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 Do You Think?


Wildgirl

Recommended Posts

Wildgirl Newbie

Because of having breast cancer, and the connecting with low vit D and recurrence, I found out that my D was low. Very high levels of prescription D were barely budging it. Celiac was one of the possibilities - Blood tests showed the deaminated gliadin iga to be >150 (normal 0-19). So I had an endoscopy at our local hospital which was negative. I had been avoiding gluten up to two weeks before the endoscopy, when I was told to start eating it. Not sure if avoiding gluten could cause such a high iga but neg iga -? (Other blood tests were normal). Soooo, my endocrinologist and GI drs (at a larger teaching hospital) both still suspect celiac. I was told to go all out with gluten for 6 weeks and they redid the blood tests - basically the same results. So now I'm going to be seeing the GI dr again next week.

What should I expect? Is it unreasonable to have another endoscopy at this better hospital? My endocrinologist thought the GI dr might just say to do a celiac diet - but I'm afraid to go on such a strict diet without more evidence that im really celiac. What would be reasonable at this point? What questions should I ask the GI dr?


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

My tTG tests were negative.  Just one of the DGP's was positive, yet I had a Marsh Stage IIIB diagnosis per the biopsies.  The intestinal tract is vast (size of a tennis court), so celiac savvy doctors take the recommended six samples throughout.  How many did they take?  My visual endoscopy revealed nothing!  

 

How long were you gluten free?  Just gluten-free just prior to the endoscopy?  Usually you need at least four weeks of eating gluten daily before the endoscopy.  Doctors usually request that you keep eating gluten between the blood tests and the biopsies.  But many folks have to wait months for the endoscopy to get scheduled, so four weeks is usually the minimum.  

 

Exactly what celiac blood tests were ordered?   Can you post them?  

nvsmom Community Regular

Welcome to the board.  :)

 

With a deaminated gliadin peptides (DGP IgA) that high, it is most likely that it was caused by celiac disease.  False positives are very rare, around 5% of the time (and those are weak positives like a 20), whereas false negatives are more common, up to 1 in 5 endoscopies of celiacs yield a false negative, especially if 4 or fewer biopsy samples were taken.

Info on the tests is in this report: Open Original Shared Link

 

My guess is that you have celiac disease but the doctors missed it during the endoscopy.  I would guess that at least half of the people around here had a mix of positive and negative tests - it's pretty common.

 

If you need more evidence before accepting a celiac disease diagnosis, by all means, do the endoscopy again.  Make sure you are eating gluten every day in the month before the test, and ensure that the doctors take 6 or more samples to increase your odds of having an accurate biopsy.  Get the other blood tests done too: tTG IgA, tTG iGG, EMA IgA, and DGP IgG.

 

Best wishes

RMJ Mentor

Another form of evidence would be to go gluten free and see if the antibody levels normalize.

Wildgirl Newbie

Here are the blood test results

Component Results

Component Standard Range Your Value

DEAMINATED GLIADIN ABS, IGA 0 - 19 units >150

Negative 0 - 19

Weak Positive 20 - 30

Moderate to Strong Positive >30

DEAMINATED GLIADIN ABS, IGG 0 - 19 units 2

Negative 0 - 19

Weak Positive 20 - 30

Moderate to Strong Positive >30

t-TRANSGLUTAMINASE IGA 0 - 3 unit/mL <2

Negative 0 - 3

Weak Positive 4 - 10

Positive >10

Tissue Transglutaminase (tTG) has been identified

as the endomysial antigen. Studies have demonstr-

ated that endomysial IgA antibodies have over 99%

specificity for gluten sensitive enteropathy.

