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Blood Test Results Help


kbial

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kbial Newbie

I had a endoscopy done due to random stomach pains every so often and my doctor said everything looks fine but said the biopsy is showing some minor problems with the lining in my small intestine. He asked that I get a celiac blood test done and I got the results back today and am very overwhelmed/ confused.

both the IgA immunoglobulin and Deamidated Gliadin are within normal range but my Transglutaminase antibodies are very high.

IgA Immunoglobulin: 2.55 g/L. Normal Range: 0.69-3.82

Deamidated Gliadin IgG Antibodies: 6.5 u/ml. Negative: <15 u/ml, Positive >=15 u/ml

Transglutaminase IgA Antibodies: 80 u/ml. Negative: <15 u/ml, Positive >=15 u/ml

 

Has anyone had similar results? My follow up with my doctor is in 2 weeks and these results have been making me incredibly anxious. Is this for sure celiac or could it be something else? Any insight would be appreciated.


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trents Grand Master
(edited)

"The finding of tissue transglutaminase (tTG)-IgA antibodies is specific for celiac disease and possibly for dermatitis herpetiformis. For individuals with moderately to strongly positive results, a diagnosis of celiac disease is likely and the patient should undergo biopsy to confirm the diagnosis.https://www.mayocliniclabs.com/test-catalog/Overview/82587

Biopsy results can be affected by the skill and thoroughness of the one doing the biopsy in that some practitioners don't take the samples from the right areas. They can also be affected by the length of time you have been eating gluten sense the Celiac Disease was triggered and became active. And if someone was already eating gluten free beforehand there may have been a degree of healing.

Edited by trents
DJFL77I Experienced

80 is most probably celiac..

mine was 100+...

now its down to 13 after going gluten free for like 4.5 months an getting checked again for the first time...

my Dr said how high the number is at diagnosis doesn't really matter..  only that it begins dropping once starting gluten free 

kbial Newbie
5 hours ago, DJFL77I said:

80 is most probably celiac..

mine was 100+...

now its down to 13 after going gluten free for like 4.5 months an getting checked again for the first time...

my Dr said how high the number is at diagnosis doesn't really matter..  only that it begins dropping once starting gluten free 

Thanks for the response. Was your DGP IGg also negative?

DJFL77I Experienced

Dunno.. never had that tested . It's not in my latest panel results either

Kate333 Rising Star

Hi kbial.  Only your GI doc can give you a definitive diagnosis. 

My test results were similar to yours.  At its highest (last fall, at the time of my first blood test and endoscopy) my TTG level was 224.  My DGP level has always been in "normal" range.   My scope was negative for celiac sprue.

But don't panic because the good news is that your TTG blood level should rapidly plunge back down to "normal range" once you adopt and stick to a STRICT gluten-free diet and, hopefully, you will feel much better as you heal.  It took me about 6 months for my TTG test result numbers to decline from over 200+ to .50 (nearly zero), from March '20 to Sept. '20.   I say "strict gluten-free" because IMO continuing to eat packaged foods, even those labeled "gluten-free" or "certified gluten-free" still carries an unreasonably high risk of gluten exposure, esp. for newly-diagnosed patients in early stages of healing.     And you cannot "cheat" on the gluten-free diet (even "only a little bit") and expect to heal or your blood level to return to normal.  

After my first blood test, I just assumed I could safely continue eating packaged foods, as long as I checked (and believed) food manuf. labels/claims.  But then I noticed my TTG numbers didn't completely return to normal until AFTER I began buying, cooking, and eating 100% strictly fresh, unpackaged foods and avoiding eat out altogether (even carryout). 

I wanted to hasten my healing/recovery and I was tired of reading/stressing about labels, worrying about the possibility of cross-contamination, or suspect food manuf. claims etc.   I also don't like the taste or contents of gluten-free-labeled foods, which also tend to be very expensive and full of sugar, artificial color, flavors etc.  But to each his/her own.

 

 

 

DJFL77I Experienced
9 hours ago, Kate333 said:

 My scope was negative for celiac sprue.

 

 

 

celiac sprue is just another name for celiac disease.....

and there's no way you can't have damage to your gut.. with a 224 ttg......   if they didn't see it.. they simply missed it with the biopsies

 


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  • 2 months later...
MADMOM Community Regular

i agree - i’ve been  gluten free 6 weeks almost and have been learning from trial and error - in my 2-3 week i had some seeded veggies - night shades that just did not agree with me / i also eat very min dairy and more lactose free yogurts and milk since i don’t really get a reaction - i also started cooking more fresh veggies and meats and so far thank god have been improving - weeks 4-now are so much better - ofc i still have sore tummy from time to times but no GI issues as i didn’t really have much to start with - my GI says it takes time and you will have good and bad days- so far i’m learning what not to have and that’s less packaged foods more fresh - i also got great feedback from a lot of ppl on this site which i appreciate so much - puts my mind at ease when i’m stressing out 

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    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
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      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
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