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

What can these test results tell me?


CatchyUserName

Recommended Posts

CatchyUserName Rookie

Hi,

I'm newly diagnosed.

Had endoscopy & colonoscopy first, then one week later GI's office called and told me to go have bloodwork done. About one week after the bloodwork GI's nurse called saying I have Celiacs and to go ahead and start a gluten-free diet. Didn't speak to the doctor, I follow up with him  July 27th.

Test Results:

EMA Titer 1:20

Gliadin Deamidated AB - IgA 17 (<20 antibody NOT detected); IgG 68 H (>20 antibody detected)

Tissue Transglutaminase AB - IgG 1 (<6 antibody NOT detected); IgA 28 H (>4 antibody detected)

Total IgA 153 (Range 81-463) 

I've done some reading and *think* I understand these results, except for one thing... Does it tell me anything that my TIgG and Gliadin IgA are lower (not detecting antibodies)? I would have assumed both test IgAs would be low or both IgGs but not flip flopped. 

I didn't follow a gluten-free diet prior to bloodwork, however, I do follow a predominately whole food based diet, could that account for any of these numbers? I guess my real question is: can these numbers tell me anything other than, "you have Celiac Disease" ?

My understanding is that these numbers cannot tell you anything about the severity, gluten sensitivity or level of damage... is that correct? I would like to extrapolate the most I can from this test. Is there anything else I might be able to surmise before I see my GI in a few weeks?

Thanks so much, I've already learned a lot from poking around on these forums!


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



Celiac.com Sponsor (A8-M):



plumbago Experienced

I am still learning myself, but one thing I don't understand is why your tTG IgA is high but the tTG IgG is low. Also, I don't hear of many cases where the 'scopes precede the bloodwork ! Doctors should be telling you about abnormal labwork and most especially new diagnoses, not nurses.

Plumbago

ravenwoodglass Mentor

We don't have to be positive on all blood tests for a diagnosis. That is why they run a panel rather than just one test. It sounds like your doctor may have suspected celiac and saw damage during the endoscopy that prompted him to do biopsies that were positive. He then ordered the blood work to confirm. Kind of backwards but at least you know you have ruled out other posible problems.  You should go to the Coping section of the board and check out the Newbie 101 thread at the top. It will have a lot of good info for you. Ask any questions you need to ask and I hope you heal quickly.

emma6 Enthusiast

i dont think its that unusual, mine was similar, my TTG IgA was >250 and my TTG IgG was 2 with the negative range being <15  everyone tests differently :)

tessa25 Rising Star

To me, not a doctor, you failed 3 out of 5 celiac tests. You only have to fail one test to have a gastro want to do an endoscopy to confirm celiac.

EMA positive

DGP IGG 68 is very high

TTG IGA 28 high

Everybody tests different, that's why there are so many tests, to catch everyone. They don't indicate severity. The endoscopy results will tell you how much damage. Just ask them to send you a copy of all records for your files.

As said above, check out the Newbie 101 thread. There is a gluten free equivalent or recipe for most foods out there, so you just have to switch brands and be careful eating out.

TexasJen Collaborator

Actually, I was diagnosed the same way: endoscopy first then labs. I was anemic so they did a scope looking for the source. Since I do not have GI Symptoms(which is true for 1/2 of celiacs)  and I have no family history, no one was suspecting it. Once the gastroenterologist got the results of the small bowel biopsy showing villous atrophy, he suspected celiac and ordered the labs to confirm. There are other malnutrition syndromes that can cause villous atrophy. It is common for the nurse to call with preliminary results or brief discussion and then to make a followup appointment with the doc to go over the results in more detail. 

I agree with getting a copy of the pathology report. If the pathologist did their job, it will reveal the villous atrophy and the extent of the damage (either staging it with Marsh staging system or categorizing - mild, moderate, severe).  That is the way to tell how bad it is - not through the blood work.

I think it's good in this case to do your research before the appointment and then make a list of questions that you have so that you make sure to get everything answered. Also, look at your insurance and see if you can get a list of dietitians in the area that are covered by your insurance. Then compare that list with the ones that the GI recommends. Since diet is the primary treatment and the diet is hard to follow, it is good to get solid advice from the beginning to start your healing.

Good luck!

 

Gemini Experienced
On 7/4/2017 at 8:56 AM, tessa25 said:

To me, not a doctor, you failed 3 out of 5 celiac tests. You only have to fail one test to have a gastro want to do an endoscopy to confirm celiac.

EMA positive

DGP IGG 68 is very high

TTG IGA 28 high

Everybody tests different, that's why there are so many tests, to catch everyone. They don't indicate severity. The endoscopy results will tell you how much damage. Just ask them to send you a copy of all records for your files.

As said above, check out the Newbie 101 thread. There is a gluten free equivalent or recipe for most foods out there, so you just have to switch brands and be careful eating out.

With a positive on both the EMA and the tTg/IgA, that is a slam dunk for Celiac without the biopsy.  On the EMA testing, no other disease but Celiac will cause a positive.  They test the IgG antibodies in case you are IgA deficient, which you are not.  If you are IgA deficient, the IgA testing will never pop positive, even with full blown Celiac, so this is why they add the IgG antibody testing into the panel.


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



Celiac.com Sponsor (A8-M):



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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    4. - Scott Adams replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

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

    • Total Members
      132,912
    • Most Online (within 30 mins)
      7,748

    journaljenny
    Newest Member
    journaljenny
    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

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.