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

Confused About Genetic Testing Results


DebW

Recommended Posts

DebW Newbie

We did genetic testing on my husband and son through Enterolab, and now that I have the results, I'm thrown as to the difference between celiac/gluten intolerance/gluten sensitivity. (Is there even a difference between the last two?)

I know celiac disease involves damage to the intestine, but can gluten intolerance do the same? What ARE the manifestations of gluten intolerance, and what would happen if someone who was double-gened gluten sensitive continued consuming gluten?

Here are the results:

Husband:

Gluten Sensitivity Gene Test

HLA-DQB1 Molecular analysis, Allele 1 0502

HLA-DQB1 Molecular analysis, Allele 2 06xx

Serologic equivalent: HLA-DQ 1,1 (Subtype 5,6)

Son:

Gluten Sensitivity Gene Test

HLA-DQB1 Molecular analysis, Allele 1 0301

HLA-DQB1 Molecular analysis, Allele 2 0502

Serologic equivalent: HLA-DQ 3,1 (Subtype 7,5)

Both had this message:

Interpretation Of HLA-DQ Testing: Although you do not possess the main genes predisposing to celiac sprue (HLA-DQ2 or HLA-DQ8), HLA gene analysis reveals that you have two copies of a gene that predisposes to gluten sensitivity (DQ1 or DQ3 not subtype 8). Having two copies of a 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 the gene. Two copies also means there is an even stronger predisposition to gluten sensitivity than having one gene and the resultant immunologic gluten sensitivity may be more severe.

We all eat gluten-free at home, but my husband consumes gluten at work. (The rest of us are entirely gluten-free.) My son had symptoms which improved on the gluten-free diet. My husband had no symptoms.

The more I read about this, the more confused I am. Some articles seem to indicate that gluten sensitivity to celiac disease is a progression of sorts, while others seem to draw a clear line between the two, with gluten intolerance being rather vaguely defined.

Any light you could shed on this would be most appreciated!

Thanks!

Deb


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



Celiac.com Sponsor (A8-M):



confused Community Regular

Ok from the research I have done and conclusions I have made, it looks like your hubby needs to stay away from gluten all the time. Two DQ1 genes are linked to many neurological problems. Your husband may have symptoms that he is not aware of that are not Gi related.

I am sure ohters will have more information. But i just wanted to respond with the little that I know.

Are you gluten free cause you are celiac, have u had the gene test done?

paula

gfp Enthusiast
Ok from the research I have done and conclusions I have made, it looks like your hubby needs to stay away from gluten all the time. Two DQ1 genes are linked to many neurological problems. Your husband may have symptoms that he is not aware of that are not Gi related.

I am sure ohters will have more information. But i just wanted to respond with the little that I know.

Are you gluten free cause you are celiac, have u had the gene test done?

paula

Hey... can you point any links :D .....

I never bothered with genetic testing since it seemed superfluous (having positive blood tests).... however I always feel the neuro-symptoms hit me harder than the GI ones... (I do get GI .. I just don't seem so bad as some here)...

This really is interesting, it might be worth me getting the gene test afterall ....

Nantzie Collaborator

I have DQ1 (double). The neuro problems are the worst part for me. I came across celiac as a way to stop my GI problems, but it turns out my mobility problems (I could barely walk by the time I found out about celiac), fibro-type pain, insomnia, nightmares, headaches, anxiety, depression, anger, memory problems, social anxiety, etc. were all due to gluten. Never would have suspected that.

The mood issues I always just thought were my charming personality. ;)

I think if you can do it, the gene test through enterolab is worth is just for scientific curiosity's sake.

You can also do a search on the web for your gene type and come up with all sorts of information. For example I found out that one of my genes ( HLA-DQB1*0602 ) seems to be protective against diabetes, but some people with that gene develop narcolepsy. And the other one ( HLA-DQB1*0609 ) is an Ashkenazi Jewish gene, which lets me know that my mom's breast cancer was likely genetic, and I need to be especially careful in that regard. There are also a lot of other genetic diseases in the Ashkenazi group. This was a huge surprise because nobody in my family ever heard anything about anyone being Jewish. It must have been someone who married and converted to Luteranism, because both sides of that family are from Sweden and everyone was Lutheran.

So it is kind of fun to learn about.

