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

Enterolab Results


jitters

Recommended Posts

jitters Apprentice

Okay, my mom has Celiac disease. I've been off and on gluten free for about five years now. Long enough to know that I definitely have a problem with gluten. I have all the classic symptoms from intestinal to physical to neurological. Long story short I thought I was noticing some signs in my daughter that could be gluten related so we decided to test through Enterolab, we chose Enterolab because it is nonevasive. Here are our results:

Hubby- 45

Daughter- 30

Me- 8

Normal is less than 10 so I am in the normal range. Funny thing is I"M THE ONLY ONE IN MY FAMILY WHO HAS OBVIOUS PROBLEMS WITH GLUTEN!! I have DH and everything. So now I look like a total hypochondriac. Yes, I could be that lucky 1 in 500 people that doesn't make the antibodies but try telling that to people who already think I'm crazy. I'm sure they'll believe me then...

Anyway, I know a lot of people are curious about Enterolab and like to see the results others get so I hope this helps out in some way.

Jitters


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



Celiac.com Sponsor (A8-M):



Nancym Enthusiast

Have you been gluten-free awhile? Your antibody levels will go down after awhile.

lonewolf Collaborator

If you've been gluten free on and off for 5 years it's going to skew the results. I wouldn't be mad. Enterolab says that the test is accurate if you've been off gluten for up to a year. You probably just don't have enough antibodies, although you are at the high end of "normal".

AndreaB Contributor

I would agree with the others. You wouldn't get accurate results if you've been off of gluten most of the time in that 5 years.

ravenwoodglass Mentor

Just another voice saying the same thing. In addition the positive numbers do not always corelate to the degree of illness. Someone who shows only a 1 point positive may be sicker than someone who shows a 40. Different people have different systems effected, some are much more obvious like the tummy problems but for example with the neuro issues folks may not realize how severely they are impacted until they are gluten-free. My DS and DH both thought they were symptom free for the most part, until they went gluten-free and felt the difference.

holiday16 Enthusiast
Just another voice saying the same thing. In addition the positive numbers do not always corelate to the degree of illness. Someone who shows only a 1 point positive may be sicker than someone who shows a 40. Different people have different systems effected, some are much more obvious like the tummy problems but for example with the neuro issues folks may not realize how severely they are impacted until they are gluten-free. My DS and DH both thought they were symptom free for the most part, until they went gluten-free and felt the difference.

Have to add my agreement to this. I tested positive with only an 11 and yet I react severly to gluten with mostly neuro. symptoms. I didn't have any idea how much my gut was affected until I went off of it. The NP kept asking me if my stomach hurt and I kept telling her no. I had gotten so used to it that for me it was "normal". Now that I'm better I'm amazed at how much my stomach hurts if I accidentally get even trace amounts of gluten and I have no idea how I tuned that out for so long!

My numbers were so low and there seemed to be a trend in our family towards that with Enterolab testing so I had my IGA tested and it turns out that I do have low IGA so that explains my low number. My mother tested negative with a 9, but I talked with Enterolab and they recommend that you still do the diet and see if there is an improvement and if you do then you need to be on the diet regardless of the number. Basically, they had to make a cutoff, but it's not perfect for everyone. I understand the frustration with the negative number, but dietary response really is the true test.

Miriam3 Rookie

Same here. I only got an 10 for gluten antibodies, but I know that I'm not just being a hypochondriac about the gluten. I've been slowly but surely avoiding bread and other "junk foods" for years because they just didn't seem to make me feel good. I didn't know about celiac, so I thought I was just having "food coma" from too much starches. Rarely I would have a sandwich but mostly I was only getting the hidden gluten in certain foods I was still eating.

Now that I've been gluten free a piece of bread would half kill me-- I've felt it.

I'm considering having my IgA checked because of it, and I understand your frustration, Jitters. I would rather have it clear in black and white than be wondering. And with my family I could be the world's most famous celiac doctor to the family reunion and have him swear on the bible that I had celiac and my family would still think I was just trying a fad diet. They only believe in medical conditions they have heard of before and cures that come in pills.

