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

Test Results


HelenS

Recommended Posts

HelenS Newbie

I just received test results for celiac disease... two were normal (tTg AB, IgA <3 u/ml, IgA Serum 144 mg/dl, but one was not... Gliadin Ab IgA was 18 u/ml, just a tad higher that the 11-17 " equivocal" result. The problem is I'm away from home for another month and a half, my dr. doesn't do phone consults, and I'm not sure what this all means. I know this isn't a medical site, but is this result really significant? What does it mean? Should I stop eating gluten (only symptom is diarrhea).


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

If you are going to pursue more celiac testing do not go gluten free yet. You need to be on a full gluten diet for any chance of an accurate result on an endoscopy. If you are not going to do more testing then you should give the diet a good strict try for a couple of months. After all testing is done give the diet a shot no matter what the results are. False negatives with testing are common, false positives are almost unheard of.

carecare Enthusiast

I asked my son's ped GI dr this a couple weeks ago. I had my daughters celiac panel and wanted to know why her high gliadin ab IgA which was flagged as abnormal yet I was never told this. He said that there is a high rate of false positives with the gliadin ab IgA and they don't rely on that for a diagnosis. One person's high positive number could mean they are reacting to gluten and another person could have a high number and gluten isn't an issue. That's how I understood what he said. Most likely he's going to tell you your overall test is negative. However, it doesn't mean you aren't because the endoscopy is really what will let you off the hook or not. Like others always say....don't go off of gluten until you get all the testing done. So unfortunately you'll need to continue on gluten if you want the endoscopy.

My husband didn't do any testing but just went gluten free on his own. He knows without a doubt he reacts to gluten. It took him a good 5 months for the diarrhea to clear up completely but his indigestion cleared up immediately upon starting the gluten free diet. He also just felt better overall. His bouts of diarrhea weren't as frequent when he started the gluten free diet and eventually that cleared up completely as well...just took longer for him to heal I guess.

Good luck!

I just received test results for celiac disease... two were normal (tTg AB, IgA <3 u/ml, IgA Serum 144 mg/dl, but one was not... Gliadin Ab IgA was 18 u/ml, just a tad higher that the 11-17 " equivocal" result. The problem is I'm away from home for another month and a half, my dr. doesn't do phone consults, and I'm not sure what this all means. I know this isn't a medical site, but is this result really significant? What does it mean? Should I stop eating gluten (only symptom is diarrhea).

Mari Contributor

When I had the blood tests done the anti-gliadin was elevated but the other test were negative and it also showed an allergy to cow's milk. Within a few days of starting the gluten-free diet I felt so much relieved and better that I did not want to eat gluten again. I read online that some experts were saying the endoscopy biopsy wasn't always necessary and decided to have the genetic tests done. They showed I had two DQ2 markers and had a very high predisposition to develop gluten sensitivity and besides one brother had autoimmune diabetes which one of my markers showed that I had a chance of developing that, too. This was four years ago and now more of the experts are backing off the endoscopy as a necessary test.

ravenwoodglass Mentor

I asked my son's ped GI dr this a couple weeks ago. I had my daughters celiac panel and wanted to know why her high gliadin ab IgA which was flagged as abnormal yet I was never told this. He said that there is a high rate of false positives with the gliadin ab IgA and they don't rely on that for a diagnosis. One person's high positive number could mean they are reacting to gluten and another person could have a high number and gluten isn't an issue. That's how I understood what he said. Most likely he's going to tell you your overall test is negative. However, it doesn't mean you aren't because the endoscopy is really what will let you off the hook or not. Like others always say....don't go off of gluten until you get all the testing done. So unfortunately you'll need to continue on gluten if you want the endoscopy.

My husband didn't do any testing but just went gluten free on his own. He knows without a doubt he reacts to gluten. It took him a good 5 months for the diarrhea to clear up completely but his indigestion cleared up immediately upon starting the gluten free diet. He also just felt better overall. His bouts of diarrhea weren't as frequent when he started the gluten free diet and eventually that cleared up completely as well...just took longer for him to heal I guess.

Good luck!

I believe your doctor is misinformed. The biopsy is certainly not the absolute the doctor thinks. There are many instances of false negative on both the blood and biopsy. In some cases it is because the damage in patchy and a damaged area wasn't biopsied. In others there are changes present, like inflammation, scalloping, high esinophils etc that some doctors don't recognize as related to celiac. There are even times when a doctor will tell a person to continue eating gluten until the villi are totally destroyed before they will make a diagnosis. There are also folks who no matter how sick they are will show a false negative on blood tests. I was told over and over again that there was no way I was celiac because of negative blood tests. It cost me many years of pain and left me with some permanent damage. I hope you gave the diet a good strict try after all the testing was done. The body does know the answer that sometimes doctors can't tell us.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,161
    • Most Online (within 30 mins)
      7,748

    DAR girl
    Newest Member
    DAR girl
    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

    • 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/   
    • trents
      A lot to think about here. Does anyone have any recommendations for third party laboratories that will do full panel celiac screens private pay in the U.S.?
×
×
  • Create New...