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

Gliadin Ab IgA


Marmee

Recommended Posts

Marmee Rookie

Hello,

I’m new to the forum and have a question about Gliadin Ab IgA.  If  the results are weak positive does that mean I have Celiac Disease?


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Welcome to the forum, Marmee!

One challenge in interpreting lab results is the variations found in terminology from lab to lab.

I think the test you are referring to is also called Deamidated gliadin peptide IGA. https://celiac.org/about-celiac-disease/screening-and-diagnosis/screening/

It is a secondary diagnostic test for celiac disease that is sometimes run in addition to the tTG-IGA, the latter being the most popular test run by docs because it combines good specificity with good sensitivity. And it is economical. The test you report in your post is not as specific for celiac disease, meaning a positive can be caused by other things, and is often run when what's called "total serum IGA" is low. In addition, your score is a low positive.

This certainly could mean you have celiac disease but it could also point to other medical conditions as mentioned in the link above.

Were you eating significant amounts of gluten in the weeks and months leading up to the blood draw? If you were not, then it would have the effect of sabotaging the testing with false negatives. Also, was there a test done for total serum IGA? Is the information you gave in your first post complete? Seems like there should be more.

Right now, it looks kind of inconclusive and you may be asked to have an endoscopy with biopsy done of the small bowel lining  to check for damage to the villi that line the small bowel. This is considered to be the hallmark of celiac disease and the biopsy is considered to be the gold standard diagnostic test.

knitty kitty Grand Master

@Marmee,

A positive is a positive.   

Like being a little bit pregnant. 

😸  Welcome to the club.

You can double check with a genetic test.  Most Celiacs have HLA DQ 2 or 8, though there are more rare Celiac genes out there.  

You don't have to be eating gluten to get a genetic test.  Some people can't complete a gluten challenge if they've been gluten free for a short time.  The autoimmune response is much worse if gluten is reintroduced.  

Marmee Rookie

Thank you for the input. A little back story on my stomach issues.  I have always had stomach issues but it became progressively worse eight years ago when I had my gallbladder out.  I was sick all the time and went to my doctor a year later.  She ordered  tests to check for Celiac.

test results:

Tissue Transglutaminase Ab IgA / <2

IgA/ 374

Gliadin Ab IgA/ 24

Fecal Fat / increased

When the test came back she gave me referral to see a GI doctor.  He looked at my results and told me I have Celiac but they would have to do a scope to see how much damage.  He also told me to go gluten-free , which I did. I was off gluten for about 20 days. My scope came back with no abnormalities so he told me to stay off gluten because I had an allergy to it. 
Fast forward to the present. I have been off gluten for seven years. I’m having trouble with reflux etc. so I went to another GI doctor. He wants to check for  ulcers etc. I told him about my experience with the previous GI and he was shocked that he told me to go gluten free before my scope.  My new doctor wants to check for celiac  so I  went back to eating gluten. Needless to say I am sick. Nauseated, vomiting, fatigue, headaches and my face has also developed bumps. I’ve been back on gluten for 5 weeks and my scope is next week. I also have Rheumatoid Arthritis and I have bloodwork done every three months. My bloodwork is all out of wack and my liver enzymes are high. I have never had that before. It’s just so frustrating and I feel like the scope will be a waste of time considering the tests that were done seven years ago. 
 

 

knitty kitty Grand Master

@Marmee,

I am so sorry you're going through this.  Lots of us have been misdiagnosed, misdirected, and mistreated by doctors ignorant of Celiac Disease.  My heart goes out to you.  

You're almost done with the gluten challenge, so stay strong.  You can make it through.  You will have a baseline endoscopy with which to compare future endoscopies if problems arise (heaven forbid).  

Make sure all testing (endoscopy and additional antibody blood tests) are done before going gluten free.  

I'm sure many of your symptoms will improve as soon as you're off gluten.  Others may improve further if nutritional deficiencies are addressed.  

