response to Gliadin. And I could be totally wrong, but that's how I explain it is, does that make sense to you? Yeah.
I mean, I would test total immunoglobulins in the blood look at total IgA, total IgG, total, IGN, total IgE, because that's going to give you a better snapshot. Secretory IgA is similar, but different. It's a different than a total like than an IGA molecule, but, yeah, they should. I mean, sometimes they correlate, sometimes they don't,
but if they're but if we're looking at fecal anti Gliadin, we're looking at antibodies to Gliadin. Yes, right? So if, if their immune response, and we're just looking at the test and in the Gliadin is with, if it's within the reference range, but the secretory IgA is weak.
Does, does it? I mean, if it, if it correlates clinically Absolutely, you could indicate that for sure. I mean, even just a slightly like, if it's in the green, but it's high green, that means something too, sure.
Yeah, you're still responsive, right? Yeah,
it's not zero. It's not at the very low end. It means there's some reaction. And is it a some reaction, but would have been higher if your immune system was more robust, or is it right? What's the reason for it to be a high green, high normal, right?
I agree, and that's where it comes down to the interpretation piece, right? Not just saying, Oh, it's in the green, you're good, but saying, How much do you eat? I don't eat much, and it's this high in the green, hmm. And you're seeing maybe your immune system's compromised, you might be, and you guys are only testing one peptide on here, correct? Yeah,
right. And there's multiple breakdown products of wheat. So the important part is, if you feel wheat reactive, but this component is normal, it doesn't mean you're not reactive, right? We'd look at, right? Might be better to look at an antibody test, yes. And we'd look at maybe the breakdown, all the breakdown products, and see, are you reacting to other components of wheat, but not this Gliadin piece that you're looking at here, like
when there's scattered thunderstorms, you might be in a sunny spot, doesn't mean it's not raining somewhere else in
your body. Yeah, perfect. Alright, so let's wrap this up. Let's do two things. What if you wanted to give some final insight into the benefits of the gut Zoomer test, maybe over some of the other tests that are out there, and then maybe three tips for somebody who's struggling with chronic GI issues, should they run a test? Should they not run a test? When did they run a test. Yeah,
so vibrant. Gut Zoomer is just very comprehensive. It includes more microorganisms and more of these extra markers to look into digestion, absorption, immune response than pretty much every other test, any other test on the market, in terms of whether or not to run a test, I'd say everyone could benefit from gut zoom or testing. Everyone can
benefit from knowing what's going on in the microbiome. And then in terms of when to test, I would definitely not do it right after a colonoscopy, because that will wipe out everything in your gut, so wait at least two weeks for the microbes to grow back. And as a side note, after a colonoscopy is a great time to feed your microbes, all of the healthy things, so they grow back in the way you want them to, as opposed to eating a poor
diet, which then would continue to decimate them. So not right after colonoscopy, and then I would do it, eating your normal diet. Some people, some providers, will say, avoid anything that could possibly contribute to a change in the gut. But you want, you want to do a baseline, or you want to do like in your normal, like, you know, like washout, or just like eating your normal. What does that look like? So I would say, maintain your normal routine, what you're currently doing. I
would not change anything. Personally for my clients, they just eat normal. Um. And that will give you the best insight into what your current diet, lifestyle habits, what impact that's having on your gut microbiome. And
I agree with that, like, I don't want to test you on your like, two weeks on a AIP diet that doesn't tell you were struggling with on your nerve, on your on your diet. I want to test you on your diet. Last question, so many people taking supplements? Okay, so they're taking lots of supplements. How do you recommend? I I give different answers here based on the on the individual. But should somebody,
if somebody's testing, they're doing the test. Are there supplements that are going to interfere with the test that they shouldn't take? And if somebody's coming in, I'm taking this probiotic, that probiotic. I'm taking this. I'm taking that, taking this. Do you have them stop those things, or do you have them take those things? I'd like to get your opinion on
that. Yeah. So if you want to know if your gut needs a particular supplement, I would say test without the supplement to see what it's doing baseline. I think baseline information is more helpful because if you're taking you know digestive enzymes, if you're taking pro kinetics, if you're taking probiotics like that's going to impact the
results. And it might say it looks great, but that means maybe you need to be on digestive enzymes the rest of your life, or taking that pro probiotic the rest of your life. But that's really not sustainable. We want you to be in homeostasis without the need for extra stuff. It's a supplement. Because it's supplements. It's not a long term thing you have to do all the time. So I love, like, just baseline, no supplements.
Yeah, I agree. So I'll do the I'll tell most people listening, I don't want if I can get them all. My starting point is, usually you're on 30 supplements. If you need 30 to feel this awful, you don't need any of them. Let's wean you off of them first. But if I have somebody who says, Listen, I this is a really good probiotic. I'm taking this. I
need my digestive enzymes. I'm then I may. If they're not willing to not do those things, I'm like, Great, take it, because I want to show them that what they're doing isn't having the intended impact. I They think it is right. And so typically I'd say, Look, don't take anything week or so, and then we'll get the stool test done. Just eat your normal diet. We don't need all the extra support in there. And let's just see where you're at. But if somebody says, I can't live
without it, great, take your stuff. Let's see how it changes. See how if it makes the test look perfect, then we know there's problems, and what you're doing is managing it. But then we have to talk about whether you want to recover, you just want to manage but many times, the reason they're coming to you or is because they they're managing their symptoms with supplements, but it's not really restoring a functional, healthy,
functional state. No one goes to a doctor if they're feeling right.
Yeah. So, Dara, I want to wrap this up. I want to respect your time. We got like two minutes left, so tell everybody a little bit about you and where you're located. So if they want to hear more about you and what you do, they can reach out. Alright,
so I'm located in Washington, DC. My private practice is called eating with integrity. The website's www, dot eat honest.com. You can schedule a free consultation to learn if my program is right for you and I resolve functional gut disorders like idea. So helping people be able to live a normal life again after suffering from all that digestive issues,
awesome. Well, I appreciate you coming on the podcast. We got through a lot of this test and some of the markers on there and the importance, but I appreciate you coming on and sharing your wisdom with us. All right, thanks for having me. You
