Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Are Enterolab Tests Ever False Positive?


dennymel

Recommended Posts

dennymel Rookie

Hi all,

I got my results back today and I am gluten sensitive. Can I be SURE these tests are right? Are there false positives?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I'm wondering myself. I know gluten makes me sick, but I got off dairy for months and have been challenging it lately. Today I had an eggnog latte and some gluten-free pasta with cheese. I've had no problems whatssoever and this is the third or fourth time I've challenged it. My dairy results were NOT borderline either.

Gluten does make me sick, however.

Nantzie Collaborator

Would you be comfortable posting your results? We could probably be more helpful with more information. There is controversy about going just by the genetics because it seems like most people (at least the ones who are on this board have at least two copies of the gluten sensitive genes, which may not be very helpful in figuring out if you have an active gluten intolerance), but the fecal tests seem to be pretty accurate.

Nancy

dennymel Rookie
Would you be comfortable posting your results? We could probably be more helpful with more information. There is controversy about going just by the genetics because it seems like most people (at least the ones who are on this board have at least two copies of the gluten sensitive genes, which may not be very helpful in figuring out if you have an active gluten intolerance), but the fecal tests seem to be pretty accurate.

Nancy

Sure,

I didn't do the gene part of the test ($$$)

Fecal Antigliadin IgA 64 (normal range <10)

Fecal Antitissue Transglutaminase IgA 33 (normal range <10)

Quantitative Microscopic Fecal Fat Score-NORMAL <300 units

I'm wondering myself. I know gluten makes me sick, but I got off dairy for months and have been challenging it lately. Today I had an eggnog latte and some gluten-free pasta with cheese. I've had no problems whatssoever and this is the third or fourth time I've challenged it. My dairy results were NOT borderline either.

Gluten does make me sick, however.

That's odd. I keep worrying that it's a scam for them to make money. Maybe I don't want to admit I'm really sick...?

Maybe you're only allergic to certain dairies. I can eat cheese, eggs, but NO milk, ice cream or I get ill. But oddly enough since I've gone gluten free, I ate ice cream the other day with no problems...? egad...

CarlaB Enthusiast

Well, the test said I was intolerant to casein.

I would try the gluten-free diet if I were you and let the dietary response confirm your result. If you're not strict with it, it will do no good, so eliminate 100% of the gluten and see what happens. After a few months, eat some gluten again to challenge it and notice again how you feel. That way you have a solid test of your dietary response.

Nancym Enthusiast

He's done a lot of work correlating symptoms to results, and then following up to see if the gluten-free diet worked. His results are quite good. I think he's got a slide on how many fail to respond to the diet and it ain't much. Even more surprisingly he's had a few people test negative that felt better on the diet.

I'm sure if you sent an email they could tell you more about false postives or negatives.

Nantzie Collaborator

I did JUST the gene test. I had already done some trials of the gluten free diet and knew for sure that gluten was my problem. My husband thougth I was off on another health kick and wasn't being supportive. I did the genetic test (showed gluten sensitivity, not celiac) pretty much just to shut him up. :P

We tested our kids this past summer with just the Fecal Antigliadin IgA test. My 4yo daughter's was 15 and my son's was 41. My daughter was having tummy aches and was always anxious. That went away. My 2yo son didn't seem to have any symptoms, but we tested him because our daughter tested positive. He had a complete personality change. He used to be shy and kind of withdrawn. After going gluten-free, he's a normal goofy, active little 2yo boy.

I would trust your test results and go gluten free. You will never know how gluten effects you personally until you do that. After you're gluten-free for about a month, you can challenge it by eating something with gluten in it (not too much) and you'll have your answer. To be honest, when you first go gluten-free, there are so many times when you accidentally get "glutened" that you'll probably have at least one inadvertant gluten-challenge long before a month is over.

As far as dairy, I had dairy intolerance at first (soy too). I was able to add them both back in eventually. Dairy was hit and miss for a while, but now, about a year later, I don't have any issues with it at all.

