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

My Wife's Test Results And Questions


CaeZaR

Recommended Posts

CaeZaR Newbie

My wife has been feeling terrible all of 2014: bloating, loose bowels, floating, light coloured stools, general aching, abdominal cramping (especially LLQ), fatigue, loss of libido, feelings of depression and anxiety. Many symptoms started mid 2013, but they have gotten worse this year.

 

She had a blood test for celiac, and here are the results:

 

tTg-Iga Ab 5

tTg-IgG Ab 3

DGP-IgA Ab 162

DGP-IgG Ab 3

 

Result Range indication for tTG and DPG

Negative < 20

Weak Positive 20-30

Moderate to Strong Positive >30

 

Test results: Positive

 

Feelings towards test results: :,(

 

My first question is: Could anything other than Celiac produce these results? How positive is the test (90%, 99%, 99.9%)?

 

She will have a GI appointment where they will do a biopsy in a month or so (date not confirmed yet). So far this week, she has been off gluten and it seems already she has noticed improvement. The GI's office wants her to keep eating gluten until the appointment (the receptionist said that it might be an allergy and not Celiac). What are your thoughts? Can she just start eating gluten again a week before the appointment if need be, or does she have to feel terrible for another month?

 

I'm sure she'll create her own account here soon, but I had a bit of time, so I thought I'd ask on her behalf. Thanks community.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi CeZaR,

 

She should keep eating gluten until the testing is completed.  She might be able to get in sooner if they have a standby list for openings.  Often people have worse symptoms from returning to eating gluten after being off it for awhile.  So stopping gluten for a couple weeks and restarting it won't be fun.  She doens't need to eat a lot fo gluten.  They often say something like 2 slices of wheat bread per day.

 

DGP is deminated gliaden protein antibodies.  It is very specific and very low chance of a false positive.  Plus she had symptoms change after stopping gluten.  That means that gluten is casuing a reaction for some reason.

 

She might feel somewhat better if she stops eating dairy now.  That won't affect her celiac testing.  But often people have problems with dairy at first.  She can also try taking pepto bismol   If she has problems with trapped gas she can try peppermint tea.

nvsmom Community Regular

That DGP IgA tests is 93-96% specific to celiac disease as seen on page 12 of this report: Open Original Shared Link  That's pretty specific, especially combined with those classic celiac disease symptoms you listed. It's not uncommon for celiacs to test positive in only a few tests, or even just one so don't worry about those others being negative. The DGP tests in particular are very good at picking up early celiac disease unlike the tTG tests.

 

She should keep eating gluten prior to the biopsy. Most doctors recommend a minimum two week gluten challenge prior to testing; some want as much as 4 weeks. If she needs to go a bit lighter on the gluten now just make sure to add more gluten (about 2 slices of bread per day) back into her diet about three weeks prior to testing. The more gluten she eats now, the better chance of damage showing up in the biopsy.

 

The comment about the allergy makes no sense at all. That receptionist has no clue!  The allergy response is IgE based and not related to the IgA and IgG immune response that is tested for in celiac disease.  It is possible to have a wheat allergy and a gluten sensitivity (like celiac disease) but the tests she had done would not show an allergy... It would be like taking a urine sample to check your blood counts - totally unrelated. ;)

 

Ditto the the dairy idea. About half of all celiacs are lactose intolerant when diagnosed (the damaged villi can't make lactase) but many celiacs regain the ability to digest milk sugars after they have healed, which usually takes at least 6 months.

 

Welcome to the board!

Archived

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

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

    • Total Members
      133,076
    • Most Online (within 30 mins)
      7,748

    Monica L
    Newest Member
    Monica L
    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

    • cristiana
      Thank you for your thoughtful contribution, @Tazfromoz. I live in the UK and the National Health Service funds free vaccines for people deemed to be at heightened risk.  I was pleasantly surprised to discover that as a coeliac in my 50s I was eligible for this vaccine, and didn't think twice when it was offered to me.  Soon after diagnosis I suffered mystery symptoms of burning nerve pain, following two separate dermatomes, and one GP said he felt that I had contracted shingles without the rash aka zoster sine herpete.  Of course, without the rash, it's a difficult diagnosis to prove, but looking back I think he was completely spot on.  It was miserable and lasted about a year, which I gather is quite typical. For UK coeliacs reading this, it is worth having a conversation with your GP if you haven't been vaccinated against shingles yet, if you are immunosuppressed or over 50. I have just googled this quickly - it is a helpful summary which I unashamedly took from AI, short for time as I am this morning!   My apologies. In the UK, coeliac patients aren't automatically eligible for the shingles jab unless they're severely immunosuppressed or over the general age for vaccination (currently 50+) but Coeliac UK recommends discussing the vaccine with a GP due to potential splenic dysfunction, which can increase risk, even if not routine for all coeliacs. Eligibility hinges on specific criteria like weakened immunity (chemo, certain meds) or age, with the non-live Shingrix vaccine offered in two doses to those deemed high-risk, often starting from age 18 for the immunocompromised.
    • 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. 
×
×
  • 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.