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

IGA vs. IGG. Questions...please help! :)


kaelynrose89

Recommended Posts

kaelynrose89 Newbie

A little background...I'm a 28 year old female, and have always had stomach issues (bloating/constipation/sharp pains). Always felt like I had just eaten a huge cheeseburger, xl fry and a shake, when I just ate a bowl of cereal. My mom recently informed me that when I was 12 months old I was diagnosed celiac, but I outgrew it. Last week, I went in to ask my doctor to run a test to see if that's the reason I've been having issues all these years. Results were that my IGA was <1 (would have been > or = 4 to detect an antibody), but my IGG was high at 22 (antibody detected at > or = 6).

She noted that I have increased levels of immune transglutaminase without acute celiac disease and to follow a gluten free diet. I'm wondering if I should just leave it alone or push for the biopsy just to be clear. Any suggestions? I'm conflicted because my doctor doesn't seem concerned, but my husband works at a hospital and asked some of the doctors there and they seem to think there's a good possibility it could be Celiac.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi,

You only have to be positive on 1 antibody test to have celiac disease.  One kind of immune cell attacking your gut can do plenty of damage.  They are powerful little buggers!

People don't get over celiac disease, although that was thought to be true in the past.  What does happen is sometimes a person's immune system will take a break from attacking for an while.  That doesn't last forever though and at some point the immune attack will resume.  The same thing happens in other AI diseases at times.  That resumption of symptoms is sometimes called a "flare-up" in other conditions.

If you are unsure of your diagnosis, then get the endoscopy done.  But don't stop eating gluten until the endoscopy is complete.  The GI will generally take from 4 to 6 biopsy samples of the small intestine for microscopic examination.

There is some info in the Newbie 101 thread posted in the Coping With section that may help.

kaelynrose89 Newbie
7 minutes ago, GFinDC said:

Hi,

You only have to be positive on 1 antibody test to have celiac disease.  One kind of immune cell attacking your gut can do plenty of damage.  They are powerful little buggers!

People don't get over celiac disease, although that was thought to be true in the past.  What does happen is sometimes a person's immune system will take a break from attacking for an while.  That doesn't last forever though and at some point the immune attack will resume.  The same thing happens in other AI diseases at times.  That resumption of symptoms is sometimes called a "flare-up" in other conditions.

If you are unsure of your diagnosis, then get the endoscopy done.  But don't stop eating gluten until the endoscopy is complete.  The GI will generally take from 4 to 6 biopsy samples of the small intestine for microscopic examination.

There is some info in the Newbie 101 thread posted in the Coping With section that may help.

I really appreciate your feedback! I feel like I have to push my doctor at times to thoroughly examine my concerns, so I'll have to fight for that referral to a GI doc, just for my own peace of mind. I go back and forth wondering if it even matters to get a final diagnosis since the only way to keep it under control is with a gluten free diet, which I think I'll try to follow anyways. It's only been 3 days since I've officially eliminated gluten from my diet, so I need to figure out what I'm going to do.... =/ Thank you so much for taking the time to respond!

cyclinglady Grand Master

I just wanted to add that when I was diagnosed, I only suffered with anemia that was always blamed on my being a female.  Seriously.  It is amazing that I was able do triathalons and century rides.....I think it was due to true grit and the bodies ability to cope. 

If my doctor had not ordered the complete celiac panel, my diagnosis would have been missed.  It looks like you just got the screening TTG tests which catch most, but not all celiacs.  Often only a GI can order the complete panel depending on your provider.  Found that out when my family went in for testing (that would be Kaiser....).

Get to a GI!  Ask for the rest of the panel (DGP IgA/IgG and EMA).   I test positive to only the DGP IgA even in follow-up testing, yet I had severe damage.  

Finally, keep in mind that some 10% of celiacs are seronegative.  Proceeding to an endoscopy would be the next step.

What was your total IGA (Immunoglobulin A)?  Was that test given?  If you are IgA deficient, you will NOT get a valid response out of any of the IGA type tests (e.g. TTG IgA).  

kaelynrose89 Newbie
19 hours ago, cyclinglady said:

I just wanted to add that when I was diagnosed, I only suffered with anemia that was always blamed on my being a female.  Seriously.  It is amazing that I was able do triathalons and century rides.....I think it was due to true grit and the bodies ability to cope. 

If my doctor had not ordered the complete celiac panel, my diagnosis would have been missed.  It looks like you just got the screening TTG tests which catch most, but not all celiacs.  Often only a GI can order the complete panel depending on your provider.  Found that out when my family went in for testing (that would be Kaiser....).