Nancy


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



bklynceliac Apprentice

In short, no. You can't be sure. There has been no peer-testing of his methods. But a lot of his patients swear by enterolab. So, it's a bit of a toss up. I would add however that there aren't a whole lot of medical tests that you can be completely certain about.

lonewolf Collaborator

My son tested negative through Enterolab for gluten sensitivity, so I know they don't tell everyone that they're positive. Funny thing is, my son is doing better on the gluten-free diet, so I don't know what's up. He did show two copies of the same gluten sensitive gene.

dennymel Rookie
My son tested negative through Enterolab for gluten sensitivity, so I know they don't tell everyone that they're positive. Funny thing is, my son is doing better on the gluten-free diet, so I don't know what's up. He did show two copies of the same gluten sensitive gene.

By the way your doggie, is VERY cute. I often wonder if I handle dry dog food, if that can affect my gluten? I feed them Beneful....

Anyways, I honestly think from gathering data and reading these type boards, that a lot of sick people have allergies to preservatives or chemicals. So going Gluten free sometimes makes them go organic, thus the relief in symptoms. Either way, if you feel better, go with it. I'm going to work on honing in on the other things that might be making me sick also. I didn't get a Casein screening, or Soy. I will start removing these from my diet and keeping a diary of how I feel. Do you think I should get the gene test after the diagnosis of the Gluten Sensitivity? Or is it a waste of money at this point?

CarlaB Enthusiast
By the way your doggie, is VERY cute. I often wonder if I handle dry dog food, if that can affect my gluten? I feed them Beneful....

Anyways, I honestly think from gathering data and reading these type boards, that a lot of sick people have allergies to preservatives or chemicals. So going Gluten free sometimes makes them go organic, thus the relief in symptoms. Either way, if you feel better, go with it. I'm going to work on honing in on the other things that might be making me sick also. I didn't get a Casein screening, or Soy. I will start removing these from my diet and keeping a diary of how I feel. Do you think I should get the gene test after the diagnosis of the Gluten Sensitivity? Or is it a waste of money at this point?

I actually went organic and healthy years before I went gluten-free, but I think what you say is true for many. I was always considered a health food nut before ... I always felt better eating that way.

Some are bothered by the dog food ... dog gets it on his paws, tracks it around the house ...

I would skip the gene test ... I have yet to meet someone who didn't at least have two copies of the gluten sensitive genes ... it would be helpful to confirm you had a celiac gene, though, so it's really your call whether it's worth it to you.

BTW, my daughter also came out negative on the Enterolab test.

lonewolf Collaborator
By the way your doggie, is VERY cute. I often wonder if I handle dry dog food, if that can affect my gluten? I feed them Beneful....

Anyways, I honestly think from gathering data and reading these type boards, that a lot of sick people have allergies to preservatives or chemicals. So going Gluten free sometimes makes them go organic, thus the relief in symptoms. Either way, if you feel better, go with it. I'm going to work on honing in on the other things that might be making me sick also. I didn't get a Casein screening, or Soy. I will start removing these from my diet and keeping a diary of how I feel. Do you think I should get the gene test after the diagnosis of the Gluten Sensitivity? Or is it a waste of money at this point?

Thanks - we think our pup is pretty cute too. He gets mostly raw meat and we only have gluten-free dry food, so I don't have to worry. I think it's a good idea to get gluten-free pet food because their digestive systems aren't really designed to digest wheat anyway - and it's an unneccessary risk for people who are gluten intolerant.

Like Carla, I went organic (mostly) and as chemical free as possible years before going fanatically gluten-free. My kids have been raised that way and two of them still feel better off gluten.

Keeping a food diary is a great idea and much cheaper than paying for testing. As for the gene testing, it's interesting, but I don't think neccessary.

sunshinen Apprentice
Anyways, I honestly think from gathering data and reading these type boards, that a lot of sick people have allergies to preservatives or chemicals. So going Gluten free sometimes makes them go organic, thus the relief in symptoms. Either way, if you feel better, go with it. I'm going to work on honing in on the other things that might be making me sick also. I didn't get a Casein screening, or Soy. I will start removing these from my diet and keeping a diary of how I feel. Do you think I should get the gene test after the diagnosis of the Gluten Sensitivity? Or is it a waste of money at this point?

