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

Gene Test


MyMississippi

Recommended Posts

MyMississippi Enthusiast

I'm thinking I might go for the gene testing since I am allergic to wheat and can't do the eating gluten thing. I really would like to know if I have the genes.

I certainly have a suspicious family history for celiac----I've had abd. cramps, bloating, and "gurgling" intestines since I was 18. My son has had recurrent mouth ulcers since childhood- (celiac symptom). My sister is anemic with gut problems too. My father (of Irish decent )had same problems as well as most of his siblings did. His own father (my grandfather ) had issues too and referred to it as the "Carr Belly " :D So apparently these bellyaches go way back ! :)

Is the test expensive--- I have insurance--- but not sure if I will ask my MD for the test or just do it myself.

Thanks !


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



Celiac.com Sponsor (A8-M):



brendygirl Community Regular

I've been thinking about doing this, too. My parents are both Norwegian, so wondering if I have two of the genes or just one.

There are articles about genetic testing and labs on the homepage on this site. Very informative.Good luck!

lizard00 Enthusiast

My doctor uses Prometheus. I believe that there are only 3 labs int the US that are capable of doing this test:

Enterolab (which is still controversial), Prometheus and Kimball. (If I'm wrong on that, I apologize and please correct me)

The next question is how much will my insurance pay??? :huh::lol:

happygirl Collaborator

Many other labs do it as well - including

Quest Open Original Shared Link

Labcorp Open Original Shared Link

And most labs that your doctors office uses. Go to your doctor and ask to him to test you for HLA DQ2 and DQ8. :)

Otherwise, use Kimball Genetics - they are recommended by the Celiac Center at the University of Chicago. Open Original Shared Link

MyMississippi Enthusiast

Thanks for the info !

Will look into it--- :)

blueeyedmanda Community Regular

I had my testing done through AML labs which has since converted to Quest Diagnostics. It is the lab our hospital uses, my insurance covered the entire panel.

*lee-lee* Enthusiast

i used Prometheus. my GI doc ordered the tests and i went to a local hospital to have the blood drawn. Supposedly the doctors office and the hospital have some kind of agreement where they don't give Prometheus any patient info and all the billing is through the doctor and the hospital. i was confused as far as what that meant for me and what i'd have to pay but i bit the bullet and went ahead with the testing. i just got the initial EOB from my insurance company and sure enough, $788 was billed from the hospital. no mention of Prometheus. insurance hasn't paid yet so i don't know what is my portion. i'm hoping it's not more than a $10 or $25 co-pay.


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



Celiac.com Sponsor (A8-M):



givenupgluten Explorer

I go to Dr. Green in NY, and he orders the tests through Kimball Genetics. I didnt end up having to pay anything at all, b/c I went through my insurance and they covered it. When you receive the tests, you can get codes for the test, so that you can contact your insurance co. and find out if they will cover it. I called before I sent in the test just to make sure. I'm not sure about the other genetic testing labs, but i've heard Enterolab is also pretty well known and respected.

nora-n Rookie

https://www.celiac.com/articles/21628/1/Cel...tics/Page1.html is an article that had been in a newsletter but now it has been published on the website.

Some labs only test for DQ2 and 8, and some only for the beta chain, and those with the half gene are missed, and those with the gluten sensitive genes will just get an answer that they are negative for celiac gennes without further expnanation. Some labs have changed their testing and reporting now (those that calculate your risk now. The old way of reporting or not reporting results was ovten very confusing)

I am thinking about ordering a gene test from enterolab as I am in europe and only got the test for DQ2 and 8, and now my doctors think they excluded celiac and it is all in my head, and have referred me to the shrinks. The article comments on negative resutls, that they still cannot be used to exclude celiac like my doctors think. ( they say it si absolutely impossible for me to be celiac. My daughter is diagnosed celiac, and I have DH but without diagnosis so I disagree)

nora

jbuckeye Newbie

I thought I'd share my experience on gene testing again since this topic pops up from time to time. I know Kimball Labs is very respected, but they misdiagnosed me the first time they did my testing. I was a biopsy and blood test proven Celiac, and they told me that I was non DQ2 and 8. When I told them that I'd already been diagnosed, they reran the test and found DQ8. They said that it was "acting like another gene" that I had and they needed to do a more sophisticated test.

I tested my kids and myself through Enterolab, and the test results showed that Enterolab uses the American Red Cross for the gene testing. If you can't trust the American Red Cross, who can you trust? :)

nora-n Rookie

jbuckeye, I have been wondering for several months now what the enterolab test said about you (assuming you did some gene tests through them)

and what genes Kimball thought you had initially.

I remember thye sent the sample on to a bigger lab and they found DQ8.

I guess Kimball used a rapid test, a commercial test kit, I found it when googling.

I guess the bigger lab actually carried out a proper test.

There is an article where it is mentioned which lab Enterolab uses, https://www.celiac.com/articles/21628/1/Cel...tics/Page1.html , Bonfils does testing for Enterolab

and see the next article Ten facts

https://www.celiac.com/authors/45/Dr.-Scot-Lewey

I was negative on a test that seems identical to kimball's test, so the question is a bit relevant to me.

