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

Help Understanding Blood Panel Results


Sulbin

Recommended Posts

Sulbin Newbie

Thank you in advance for any help understanding my son's celiac disease blood panel.  He is 2 years, 3 months and has stomach issues since birth.  I have not been formally diagnosed myself, but went gluten free to become pregnant (after 3 years of unexplained infertility), and have stomach issues and what I suspect is DH when if I eat gluten.

 

I've googled, read, re-read how to read the results, but I just can't seem to figure it out.  We will be scheduling him to see a GI (as suggested by the asthma/allergist specialiast per these results).  While we wait, I'm hoping somebody can break these results down for me:

 

Serological evidence for celiac disease is present.  Consider IgA deficiency.

 

Tissue Transglutaminase AB, AGA <1 U/ML

<4 No antibody detected.... > or = 4 Antibody detected

 

Immunoglobulin A 21 mg/dl

24-121 is the range given with that result

 

Gliadin (deamidated) AB (IGA) 1 U

reference ranges for Gliadin (Deamidated peptide) Antibody (IGA) < 20 U Antibody not detected >=20 antibody detected

 

Immunoglobulin E 29 kU/L

<or = 93 was written after that

 

Tissue Transglutaminase AB, IGG 7 U/ml

Range given <3 No antibody detected, > or = 6 Antibody detected


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Welcome to the board. :)

 

About 5% of celiacs are deficient in immunoglobulin A (IgA) which is the part of the immune system that deals with the mucosal linings such as in the nose, mouth, and intestinal tract. It's not something that will have a large impact on someone's health, except maybe an immune "under-reaction" when an infection is in those areas.

 

What an IgA deficiency means to a celiac is that the celiac tests that are based on the the IgA part of the immune system (tTG IgA, DGP, IgA, and EMA IgA) will not be accurate (possibly give a false negative) because there won't be enough autoantibodies to register on the tests. Those who are low in IgA will need to rely on the IgG based tests or the endoscopic biopsy.

 

It looks like your son's tTG IgG test was positive. That's a pretty specific test to celiac disease. Chances are he'll need to be gluten-free once all testing (biopsy if warranted) is done.  :( If you want more blood tests for him, you could always request the EMA IgG and the DGP IgG tests.

 

This report has more info on the tests starting on page 10:

Open Original Shared Link

Sulbin Newbie

Thank you for your welcome, and thank you for your response as well!

 

I'm going to throw out a clarifying statement.  Please let me know if I understand or not:  His results show he has an IGA deficit.  Because of this, his testing may not be acurate.  However, his Tissue Transglutaminase AB, IGG shows antibodies, so that trumps the other tests, and means highly probable chance of celiac disease?

 

I just want to be informed before going to the GI.  My own curisoity, but also because I want to make an informed choice when we are there.  I want the least invasive testing for the most relable results.  (Don't we all, but especially for a 2 year old.)

 

And... don't give a frown face for having to go gluten free.  We were already 95% gluten-free anyway.  I make a mean pancake and lemon loaf  ;) .  I'm hoping that totally gluten free will heal him up enought to have cheese someday.  A momma can dream!

nvsmom Community Regular

 

I'm going to throw out a clarifying statement.  Please let me know if I understand or not:  His results show he has an IGA deficit.  Because of this, his testing may not be acurate.  However, his Tissue Transglutaminase AB, IGG shows antibodies, so that trumps the other tests, and means highly probable chance of celiac disease?

 

That is completely correct. There are a few parts to the immune system that the immunoglobulins measure (IgA, IgE, IgG, IgM), and celiac disease is testable is two parts: IgA and IgG. Many people are positive in the IgG version of the tests even when they don't have an IgA deficiency.

 

Below is the full panel of celiac tests that can be run; as you can see almost half are IgG based - it's a very valid and accurate way to test.

 

tTG IgA and tTG iGG

DGP IgA and DGP IgG

EMA IgA

total serum IgA (the control test to look for IgA deficiency)

AGA IgA and AGA IgG (older and less reliable test)

 

And about the cheese, it took me a year but I got cheese back.  :D

Sulbin Newbie

And about the cheese, it took me a year but I got cheese back.   :D

 So there is hope!

