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. - badastronaut replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Still unsure.....

    2. - knitty kitty replied to cristiana's topic in Related Issues & Disorders
      28

      Ectopic heartbeats - any relation to digestive issues?

    3. - knitty kitty replied to Jhona's topic in Introduce Yourself / Share Stuff
      26

      Does anyone here also have Afib

    4. - knitty kitty replied to Jhona's topic in Introduce Yourself / Share Stuff
      26

      Does anyone here also have Afib

    5. - thejayland10 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      TTG IgA and IGA elevated mildy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,736
    • Most Online (within 30 mins)
      7,748

    Phyliss
    Newest Member
    Phyliss
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • badastronaut
      Ok so I couldn't find the thiamine you suggested but I was able to buy a bottle of 'standard' thiamine (100 mg). Should I just try half a tablet to see if I notice any difference? If it turns out it does have effect I can always buy the more expensive stuff. Or is that not a smart idea?
    • knitty kitty
      @cristiana, Yes, I found high carbohydrate meals would trigger mine as well.  I learned from Dr. Lonsdale that high carbohydrate diets can deplete thiamine.  Heart palpitations are a symptom of thiamine insufficiency.  Diets high in refined simple carbohydrates (empty calories) need additional Thiamine to process the carbs into energy.  The more carbs one eats, the more Thiamine is required to process the additional calories.  500 mg more Thiamine is required for every additional one thousand calories.  This is named "High Calorie Malnutrition."  Sufficient calories are being consumed, but not enough of thiamine to burn the carbs for energy.  Instead to ration out the small supply of thiamine, the additional calories are stored as fat.  It takes less thiamine to burn fat than to burn carbs.    Do read Dr. Lonsdale' article here... Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/
    • knitty kitty
      I used to suffer with migraines, but I have rarely had one since I started taking additional Thiamine.  The form called TTFD (tetrahydrofurfuryl disulfide) can improve neurological functions in the brain.  Benfotiamine is another form that improves migraines. Look at the label on your B Complex vitamins.  It should tell you what form of thiamine is in it.  If it says thiamine mononitrate, you're probably not getting sufficient thiamine.  Thiamine Mononitrate is a form used in vitamin supplements and foods because it is shelf stable.  Shelf stable means it won't break down when exposed to heat and light sitting on a shelf waiting to be bought in a store or warehouse.  It also is very difficult for the body to break it down and utilize it.  Only about thirty percent of the amount of thiamine mononitrate on the label is absorbed.   Do take a look at Dr. Lonsdale and Dr. Marrs' website hormonesmatter.com.  Dr. Lonsdale has done much research on Thiamine.   Keep us posted on your progress!
    • knitty kitty
      @DebJ14 The Spectracell Test for Micronutrient Deficiencies tests  intracellular levels of the nutrients INSIDE Leukocytes (white blood cells) which are in the bloodstream.  This still is not reflective of current stored vitamin levels inside organs.   The genetic MTHFR mutation does occur frequently with Celiac Disease.  Taking the methylated (activated) forms of the B vitamins is necessary.   A good multivitamin may not be sufficient to correct deficiencies.  Malabsorption due to the intestinal damage of Celiac Disease may prolong deficiency states.  Vitamin deficiencies need to be corrected quickly to prevent long-term problems.  Taking a B Complex twice a day increases absorption.  Taking a multivitamin as well is fine as multivitamins usually also contain some necessary minerals.
    • thejayland10
      My TTG IgA and IGA are elevated mildly, right at borderline positive,e but my EMA is negative. All my vitamin levels are normal as well as cbc and metabolic panel. What is the likely cause of this? I have been on gluten-free diet for 15 yrs nearly. 
×
×
  • Create New...