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

Test Result Confusion


mythreegems

Recommended Posts

mythreegems Newbie

Hi there - I am a new member. But I have googled and googled to death everything related to Gluten and celiac disease. I was thought to be gluten intolerant and was off gluten for 2 years, but was still having some issues. I then was referred to GI at the hospital I work at. I had the Celiac Panel, and EGD with biopsies, Hydrogen breath tests, and most recently they added an IgE Wheat test. First before the Celiac Panel I went back on gluten a full 2 weeks for testing purposes.

But I am confused.

I was negative on EVERYTHING but:

IgA deamiated Gliadin - after 2 weeks on Gluten I was 46.6 which is positive.

The rest of those tests were negative on the panel.

EGD was negative and all biopsies (I was eating gluten for 5 weeks before that).

This week I had the IgE Wheat test which was only 0.35 as result so pretty much negative.

SO based on all my research the IgA DGP being positive is positive for celiac disease and is most sensitive. but then why would the wheat test be basicially negative? She finally just referred me to a dietician for Celiac Diet and told me to go back to no gluten. I just dont get how that was positive and wheat negative. CONFUSED :-) They told me to get new pots and pans ect. Most places in MN that I know quit doing the EGD when the IgA DGP was positive - we are just old school.

I dont know, just have a lot going on and want to understand better.

Any help is appreciated!!!

Kelli

Mom to 8 year old GGB Triplets.


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



Celiac.com Sponsor (A8-M):



EmiPark210 Contributor

There are other people who know more about the specific blood tests so I'll let them answer to those more specifically. The IgE Wheat test is for an allergy which is different and separate for celiac's though it is possible to have both. Open Original Shared Link

But if you are wanting to have a endoscopy to confirm damage within the small intestine (the "gold standard" of celiac's diagnosis, as my PCP told me), then you need to maintain at least a low level of gluten within your diet. 

 

Welcome to the forums!

 

Also... the University of Chicago Celiac Disease Center recommends a 12 week gluten challenge for any antibody tests and 2 weeks prior to a biopsy Open Original Shared Link for if you're wondering about the biopsies 

mythreegems Newbie

Thanks, I did have an EGD with biopsy which was negative.  Which is another reason I am so confused :-)

There are other people who know more about the specific blood tests so I'll let them answer to those more specifically. The IgE Wheat test is for an allergy which is different and separate for celiac's though it is possible to have both. Open Original Shared Link

But if you are wanting to have a endoscopy to confirm damage within the small intestine (the "gold standard" of celiac's diagnosis, as my PCP told me), then you need to maintain at least a low level of gluten within your diet. 

 

Welcome to the forums!

 

Also... the University of Chicago Celiac Disease Center recommends a 12 week gluten challenge for any antibody tests and 2 weeks prior to a biopsy Open Original Shared Link for if you're wondering about the biopsies 

mushroom Proficient

An EDG with biopsy performed five weeks after beginning a gluten free diet is not to be relied upon.  Healing begins to take place immediately upon the removal of gluten, and by five weeks could be not observable as damage.  If you combine that with the element of luck involved in the GI doing the biopsy of the damaged areas (the damage often has a patchy distribution) it really means nothing, compared to the fact that your IgA DGP was so strongly positive.  All other tests being negative also does not mean anything, because the DGP is the most sensitive of all the tests and will usually be positive earlier than the others which require a greater degree of damage.

 

I would consider myself to be celiac and go gluten free immediately.

 

Welcome to the forum and please ask as many questions as you need and stay in touch. :)

 

ETA:  As the previous poster says, your IgE allergy testing is not in conflict with your celiac testing.  Celiac is an intolerance to gluten, IgE is an allergy to wheat  ~~ they are apples and bananas.

mythreegems Newbie

Thank you.  Just to mention I was off gluten for 2 years unless contamination happened.  I was eating gluten for 5 weeks every day before the EGD.  Didnt want to be confusing. :-)

An EDG with biopsy performed five weeks after beginning a gluten free diet is not to be relied upon.  Healing begins to take place immediately upon the removal of gluten, and by five weeks could be not observable as damage.  If you combine that with the element of luck involved in the GI doing the biopsy of the damaged areas (the damage often has a patchy distribution) it really means nothing, compared to the fact that your IgA DGP was so strongly positive.  All other tests being negative also does not mean anything, because the DGP is the most sensitive of all the tests and will usually be positive earlier than the others which require a greater degree of damage.

