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

Please Help!


amberlink84
Go to solution Solved by trents,

Recommended Posts

amberlink84 Newbie

These where my testing values.. The way it was worded in the test results has me concerned.. Please help..

Gliadin IgA

Value

<0.72

TISSUE TRANSGLUTAMINASE (TTG) AB IGG

Value

<0.82

Gliadin IgG

Value

3.03


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Welcome to the forum!

We cannot comment on your test scores unless you also include the reference ranges for negative vs. positive on each test used by the particular laboratory doing the analysis. Each lab concocts its own test and uses different parameters so the ranges the use for reference vary. There is no industry standard. Please repost and add this additional information. The time window for editing your original post is now closed.

Were these the only tests performed? It's a rather odd selection of tests in that the TTG-IGA and total IGA were not ordered. The ones you posted above are second level tests. Were there more that you did not post? Please post the result info exactly like it appears in the results given to you.

amberlink84 Newbie

This is all it says/copied and pasted each test:

TISSUE TRANSGLUTAMINASE (TTG) AB IGG

View trends

Normal value: 0.00 - 4.99 FLU

Value

<0.82

INTERPRETIVE INFORMATION: Tissue Transglutaminase Ab, IgG

 

In individuals with low or deficient IgA, testing for tissue

transglutaminase (tTG) and deamidated Gliadin (DGP) antibodies of

the IgG isotype is performed. Positive tTG and/or DGP IgG antibody

results indicate celiac disease; however, small intestinal biopsy

is required to establish a diagnosis due to the lower accuracy of

these markers, especially in patients without IgA deficiency.

Performed By: ARUP Laboratories

500 Chipeta Way

Salt Lake City, UT 84108

 

Gliadin IgG

View trends

Normal value: 0.00 - 4.99 FLU

Value

3.03

INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide

(DGP) Ab, IgG

 

In individuals with low or deficient IgA, testing for tissue

transglutaminase (tTG) and deamidated Gliadin (DGP) antibodies of

the IgG isotype is performed. Positive tTG and/or DGP IgG antibody

results indicate celiac disease; however, small intestinal biopsy

is required to establish a diagnosis due to the lower accuracy of

these markers, especially in patients without IgA deficiency.

Performed By: ARUP Laboratories

500 Chipeta Way

Salt Lake City, UT 84108

 

Gliadin IgA

View trends

Normal value: 0.00 - 4.99 FLU

Value

<0.72

Low IgA antibody levels suspected. Tissue transglutaminase, IgG

and deamidated gliadin peptide, IgG tests to follow.

INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA

 

A positive deamidated gliadin (DGP) IgA antibody result is

associated with celiac disease but is not to be used as an initial

screening test due to its low specificity and only occasional

positivity in celiac disease patients who are negative for tissue

transglutaminase (tTG) IgA antibody.

Performed By: ARUP Laboratories

500 Chipeta Way

trents Grand Master

Is this the first round of antibody testing you have had done? Have you already had any IGA antibody testing done? The reason I ask is from the statement found in your lab report from your second post: 

"Low IgA antibody levels suspected. Tissue transglutaminase, IgG

and deamidated gliadin peptide, IgG tests to follow."

But I see no IGA test scores in the information you have provided.

At any rate, your IGG antibody tests do not indicate celiac disease. They are all within normal range and therefore negative. What symptoms do you have? Have you considered that you might not have celiac disease but NCGS (Non Celiac Gluten Sensitivity) instead. There are no tests available for NCGS yet. Celiac disease and NCGS share many of the same symptoms but NCGS does not damage the villous lining of the small bowel and therefore not antibodies are produced. NCGS is 10x more common than celiac disease. Arriving at a diagnosis of NCGS involves first ruling out celiac disease which the test results you have supplied seem to have done.

If you have already had IGA antibody tests run and they were negative there is one more diagnostic procedure that can be done to look for celiac disease and that is an endoscopy with biopsy of the small bowel lining to microscopically look for damage. A small percentage of people who actually do have celiac disease are seronegative and don't throw antibodies.

Again, what are your symptoms? Why have you been pursuing a celiac diagnosis?

I am including an article attachment that explains celiac disease antibody testing: 

 

amberlink84 Newbie

Gliadin IgA

View trends

Normal value: 0.00 - 4.99 FLU

Value >0.72

<A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening. 