Yeah, I too, had tried to go to a very healthy diet before going gluten free. Ironically, I eat much worse in this sense than I did before. And I feel better than I thought imagineable after going gluten free.

I do think you should get the gene test. If you have triggered a celiac gene, you really want to know that. I don't think normal fat counts is enough to say that it is "just" gluten sensitivity and not celiac. And if you are not willing to accept Enterolab results, then you should go have the biopsi before you go gluten free. With celiac, you can't cheat. And if you are not convinced, you need to KNOW that this is the problem or you could be putting your health at serious risk. I have seen people who had negative gene results, so I don't think this is a scam. I was also skeptical at first, but Dr. Fine publishes [edited to retract "and seems to be a respected member of the medical community." -- I have seen him treated this way, but it seem like others are saying the lab is not taken seriously, but they are also saying "everyone tests positive" which I know is not the case. I have seen many people reporting negative tests from Enterolab.]

I had an 800% turn around in health. I have terrible results when I make gluten mistakes, and yet I wish I had known about the biopsi gold standard before I went gluten free. Given the dramatic turn around I had, I didn't think I would care. But I find I still want to have excuses for why I don't have to be THAT careful. It's denial, but it's there (even when I'm suffering from a mistake). Knowing I have the gene for celiac helps fight the denial. So I recommend shelling out the money to get as much evidence as you can get.

CantEvenEatRice Enthusiast

Does everyone have the 2 gluten sensitivity genes if they do not have a Celiac gene? It just seems that way on this board through Enterolab.

ravenwoodglass Mentor

"I had an 800% turn around in health. I have terrible results when I make gluten mistakes, and yet I wish I had known about the biopsi gold standard before I went gluten free. Given the dramatic turn around I had, I didn't think I would care. But I find I still want to have excuses for why I don't have to be THAT careful. It's denial, but it's there (even when I'm suffering from a mistake). Knowing I have the gene for celiac helps fight the denial. So I recommend shelling out the money to get as much evidence as you can get."

You really need to be just as careful with a gluten sensitivilty as you do with full blown celiac. Being only sensitive on the gene results does not give a reason to be less cautious or to cheat on the gluten-free diet. As many with only the gluten-free sensitivity genes will tell you you can do just as much harm with 'a little gluten' if you are sensitive as if you are a full blown celiac. Your reaction to the diet should be enough to keep you away.

CarlaB Enthusiast
Does everyone have the 2 gluten sensitivity genes if they do not have a Celiac gene? It just seems that way on this board through Enterolab.

We had a thread on this a couple weeks ago, and I believe this was the conclusion we came to -- it seems you either have two gluten sensitive genes, or two celiac genes or one of each ... we couldn't find one person who had a non-gluten sensitive gene.

Nancym Enthusiast

There's one genetic combination that Dr. Fine says doesn't correspond to Gluten Sensitivity or Celiac, that's a double DQ4, which is very rare except in Asia.

chrissy Collaborator

everyon keeps referring to the "gluten sensitive" genes that enterolabs has named. is there ANY scientific proof that what dr. fine claims to be the gluten sensitive genes really ARE gluten sensitive genes? i don't think that any other medical institution or celiac research center acknowledges gluten sensitive genes. i kind of think we are back to needing to see his scientific proof, which he refuses to give to anyone. we are involved in a celiac study with a reputable college---university of california, irvine. i asked specifically about gluten sensitive genes, and they do not believe that there are any gluten sensitive genes identified. i am not saying that there aren't people who are non-celiac and gluten sensitive----but the reputable institutions aren't recognizing any gene for it.

