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

Help Interpreting Lab Results


tpogo

Recommended Posts

tpogo Newbie

Hi all,

I was given a celiac panel last year and received a phone call that I'm 'positive' and i should go to a GI dr to get a biopsy. I didn't know much about the results and immediately went on a gluten-free diet as I just didn't want to go through the process of something so invasive (especially when I read of so many false negative results).

But over the last year of trying to be gluten-free, I've noticed some things w/ my children and wanted to get them tested also. So I've been doing research to understand what's involved w/children and also dug into my lab results to figure out if a genetic test would be a better alternative.

~Now that I have my results, I'm completely confused~

I could use some advice from this forum of experience in how exactly to interpret these results. My lab results report : For a Reference range of 0-15 U/ml, I basically have normal Gliadin IgA (8.92 U/ml) & Gliadin IgG (12.36 U/ml) but very high tTg IgA (22.41 U/ml) and normal tTg IgG (9.20 U/ml).

So my question - what does it mean to have a normal Gliadin IgA/IgG but high tTg Iga? Does this mean I have Celiac or gluten sensitivity, or would the levels indicate something else?

Thank you in advance for the opinions :)!


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

Hi and welcome to the board.

Anti-gliadin is an old, inaccurate test that isn't very sensitive. It's negative in a lot of celiacs. TTG IgA is an autoimmune antibody directed at your intestine and assuming you don't have some other autoimmune disease like type 1 diabetes or rheumatoid arthritis, it indicates celiac disease. If you feel better and the TTG falls on the gluten-free diet, you definitely have celiac.

Be sure your kids are eating a full gluten diet for three months before you get them tested. They will have false negatives gluten-free.

tpogo Newbie

Hi and welcome to the board.

Anti-gliadin is an old, inaccurate test that isn't very sensitive. It's negative in a lot of celiacs. TTG IgA is an autoimmune antibody directed at your intestine and assuming you don't have some other autoimmune disease like type 1 diabetes or rheumatoid arthritis, it indicates celiac disease. If you feel better and the TTG falls on the gluten-free diet, you definitely have celiac.

Be sure your kids are eating a full gluten diet for three months before you get them tested. They will have false negatives gluten-free.

Thank you for the info! As far as I know, I don't have any autoimmune disease. I had some confusion over this because was that I was reading in one place that low IgA but high tTg could also indicate just general dietary allergies like eggs/milk/corn/etc.

Do you know if genetic tests are as reliable as the biopsy in diagnosis? i've read so much of false negatives in biopsy method and that Dr's today do not recommend the genetic testing yet. ...

Skylark Collaborator

Thank you for the info! As far as I know, I don't have any autoimmune disease. I had some confusion over this because was that I was reading in one place that low IgA but high tTg could also indicate just general dietary allergies like eggs/milk/corn/etc.

Do you know if genetic tests are as reliable as the biopsy in diagnosis? i've read so much of false negatives in biopsy method and that Dr's today do not recommend the genetic testing yet. ...

I don't know what you've been reading but it's dead wrong. TTG is an enzyme in your body, not a food substance. If you have anti-TTG you definitely have autoimmunity. The only question is which kind of autoimmunity and most often TTG is a sign of celiac autoimmunity. Your GI doctor should be able to confirm what I'm telling you.

Genetic tests are not diagnostic. All they can do is stratify risk. 30% of the US population has a so-called celiac gene and 1% of celiacs do NOT have a so-called celiac gene. In a sense your kids already have positive genetic tests, since celiac runs in families and first-degree relatives of celiacs have at least a 1 in 20 chance of getting celiac. The chance of gluten intolerance is probably higher.

What you need to do with the kids is make sure they're eating a full gluten diet for three months and then get them celiac panels. Since you're positive for TTG, your kids have a little better chance of having TTG show up if they're celiac too. If your kids are tested, be sure they also get the newest deamidated gliadin IgG and IgA. It is much more sensitive and has a lower false negative rate.

There are false negatives by biopsy if 1) your doctor caught your celiac symptoms early and the autoimmune damage is very mild or 2) the biopsy simply misses patchy damage. People with anti-TTG have been followed in prospective studies and they almost invariably go on to develop positive biopsies, suggesting that sometimes anti-TTG precedes the onset of damage. They also usually have metabolic markers consistent with celiac disease. This is why there are a lot of medical papers now suggesting that celiac be diagnosed if a person has anti-TTG or anti-EMA, responds to a gluten-free diet, and the TTG antibodies go away gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,991
    • Most Online (within 30 mins)
      7,748

    ZENken
    Newest Member
    ZENken
    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

    • Wheatwacked
      Testing can't alone be trusted.  Else why would it take so many years of testing and retesting and misdiagnosis to finally be told, yes you have Celiac Disease. As to what to eat, I like pre 1950 style food.  Before the advent of TV dinners.  Fresh food is better for you, and cooking from scratch is cheaper.  Watch Rachel Ray's 30 Minute Meals for how to cook.  Keep in mind that she is not gluten free, but her techniques are awesome.  Just use something else instead of wheat, barley, rye. Dr Fuhrman is a ex cardiologist.  His book Eat to Live and Dr Davis' book Wheatbelly were instrumental in my survival.
    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch--thanks for the tip about Dupixent, and I've added it to the article:  
    • Scott Adams
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
    • knitty kitty
      @tiffanygosci, Thiamine deficiency is a thing in pregnancy for "normal" people, so it's exponentially more important for those with celiac disease and malabsorption issues. I studied nutrition before earning a degree in Microbiology because I was curious what the vitamins were doing inside the body.  See my blog.  Click on my name to go to my page, scroll to drop down menu "activities" and select blog.   So glad you're motivated to see the dietician!  We're always happy to help with questions.  Keep us posted on your progress! 
×
×
  • 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.