This is 1st screening in all testing.  This was IGA Antibody >0.72... 

I have bloating, Stomach pain, constant diarrhea, nausea, vomiting, in and out of hospitals, different test, different meds, different diagnosis. I'm tired.

@trents

  • Solution
trents Grand Master

Yes, missed that. But still, no TTG-IGA? No total IGA? Who ordered these tests anyway? Doesn't seem like they know what they are doing. 

At a bare minimum, an initial celiac blood antibody testing panel should include a test for total IGA to check for IGA deficiency and the TTG-IGA test. The normal protocol is that if the TTG-IGA is negative but total IGA shows an IGA deficiency then other tests are ordered reflexively such as the DGP-IGA and the DGP-IGG.

I would ask for a total IGA test and a TTG-IGA test to be done or better, yet, an endoscopy with a biopsy of the small bowel lining. If you get no cooperation, trial a gluten free diet for a few months and see if your symptoms improve.

Speaking of trialing a gluten free diet, I should ask you, have you already been cutting back on gluten significantly for a significant period of time? If so, know that doing so would have invalidated the blood antibody testing. All testing for celiac disease, whether the blood antibody testing or the endoscopy/biopsy requires being on regular amounts of gluten for significant periods of time (weeks/months).

But something else just now occurred to me as I was looking at your avatar. Are you African American by any chance? If so, I remember reading somewhere that celiac serum antibody testing doesn't work well for those with African heritage. If I remember correctly, the article said it misses about 80% of those of African decent who actually do have celiac disease.

amberlink84 Newbie
1 hour ago, trents said:

Yes, missed that. But still, no TTG-IGA? No total IGA? Who ordered these tests anyway? Doesn't seem like they know what they are doing. 

At a bare minimum, an initial celiac blood antibody testing panel should include a test for total IGA to check for IGA deficiency and the TTG-IGA test. The normal protocol is that if the TTG-IGA is negative but total IGA shows an IGA deficiency then other tests are ordered reflexively such as the DGP-IGA and the DGP-IGG.

I would ask for a total IGA test and a TTG-IGA test to be done or better, yet, an endoscopy with a biopsy of the small bowel lining. If you get no cooperation, trial a gluten free diet for a few months and see if your symptoms improve.

Speaking of trialing a gluten free diet, I should ask you, have you already been cutting back on gluten significantly for a significant period of time? If so, know that doing so would have invalidated the blood antibody testing. All testing for celiac disease, whether the blood antibody testing or the endoscopy/biopsy requires being on regular amounts of gluten for significant periods of time (weeks/months).

But something else just now occurred to me as I was looking at your avatar. Are you African American by any chance? If so, I remember reading somewhere that celiac serum antibody testing doesn't work well for those with African heritage. If I remember correctly, the article said it misses about 80% of those of African decent who actually do have celiac disease.

You haven't paid attention to any of the question, or response... All test are done, just not the biopsy. These are just the numbers on me- THE TEST

IGA, (TTG) AB IGG, & IGG

Gliadin IgA

Value

<0.72

TISSUE TRANSGLUTAMINASE (TTG) AB IGG

Value

<0.82

Gliadin IgG

Value

3.03

I've had scopes "upper and lower".

All test are from Texas. Nevermind, I'll just delete this. Again, not paying attention. Ignoring what I type out, like the doctor's Ignoring everything I go through daily. Thanks 🤷‍♀️


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

Good for your doctor in ordering a complete celiac panel! Many just order TTG IgA. The four celiac tests are all normal, i.e. not indicating celiac disease (as long as you were eating gluten prior to the tests). I’m not sure why the lab said low total IgA was suspected, but even if the total IgA was low, the correct tests were done to account for that.

I hope your doctor can figure out why you’re having gastrointestinal issues.

trents Grand Master

I certainly was paying attention to everything you posted but apparently the formatting and the terminology deployed is unusual and not what we are used to seeing on this forum. It was very confusing to me and I'm sorry for the confusion it all caused in our interaction. But, if you go back and read my several posts you will see that I agree with RMJ that your test results do not indicate celiac disease. And it is unfortunate that no one did a biopsy while doing an upper GI since some celiacs are seronegative. 

Wheatwacked Veteran

Welcome to the forum.

On 7/27/2024 at 11:44 AM, amberlink84 said:

The way it was worded in the test results has me concerned.

What is your concern?

