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

Questions Regarding Blood Tests And Celiac Diet


Hardeep

Recommended Posts

Hardeep Newbie

Hi everyone. I am 27 years old and suffering from a number of celiac-like symptoms, the worst of which is joint pain (scattered all over the body). I have a lot of intestinal problems as well, bloating, diarrhea, constipation etc. Anyways, I have had all the relevant blood tests done and everything came out negative (save a red blood cell count that was very slightly below the normal range). Specifically, my IgA and IgG levels were normal. I was wondering what percentage of celiac sufferers have a normal levels for these two tests? Also, if one had the disease and the joint pain, how long does the pain typically take to go away after the switch to the gluten free diet?

I have tried the celiac diet for the last 5 weeks, and not much seems to have changed (definitely nothing regarding the joint pain). One of the main reasons I thought I might have the disease was because my mother has been conclusively diagnosed with it.

Thanks.


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



Celiac.com Sponsor (A8-M):



Mother of Jibril Enthusiast

Actually, it's not that uncommon to test "negative" on a celiac panel, even if you have a problem with gluten. The reference numbers are set pretty high to correlate with visible damage to your villi. You could easily have damage that just isn't visible yet! Some people even have a negative blood test and a positive endoscopy.

Also, gluten can damage a lot more than your intestines. Have you considered seeing a doctor... like a rheumatologist... about the joint pain?

If you're strict about a gluten-free diet, your immune system should stop making antibodies in 3-6 months. However, some types of damage are not reversible. You just have to wait and see. Check out the signature of "ravenwoodglass" for some inspiration :)

Hardeep Newbie

Thanks for the response. The reason I asked the question was that my GI doctor told me that the blood test catches 95% of celiacs. I found that number to be pretty high.

I am scheduled to see a rheumatologist, but it will be a while before the appointment. I am now trying to go off all foods that give me issues, and may try reintroducing gluten once I done with that and see how that goes.

I had another question: Does anyone find that the lactose free milk still gives them problems? I had to switch to soy milk.

julirama723 Contributor

My tests came back negative, but I'm IgA deficient, and I'm still awaiting test results to find out just how deficient I am. I don't know exact numbers, but 95% seems a little steep. I know there are a LOT of false negatives with the serological testing. (Even if I don't ever get an official celiac diagnosis, I am sticking with gluten-free eating, as I finally feel like my old self!)

I discovered that I can't handle basically ANY dairy after going gluten-free. My body doesn't like lactose OR casein! Soy milk has casein, so if you're still having problems, it might be due to casein or the soy itself. (Soy is a problematic food for many.)

ravenwoodglass Mentor

The actual number for false negatives according to the NIH is about 30%. It can take a while for the antibody reaction and the inflammation to leave the joints. It took about 3 months for me to really notice the difference in my arthritis and by 6 months it was in remission. The only time I have any flares now is with severe glutening. I have been able to add back in a bit of dairy with no issues but soy is a big problem for me and will cause the same joint pain that gluten does but different GI symptoms and of course no DH. You may for the time being want to go with a gluten free rice, almond, hemp or other alternative milk, Don't get Rice Dream though that is not really gluten free. After your pain eases then go ahead and add back in soy to see if it is a problem also.

Mother of Jibril Enthusiast
Soy milk has casein, so if you're still having problems, it might be due to casein or the soy itself. (Soy is a problematic food for many.)

I've never seen a brand of soy milk that has casein... I have to be careful about it because my (breastfed) son is very sensitive to casein. He's fine with soy.

Have you noticed a particular brand that does have casein?

lizard00 Enthusiast

Have you been tested for any food allergies?

I have a friend who is allergic to egg whites. (I am too, which is how we got on the topic)

Her symptom was joint pain. Sounds random, but allergic reactions create inflammation... inflammation does bad things.

It may be worth looking into.