CantEvenEatRice Enthusiast
everyon keeps referring to the "gluten sensitive" genes that enterolabs has named. is there ANY scientific proof that what dr. fine claims to be the gluten sensitive genes really ARE gluten sensitive genes? i don't think that any other medical institution or celiac research center acknowledges gluten sensitive genes. i kind of think we are back to needing to see his scientific proof, which he refuses to give to anyone. we are involved in a celiac study with a reputable college---university of california, irvine. i asked specifically about gluten sensitive genes, and they do not believe that there are any gluten sensitive genes identified. i am not saying that there aren't people who are non-celiac and gluten sensitive----but the reputable institutions aren't recognizing any gene for it.

This is exactly what I am curious about! If you do not have the actual Celiac genes, can you still have Celiac or gluten intolerance? I just posted a link to the glutensensitivity.net page and there is a story of a girl who has NO Celiac genes, but is a blood and biopsy proven Celiac. So what is the research saying about people who do not have Celiac genes, but seem to be intolerant to gluten? That is what I am so confused about. My son does not have any Celiac genes, but seems to be better on the gluten free diet. However, I question whether I should challenge the gluten at some point since he doesn't have Celiac genes. I am so confused!

e&j0304 Enthusiast

Actually, there is a woman who posts on this board who has a double copy of DQ-1 which Dr. Fine says is a gluten senstivity gene and she is blood and biopsy proven celiac.

So....who knows?

Tim-n-VA Contributor

When it comes to statistical tests, I'd avoid saying always or never. With that caveat, I'd be extremely surprised if there was a medical test that didn't have some false results - both negative and positive.

nikki-uk Enthusiast
This is exactly what I am curious about! If you do not have the actual Celiac genes, can you still have Celiac or gluten intolerance? I just posted a link to the glutensensitivity.net page and there is a story of a girl who has NO Celiac genes, but is a blood and biopsy proven Celiac. So what is the research saying about people who do not have Celiac genes, but seem to be intolerant to gluten? That is what I am so confused about. My son does not have any Celiac genes, but seems to be better on the gluten free diet. However, I question whether I should challenge the gluten at some point since he doesn't have Celiac genes. I am so confused!

Although there has been two main genes identified to celiac disease I think it's fair to say there may be more genes (or combinations) that as yet have not been discovered.

(Just my opinion though) :)

celiacgirls Apprentice
Although there has been two main genes identified to celiac disease I think it's fair to say there may be more genes (or combinations) that as yet have not been discovered.

(Just my opinion though) :)

I agree with this. I have done all of my testing with Enterolab so obviously I believe it is valid. However, as far as the gene testing goes, since he identifies almost all genes as gluten intolerant genes, to me the most valid information I got from him was that I have the DQ8 gene, which is a widely accepted celiac gene.

There is so much that is unkown about celiac disease and gluten intolerance that I think everyone needs to do their own research and come to their own conclusions about their situation if they don't meet the widely accepted standards for celiac. You can believe you should avoid gluten completely to avoid future problems if you are only "gluten intolerant" or you can take your chances that it won't cause future problems and have a little bit now and then or ignore it completely. For us, having even a trace of gluten causes enough noticeable problems that I am willing to avoid it completely for that alone, never mind the whole issue of future problems.

sunshinen Apprentice
You really need to be just as careful with a gluten sensitivilty as you do with full blown celiac. Being only sensitive on the gene results does not give a reason to be less cautious or to cheat on the gluten-free diet. As many with only the gluten-free sensitivity genes will tell you you can do just as much harm with 'a little gluten' if you are sensitive as if you are a full blown celiac. Your reaction to the diet should be enough to keep you away.

It's true that many people with gluten sensitivity have more severe reactions than many with celiac and many need to be just as careful. BUT there are degrees of sensitivity. Many other people are fortunate enough to be able to have some gluten without any negative effects. And unlike celiac, food sensitivities can go away. For example, many of us are sensitive to milk when we are first diagnosed, but that sensitivity often goes away as we heal. When I consider whether to have dairy or not, I know that I can have it as long as I can handle the symptoms; antibodies are not going to start damaging my intestines. With celiac, you can have damage when you have no symptoms.