Nancy

gfp Enthusiast
I have DQ1 (double). The neuro problems are the worst part for me. I came across celiac as a way to stop my GI problems, but it turns out my mobility problems (I could barely walk by the time I found out about celiac), fibro-type pain, insomnia, nightmares, headaches, anxiety, depression, anger, memory problems, social anxiety, etc. were all due to gluten. Never would have suspected that.

The mood issues I always just thought were my charming personality. ;)

I think if you can do it, the gene test through enterolab is worth is just for scientific curiosity's sake.

You can also do a search on the web for your gene type and come up with all sorts of information. For example I found out that one of my genes ( HLA-DQB1*0602 ) seems to be protective against diabetes, but some people with that gene develop narcolepsy. And the other one ( HLA-DQB1*0609 ) is an Ashkenazi Jewish gene, which lets me know that my mom's breast cancer was likely genetic, and I need to be especially careful in that regard. There are also a lot of other genetic diseases in the Ashkenazi group. This was a huge surprise because nobody in my family ever heard anything about anyone being Jewish. It must have been someone who married and converted to Luteranism, because both sides of that family are from Sweden and everyone was Lutheran.

So it is kind of fun to learn about.

Nancy

I already know my great grandfather was Jewish :D but not which branch genetically.

So far as the family know anyway... Its not like people have to even convert since its done for them... especially because of the maternal requirement...so I doubt its anywhere as uncommon than we think...

I do think its fun though....

hathor Contributor

Might I suggest your husband going gluten-free for a period of time & see how he feels. There are so many symptoms for gluten intolerance; he just may not be aware of what it is doing to him because, to him, this is how he always feels. I remember getting my Enterolab result back for soy. I never noticed any reaction from soy. I went off it and a few things changed for the better.

If he is unwillling to do that, he could get the gluten intolerance testing from Enterolab and see if he is creating the antibodies and has any malabsorption. If he doesn't test as showing intolerance, then there would be no reason for him to go gluten-free. Practically everyone in the US either has celiac or intolerance genes.

DebW Newbie

Thanks so much to everyone who replied -- I have some info from other listservs and sources, too, and I'll post it here when I put together the summary. (So watch for those links, GTP. ;) ) The double DQ1 combo is actually quite interesting...

To Confused, I'm next for the genetic testing. We know I have at least one gene for gluten sensitivity since my son was double gened, and that's no shock at all. I have a whole laundry list of chronic and severe symptoms that disappeared when I stopped eating gluten. We'll eventually get everyone tested, but we figure that if I show up as double-gened as well, then we'll know all our children are, too. (Since my husband has the double, too.) My daughters both had intense symptoms which cleared in the absence of gluten as well.

To Hathor, my husband's going to go gluten-free anyway. Since he's double-gened, he doesn't want to take the risk, and frankly, since we have a gluten-free household already, and he was only eating gluten occasionally at work, this is not a major change for him -- just a little more dedication. :rolleyes: He hasn't noticed a lot of symptoms, but that's primarily because he was looking at gastro symptoms and not the neurological ones. Now that he's considering that angle, he's realized that he had started to automatically avoid all carbs on days he wanted to be particularly alert to avoid the "brain fog" and he has some peripheral neuropathy issues as well.

Nantzie, thanks so much for sharing your symptoms and experience with this type -- it helped us a lot ! Now that we're understanding that the gastro angle is only one manifestation, this is becoming much clearer.

Cheers,

Deb


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,566
    • Most Online (within 30 mins)
      7,748

    Rrenee2990
    Newest Member
    Rrenee2990
    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

    • cristiana
      That's great news, you can do this.  Let us know how things go and don't hesitate to ask if you have any more questions. Cristiana 😊
    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
    • petitojou
      Thank you so much for the information and kind message! Reading this transformed how I’ve been viewing my efforts and progress. Guess there’s still a lot to celebrate and also heal 😌  Yes, I’ve been taking it! Just recently started taking a multivitamin supplement and separated vitamin D! I also took chewable Iron polymaltose for ferritin deficiency 2 months ago but was unable to absorb any of it.  Thank you again! Hearing such gentle words from the community makes my body and heart more patient and excited for the future. 
    • ckeyser88
      I am looking for a roomie in Chicago, Denver or Nashville! 
    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
×
×
  • 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.