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



Celiac.com Sponsor (A8-M):



julirama723 Contributor

MoJ--I can't remember the brand off-hand. I haven't purchased it in a while! Let me do some research and I'll get back with you. :)

BarbaQ Rookie

Hello

You may want to consult a dietition about what foods to avoid if you have joint pain. I have read that the nightshade plants (tomatoes, potatoes, ect) cause an increase in problems related to arthritis. Also, omega 6 oils tend to increase inflammation.

Is you doctor planning to do a biopsy? Did they also do the transglutaminase or only anti-gliadin?

Barb

sbj Rookie

Have you considered illnesses other than celiac disease? I was just reaidng another thread about ulcerative colitis - you have some of the symptoms:

The clinical presentation of ulcerative colitis depends on the extent of the disease process. Patients usually present with
diarrhea
mixed with blood and mucus, of gradual onset. They also may have signs of weight loss,
abdominal pain
and blood on rectal examination. Ulcerative colitis is a systemic disease that affects many parts of the body. Sometimes the extra-intestinal manifestations of the disease are the initial signs, such as
painful, arthritic knees
in a teenager. It is, however, unlikely that the disease will be correctly diagnosed until the onset of the intestinal manifestations.

Have you ever had a colonsoscopy? You may want to plug some of your symptoms into the WebMD symptom checker and see if any of their suggestions make sense.

ang1e0251 Contributor

For the milk question, I also cannot tolerate Lactaid but my daughter can. ??

Hardeep Newbie

Thanks for the suggestions everyone! I have finally gotten frustrated enough to keep a diary of what I eat and how I feel afterwards. I found that even after eating non-dairy, non-gluten (as far as I can tell) foods, I could feel nauseous, bloated etc.

I have never been tested for allergies, though I may have to find out, especially about the nightshade allergy. The joint pain I get seems to occur typically in those joints I use the most (makes sense I suppose); first the knees (3.5 years ago) which I attributed to playing too much squash, then a shoulder which I attributed to too much swimming. Then my finger joints...which I blamed on using the computer too much (though I don't use it that much, as I don't really need one too much in day to day life) and finally my elbows, which I thought may be due to Yoga. None of those ever heals given time. I have no swelling, no noticeable inflammation, just pain every so often when the joints are used.

BarbaQ: The doctor ran this test and got the result:

Immunoglobulin A 2.01 [0.70-4.00] g/L

Immunoglobulin G 10.3 [6.7-15.2] g/L

sbj: I just looked into the symptoms for ulcerative colitis. They seem much harsher than anything that I have ever displayed (even the joint pain is bearable without medication, though it prevents me from doing almost all physical activities). My doctor has scheduled a gastroscopy, but not a colonoscopy in a few months (he is giving me time to see if eliminating more foods helps).

ang1e0251 Contributor

My joint pain went away with the gluten-free diet but I do have muscle pain now if I don't take my B12 or other vitamins.

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. - rei.b replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      High DGP-A with normal IGA

    2. - knitty kitty replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      High DGP-A with normal IGA

    3. - rei.b replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      High DGP-A with normal IGA

    4. - knitty kitty replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      High DGP-A with normal IGA

    5. - rei.b replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      High DGP-A with normal IGA


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
    • knitty kitty
      Food and environmental allergies involve IgE antibodies.  IgE antibodies provoke histamine release from mast cells.   Celiac disease is not always visible to the naked eye during endoscopy.  Much of the damage is microscopic and patchy or out of reach of the scope.  Did they take any biopsies of your small intestine for a pathologist to examine?  Were you given a Marsh score? Why do you say you "don't have intestinal damage to correlate with lifelong undiagnosed celiac disease"?   Just curious.  
    • rei.b
      I was tested for food allergies and environmental allergies about 7 months before I started taking Naltrexone, so I don't think that is the cause for me, but that's interesting!  The main thing with the celiac thing that is throwing me off is these symptoms are lifelong, but I don't have intestinal damage to correlate with lifelong undiagnosed celiac disease.
×
×
  • 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.