T-TRANSGLUTAMINASE IGG 0 - 5 unit/mL <2

Negative 0 - 5

Weak Positive 6 - 9

Positive >9

ENDOMYSIAL ANTIBODY IGA Negative Negative

IMMUNOGLOBULIN A QT 91 - 414 mg/dL 143

So you really think I could be celiac? Considering how extremely strict the diet is, would you want another endoscopy to prove it?

cyclinglady Grand Master

Well, I am not a doctor, but based on what you presented....Yes, I think you could have celiac disease.  You presented the same way I did with only  DGP being positive and the tTG negative!  I understand your denial.  I was shocked when my DGP was high.  My husband has been gluten free for 14 years based on some poor advice from his GP and my allergist.  Yes, he has healed and is doing great, but wishes he had a proper diagnosis, but is not willing to do a gluten challenge.  He knows that gluten makes him sick!  So, I needed that endoscopy to verify that I really had celiac disease.  I did.  

 

Perhaps, you should push for another endoscopy making sure you get at least six biopsies.  Or if your doctor is willing to give you a diagnosis without the endoscopy, go gluten free.

 

The damage that celiac disease can cause is great.  You already have been dealing with cancer.  Untreated celiac disease at worst, can cause more cancer.  The diet sounds daunting, but it is manageable.  It's just going to take some time to learn.  The results can be amazing -- feeling good and healthy!  

Wildgirl Newbie

Wow. I wish it wasn't such a big deal to do the endoscopy.... I'm concerned that I will have a hard time being sooo strict - especially when eating out or going to a friends house or picnic - if I don't know absolutely. If I had absolute proof, then I know I'd be determined... But then maybe the blood test really is proof and I'm just not wanting to accept the reality...

I spent so much time researching everything about breast cancer - I was done and wanted to move on with life. I don't see how I can avoid more intense research if this is celiac - there's so many things to be aware of ...

Another. Question then - are there ant other issues that tend to go along with celiac? Like if you're celiac, you could also have this or need to watch for that?

Thank you so much for your help - I have a LOT to learn!


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Here's a link regarding symptoms:

 

Open Original Shared Link

 

Once you have one autoimmmune disorder, you tend to accumulate more.  This includes:  Hashimoto's Thyroiditis, Type 1 Diabetes, R. Arthritis, Lupus, etc.  So, it can be important to have a diagnosis, so that doctors can be "on the lookout" for new diseases.   There are some hidden potential problems.  I had fractures two months into my diagnosis.  I had no idea that I had osteoporosis!  

 

 Others are not so lucky to get a diagnosis for so many reasons, but strict adherence to the diet is a tell-tale sign that you have gluten intolerance.  

 

I know that this seems overwhelming and it is....in the beginning.   I'm sure you went through a period of grief with your breast cancer.  It's the same thing each time you are diagnosed with something!  

cyclinglady Grand Master

I forgot about vitamin defciencies. Those usually resolve on a gluten free diet. Haven't you been struggling with low vitamin D? I struggled with low iron, despite supplements, prior to going Guten free.

Wildgirl Newbie

Yes, D has been an issue - that's what began this whole process that is questioning celiac being the culprit.

That did make me wonder though - I have had other nutrient levels tested - like iron - and everything else is normal. Wouldn't they all be off if it were celiac?

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Inconclusive results

    2. - Wends replied to Heatherisle's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      30

      Blood results

    3. - Wends replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Inconclusive results

    4. - cristiana replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      63

      How Come Gluten Didnt Bother Me In Italy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,700
    • Most Online (within 30 mins)
      7,748

    RelievedP
    Newest Member
    RelievedP
    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

