Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Testing Question


Marc49

Recommended Posts

Marc49 Explorer

Here is a brief history of what led me to sign up here.

Several months ago I started seeing a new doc that is into 'functional medicine' per se. He is actually an OB/GYN medically though. I was referred by my regular doc due to some vague issues I have been having for the past year.

New doc had me do a stool profile by a company called Metametrix that supposedly looks at almost everything.

Anyway, some section of that test has a test for gluten anti-bodies I think and it showed as 'borderline' per se. Not positive or negative,.....borderline.

After that he had me do a gene test through EnteroLab in Texas. I received the results back on 1/19 and it shows I carry one celiac gene, and one non-celiac gene that is predisposing to gluten sensitivity. I can post the results here if anyone is familiar with this testing.

I have had issues with GERD for over 5 years, and also have been diagnosed with the generic GI disease of IBS due to my ever changing stomach issues. I am a 49 YO male BTW.

I had an endoscopy right before I started nexium for Gerd,.....they were looking for Barret's I believe and that was negative. I do not believe that they checked me for anything to do with celiac disease at the time though. Nothing was said about any problems though other than the GERD.

Long story short,........my question is should I have any type of blood test done to confirm/deny whether the problem is active in me since I carry the gene, or do you go from the gene test alone?

I am in the process of learning about the foods to eat, but have not started on a 100% path as of now. I have reduced some easy targets, but I am not gluten free by any stretch.

While going gluten-free doesn't appear to be that big of a deal to me, I obviously would prefer to not have to bother unless it is needed.

I figure that if I should have further testing done, I should do it while still eating my normal diet.

Thanks for any advice!


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



Celiac.com Sponsor (A8-M):



Mari Contributor

Please do post your Enterolab results. I also used Enterolab, my two b allele markers are 0302 and 602. Drs are more familiar with the molecular serology terms so these translate to HLA-DQ8 and HLA-DQ6. DQ8 indicates a main celiac gene and DQ6 confers a predisposition to non-celiac sprue also called Leaky Gut Syndrome. Both of these conditions are gluten sensitivities.

Wikipedia has some good articles - search for HLA-DQ for an overview. The Enterolab report gives the DNA HLA assay results - the marker/gene number.

Below that are the results changed to the molecular serology terms. Look at the numbers in parenthesis, mine were (8, 6). You can then search WiKipenia for HLA- your number and HLA-the other number.

Any degree of positive is considered postive but a negative result does not rule out celiac disease. Many Drs would have you go on a gluten challange diet for up to 3 months to raise the antibody level before doing the blood tests for celiac disease. Also they would order a total immunoglobulin A level to make sure you have enough IgA to make the test valid. Some Drs would do another endoscopic exam with multiple biopsies to see if you have flattened villi or other damage to the small intestine.

Even if you show no intestinal damage by the blood tests or biopsies most experts would advise you to go gluten free. If the autoimmune reaction is not causing you symptoms there is evidence that you may develop more serious problems in the future and it may reduce your risk for some types of cancers.

Hope this is not too confusing.

Marc49 Explorer

This was my result:

Gluten Sensitivity Gene Test

HLA-DQB1 Molecular analysis, Allele 1 0302

HLA-DQB1 Molecular analysis, Allele 2 0502

Serologic equivalent: HLA-DQ 3,1 (Subtype 8,5)

Interpretation Of HLA-DQ Testing: HLA-DQB1 gene analysis reveals that you have one of the main genes that predisposes to gluten sensitivity and celiac sprue, HLA-DQB1*0201 or HLA-DQB1*0302. Each of your offspring has a 50% chance of receiving this gene from you, and at least one of your parents passed it to you. You also have a non-celiac gene predisposing to gluten sensitivity (any DQ1, DQ2 not by HLA-DQB1*0201, or DQ3 not by HLA-DQB1*0302). Having one celiac gene and one gluten sensitive gene, means that each of your parents, and all of your children (if you have them) will possess at least one copy of a gluten sensitive gene. Having two copies also means there is an even stronger predisposition to gluten sensitivity than having one gene and the resultant immunologic gluten sensitivity or celiac disease may be more severe. This test was developed and its performance characteristics determined by the American Red Cross - Northeast Division. It has not been cleared or approved by the U.S. Food and Drug Administration.