Becoming low in certain nutrients can occur on the Gluten Free diet.  Since you've been gluten free for seven years, you should be checked for nutritional deficiencies as part of proper follow up care for people diagnosed with Celiac Disease.

Gallbladder dysfunction and reflux are conditions that happens in Thiamine Vitamin B 1 deficiency.  I had my gallbladder removed, and had reflux as well.  Thiamine deficiency diseases can get much worse, but supplementing with Thiamine easily improves things.  Thiamine helps with Rheumatoid arthritis and liver function.  Raised liver enzymes are a symptom of Thiamine deficiency.  (Ask for a Erythrocyte Transketolase test for Thiamine deficiency.  Blood tests are not accurate.)

Were you prescribed a PPI for your reflux?

trents Grand Master

Elevated liver enzymes is what eventually led to my diagnosis of celiac disease. But it tool 13 years from when I first became aware of the elevated liver enzymes until  the time when I was diagnosed with celiac disease. My GP was clueless and I finally scheduled an appointment with a GI doc and he tested me right away for celiac disease. But by that time I had developed osteopenia and kyphosis of the spine and number of other food sensitivity issues.

Marmee Rookie
54 minutes ago, knitty kitty said:

@Marmee,

I am so sorry you're going through this.  Lots of us have been misdiagnosed, misdirected, and mistreated by doctors ignorant of Celiac Disease.  My heart goes out to you.  

You're almost done with the gluten challenge, so stay strong.  You can make it through.  You will have a baseline endoscopy with which to compare future endoscopies if problems arise (heaven forbid).  

Make sure all testing (endoscopy and additional antibody blood tests) are done before going gluten free.  

I'm sure many of your symptoms will improve as soon as you're off gluten.  Others may improve further if nutritional deficiencies are addressed.  

Becoming low in certain nutrients can occur on the Gluten Free diet.  Since you've been gluten free for seven years, you should be checked for nutritional deficiencies as part of proper follow up care for people diagnosed with Celiac Disease.

Gallbladder dysfunction and reflux are conditions that happens in Thiamine Vitamin B 1 deficiency.  I had my gallbladder removed, and had reflux as well.  Thiamine deficiency diseases can get much worse, but supplementing with Thiamine easily improves things.  Thiamine helps with Rheumatoid arthritis and liver function.  Raised liver enzymes are a symptom of Thiamine deficiency.  (Ask for a Erythrocyte Transketolase test for Thiamine deficiency.  Blood tests are not accurate.)

Were you prescribed a PPI for your reflux?

I will have to look into Thiamine. That never crossed my mind. I was prescribed  PPl but haven’t taken it yet. Thank you so much for your suggestions.  


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



Celiac.com Sponsor (A8-M):



trents Grand Master
1 minute ago, Marmee said:

I will have to look into Thiamine. That never crossed my mind. I was prescribed  PPl but haven’t taken it yet. Thank you so much for your suggestions.  

Avoid long term PPI therapy if you possibly can. It raises gut PH which makes vitamin and mineral absorption less efficient and digestion in general. You may need to investigate other food intolerance/sensitivity issues as it is par for the course for celiacs to develop them. Also, research histamine intolerance/MCAS (Mast Cell Activation Syndrome) and SIBO (Small Intestine Bacterial Overgrowth), both of which are common in the celiac community.

knitty kitty Grand Master

I agree with @trents.  

Do not take the PPI.  It can cause more inflammation.  

Reflux or Gerd is symptomatic of low stomach acid, hypochlorhydria.  Deficiency in Niacin Vitamin B3 can cause low stomach acid.  

My Gerd resolved after supplementing with Niacin.

There are eight B vitamins which all work together.  A B Complex usually contains all eight.  Talk to your doctor before starting supplementation, in case testing is offered.  Blood tests aren't really accurate measurements for vitamins because most vitamins work inside cells, not in the bloodstream.  Taking supplements before testing will reflect the vitamins you've taken.  

Scott Adams Grand Master

This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.

