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

Maybe IGA deficient?


FieryGhosts

Recommended Posts

FieryGhosts Newbie
(edited)

About 5 years ago a holistic doctor did an IGG and IGA blood test. My results were normal, but she said to reduce gluten anyway. I used to get terrible migraines, which got much better on the new diet.

Im not strict with the diet and will have gluten with up to one meal on most days.

I’ve gotten worse with my diet in the past 2ish years. It’s hard to keep, when there was no definitive proof. I’ve also had worsening of symptoms, especially over the past year. A bout of rectal bleeding occurred about 1.5 years ago and again 1.5 months ago which set my regular doctor off on all sorts of tests.

Tests in 2014 (pre-diet)

IGG: 2 (normal range 0-19)

IGA: 5 (normal range 0-19)

Test in 2019 (post diet, but not strict)

IGA: <1 (normal range 0-19)

I started eating gluten just under 2 weeks before an upper endoscopy and almost immediately started feeling really sick. After the test, the doctor said everything looked normal, but he took a biopsy anyway. I’m still waiting on the results. 

Also, right when the rectal bleeding started (when not doing the best at following the diet) my regular doctor tested my Erythrocyte sedimentation rate which looks for inflammation, then I became very strict with my diet and the specialist tested it again 2 weeks later. 

First test (bad at diet): 9 (normal range 0-20)

second test (strict diet): 7 (normal range 0-20)

I see the specialist next week for the results of the biopsy. Could the results have been compromised by years of dieting, even if it’s not strict? Should I ask for an IGG test or would that be a waste? Everything is in the normal range, but I’ve read that IGA <1 is sometimes considered deficient. All the lab results say there’s a 10% chance of a false negative due to diet or low IGA.

 

 

 

 

 

Edited by FieryGhosts
Adding normal ranges

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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi, There are some people who are IgA deficient, meaning they don't make much IgA antibodies.  They test for that by doing a serum or total IgA count.  You could ask if they did that test.  If you are IgA deficient the yes, the IgG test is the better way to go.

cyclinglady Grand Master

What tests did you take?  

IgA and IgG refer  to Immunoglobulin.  I assume you were testing for celiac disease.  If just the TTG tests were given, you might ask for the entire panel and be sure to check your Immunoglobulin A (IgA) a control test when just checking for celiac disease.  But the ultimate test are the biopsies. 

http://www.cureceliacdisease.org/screening/

FieryGhosts Newbie

Thanks! I didn’t realize that the IGA test could be just a specific portion of your total IGA. 

I looked at at my test results and it says  with assessment of total IGA.  My follow up appointment is on Thursday, I can ask my doctor for more information when I see her.

cyclinglady Grand Master

The celiac tests are:

TTG IgA

TTG IgG

DGP IgA

DGP IgG 

EMA IgA

And....Immunogobulin A (IgA).  This test is used only as a control test when checking for celiac disease.  If your body is not producing enough IgA, the IgA celiac tests are invalid or will not work.    You would also have a immune deficiency issues too.  But that is a separate issue.  

The previous link I gave you spells out the test names which are long!  ?

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,342
    • Most Online (within 30 mins)
      7,748

    Setb1210
    Newest Member
    Setb1210
    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

    • trents
      My reaction to a gluten bolus exposure is similar to yours, with 2-3 hours of severe abdominal cramps and intractable emesis followed by several hours of diarrhea. I don't necessarily equate that one large exposure to gluten with significant intestinal lining damage, however. I think it's just a violent reaction to a what the body perceives to be a somewhat toxic substance that I am no longer tolerant of because I have quit exposing myself to it regularly. It's just the body purging itself of it rather than an expression of significant damage. Before diagnosis, when I was consuming gluten daily, I had little to no GI distress. I was, for the most part, a "silent celiac". The damage to my small bowel lining didn't happen all at once but was slow and insidious, accumulating over a period of years. The last time I got a big shot of gluten was about three years ago when I got my wife's wheat biscuits mixed up with my gluten-free ones. There was this acute reaction after about two hours of ingestion as I described above. I felt washed out for a few days and fully recovered within a week or so.  Now, I'm a 74-year-old male. So, I'm not worried about being pregnant. And I don't want to contradict your physicians advice. But I just don't think you have done significant damage to your small bowel lining by one episode of significant gluten ingestion. I just don't think it works that way.
    • Skydawg
      Wondering about some thoughts on how long to wait to try to get pregnant after a gluten exposure?  I have been diagnosed for 10 years and have followed the diet strictly. I have been cross contaminated before, but have never had a full on gluten exposure. I went to a restaurant recently, and the waiter messed up and gave me regular bread and told me it was gluten free. 2 hours later I was throwing up for the whole evening. I have never had that kind of reaction before as I have never had such a big exposure. My husband and I were planning to start trying to get pregnant this month. My dr did blood work to check for electrolytes and white blood cells, but did not do a full nutritional panel. Most of my GI symptoms have resolved in the past 2 weeks, but I am definitely still dealing with brain fog, fatigue and headaches. My dr has recommended I wait 3 months before I start to try to get pregnant.   I have read else where about how long it can take for the intestine to fully heal, and the impacts gluten exposure can have on pregnancy. I guess I am really wondering if anyone has had a similar experience? How long does it take to heal after 1 exposure like that, after following the diet so well for 10 years? Is 3 months an okay amount of time to wait? Is there anything I can do in the meantime to reduce my symptoms? 
    • ShadowLoom
      I’ve used tinctures and made my own edibles with gluten-free ingredients to stay safe. Dispensary staff don’t always know about gluten, so I double-check labels or just make my own.
    • Scott Adams
      It's great to hear that there are some good doctors out there, and this is an example of why having a formal diagnosis can definitely be helpful.
    • RMJ
      Update: I have a wonderful new gastroenterologist. She wants to be sure there’s nothing more serious, like refractory celiac, going on. She ordered various tests including some micronutrient tests that no one has ever ordered before.  I’m deficient in folate and zinc and starting supplements for both. I’m so glad I decided to go to a new GI!
×
×
  • Create New...