Daughter is a diagnosed celiac.

Here is your initial posting. Open Original Shared Link Blogspot seems to be down these days so thefoodoc's link does not work right now.

nora

glutenfreewithease Rookie
jbuckeye, I have been wondering for several months now what the enterolab test said about you (assuming you did some gene tests through them)

and what genes Kimball thought you had initially.

I remember thye sent the sample on to a bigger lab and they found DQ8.

I guess Kimball used a rapid test, a commercial test kit, I found it when googling.

I guess the bigger lab actually carried out a proper test.

There is an article where it is mentioned which lab Enterolab uses, https://www.celiac.com/articles/21628/1/Cel...tics/Page1.html , Bonfils does testing for Enterolab

and see the next article Ten facts

https://www.celiac.com/authors/45/Dr.-Scot-Lewey

I was negative on a test that seems identical to kimball's test, so the question is a bit relevant to me.

Daughter is a diagnosed celiac.

Here is your initial posting. Open Original Shared Link Blogspot seems to be down these days so thefoodoc's link does not work right now.

nora

Just a note, I was tested in August through Enterolab and both of my girls are being tested this month and Enterolab is currently using the American Red Cross. It is also listed on the bottom of my lab results. American Red Cross is not associated with Bonfils is it?

jbuckeye Newbie

Hi--Kimball originally sent a letter saying I was DQ2 and 8 negative--nothing else. When they reran the test, a new letter came saying I was DQ8 positive.

Enterolab said I was DQ8 and DQ7.

My daughter is also DQ8 and DQ7.

I'm thinking that maybe DQ8 and 7 look similar/have similar actions, but genetics is WAY over my head.

jbuckeye, I have been wondering for several months now what the enterolab test said about you (assuming you did some gene tests through them)

and what genes Kimball thought you had initially.

I remember thye sent the sample on to a bigger lab and they found DQ8.

I guess Kimball used a rapid test, a commercial test kit, I found it when googling.

I guess the bigger lab actually carried out a proper test.

There is an article where it is mentioned which lab Enterolab uses, https://www.celiac.com/articles/21628/1/Cel...tics/Page1.html , Bonfils does testing for Enterolab

and see the next article Ten facts

https://www.celiac.com/authors/45/Dr.-Scot-Lewey

I was negative on a test that seems identical to kimball's test, so the question is a bit relevant to me.

Daughter is a diagnosed celiac.

Here is your initial posting. Open Original Shared Link Blogspot seems to be down these days so thefoodoc's link does not work right now.

nora

nora-n Rookie

Thank you, I was wondering wether I should order a gene test from enterolab. Shipping is very expensive from europe.

As far as I know, DQ7 and DQ8 are not similar, but I can look at the Wiki for DR. Looks like there are several DQ8 types, so maybe this rapid test kit is not so good for all of the DQ8 types, just the more common ones. Maybe. Just a theory.

nora

nora-n Rookie

The DR wiki page is Open Original Shared Link

I even have a link that says that DQ7 is very very similar to DQ8:

Open Original Shared Link

"Eight of the 122 celiac disease patients lacked both the heterodimer and the DRB104 alleles; therefore, we further screened the DQB1 locus to investigate if other alleles were present in association to celiac disease (2)(14). Two of these eight celiac disease patients showed the DQ2 molecule (DQB10201 allele in heterozygosis); but one of them carried also the DQB10501 allele, also found in Sardinian patients to be associated to celiac disease (15); four showed the DQ7 molecule (DQB10304 or DQB10301 alleles). Another patient carried the DQ8 molecule encoded by the DQB10302 allele, and the remaining patient had the haplotype DQB10501 in homozygosis (15). The DQ8 molecule seems to be an alternative to DQ2 in influencing susceptibility towards celiac disease, being present in up to 20% of celiac patients not bearing of DQ2 in the Mediterranean area (2)(14)(16). Our data do not support an earlier finding that HLA-DQ7 is a nonsusceptible molecule (2). In fact, DQ7 was present in 50% of our celiac disease patients in the absence of the heterodimer and of the DRB104 alleles. Because the DQ7 molecule is very similar to the DQ8 molecule, it could alternatively present similar gluten-derived peptides to restricted T cells (17). DQ7 has been detected in a few celiac disease cases in the absence of DQ2 but in association with the DRB104 alleles (18). "

I also have a link that DQ9 is very similar to DQ8

Open Original Shared Link and they say right out that both DQ7 and DQ9 are very similar to DQ8.

"The DQ8 molecule is highly homologous to two other naturally occurring alleles, DQ7 (DQA1*0301/B1*0301) and DQ9 (DQA1*0301/B1*0303). These three alleles share an identical chain (DQA1*0301) and have nearly identical

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,207
    • Most Online (within 30 mins)
      7,748

    WAB19
    Newest Member
    WAB19
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.