Jump to content
  • 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

Has Anyone Seen A Negative Gliaden Iga Test From Enterolab?


Amyand2girls

Recommended Posts

Amyand2girls Rookie

I just got back our results from Enterolab, and me and both kids came back positive, for gliaden, for tTg, for casein, for genes. We had slightly different numbers, but all positive. So my husband, the skeptic, immediately asks, "What if they tell EVERYONE they are positive?" I had gotten a positive saliva test from Diagnos-Techs, but my eldest child's came back negative on the saliva and all our blood serum tests were negative (for gliaden and tTg, total IgA was normal.) I believe these results are true, but I'm just wondering if any of you have tested yourself or your family through EnteroLab and got "normal" results? We are also waiting on IgG testing from ImmunoLab, but I know that's a whole other kettle of fish.

Thanks,

Amy


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



Celiac.com Sponsor (A8-M):



Gentleheart Enthusiast

I'm sure you will be getting some specific answers soon. But there have been many people here who have reported negative results for various family members from testing with Enterolab.

But we also have to realize that most people testing with Enterolab in the first place are people who already suspect they have gluten problems. So it stands to reason that the positives might be higher than they would be if their clientelle were a more random, uninterested cross section of the general public.

We need to look at motive as well. What would Enterolab's motive be for testing everyone positive? They aren't selling anything. Maybe it could be argued that they will want you to retest in the future so they can make more money off of you by giving you positive results. But in my case, it has been quite the opposite. I emailed them to ask whether I needed to retest after it had been a year and they said no. So it's obvious they weren't trying to sell me anything! :)

Christina98 Explorer
I just got back our results from Enterolab, and me and both kids came back positive, for gliaden, for tTg, for casein, for genes. We had slightly different numbers, but all positive. So my husband, the skeptic, immediately asks, "What if they tell EVERYONE they are positive?" I had gotten a positive saliva test from Diagnos-Techs, but my eldest child's came back negative on the saliva and all our blood serum tests were negative (for gliaden and tTg, total IgA was normal.) I believe these results are true, but I'm just wondering if any of you have tested yourself or your family through EnteroLab and got "normal" results? We are also waiting on IgG testing from ImmunoLab, but I know that's a whole other kettle of fish.

Thanks,

Amy

I just got back my results as well from Enterolabs and my casein and gluten test was positive.I have to say i am wondering the same thing? (could they be just telling everyone there positive?)

I thought about it and I am doing that because I believe I am in denial.I still think I am going to have the test done else where and say nothing about having been tested for it ever before.i wanna see if it still in fact comes back positive.I am not well, never was, and am gettinf worse as the years tick on....so I wouldnt doubt its positive but I am in denial I think.

Did you say you guys are going to have the test somewhere else also to see what they say?

Christina

Fiddle-Faddle Community Regular

I never used Enterolab, but have been on this board for about 3 years, and I have seen people report back that either they, a spouse, or a child did not test positive for IgA with Enterolab.

Enterolab does say that their tests are NOT valid after being off gluten for a certain amount of time--I think it's one year? It makes sense--at that point, you've healed, and are not producing antibodies to gluten any more since you're not consuming it.

Amyand2girls Rookie
I never used Enterolab, but have been on this board for about 3 years, and I have seen people report back that either they, a spouse, or a child did not test positive for IgA with Enterolab.

Enterolab does say that their tests are NOT valid after being off gluten for a certain amount of time--I think it's one year? It makes sense--at that point, you've healed, and are not producing antibodies to gluten any more since you're not consuming it.

Yes, there is still a time limit with the gluten-consumption, but theirs supposedly is still the most sensitive. We had been eating gluten and casein for about 3 months (after being off for a year and a half) before taking this, because we also had other tests done. We all had traditional blood serum testing for celiac (the whole panel), which came back negative for all of us. I and my eldest had saliva testing done through Diagnos-Techs and mine was positive, but hers was negative. She is also only 4 1/2, though-- mine's had a lot more time to build up and cause all sorts of freaky immune issues that no one can diagnose.