Get to a GI!  Ask for the rest of the panel (DGP IgA/IgG and EMA).   I test positive to only the DGP IgA even in follow-up testing, yet I had severe damage.  

Finally, keep in mind that some 10% of celiacs are seronegative.  Proceeding to an endoscopy would be the next step.

What was your total IGA (Immunoglobulin A)?  Was that test given?  If you are IgA deficient, you will NOT get a valid response out of any of the IGA type tests (e.g. TTG IgA).  

They tested "Tissue Transglutaminase AB, IGG", results were high at 22 U/mL

"Tissue Transglutaminase AB, IGA", results were <1 U/mL

Because my IgA test came back negative, she put in her notes that I do not have celiac, but told me to follow a gluten free diet. Everything I'm reading, and every health care professional my husband works with, seems to think there's a strong possibility that it could be celiac because my IGG levels were so high. Obviously my body is fighting SOMETHING off, and I just want a conclusive answer. Challenging finding that balance between being proactive about my health and having your doctor settle for inconclusive results.

cyclinglady Grand Master

So, I am assuming Immunoglobulin A test was not given.  Your doctor can not say that the TTG test result (that was less than 1) is even accurate.  If you do not make IgA, then the IgA tests are invalid.  Again, your result is not standard, but that does not mean you can not have celiac disease.  I have never had a positive on either of the two tests that you were given.  Ever.  Taken repeatedly.  Yet, my biopsies revealed severe damage.  

Please consider another opinion from a celiac-savvy GI.  Your primary doc is way off in my non-medical opinion.  Sure you can go gluten free, but maintaining this diet for life can be very hard if you have any doubts.  

frieze Community Regular

doc wrong, find new doc.  cycling and I may not be docs, but we do know our way around a blood test or two.  good luck.  and remember her "wrongness" if anyone asks for suggestions for a doc.


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



Celiac.com Sponsor (A8-M):



KKJ Rookie

When I was tested, my IGa came back very low, nearly nil. Turns out that I have the most common form of immune deficiency called an IGa deficiency. So, my doc ran other tests to confirm/rule out celiac as well astook a biopsy, and for sure, all results showed that I have celiac.

Many of us with IGa deficiency are asymptomatic and the thought among immunologists (at least mine)  is that those of us w/o symtpoms likely have IGg in the areas were there'd be IGa and it's taken over the role of the missing / low IGa.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,634
    • Most Online (within 30 mins)
      7,748

    AmyMcG
    Newest Member
    AmyMcG
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @JenFur! You must be relatively new to the celiac journey. I wish it were as simple as just having to cut out gluten and all our gut issues magically disappear. It is very common for those with celiac disease to develop intolerance/sensitivity to other foods. Often it is because the protein structure of some other foods resembles that of gluten. Sometimes it is because damage the damage done to the gut lining by celiac disease wipes out cells that produce enzymes needed to break down those foods. Sometimes it is because the "leaky gut syndrome" associated with celiac disease causes the immune system to incorrectly identify other food proteins as threats or invaders. The two most common non-gluten foods that cause trouble for a lot of celiacs are dairy and oats. But soy, eggs and corn are also on that list. Sometimes these non-gluten food intolerances disappear with time and the healing of the villous lining of the small bowel.
    • JenFur
      I love popcorn but it doesn't love me.  Right now my gut hurts and I am bloated and passing gas.  Am I just super sensitive. I thought popcorn was gluten free 🤔 
    • trents
      Welcome to the forum, @marinke! "Type 1a diabetes (DM1) is associated with an increased risk of celiac disease (celiac disease) (1)." from: https://diabetesjournals.org/care/article/35/10/2083/38503/IgA-Anti-transglutaminase-Autoantibodies-at-Type-1 "The prevalence of celiac disease (celiac disease) in children with type 1 diabetes (T1D) is 5.1%, and it is often asymptomatic (1)." from: https://diabetesjournals.org/care/article/48/2/e13/157637/Diagnostic-Outcomes-of-Elevated-Transglutaminase So, this is 5x the rate found in the general population.
    • Mari
      Hi James47, You are less than 2 years into your recovery from Celiacs.  Tell us more about the problems you are having. Do you just want to get rid of belly fat or are you still having symptoms like gas and bloating.    For symptoms you may need to change your diet and take various supplements that you cannot adsorb from the foods you eat because of the damage caused by the autoimmune reaction in your small intestine. 
    • marinke
      My daughter (4 years old) has type 1 diabetes since she was 1. Therefore, every year a screening is done. We live in the Netherlands. Every year the screening was fine. This year here ttg is positive, 14, >7 is positive. IGA was in range. Could the diabetes cause this positive result? Or the fact that she was sick the weeks before the brood test?
×
×
  • Create New...