 

I would consider myself to be celiac and go gluten free immediately.

 

Welcome to the forum and please ask as many questions as you need and stay in touch. :)

 

ETA:  As the previous poster says, your IgE allergy testing is not in conflict with your celiac testing.  Celiac is an intolerance to gluten, IgE is an allergy to wheat  ~~ they are apples and bananas.

GFinDC Veteran

Right, the body makes several different types of antibodies cells.  Having a positive reaction on one test is a solid positive result.  You don't need a positive on all the tests to prove there is an immune reaction.  A reaction is a reaction.  Your body is doing something in response to eating gluten that is not normal.

 

It is not real uncommon for us to develop additional food intolerances beyond wheat, rye and barley.  Some of us react to oats the same way.  And other foods like nightshades, soy, corn, dairy etc can cause reactions too.  So if you don't eliminate other foods that your body reacts to, you will still have symptoms.

RobinL Newbie

My doctor told me that you need to be on gluten at least once a day for 6 weeks for the blood test to work. I did that, and had similarly inconclusive results... and the doctor said even on gluten for 6 weeks, it could be not enough time to see a reaction (this is just for a blood panel, not an endoscopy).

 

So in my experience, you might not have been on gluten enough for the blood tests to work. I have read some forums that suggest 3 months. And for the endoscopy, it depends how many samples they take, from how many different places etc.

 

 

 


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



Celiac.com Sponsor (A8-M):



mythreegems Newbie

So, a strong positive IgA DGP of 46.6 is considered celiac.

When she said the biopsies were all negative she said she didn't believe it, since the IgA was so +++ after only eating gluten again for two weeks. But when she kept saying the EGD and biopsy was gold standard. So when that was negative I felt bad. But everywhere I checked that DGP was super sensitive and accurate. I guess that is why so confused. Add that in to a family who doesn't believe in gluten/gluten free I was happy for diagnosis.

Hoping the dietician has some good ideas for me. So ready to get off it again. Bought new pots and pans and kitchen stuff last night. Just need to stock up on groceries.

She too said that possible for more intolerances. But for sure the lactose and fructose knew are fine. The wheat one negative at 0.35. She said she wasn't ordering anything else at this time. Just the dietician. She put me on protonix too. My stomach is so distended I can barely breathe. What a miserable set off issues this entails huh.

Oh well, keep on plugging. :-) thanks for your help.

Takala Enthusiast

Oh, so you have acid reflux, too, besides the bloating ?  :(

 

The family will come around, at least the immediate family, if you insist they respect your choices, the older generation tends to be nearly impossible, because they really tend to be set in their ways and they'd rather keep eating the same old thing and complaining about their indigestion  :wacko:  :rolleyes:.  There is a lot of popular media "pushback" against the gluten free concept right now, but almost all of it is being cleverly placed there by the various lobbying interests, who are playing tug of war with the farm ag subsidy budgets because they are concerned with the export market, and they see a slight slip in their domestic market.   The important thing is that you eat and cook in a way that keeps you healthy and functional. 

mythreegems Newbie

Mine said accurate blood test after a week for the sensitive ones.  For the negative ones I imagine just wasnt enough time or they just were really negative, but for as positive as that one is i guess that is what makes me most confused.  They say that specific one is very sensitive, and very accurate so that just makes me think too much HA.  It just was such a big reaction positive.  In only 2 weeks.  just seems odd.  They did 8 biopsies.  2 in one area, and 6 in another. 

 

 

My doctor told me that you need to be on gluten at least once a day for 6 weeks for the blood test to work. I did that, and had similarly inconclusive results... and the doctor said even on gluten for 6 weeks, it could be not enough time to see a reaction (this is just for a blood panel, not an endoscopy).

