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

Is There Such Thing As False Positive?


ElseB

Recommended Posts

ElseB Contributor

My bloodtests came back positive for celiac, and I'm currently waiting for the biopsy. Thing is, I have absolutely no symptoms. Could the blood test be wrong? A few months ago I got sick with antiobiotic colitis and c.difficile. Then, just when I was recovering, out of the blue the doctor says mmm, lets test you for celiac disease. Before the colitis and c.diff. I didn't have any celiac symptoms either. Anyone have any thoughts?


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



Celiac.com Sponsor (A8-M):



Ridgewalker Contributor

I don't believe there can be a false positive. Technically, there could certainly be a lab mistake, where your sample got mixed up with someone else's. The blood test looks for raised antibody levels- which simply wouldn't be there if you weren't Celiac.

Some Celiacs are "asymptomatic." They have no noticeable symptoms, but this does not mean that there is not damage being done to the intestine! Therefore, no Celiac would be asymptomatic forever. That damage will cause symptoms on its own eventually. (Intestinal damage = villi damage, which causes a myriad of problems: vitamin deficiencies, osteoporosis, dental problems, infertility, cancer...)

Also, it is possible to have symptoms that you are so used to, that you just don't really notice them. For example, upon going gluten-free, one might notice an increase in energy- when they didn't even realize they were feeling run-down. Or clearer, sharper thinking... or a cessation of "normal" occasional heartburn... migraine headaches that you may have attributed to something else... etc.

But even if you are completely symptom free-- if you are Celiac, then gluten is destroying your small intestine, whether you can see it or not. :(

Hope this helps.

HAK1031 Enthusiast

this article may help you: https://www.celiac.com/articles/32/1/How-ac...ests/Page1.html

also know that celiac can be brought on in predisposed individuals by stress or illness

hope this helps!

Tim-n-VA Contributor

The most likely thing is that the test is correct and you just don't have noticable symptoms.

There are some ways to get a false positive. Human error in reading slides on the tests that require examination of a slide. The American Celiac website says that other auto-immune diseases can theoretically cause a false positive but it says nothing about whether this has been demonstrated.

In my case, I had no outward symptoms but was tested as part of a large set of tests to try to explain some liver function issues. In retrospect, I could find things that were probably gluten reactions - upset stomach after a breakfast of pancakes or after drinking wheat-beer in Germany.

loco-ladi Contributor

Well, even concidering I have no "medically positive" results here is something to think about...

I am now 40 years old (not old if your a tree but I live with it) my first "celiac" symptoms started when I was in grade school and were ignored, had some more in high school, also ignored.... and until I was in my 30's did any major symptoms show up and they also were ignored by my doctor and misdiagnosed by him as well......

Yes I am angry about this not being found sooner and being found by the medical profession BUT

it took 5-10 years for the first symptom to appear and to be honest it could have been caused by almost anything

it took another 10 years for a few of the other symptoms to appear and again not unusual symptoms or even alarming

by the time I was 30 I knew something was going on.... diagnosed myself via diet between the ages of 35 and 38

so for 30+ years I didnt have very serious issues (but I was still destroying my intestines) why would it be found? I go to the doctor and say "I feel tired all the time" he checks my thyroid and its "borderline" and prescribes me a light dose of pills I feel better for a while then it eventually crawls back even with the pills.

It takes years to destroy everything and it takes years for it all to go back to normal and just because YOU dont recognise any symptoms or maybe even have them as yet, count yourself lucky its been found some of us weren't so lucky.

If you want to continue on a gluten containing diet go ahead its your choice but a few years down the road we will welcome you back with open arms(and keyboards) and help you start something you should be already on.

ElseB Contributor
Well, even concidering I have no "medically positive" results here is something to think about...

I am now 40 years old (not old if your a tree but I live with it) my first "celiac" symptoms started when I was in grade school and were ignored, had some more in high school, also ignored.... and until I was in my 30's did any major symptoms show up and they also were ignored by my doctor and misdiagnosed by him as well......

Yes I am angry about this not being found sooner and being found by the medical profession BUT

it took 5-10 years for the first symptom to appear and to be honest it could have been caused by almost anything

it took another 10 years for a few of the other symptoms to appear and again not unusual symptoms or even alarming

by the time I was 30 I knew something was going on.... diagnosed myself via diet between the ages of 35 and 38

so for 30+ years I didnt have very serious issues (but I was still destroying my intestines) why would it be found? I go to the doctor and say "I feel tired all the time" he checks my thyroid and its "borderline" and prescribes me a light dose of pills I feel better for a while then it eventually crawls back even with the pills.

It takes years to destroy everything and it takes years for it all to go back to normal and just because YOU dont recognise any symptoms or maybe even have them as yet, count yourself lucky its been found some of us weren't so lucky.

If you want to continue on a gluten containing diet go ahead its your choice but a few years down the road we will welcome you back with open arms(and keyboards) and help you start something you should be already on.

Hmmm, interesting points. For now, I've been instructed to keep eating gluten because I haven't had the biopsy yet. I suppose I could be asymptomatic because if I have celiac, I've maybe only had it for 2 months - ever since the colitis and c.difficile episode. Perhaps I had it before, but I certainly never had any of the problems with energy levels that people have described - I've a run a few marathons and I don't know how I could have done that if I was malnourished!!! For now, I'm still eating gluten until the biopsy, but doing my research so I have a game plan for when they tell me to stop eating gluten! Thanks for your comments!

tarnalberry Community Regular

There are a LOT of people who are either asymptomatic, have very light symptoms, or have symptoms that are not GI related at all. It affects different people very differently, and you certainly could have run marathons with it (though who knows when it really was triggered). When you read symptom lists, remember that those are the symptoms that get doctors to pay attention and say "oh, something's really wrong", instead of writing it off as being a "bit off normal, but not really wrong", even though it is for a particular person.

I think you're on the right track - keep eating gluten for the biopsy while educating and preparing yourself. In the meantime, have something scrumptious for us all! :):D


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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,974
    • Most Online (within 30 mins)
      7,748

    LRB
    Newest Member
    LRB
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.