Yes, a positive reaction to the diet should be enough to keep people away from gluten. I have never intentionally cheated. But as you learn more and more about this, it is often really hard to believe you have to worry about shampoo or kissing someone who has eaten gluten. Denial is powerful, and anything we can do to overcome it is a good thing. We all know how unaccepting many people are of our new, "extreme" diet and having that extra evidence is always nice to have if you can get it. Some people don't have that luxury, and have to base it on dietary response alone. All I'm saying is that it can make things much simpler if you learn as much as possible about what reaction is happening in your body and acquire whatever medically accepted evidence you can to support yourself against the ney-sayers. Knowing whether your reaction is immune, autoimmune, or digestive can make a big difference on what the right course for you is.

To get back to the topic of the thread (sorry to have participated in the hijack) on the reliability of Enterolab, here are some opinions from other doctors:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

sunshinen Apprentice

PS. I got these links from Open Original Shared Link, which seems to have a lot of good links to studies and articles related to celiac. So you can see the data and conclusions of researchers rather than just reading people's opinions.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,836
    • Most Online (within 30 mins)
      7,748

    RyanOB
    Newest Member
    RyanOB
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Dawn Meyers
      Hi I have celiac disease and the dermatitis herpetiformis rash Also other autommune diseases.  I have had bad side effects to all the vaccines I have had and now my Doctor wants me to have the pneumonia vaccine.  I am concerned because of some of the bad side effects I have had in the past example Hep B after shot couldn't  move arm for several months.  Flu shot and COVID was sick right after shot. Told not to get anymore. My lung is inflamed and have a cough I can't seem to get rid of. Very concerned 😟. 
    • knitty kitty
      @Manaan2,  I'm so happy to hear you're going to try thiamine and magnesium!  Do let us know the results!   You may want to add a B 50 Complex with two meals of the day to help boost absorption.  Thiamine interacts with each of the other B vitamins which are all water soluble.   When supplementing magnesium, make sure to get sufficient calcium.  Calcium and magnesium need to be kept in balance.  If you choose a calcium supplement, take two hours apart from magnesium as they compete for absorption.  Take Calcium with Vitamin D.  Vitamin D helps calm the immune system.   For pain, I use a combination of thiamine, B12 Cobalamine, and Pyridoxine B6.  These three vitamins together have analgesic effects.  My preferred brand is "GSG 12X Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets".  Alinamin is another form of thiamine.  It really is excellent at relieving my back pain from crushed vertebrae without side effects and no grogginess.   Look into the low histamine version of the Autoimmune Protocol Duet (Dr. Sarah Ballentyne, a Celiac herself, developed it.)  It really helps heal the intestines, too.  It's like a vacation for the digestive system.  Add foods back gradually over several weeks after feeling better.   I'm so happy to have pointed the way on your journey!  Let us know how the journey progresses! P. S. Add a Potassium supplement, too.  Potassium is another electrolyte, like magnessium, that we need.
    • Manaan2
      @knitty kitty I can't thank you enough!  My husband and I already started looking into those supplements.  We definitely plan to give it a try.  We've been against the Miralax since it was originally advised by PCP, but because of the level of pain she experienced on a daily basis, we decided to try it.  We've made many attempts to gradually decrease but due to her pain and related symptoms, we've kept her on it while trying all sorts of other dietary adjustments pre and post diagnosis specific to food; so far none of those efforts have made a significant difference.  I will definitely share how she's doing along the way!
    • BIg Nodge