 

So in my experience, you might not have been on gluten enough for the blood tests to work. I have read some forums that suggest 3 months. And for the endoscopy, it depends how many samples they take, from how many different places etc.

mythreegems Newbie

My husband and HIS family are amazing about it.  My kids are too.  Just my parents and grandma.  We all know how crappy I been feeling - so I am not alone here.  :-)

Oh, so you have acid reflux, too, besides the bloating ?  :(

 

The family will come around, at least the immediate family, if you insist they respect your choices, the older generation tends to be nearly impossible, because they really tend to be set in their ways and they'd rather keep eating the same old thing and complaining about their indigestion  :wacko:  :rolleyes:.  There is a lot of popular media "pushback" against the gluten free concept right now, but almost all of it is being cleverly placed there by the various lobbying interests, who are playing tug of war with the farm ag subsidy budgets because they are concerned with the export market, and they see a slight slip in their domestic market.   The important thing is that you eat and cook in a way that keeps you healthy and functional. 

Cara in Boston Enthusiast

your children need to be tested too.

frieze Community Regular

yup, and those rascally parents as well, like that is very likely!

your children need to be tested too.

mythreegems Newbie

Well now I am more confused. Went to the dietician as they ordered and she saying only non celiac gluten intolerance. Grrrrr. I like where everything else I see with my positive IgA DGP of 46 says celiac disease and hospital where I go and work only says intolerance.

Frustrating

GFinDC Veteran

Hi,

 

Celiac disease testing is not perfect.  You don't automatically get perfectly accurate test results.  It's not an exact science.  Your body and mine are different, and the tests may show very different results if we both eat the same gluteny food for 2 weeks.  Some of the celiac disease centers here recommend 3 months eating gluten before doing an endoscopy.

nvsmom Community Regular

A lot of the medical community is not up to date on celiac testing. You are correct in that the DGP IgA test is very specific to celiac and very sensitive - meaning you have celiac. Other tests, like the (anti-gliadin) AGA IgA, are often mixed up with the newer (deaminated gliadian) DGP IgA tests, and were not nearly as reliable. DGP testing, and EMA testing are thought to be the most accurate tests out there.

 

Your intestine damage was probably patchy. I highly doubt the villi blunting is uniform throughout the guts of most people. When you consider that the surface area of the small intestine is roughly the size of a tennis court, it's easy to imagine how a tiny biopsy sample could miss the damage.

 

On the other hand, even if it is NCGI, that is still a serious health problem (although it doesn't cause a positive DGP) and requires the same treatment as celiac disease. I would just declare yourself a celiac and move forward with the gluten-free diet.

 

Best wishes.  :)

mythreegems Newbie

Thank you. That was the response I hoped for. :-) yes my result even says deamiated gliaden IgA :-) whohoo. Never been so happy to have a disease lol. Proof to that family of mine ha. Thanks again. I appreciate it and am sure I will have more questions to come.

nvsmom Community Regular

LOL :lol:  Woohoo isn't the usual response to a positive DGP test! LOL  I know what you mean though. it is nice to have answers after all that time... and if you have to have an illness, celiac isn't the worst - at least we, the patients, have full control over how we treat the disease.  :)

mythreegems Newbie

At this same time I also have mono for the 9th time mixed with the flu. Yeah I'm so lucky lol.

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

      how much gluten do I need to eat before blood tests?

    2. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      how much gluten do I need to eat before blood tests?

    3. - trents replied to McKinleyWY's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Accuracy of testing concerns

    4. - Theresa2407 replied to chrish42's topic in Doctors
      4

      Doctors and Celiac.com

    5. - Scott Adams replied to suek54's topic in Dermatitis Herpetiformis
      4

      Awaiting dermatitis herpetiformis confirmation following biopsy

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

    • Total Members
      133,254
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
    • Theresa2407
      Our support groups in Iowa have tried for years to educate doctors and resource sites like this one.  We have held yearly conferences with continued education classes.   We have brought in Dr. Murray, Dr. Fasano, Dr. Green and Dr. elliott.  In those many years we may have had 2 doctors attend.  We sent them information, with no response.  I talked to my personal doctor and she said their training for Celiac was to show them a skinny man in boxer shorts and a huge stomach.  Saying if you see this, it is Celiac.  If it isn't in their playbook then they don't care.  Most call it an allergy with no mention of our immune system.  There is so much false information on the internet.  Then people don't understand why they can't get well and are acquiring more immune diseases. I mention this site to everyone.  Scott has working hard for the Celiac community.
    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
×
×
  • 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.