Christina,

Enterolab is the only lab I know of that does the stool testing that is supposedly the most sensitive, so I can't tell you where to go to double check this exact test. The IgG Elisa test we're having done by ImmunoLab really isn't the same thing. I could be IgG negative or positive and it doesn't necessarily reflect on my IgA levels, from what I understand: they are responses mediated by different parts of the immune system. IgE, IgA, IgG...it's quite confusing at first and even after a while. If I'm wrong here, someone else feel free to correct me! If you want something else to confirm that a "normal" doctor will accept, you would want to go with blood serum panel for celiac...but mine was negative, as was my biopsy. However, I do believe, deep down, that Entero's results are accurate. I KNOW my eldest responds to casein and gluten (autism like symptoms appear after being on these foods and disappear mostly when off them) and I suspected my youngest might inherit the same set of issues. You might look into Diagnos-Techs or ImmunoLab, though, because the saliva test is also supposedly more accurate than bloodwork...but I will warn you that a traditional gastrointestinal specialist will tell you that these tests "mean nothing," as he told me. Then he told me to go on the diet anyway for a year and see how that goes. So that's what we're doing, which we would have done without his suggestion. But for me, it helps to have this test showing positive, even as non-standard and unrecognized as it is among most traditional Western medicene docs...it gives me the back up my husband needed to feel at peace about the restricted diet. AND as I've just discovered Nearly Normal flour and made some awesome muffins today, I no longer feel quite as depressed about the "immediate and lifelong" aspect of the diet. Hope that helps some!

Thanks guys for the other responses-- you're right of course, Gentleheart...what would be their motiviation to show a bunch of positives? Good point!! And also an excellent point about the people who are likely to be taking this test!

Lisa Mentor

Not to dig up old bones here, but I have never seen an independent study as to the accuracy of Enterolabs stool testing. :ph34r:

Mike M Rookie
I just got back our results from Enterolab, and me and both kids came back positive, for gliaden, for tTg, for casein, for genes. We had slightly different numbers, but all positive. So my husband, the skeptic, immediately asks, "What if they tell EVERYONE they are positive?" I had gotten a positive saliva test from Diagnos-Techs, but my eldest child's came back negative on the saliva and all our blood serum tests were negative (for gliaden and tTg, total IgA was normal.) I believe these results are true, but I'm just wondering if any of you have tested yourself or your family through EnteroLab and got "normal" results? We are also waiting on IgG testing from ImmunoLab, but I know that's a whole other kettle of fish.

Thanks,

Amy

I personally know of 2 people that tested negative via Enterolab. One had symptoms of celiac and/or a gluten intolerance. Test came back negative and still having issues, she then went to the GI. Last month she was diagnosed with Crones disease. The other was curious and just wanted to be tested. Mike


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



Celiac.com Sponsor (A8-M):



jitters Apprentice

My husband, my daughter, and I all got tested. They both came back positve and I came back negative. I am the one with obvious gluten issues...

My daughters specialist said enterolab is "voodoo". I'm not sure what to think about it. I had been eating gluten for a long time before I did that test and I was SO sick from it. I even put in their little thing that I have family members with it. Part of me thinks that if they did make up results they would have definitely put me as postive. The other part of me thinks that maybe it isn't as great as people think and they just picked me to come back negative. Hard to say!

In defense of enterolab I DO think my husband has issues, and my daughter as well although they are not as obvious as mine.

Amyand2girls Rookie

Yes, I'm aware that he has not pursued publications in journals, for whatever reason. I knew that going in-- I think I'm just curious if there is perhaps many, many more people with a minor response to gluten that would show up in their stool that might never, ever be strong enough to show up in a serum test. In other words-- does this low level of response, only showing up in a stool test, truly mean "an immediate and life-long adherence to a gluten free diet."

My husband, for example, based on our daughter's gene test, probably has at least one gene for gluten sensitivity, but he has no symptoms at all. I think we are going to get him tested, sort of as a control-figure, though it would probably undermind his belief in this test even further if he DID come back positive. His mom, though, I'm sure is positive to gluten, but she wont' believe me. Rhuemtoid arthritus, fibra mialgia (sp), a host of other autoimmune issues...if he came back positive, she'd at least get a regular, traditional celiac test done. She's in such poor health, it wouldn't surprise me if it came back positive, despite a negative biopsy (since we know those are not truly conclusive with a negative.)

So I didn't mean to stir the water about their testing methodology being trustworthy or not...though I guess I DID wonder about their scrupulousness abut actually doing the test they describe on each person honestly. Their logic about why they test the stool makes sense to me, so that part doesn't bother me. Thanks for the warning, though!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,861
    • Most Online (within 30 mins)
      7,748

    Priscilla Buxton
    Newest Member
    Priscilla Buxton
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.