    • deanna1ynne
      The first negative biopsy in 2021 just said "no pathological change" for all the samples, and the second one in 2022 said "Duodenal mucosa with mild reactive change (focal foveolar metaplasia) and preserved villous architecture." So I think Marsh score 0 in both cases, though it's not actually written in the pathology reports. I'm really hoping to get a clear positive result this time, just for her sake.  
    • Wends
      Hopefully the biopsy gives a conclusive and correct diagnosis for your daughter. Im in the UK and have been in the situation a few years ago of trying to rule celiac in or out after inconclusive results. Many symptoms pointing to it including the classic symptoms and weight loss and folate and iron deficiency. You have to play a waiting game. I also had the label of IBS and likely food allergy. Genetic test showed low risk for celiac but not no risk. It sounds like the Gastroenterologist is on it and hopefully will diagnose what it is correctly. Food hypersensitivity (allergy) can also cause similar symptoms and inflammation as well as mimicking IBS. Milk / dairy and wheat (cereal grains) being the biggest culprits. The “oesophagitis” and “gastritis” you mentioned can be caused by another gastrointestinal disorder called “eosinophilic gastrointestinal disorders”. These are named depending on which part of the gastrointestinal tract is affected. For example eosinophilic oesophagitis, eosinophilic gastritis, eosinophilic gastroenteritis, and more rare eosinophilic colitis. They are antigen (allergen) driven. When the blood test measuring anti-ttg antibodies is positive in absence of a positive ema test - which is more specific to celiac, this can also suggest food hypersensitivity (allergy). Usually delayed type allergy similar to celiac but not autoimmune if that makes sense. In this case the ttg antibodies are transient. Which happens. I’ve first hand experience. For info, evidence of villous atrophy too can be caused by food hypersensitivity. Not just by celiac disease. In Egid disorders the six food elimination diet, under a dietitian and gastroenterologist care, is the dietary protocol to figure out the culprit or culprits. Sometimes only two food elimination diet is used at first. The number one culprit is milk protein / dairy. Followed by wheat, eggs, soy, fish and seafood, and nuts. Most are only reactive to one food group or two. Most are only reactive to milk. Hope this is a helpful reply.
    • Bennyboy1998
      Yes gene HLADQ2 was positive 
    • Wends
      Wow, the system is crazy isn’t it? Maybe switch Doctors if you can. It’s surprising from what you’ve written it seems obvious it’s celiac disease. The “potential” diagnosis means celiac is developing and it basically just hasn’t done enough gut damage to be captured on the biopsy yet, and meet that “criteria” to satisfy the current system! Given the overwhelming evidence already - family history, positive ttg and ema. And your own experience and intuition which counts far more. And the labs being reproduced after gluten elimination and reintroduction- elimination and reintroduction diet is the gold standard too. Shame on the Doc and the system. What was the Marsh score? I’m guessing not 0 if it’s potential celiac. Meaning the autoimmune process has been triggered and started. Your daughter is obviously very healthy and her immune system is putting up a good fight. It can take years for the gut damage to build to a point where there’s overt symptoms and then a conclusive diagnosis, hence why many celiacs receive diagnosis later in life. You can prevent it. See the positive and the gift in that. Hopefully the gluten challenge confirms it, but if it doesn’t maybe get a second opinion?
    • cristiana
      @Gigi2025  Thank you for your interesting post.  Some of what you say chimes with something my gastroenterologist tells me - that he has clients who travel to France and find the same as you  - they will eat normal wheat baguette there without issue, for example.  His theory was he thought it might be to do with the locally sourced wheat being different to our own in the UK? But I have to say my own experience has been quite different. I have been to France twice since my diagnosis, and have been quite ill due to what was then (pre-2019)  poor labelling and cross-contamination issues.  My TTG test following my last visit was elevated - 'proof of the pudding', as we say in the UK!  It was not just a case of eating something like, say, shellfish, that disagreed with me - gluten was clearly an issue. I've also been to Italy to visit family a couple of times since my diagnosis.  I did not want to take any chances so kept to my gluten free diet, but whilst there what I did notice is that coeliacs are very well catered for in Italy, and many brands with the same ingredients in the UK are clearly marked on the front of their packaging that they are 'senza glutine'.  In the UK, you would have to find that information in the small print - or it puts people off buying it, so I am told!  So it seems to me the Italians are very coeliac aware - in fact, all children are, I believe, screened for coeliac disease at the age of 6.  That must mean, I guess, that many Italian coeliacs are actively avoiding gluten because, presumably, if they don't, they will fall ill?        
×
×
  • 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.