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

Validity Of Blood Tests And Gene Test?


bluegreensea

Recommended Posts

bluegreensea Newbie

I was diagnosed a few years ago with Celiac. My sister who had a few of the same symptoms was diagnosed with it too. (incidentally the rest of my immediate family refuses to get a blood test done) She then got a few more tests done which came back pos, neg and inconclusive and even a low number on the blood test. Not one to accept her diagnosis, she then got a genetic test that showed she does not even carry the gene that would ever give her Celiac in her lifetime.

My question is if her blood tests came back positive, negative, inconclusive and then is being told she does not have the gene for Celiac, what are the chances I have/don't have the genes that would give me Celiac? I accepted the one blood test results I had, which said I had a "low number" of antibodies present, which my doctor interpreted as positive and to completely avoid gluten for the rest of my life. But I am now questioning my sister's results and the gene test. Aren't we supposed to have the same gene family? Can anyone shed some light on this for me? Thanks!


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



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator

You could still carry the gene even if your sister doesnt have it. Also a small number of proven Celiacs have neither of the main Celiac genes. Not having the gene doesnt necessarily mean you you have a 100% chance of never getting celiac disease. There are other genes involved and not all genes have been identified yet.

Do you get symptoms from consuming gluten? Do the symptoms go away when you follow the diet? If so, then you have your answer right there.

tarnalberry Community Regular

Just because she doesn't have those genes doesn't mean that you don't have at least one of them. You both got your genes from your parents, but you certainly don't have all the same ones. That being said - not all of the genes that contribute to celiac disease have been identified. A small percentage (1-2%, as I recall) of biopsy proven celiacs do not have either of the genes that are tested for in "the gene test". In addition to that, there may be other genes that are correlated to gluten intolerance that does not fall under the classic definition of celiac disease (with, classically, requires sufficient damage to the intestines to be called celiac disease). The fact is, if she had antibodies to gluten while she was eating gluten, her body is reacting to it, and reacting enough that the antibodies are able to escape the usually relatively closed system of the intestines into the bloodstream. (Were her second/third tests after she had stopped eating, or greatly reduced the amount of, gluten?)

bluegreensea Newbie

Thanks to you both for your replies. I'm going to look further into it for her.

  • 2 weeks later...
tiredofdoctors Enthusiast

From what I have read and been told, antibodies can develop and escalate at any time, and at any rate. My initial antigliadin antibodies were high, but follow-up testing only three months later found them through the roof. I haven't been genetically tested yet (that's next) -- because I'm not celiac, only gluten ataxia. The anti-transglutaminase and antiendomysial cell antibodies were negative as well as my small intestine biopsy. I do want to know if I show or carry any of the genes (and there are quite a few), because I have kids who are 19 and 23. I want to know whether they need to be genetically tested and also tested for antibodies.

You may have had a "low" number of antibodies (I'm presuming they were antigliadin) during your first testing -- of course, your body may have just begun to produce them. The more you ingest gluten, the more antibodies to it your body will produce. I would suggest to your sister to monitor symptoms, but ultimately, I would encourage her to at minimum have her antigliadin antibodies tested. When you start talking "genetic testing", for some reason, people get freaked out! :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,163
    • Most Online (within 30 mins)
      7,748

    Estee
    Newest Member
    Estee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...