Quote

The DGP-IgA test is considered to have high sensitivity and specificity. In general, the DGP-IgA test has been reported to have a sensitivity ranging from 75% to 95% and a specificity ranging from 90% to 100%. The DGP tests have been found to have a sensitivity of around 85-95% and a specificity of around 95-98%.

 

 

Marmee Rookie
3 hours ago, Scott Adams said:

This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.

 

 

The article was very informative. Thank you for posting it.  

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - PixieSticks replied to PixieSticks's topic in Super Sensitive People
      2

      Working in a kitchen with gluten?

    2. - BoiseNic replied to BoiseNic's topic in Dermatitis Herpetiformis
      11

      Skinesa

    3. - knitty kitty replied to Whyz's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Feeling ill

    4. - Scott Adams replied to Brianne03's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Advantages vs. Disadvantages of having an official Celiac diagnosis

    5. - Scott Adams replied to Whyz's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Feeling ill


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,536
    • Most Online (within 30 mins)
      7,748

    Annette Smith
    Newest Member
    Annette Smith
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • PixieSticks
      Hi yes! I was diagnosed 10 years ago through a biopsy. I’ve been gluten free ever since but no one I’m around is gluten free. I sometimes wore a surgical mask in the kitchen. but I believe particles were still getting through. I’ll definitely look into n95 instead. thanks for the reply. 
    • BoiseNic
      Ya I used to react to iodine, but it doesn't bother me anymore after strict adherence to a gluten-free diet for many years now. I am happy to report that for the first time ever in my life, a probiotic formula is not making me break out, but actually seems to be helping. The strains in this formula have been specifically tested to help with skin issues. It is gluten and dairy free also. 
    • knitty kitty
      @Whyz, I take a combination of Thiamin (Benfotiamin), B12 Cobalamine and Pyridoxine B6 for my pain and headaches.  Really works well without hurting the digestive tract.  Riboflavin B2 also helps with migraines.  Most newly diagnosed people have vitamin and mineral deficiencies.  Check with your doctor and nutritionist.   If you follow the updated gluten challenge guidelines, you can wait until two weeks (minimum) before your appointment, then eat lots of gluten, like six slices of gluten containing bread or "name your poison".   Here's the Updated Gluten Challenge Guidelines: Recommended intake of gluten should be increased to 10 grams of gluten per day for at least two weeks. Or longer. While three grams of gluten will begin the immune response, ten grams of gluten is needed to get antibody levels up to where they can be measured in antibody tests and changes can be seen in the small intestine.   Keep in mind that there are different amounts of gluten in different kinds of bread and gluten containing foods.  Pizza crust and breads that are thick and chewy contain more gluten than things like cake and cookies.   References: https://www.beyondceliac.org/celiac-disease/the-gluten-challenge/ And... Evaluating Responses to Gluten Challenge: A Randomized, Double-Blind, 2-Dose Gluten Challenge Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878429/?report=reader  "In our study, limited changes in Vh:celiac disease (villi height vs crypt depth - aka damage to the small intestine)  following 14-day challenge with 3 g of gluten were observed, in accordance with Sarna et al.  While the 3 g dose was sufficient to initiate an immune response, as detected by several biomarkers such as IL-2, the 10 g dose was required for enteropathy within the study time frame. Based on our data, we would suggest that gluten challenge should be conducted over longer durations and/or using doses of gluten of ≥ 3 g/day to ensure sufficient histological change can be induced." Keep us posted on your progress!
    • Scott Adams
      I don't believe that existing life insurance policies require such notifications--health checks are typically done before such policies are obtained. I believe it would primarily affect any new policy you get, and perhaps any policy renewal.
    • Scott Adams
      You could go gluten-free now, and then start eating lots of gluten for at least 2 weeks before your endoscopy--just be sure to tell your doctor about this beforehand. If your symptoms go away on a gluten-free diet, it is further evidence of celiac disease and/or non-celiac gluten sensitivity.  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.  
×
×
  • Create New...