      Hi, I have recently embarked on the gluten-free journey. I have what to me seems like a somewhat confusing set of test results and symptoms. I have been impressed by the accumulated knowledge and thoughtfulness as I browse this forum, so I figured I'd make a post to see if anyone can offer any insight. I know there are many posts like this from new users, so I have tried to do my baseline research first and not ask super obvious questions.  I'm 43, overall very healthy. No history of gluten sensitivity or really any of the classic GI symptoms. About three years ago I started to experience intermittent bouts of fatigue, chills/cold intolerance, and shortness of breath/air hunger (sometimes feels like a hollowness in my chest, hard to describe). The symptoms over time have become fairly significant, though not debilitating, I am able to exercise regularly and am fairly physically active, continue to perform well at work. But for example I have gone from someone who consistently ran hot, was always cranking the a/c, to someone who wears a down vest inside at work in winter and get chills if the a/c even blows on me in summer. I get tired and lose energy even when getting decent amounts of sleep, and have to have my wife take over on long drives that I could previously handle with no problems. More generally when I am experiencing these symptoms they seem to crowd out space in my mind for focusing on my family, my hobbies/activities etc, I sort of withdraw into myself.   I happened to be experiencing these symptoms during an annual physical with my PCP a few years ago, he observed post nasal drip and suggested it was allergies and that I treat it with claritin. At first it seemed to respond to claritin (though not zyrtex), but over time I became unsatisfied with that answer. There didn't seem to be any seasonal rhyme or reason to my symptoms, and I felt like I was on an endless loop of taking claritin, then stopping, not being sure if it was even making a difference. I did eventually get allergy tests and found modest allergies to dust and pollen, which didn't feel like a smoking gun.  I then started seeing a natural medicine doctor who was much more willing to explore my symptoms via testing. The first thing that came back abnormal was elevated thyroid peroxidase antibodies/TPOs, 137 IU/mL vs a reference range of <9. At the same time my thyroid panel showed normal thyroid hormone levels. So it appears my immune system is attacking my thyroid even though it is working fine. I got a thyroid ultrasound at the time, it was clear, but with some abnormalities such that they suggested I get is scanned again in a year. These are certainly risk factors for a thyroid autoimmune disease, though my thyroid seems to be working fine for now.  From here my doctor considered celiac due to the murky thyroid/celiac links, so we did a panel. Results were as follows: TT IGA <1 U/ml, TT IGG <1 U/ml, deamidated gliadin IGA 24.6 U/ml, deamidated gliadin IGG <1 U/ml, IGAs 170 mg/dL. Readings greater than 15 considered high by my lab for the first four, my IGAs are within reference range. So basically just the deamidated IGA popped, but my IGAs are normal. I also notice on the tests that my thyroglobulin was high, 86.7 ng/ml vs a range of 2.8 - 40.9.  My doctor suggested that it certainly wasn't conclusive for celiac, but it was possible, and likely that I have some sort of gluten sensitivity. She suggested going gluten free and seeing how I felt as opposed to doing a biopsy. The best theory I can come up with is perhaps I am a silent celiac or just have a gluten sensitivity that doesn't produce immediate GI symptoms, but is still doing damage and over time has caused leaky gut. So now gluten is getting into my blood, and my immune system is attacking it but also mistakingly attacking my thyroid.  So that's what I did, went gluten free in October. It's been about four months, and I am really not feeling any difference. I still get the same symptoms that come and go. My bowel movements may be a bit more regular, but it was never a major issue before so I would consider that a minor improvement. I know that it can take a while to see improvements, and I am going to remain gluten-free and see how I feel. But I am definitely questioning whether I really understand what is going on, and am open to any thoughts or suggestions from the forum. Sometimes I wish I just went ahead with the biopsy before going gluten-free. While I would certainly be down to start drinking IPAs again ahead of a biopsy, you know, for science, I feel like at this point I would be throwing away four months of work and am better off staying the course and seeing what happens. But I'm really not sure.  I know there is a lot of thyroid knowledge on these boards, along with the celiac expertise, so I'm curious if this resonates with anyone's experience. And I'm interested in what sort of timelines people have experienced in terms of feeling improvements for some of these non-GI symptoms like chills, SOB, brain fog etc. Thanks in advance. 
    • cameo674
      Does it taste like black licorice?  It said it was chewable.  I do not like that flavor.     Since the burn at the back of my throat is there everyday, I usually only take something when it is unbearable and keeping me from ADL especially sleep.  
×
×
  • Create New...