For more information about result interpretation, please see Open Original Shared Link

Stool analysis performed and/or supervised by: Frederick Ogunji, Ph.D., EnteroLab

Molecular Gene Analysis performed by: American Red Cross

Interpretation of all results by: Kenneth D. Fine, M.D., EnteroLab

I am glad you saw this as I don't really know about the subtypes,.....maybe you can chime in on my resluts when you get a chance!

Thanks.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,197
    • Most Online (within 30 mins)
      7,748

    Crazygeminimom1981
    Newest Member
    Crazygeminimom1981
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Lindquist
      Hi im from northern europe are blood type 0+ have celiac with code K900 on the paper from doctor, have low vitamin D and b12 and folate, zinc, manganese and high copper it say in test. The best food i have eaten for now is LCHF, i tried paleo but i was missing the dairy. And i love the cream in sauces. LCHF is good choice there is no grains in the dishes. It's completly gluten free lifestyle i say. Because i feel good to eat it.
    • WednesdayAddams13
      Hello,   I contacted the makers of Alpine Original Spiced Cider Drink Mix and they sent me this email.....   Subject: [EXTERNAL] Fw: Ref. ID:1335211 Alpine Original Spiced Cider Drink Mix.               On Friday, December 6, 2024, 1:04 PM, Consumer <baking@continentalmills.com> wrote: December 06, 2024   Dear Janie, Thank you for taking the time to contact us regarding our Alpine Original Spiced Cider Drink Mix. We appreciate your interest and are happy to provide you with additional information. This product does not contain gluten. However, it is not manufactured in a gluten free facility. If I can be of further help, please contact me at 1 (800) 457-7744, weekdays 7:00 a.m. to 4:00 p.m. (PT), or visit www.alpinecider.com and select "Contact Us." Sincerely, Kristin Kristin Consumer Relations Specialist Ref # 1335211   I hope this helps everyone.  I am currently looking for a spiced hot apple cider drink and have yet to find one that is not made in a plant that manufactures other gluten products.  It's so frustrating. 
    • trents
      @Rogol72, dermatitis herpetiformis occurs in a minority of celiac patients and if the OP hasn't developed it yet I doubt it will show up in the future. I think it unwise to use a scare tactic that probably won't materialize in the OP's experience. It has a good chance of backfiring and having the opposite effect.
    • Rogol72
      Hi @trents, You're correct. The OP mentioned fatigue and vitamin deficiencies as the only symptoms at the time of diagnosis. Since the family are not taking him/her seriously and find them to be too fussy, I suggested showing them pictures of dermatitis herpetiformis as one of the consequences of not taking the gluten-free diet seriously ... would make life easier for him/her, and the family might begin to take his/her strict gluten-free diet more seriously. A picture says a thousand words and the shock factor of dermatitis herpetiformis blisters might have the desired effect. The OP did say ... "How do you deal with people close to you who just refuse to understand? Are there any resources anyone could recommend for families that are short and easy to read?".  @sillyyak52, It might also help mentioning to your family that Coeliac Disease is genetic and runs in families. Any one of them could develop it in the future if they have the HLA DQ 2.5 gene. Here's a Mayo Clinic study calling for screening of family members of Coeliacs ... https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-minute-celiac-disease-screening-for-family-members/ https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/ I got glutened a few months ago because I missed the may contains statement on a tub of red pesto. It was my own fault but it happens.
    • peg
      Thank you, Scott!  This is just what I needed.  Appreciate your site very much and all of your time and energy that goes into it! Kind Regards, Peg
×
×
  • Create New...