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

Finally Got My Blood Test Results Back/need More Testing?


MoMof2Boyz

Recommended Posts

MoMof2Boyz Enthusiast

I had an endoscopy back in October and am just now got the results mailed to me....I am disappointed that I was only sent the blood test results and not the biopsy results....I have an appt. at the beginning of March so will make sure I get those copies.

Anyway, everything looks negative, but total serum IgA was marked low. hm. mine is 76 and the range is 91-414

Here is what was tested, please tell me if I need other testing as I know low IgA can make the tests false negative

Deamidated Gliadin Abs, IgA 2 units range is 0-19

Deamidated Gliadin Abs, IgG 3 units range is 0-19

**I"m not sure why they give the range as 0-19 but then it says that 0-19 is negative with 20-30 being a weak positive and >30moderate to strong positive***

T-Transglutaminase(tTG)IgA<2 U/mL range is 0-3

Tissue Transglutaminase(tTG) IgG <2U/mL range is 0-5

Endomysial Antibody IgA(this one didn't give a range and just said negative)no numbers were given for this it just says negative

Immunoglobulin A, Qn, serum(which I guess is the total serum IgA??) 76 range is 91-414

Thank you for looking! :)


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

It looks like they ran all the important tests. Yes, Immunoglobulin A Qn serum is the total IgA. Since they already ran the IgG versions of the DGP and the tTG, you do not need any further testing; this is the additional testing they would do to compensate for your low IgA. If your biopsy was also negative (do post the results when you get them) then it would appear that you are non-celiac gluten intolerant.

nvsmom Community Regular

Those are all the tests that I know too. I think your testing is done.

Because your IGA levels are so low, your ttg IgA, EMA IgA, and DGP IgA tests will not show if you are a celiac; your IgA levela are too low to be tested (about 5% of celiacs' IgA levels are low... higher than the regular population). I would completely discount those tests; if they are in the high end of the normal range (a 33 in a range of 0-34 for example) you might want to consider if that is telling you something though.

Unless you have a positive biopsy, it looks like you are NCGI as Mushroom said... same treatment plan. :) Good luck.

MoMof2Boyz Enthusiast

If the biopsy was negative, how would I know if I am non celiac gluten intolerant? Are you going by the low total serum IgA?

mushroom Proficient

If you do not test positive for celiac, and if you are intolerant to gluten, you are called non-celiac gluten intolerant. There is currently no test for this condition (although they are working on it, now they have identified it :P )

nvsmom Community Regular

The serum IgA just tells you if you have enough IgA in your body to show a positive test for celiac in the tests that refer to the IgA (like ttg IgA, EMA IgA, and DGP IgA) and you don't have enough IgA to get a positive tests in those. It is possible that you would have had a positive celiac test (in ttg IgA, EMA, and DGP IgA) but I'm afraid you'll never know because your IgA levels are deficient. These sites discuss the tests a bit and might help you;

Open Original Shared Link

Open Original Shared Link

I just assumed that you were having symptoms (GI, neuropathies, headaches, aches and pains, etc) that you had linked back to gluten and that's why you were tested for celiac. It appears you don't have celiac (although you can't be sure because of your low IgA) so i figured you are NCGI then, which occurs in between 8% and 30% of the population... it's much more common than celiac, and every bit as uncomfortable.

If you have had gluten intolerance symptoms, you should consider trying the gluten-free diet for a few months. I would give it at least four months; I'm 7 months in and still noticing minor improvements, and my arthritic like joints didn't start to improve until I was 6 months gluten-free.

Best wishes.

beachbirdie Contributor

I had an endoscopy back in October and am just now got the results mailed to me....I am disappointed that I was only sent the blood test results and not the biopsy results....I have an appt. at the beginning of March so will make sure I get those copies.

Anyway, everything looks negative, but total serum IgA was marked low. hm. mine is 76 and the range is 91-414

Here is what was tested, please tell me if I need other testing as I know low IgA can make the tests false negative

Deamidated Gliadin Abs, IgA

Deamidated Gliadin Abs, IgG

T-Transglutaminase(tTG)IgA

Tissue Transglutaminase(tTG) IgG

Endomysial Antibody IgA(this one didn't give a range and just said negative)

Immunoglobulin A, Qn, serum(which I guess is the total serum IgA??)

Thank you for looking! :)

Dumb questions. Had you been eating gluten before you got your testing? I know you posted other topics, but I haven't been around for a while and can't remember what I've read!

Were you having symptoms? (Edited to answer my own dumb question...) Ahh, yes, I went to find your older posts and see you were eating gluten!

Next dumb question...do you have the actual numbers for the other blood tests? I'll be interested to hear what the biopsy report shows, since they had told you they were only going to take two samples. Do you know how many they actually did?


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



Celiac.com Sponsor (A8-M):



MoMof2Boyz Enthusiast

ok, I looked through my papers and I do have the biopsy result. I'm not sure how I missed it, I guess I was expecting all the samples to be listed and they weren't. Turns out, 4 samples were taken. I requested the biopsy for Celiac because I have Hashimoto's(which I know is in the risk group for Celiac) and heartburn/ very severe reflux. I had to have an endoscopy done anyway because i Had a stricture in my esophagus because of the reflux.

The biopsy for celiac reads as this: Small intestine, unspecified, biopsy. Duodenal mucosa with intact villous architecture and no significant abnormality.

All of the blood test results were pretty low , I"ll go back and try and edit my first post but I know these results are negative...I do understand that it's possible my IgA tests *could* be positive, but with the deficient total serum IgA, they'lll never show up positive. I did read on Dr. Rodney Ford's site that one should get the anti gliadin test if everythingone is IgA deficient...it's the test that the deamidated gliadin test replaced(hope I got that right) should I request it?

beachbirdie Contributor

ok, I looked through my papers and I do have the biopsy result. I'm not sure how I missed it, I guess I was expecting all the samples to be listed and they weren't. Turns out, 4 samples were taken. I requested the biopsy for Celiac because I have Hashimoto's(which I know is in the risk group for Celiac) and heartburn/ very severe reflux. I had to have an endoscopy done anyway because i Had a stricture in my esophagus because of the reflux.

The biopsy for celiac reads as this: Small intestine, unspecified, biopsy. Duodenal mucosa with intact villous architecture and no significant abnormality.

All of the blood test results were pretty low , I"ll go back and try and edit my first post but I know these results are negative...I do understand that it's possible my IgA tests *could* be positive, but with the deficient total serum IgA, they'lll never show up positive. I did read on Dr. Rodney Ford's site that one should get the anti gliadin test if everythingone is IgA deficient...it's the test that the deamidated gliadin test replaced(hope I got that right) should I request it?

Well, you could ask for the gliadin antibodies IgG, and you could also beg for the anti-EMA IgG version (yes, there actually IS one!).  But, if you are willing and motivated to go with a gluten-free lifestyle, then you could stop here and be non-celiac gluten-intolerant.  NCGI is NOT a "lesser stepchild", it is a real condition.  And in order to feel well, it is important to be as gluten free as an officially diagnosed celiac.

 

Did you by chance get any of the genetics done?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,540
    • Most Online (within 30 mins)
      7,748

    Barrie S
    Newest Member
    Barrie S
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • 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.