Your tests indicate no Celiac, they don't find anything in the endoscopy or colonoscopy so they say there is nothing wrong with you?  Maybe they think it is all in your head? Welcome to the club.  

On 7/27/2024 at 3:08 PM, amberlink84 said:

I have bloating, Stomach pain, constant diarrhea, nausea, vomiting, in and out of hospitals, different test, different meds, different diagnosis. I'm tired.

"Researchers have also linked IgA deficiency to autoimmune health problems. These are health problems that cause your body’s immune system to attack your body by mistake."   Immunoglobulin A Deficiency

As  I understand it, according to the tests, you may have an autoimmune disease (low IgA),  but the testing does not prove Celiac Disease.

So many on the forum have gone through similar periods.  Some 10 years or more.

As nothing they do helps, take your health into your own hands.  Wheat has an omega 6:3 ratio of 22:1.  HIGHLY INFLAMMATORY.  Many get relief from just stopping wheat, barley and rye, whether it is Celiac Disease, Chrohns, Non Celiac Gluten Sensitivety.

Whatever is causing it, by now you are also suffering from malnutrition of multiple vitamins and minerals.  Not because you don't "eat heathy", but because you don't absorb what you eat.  Give yourself a defacto diagnosis of at least Non Celiac Gluten Sensitivity, as Trents suggested as a possibility, and go gluten free.  Preferably no procesed foods for a while.  There is no pill or treatment except for avoiding foods that hurt and to take extra vitamins.  You can get better.

Ubiquitous with all Autoimmune Disease is Vitamin D deficiency.  Do you have test results for vitamin D?

Thiamine Deficiency is common in those with digestive issues.  Possibly causing Gastrointestinal Beriberi.  But beriberi is the symptom, not the cause.  There is a test, whole blood or erythrocyte transketolase activity,  but a trial of high dose Thiamine (vitamin B1) or Benfothiamine will reverse some of those symptoms in days.  Faster than you can get a doctor to schedule the test.

Is your goal to get unsick, or to prove to doctors that you are sick?

Quote

We suggest that a suspicion for gastrointestinal beriberi should arise if gastrointestinal symptoms (anorexia, nausea, vomiting and abdominal pain) are refractory to the usual therapies.   Gastrointestinal beriberi

The third common cause of GI distress, mostly disregarded by doctors is Choline.  Following "healthy eating" by avoiding eggs, meat, and milk causes gall bladder type issues. Poor digestion of fats. Gut Pain, stinky poop brain fog are common symptoms.  Even Non Alcoholic Fatty Liver.     Choline is essential for healthy liver function, and research links choline deficiency to fatty liver disease.

So, if you want a suggestion, these helped me:

  1. Gluten Free Diet
  2. 10,000 IU a day of vitamin D.
  3. 250 mg of Thiamine or Benfothiamine or more a day. There is no upper limit.
  4. 500 mg of Choline or 1800 mg of Phostidyl Choline or more.  Safe Upper Limit is 3500 mg of Choline.

These are not some medications, they are essential nutrients you should be getting in your daily diet from foods you eat.  

As the doctors found no damage to your small intestine, improvement will come quickly, and you can start to investigate other deficiencies, like Iodine, B2, B3, B5, B12, zinc, potassium, magnesium for starters.

  

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

      Weird Symptoms

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

      Weird Symptoms

    3. - Scott Adams replied to More2Learn's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Celiac Maybe a Possibility?

    4. - More2Learn posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Celiac Maybe a Possibility?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,103
    • Most Online (within 30 mins)
      7,748