Stay gluten free for your family and keep looking for answers as long as you feel you still need them! We're here for support.


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



Celiac.com Sponsor (A8-M):



jitters Apprentice

I've had gluten off and on for the past five years. The longest I've been totally gluten free is probably 6 months. Other than that I've cheated now and then probably at least once a week just from not being picky in restaurants.

I guess my frustration isn't with Enterolab, its only because I was looking forward to telling the critics that I was tested and it came out higher than normal. Now, I have to tell those people that I was on the higher end of normal, but that maybe, just maybe, I have a low IGA count anyway. I can see the eyes rolling now. I also went on gluten for a month straight before I took the test and can say with certainty that I never want to do that again. The food tasted awful no matter how good it smelled, and I was so sick by the end of it I just "knew" my levels were going to be high. So it was just a surprise they weren't. I was just a little disappointed it didn't come out positive, as silly as that sounds. Of course my husband is even more convinced Enterolab is not reliable and thus his positive test is probably not right either and won't be going gluten free any time soon.

My frustration level was high when I got the results, but now I just have to deal with it and move on. I'm going to stick to my guns and stay gluten free.

Thanks for all the positive answers,

Jitters.

kevieb Newbie

were those numbers for antigliadin antibodies, or for Ttg antibodies?

lonewolf Collaborator
I guess my frustration isn't with Enterolab, its only because I was looking forward to telling the critics that I was tested and it came out higher than normal. Now, I have to tell those people that I was on the higher end of normal, but that maybe, just maybe, I have a low IGA count anyway. I can see the eyes rolling now.

I can definitely understand this. I did gene testing because I'd been gluten free for so long and wasn't going back on gluten for anything. I was sure that I'd have 2 copies of the Celiac gene and that I'd be able to tell my skeptical family, "See - here's absolute proof". But wouldn't you know it, I don't have either of the Celiac genes - just every symptom and a miraculous recovery going off gluten. I guess you just have to get to the point where you know what you have to do to take care of your own body and then stick to your guns.

happygirl Collaborator

If you are IgA deficient, it doesnt matter if you are eating gluten or not...you have a higher chance of NOT testing positive. I am IgA deficient also.

Enterolab tests for:

Fecal Antigliadin IgA

Fecal Antitissue Transglutaminase IgA

Taken from Columbia University's Celiac page:Open Original Shared Link

Selective IgA deficiency (SIgA deficiency)

SIgA deficiency occurs 10 to 15 times more commonly among people with celiac disease compared to the general population [19]. Patients with SIgA deficiency will lack IgA antibodies including endomysial antibody, tTG and IgA AGA. To detect celiac disease in patients with SIgA deficiency an IgG antibody, typically IgG AGA, needs to be performed together with total IgA level. Alternatively, one may screen with IgG anti- EMA or IgG anti-tTG, though these are not widely available. Typically the patient with celiac disease and SIgA deficiency will have a positive IgG AGA and absent total IgA level. This combination should prompt a biopsy, whereas an isolated positive IgG AGA would usually not.

kevieb Newbie

i have a son who is IgA deficient. he didn't just test low---his levels are almost non-existent. i think that there is a definite difference between being IgA deficient and having low IgA levels. since enterolab does not test IgA serum levels and dr. fine goes on and on saying he is going to publish---without ever publishing---i think you would be far better off having blood work done through a reputable lab if you want family members to believe you. it may just be easiest to not discuss your diet with them.

our ped gi tells me it does NOT take much gluten to raise Ttg levels in a celiac. my daughter went into the hospital with Ttg levels nearly normal. after 3 months of the hospitals "gluten free food", she came out with her Ttg levels over 100. i really think that if you have been having symptoms for 5 years and been getting gluten approx once a week and your levels are still in the normal range that you probably do not have celiac disease. that does not mean that you do not have a problem with gluten, just that you don't have any evidence to show your family.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,957
    • Most Online (within 30 mins)
      7,748

    konny heigle
    Newest Member
    konny heigle
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.