 

Thank you for your responses.  Very helpful.

frieze Community Regular

if he has been that close to gluten free for any length of time, it could be a false neg. on the IgA testing, since he is very narrowly under.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Tazfromoz replied to Ginger38's topic in Related Issues & Disorders
      14

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - hjayne19 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Celiac Screening

    3. - yellowstone posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Cold/flu or gluten poisoning?

    4. - Churro replied to Churro's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      17

      Celiac disease symptoms

    5. - Wheatwacked replied to Churro's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      17

      Celiac disease symptoms

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,073
    • Most Online (within 30 mins)
      7,748

    amaryliss
    Newest Member
    amaryliss
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Tazfromoz
      My understanding, and ex I erience is that we coeliacs are likely to suffer more extreme reactions from viruses. Eg we are more likely to be hospitalised with influenza. So, sadly, your shingles may be worse because you are coeliac. So sorry you had to go through this. My mother endured shingles multiple times. She was undiagnosed with coeliac disease until she was 65. Me at 45. I've had the new long lasting vaccine. It knocked me around badly, but worth it to avoid shingles.
    • hjayne19
      Hi all,  Looking for some advice. I started having some symptoms this past summer like night sweats and waking at 4 am and felt quite achy in my joints. I was training heavily for cycling for a few weeks prior to the onset of these symptoms starting. I have had low Ferratin for about 4 years (started at 6) and usually sits around 24 give or take. I was doing some research and questioned either or not I might have celiac disease (since I didn’t have any gastric symptoms really). My family doctor ran blood screening for celiac. And my results came back: Tissue Transglutaminase Ab IgA HI 66.6 U/mL Immunoglobulin IgA 1.73 g/ My doctor then diagnosed me with celiac and I have now been gluten free for 3 months. In this time I no longer get night sweats my joint pain is gone and I’m still having trouble sleeping but could very much be from anxiety. I was since referred to an endoscopy clinic to get a colonoscopy and they said I should be getting a biopsy done to confirm celiac. In this case I have to return to eating gluten for 4-6 weeks before the procedure. Just wanted some advice on this. I seem to be getting different answers from my family physician and from the GI doctor for a diagnosis.    Thanks,  
    • yellowstone
      Cold/flu or gluten poisoning? Hello. I've had another similar episode. I find it very difficult to differentiate between the symptoms of a cold or flu and those caused by gluten poisoning. In fact, I don't know if my current worsening is due to having eaten something that disagreed with me or if the cold I have has caused my body, which is hypersensitive, to produce symptoms similar to those of gluten poisoning.        
    • Churro
      I'm no longer dealing with constipation. I got my liver test last month and it was in normal range. Two years ago I did have a vitamin D deficiency but I'm know taking vitamin D3 pills. Last month I got my vitamin D checked and it was in normal range. I don't believe I've had my choline checked. However, I do drink almond milk eat Greek yogurt on a daily basis. 
    • Wheatwacked
      Non-Celiac Gluten Sensitivity (NCGS) can be associated with low ferritin and iron deficiency. Once Celiac Disease (1% of the population affected) has been ruled out by tests the next step is to check for Non Celiac Gluten Sensitivity (10% of the population affected) by eliminating gluten for a trial period, then re-introduce Gluten Challange. Have you been supplementing Iron? How are your liver enzymes? Low levels of ferritin indicate iron deficiency, while  59% transferrin saturation indicates high iron levels.  Possibly indicating Fatty Liver Disease.  Choline is crucial for liver health, and deficiency is a known trigger for Non-Alcoholic Fatty Liver.  Some experts say that less than 10% eat the the Food and Nutrition Board established Adequate Intake that are based on the prevention of liver damage. Severe constipation and hemorrhoids may be linked to a bile or choline deficiency.  "Ninety-five percent of phospholipids (PLs) in bile is secreted as phosphatidylcholine or lecithin."  Fatty acid composition of phospholipids in bile in man   Deficiency of these bile salts causes the bile to get thick. Some people with Celiac Disease are misdiagnosed with Gall Bladder bile issues.  Removal of the gallbladder provides only temporary relief. Whether or not celiac disease or NCGS are your issues you need to look at your vitamin D blood level.   
×
×
  • 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.