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

Please Help Me Figure Out These Results


Laura--G

Recommended Posts

Laura--G Rookie

Hey everyone! I have 2 sons. One is a type 1 Diabetic and tested positive for Celiac and he's having his biopsy tomorrow. I decided to have the other one tested this week. His doctor isn't familiar with Celiac so she couldn't really help me with the test results but is having a GI speicialist call me....I can't wait that long so I'm here hehe. She did a Celiac panel with 5 blood tests. 4 came back negative but the IGG (is that rigjt???) came back strong positive. So, my question is does he have Celiac or not...what else could a positive IGG mean? Thanks for any help you guys may have!


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



Celiac.com Sponsor (A8-M):



slpinsd Contributor

I would say that he is definitely gluten sensitive. Other markers like tTg and IgA are more specific for Celiac, but you can have celiac and have only an elevated IgG. Since one of your sons has Celiac, it is likely that the other has the genes for it, as well. I would put him on a gluten-free diet and see the positive changes. Even if he is not Celiac at this point, with a positive genetic makeup, he could develop Celiac if he continues to eat gluten. Your son could even have a positive biopsy, and still have Celiac, because damage can be missed in early stages, and also the damage could be spotty and be missed. A negative blood test or biopsy doesn't rule out Celiac, but a positive biopsy rules it in.

It is also possible that he is IgA deficient, in that case, it would skew the results of the other tests.

Guest Robbin

Laura, I have 2 sons and one is a type 1 diabetic also. I am wondering if the diabetes may cause an IgA deficiency? It sure affects so many other things. I am glad you are able to convince him to be tested. (mine is 21 and won't listen to me) Maybe yours are very young or at least reasonable(!) Keep us posted on how you are all doing. :)

Laura--G Rookie
Laura, I have 2 sons and one is a type 1 diabetic also. I am wondering if the diabetes may cause an IgA deficiency? It sure affects so many other things. I am glad you are able to convince him to be tested. (mine is 21 and won't listen to me) Maybe yours are very young or at least reasonable(!) Keep us posted on how you are all doing. :)

:D My son is only 5 and he had no idea he was going in to be tested. I figured it was easier to just take him in and spring it on him instead of letting him make that decision. Unfortunately, my kids are also allergic to peanuts and fish and milk so our menu will be very limited with Celiac now. Thanks for the replies, I guess it doesn't matter if he definitely has it or not. I don't have time to make 2 meals for dinner so we are all going gluten-free I think.

heli Newbie

IgG positive really is not specific enough. What you want to know is, "which antibodies were positive?" The panel should have included tissue trasnglutaminase (tTg), antigliadin antibodies, anitendomysium antibodies, and I can't think of the other one right now that is in the standard panel. I'm not sure what the fifth one would be either, unless it is IgA.

Again, you want to know which anitbodies reacted. Saying IgG is too general. Lots of things can make IgG react. As a comparative, it would be like saying my IgE reacted. (IgE is the true allergy reaction like hives, itching, or anaphylaxis). What you really want to know about IgE is what food triggered it. So, with IgG you want to know which antibodies are causing the IgG to react.

Laura--G Rookie

Just got the numbers from our doctor. His IgG was 24, she said positive was 9. His tTG was only a 2.

ebrbetty Rising Star

this is what I read online when I got my tests back

Testing for Coeliac.

while an intestinal biopsy is the ‘gold standard’ for diagnosing celiac disease, there are now blood tests available to screen for celiac disease.

Testing is simple and involves either screening a pin-prick of blood for Anti-gliadin (AGA) or tTG-IgA Antibodies.

Transglutaminase IgA test (tTG-IgA)

This is a new immunological marker for the identification of patients with celiac disease. External studies have shown that our Transglutaminase IgA test results show a 99% – 100% correlation with the "gold standard" endomysial antibodies tests. A positive tTG IgA result is compelling evidence of celiac disease, provided the patient is not already on a gluten free diet.

Some Celiac patients suffer from IgA deficiency and in these cases, tTG-IgA will be falsely negative. In such cases, the Anti-gliadin test may prove more useful.

Anti-gliadin test

Gliadin is a major protein found in the gluten fraction of wheat. Gliadin antibodies are found in 95% of coeliac patients, provided the patient is not on a gluten free diet, but they are also present in some other diseases. For this reason both classes of antibodies are measured. The test measures the two key antibodies (IgA & IgG) to gliadin.


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



Celiac.com Sponsor (A8-M):



Guest alex j

Laura,

This is kind of freaky. I have two sons (and a daughter), the older son has type 1 diabetes, was recently diagnosed with celiac through positive blood tests confirmed by biopsy; I had his brother tested and everything was negative except his IgG gliadin which was positive. I came here to ask exactly the same question you did.

Oh, and my oldest son is also allergic to fish, tree nuts, egg and peas/lentils/some beans, and the youngest is allergic to milk (which you're right, doesn't make the diet any easier).

If you find anything useful out please post. I called the GI to ask if I should keep the little one on gluten so we could investigate further. The GI said it's not necessary for the little one to go gluten free, but if I want to then go for it; in either case retest in 6 mos. Of course I won't be able to if he goes gluten free. He's basically gluten free anyway; I'm unsure whether to make him strictly gluten free to in an attempt to resolve his horrible constipation, or push for more testing.

I know with my older son I needed definitive test/biopsy results because he was virtually asymptomatic. (He tested through the roof on TTG; positive on everything else except I think IgG). He was only tested because his endo thought malabsorbtion might have been the culprit with our blood sugar control problems - and even he was surprised it was positive.

I don't have any problem maintaining a gluten free diet for the little one now, with no testing to back it up. Relief of symptoms would certainly be motivation enough. But if it is possible to find out if it is celiac now, I would like to - I know that otherwise we will end up challenging gluten when he is older, and if he has celiac that will not be good for him.

Alex

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. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.

    2. - Scott Adams replied to Ginger38's topic in Related Issues & Disorders
      2

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
×
×
  • 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.