    DDysard
    Newest Member
    DDysard
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jeff Platt
      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
    • cristiana
      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
    • Scott Adams
      Welcome to the forum, and thank you for sharing your story! It sounds like you’ve been through an incredible journey with your health, and it’s no wonder you’re starting to piece things together and wonder about celiac disease. Your experiences—from childhood through adulthood—paint a picture of symptoms that are often associated with celiac disease, though they can overlap with other conditions as well. The recurring sinus infections, being underweight as a child, chronic gastrointestinal issues, nutrient-related symptoms like cramps, and the persistent fatigue and brain fog are all things that many people with undiagnosed celiac report. Your reactions to gluten also stand out. The improvement in symptoms when you reduce or remove gluten, followed by the resurgence of pain and other problems when you reintroduce it, is a common experience for those with celiac or gluten intolerance. While your frustrations and trials with elimination diets might not have given you concrete answers yet, they’ve provided valuable clues. It’s also worth noting that celiac disease doesn’t always present in the classic way. Many people, like yourself, may not experience severe gastrointestinal distress but instead have “atypical” or extraintestinal symptoms like joint pain, menstrual irregularities, fatigue, and more. It’s a condition that can go undiagnosed for years, especially when symptoms are subtle, sporadic, or mistakenly attributed to other issues. The fact that you’ve sought alternative approaches to feel better shows just how determined you’ve been to find relief, even without a definitive diagnosis. Given your history and how your body responds to gluten, it would be worth exploring celiac disease further with a medical professional. Before removing gluten completely, it’s important to get tested while you’re still eating it, as going gluten-free beforehand can affect the accuracy of the results. A blood test for celiac antibodies (like tTG-IgA) is usually the first step, and if positive, an endoscopy may follow to confirm the diagnosis. If the testing process feels daunting, keep in mind that getting answers could give you clarity and help guide your health decisions going forward. Whatever the outcome, you’ve already made significant strides in identifying triggers and managing your symptoms. Your awareness and persistence are key, and this community is here to support you as you continue to seek answers. This article might be helpful. It breaks down each type of blood 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.    
    • More2Learn
      Hi, I am new!  (Although I've used this forum as a reference over the past couple of years.) I'm just looking for some initial reactions to if I actually might possibly have Celiac Disease, or if I'm reaching here.  I have had lifelong health issues and not once has a doctor suggested I look into celiac. I always thought it was basically an extreme allergy that needed an EpiPen, and I know that's not me.  However, I stumbled upon some symptoms, realized I was wrong, and after some research I'm almost shocked at what I have found.  It seems like anything I've ever struggled with has a potential correlation to this disease!  I'm in my 40's, now.  Here is my journey to date... Issues as a Kid: tons of allergies, and had sinus infections all the time... however I didn't have hayfever-like allergies and the scratch tests didn't register much, it was more that when I was exposed to allergens (like say I spent hours with a cat) I was certain to get a sinus infection and it lasted months. was extremely skinny and everyone always said I was anorexic (I wasn't) always getting sick and the illnesses hang on for a long time always cold (my favorite thing to do is sit in front of a space heater or be out in 90 degree weather) intermittent bad constipation (still happens but not as severe) horrible toe cramps that would wake me up in the middle of the night As I got older (teenage/college years): acid reflux diagnosis learned that beer made me EXTREMELY sick, cannot tolerate it horrible issues with menstrual cycle - I wasn't regular, had awful cramps and PMS, sometimes cannot function the first couple of days night terrors/sleep walking more stomach issues - I learned I couldn't have black coffee.  I often had issues especially when traveling.  For example I finally noticed a pattern that I could never, ever eat at a hotel buffet spread - it would always make me sick afterwards. More recent problems: always tired periodic pain on right side that can be so painful I can't stand up straight. Have had all kinds of scans and doctors always say I'm fine.  I was so sure I had gallstones or my liver was failing but... nope. chest pain brain fog not diagnosed but many, many ADHD symptoms lots of inflammation, am overweight now toe cramps evolved into leg/calf cramps None of my symptoms from any era of my life ever really resolved, except I went from being skinny to ~20/30 pounds overweight, and as I got older I got less outright sinus infections.  Largely due to the pain in my right side and the fact that I always, always seem to pick up every illness, especially when traveling, I started pursuing alternative medicine paths... I did the Pritikin lifestyle, I tried an elimination diet, I followed the Root Cause Protocol, I did a Leptin reset.  A lot of these paths recommend removing gluten, and in the past year or so some of my symptoms have gone away!  Specifically less issues with toe cramps, sometimes the side pain would go away for a long time, and my acid reflux got much better.  But, because I was never diagnosed with any specific intolerance, I wasn't militant about the gluten - I had cut out dairy, soy, all kinds of things.  So I would say cross-contamination is ok, or make an exception at a group outing. Then one day, I just got frustrated and ate some normal slices of pizza... and my side pain came back!  I started doing research and now I'm here and wondering... could I have actually had this my whole life??!? Thoughts and observations welcome.           
    • Wheatwacked
      "grass-fed" meat by definition cannot contain wheat as it means the animal is only fed grass  organic meat can be fed wheat feed
×
×
  • Create New...