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

Anyone Tried The Otc Test Kit For Celiac Disease


linen53

Recommended Posts

linen53 Rookie

I was reading in the Gluten Free Living Magazine about celiac disease tests and was surprised that Canada offers an over-the-counter celiac disease test. It tests for IgA antibodies in the tested blood (yes, you will have to prick your finger). The article also stated the FDA has not approved an over-the-counter celiac test in the United States.

So I went online and found the company, based in Canada that offers the test kit. You can find it at: Open Original Shared Link under Shop by Brands sub-tab (right side of the page on the blue bar).

The kit cost $61.74 in US dollars including shipping(about $75 with free shipping in Canadian dollars).

 

Anyone have any information about this?


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



Celiac.com Sponsor (A8-M):



MycasMommy Enthusiast

I was reading in the Gluten Free Living Magazine about celiac disease tests and was surprised that Canada offers an over-the-counter celiac disease test. It tests for IgA antibodies in the tested blood (yes, you will have to prick your finger). The article also stated the FDA has not approved an over-the-counter celiac test in the United States.

So I went online and found the company, based in Canada that offers the test kit. You can find it at: Open Original Shared Link under Shop by Brands sub-tab (right side of the page on the blue bar).

The kit cost $61.74 in US dollars including shipping(about $75 with free shipping in Canadian dollars).

 

Anyone have any information about this?

 

"If a patient uses the home self-testing kit for celiac disease and has a positive test result, the following steps are recommended:

  1. A serologic laboratory test, immunoglobulin A (IgA) tissue transglutaminase antibody or IgA endomysial antibody, is required. Total serum IgA should also be measured.
  2. If the serologic test result is positive, the patient should be referred for an endoscopic small intestinal biopsy to confirm the diagnosis as soon as possible.
  3. It is strongly recommended that the patient continue to consume a normal (gluten-containing) diet and not start a gluten-free or gluten-reduced diet before the biopsy is performed. A trial of a gluten-free diet before biopsy has the potential to promote intestinal mucosal healing, leading to difficulty in pathologic interpretation of the biopsy and additional delay in confirming the diagnosis.
  4. Once celiac disease is confirmed using a biopsy, the patient should see a registered dietitian with expertise on gluten-free diets. The patient should be encouraged to join a support group like the Canadian Celiac Association (Open Original Shared Link)."

 

 

From the US National Library of Medicine : Open Original Shared Link

nvsmom Community Regular

I did the home Biocard test a few years ago.  I suspected celiac disease but hated going to doctors so I was just sticking my head in the sand and ignoring the situation.  A friend discovered the Biocard tests were on sale at a local (Alberta, Canada) health / whole food store so she pushed me to buy one.  

 

I increased my gluten intake for about two weeks and then did the skin prick.  I was not able to get a big drop of blood so I did not fill the tiny test vial with blood.  Nevertheless, I did get a very faint positive line after about 10 minutes, but I had no second line at the recommended wait time.  I remember putting the tester down with a "huh", and then reading for a few more minutes.  I rechecked it and then when quickly to a lamp to make sure I was actually seeing a double line.  LOL

 

The testers look a lot like a pregnancy home test.  There is a box where two lines can appear.  The first is for total serum IgA.  It is a control test to ensure you have enough IgA for an accurate test.  The second line indicates high levels of tTG igA (tissue transglutaminase) which means your body is attacking its intestines.  That second line was a very weak positive.  Interesting enough, when I tested the tTG IgA through my doctor's office to confirm (after a month of increased gluten intake) my tTG IgA was very high at >200 when 0-20 was the normal range - not weakly positive at all.

 

I did meet another woman in my city who tried the home test.  Her result was also weakly positive but when she went to the doctor her retest was negative so they decided it must not be celiac disease.  About a month later she discovered that she had lyme disease which was probably causing her symptoms.  A weak positive tTG IgA can be caused by (5% of the time) liver disease, diabetes, thyroiditis, crohn's, colitis, or a serious infection; I've always wondered if her weak positive was caused by Lyme.

 

Anyway, I found it to be a helpful option and fairly accurate.  Just remember that the tTG IgA can miss as many as 25% of all celiacs so it is best to have multiple tests run (DGP IgA, DGP IgG, EMA IgA, tTG IgG) to make sure a negative result is accurate.

 

Best wishes.

linen53 Rookie

nvsmom, I'm wondering why you increased your gluten for a couple of weeks before taking the test.  The test is for genes not antibodies.  I'm confused.

nvsmom Community Regular

The test I took was not for genes - we might be talking about different tests. You link didn't work for me so I just assumed it was for the Biocard test which I know is available in Canada (since I used it).  The Biocard test I did was for anti-tissue transglutaminse (tTG IgA) which is positive when the body attacks the small intestine.  It also showed if levels of immunoglobulin A (IgA) was norma; this is the part of the immune system active in the mucosal linings like in the mouth and intestines.

 

I increased my gluten intake because I did not each much bread prior to that, but in hindsight, I was actually eating enough gluten without the increase.  I also increased it because the test instructions said to do so.  

 

You are correct, there is no need to increase your gluten intake for genetic testing.

 

I'm sorry.  I guess I should have clarified which test it was before I answered!  LOL  This is the test I did: Open Original Shared Link

 

I've never had genetic testing done, but since I've had positive blood tests I would never bother with them.  To be honest, I'm not a fan of genetic tests.  Less than 1% of the world has celiac disease but 30% of all people have the genes that celiacs have (DQ 2 or DQ8).  A positive result will just tell you if you are in the higher risk group or not, it can't tell you if you have celiac disease.  It even appears that a very small minority of celiacs may not even have those genes, but that is not a widely accepted belief in the medical community.

linen53 Rookie

According to what you said your test was a cheek swab.  The test I am talking about is a blood test.  Thank you so much for answering me.  I have more information now.

nvsmom Community Regular

According to what you said your test was a cheek swab.  The test I am talking about is a blood test.  Thank you so much for answering me.  I have more information now.

 

No, mine was a blood test. I pricked my hand and the blood went into a tiny tiny vial - almost like a diabetics blood glucose test.


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



Celiac.com Sponsor (A8-M):



linen53 Rookie

Okay, thanks for the clarification.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to Heatherisle's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      34

      Blood results

    2. - Known1 replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      6

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

    3. - Wheatwacked replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      31

      results from 13 day gluten challenge - does this mean I can't have celiac?

    4. - Wheatwacked replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      31

      results from 13 day gluten challenge - does this mean I can't have celiac?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,414
    • Most Online (within 30 mins)
      7,748

    EBeloved
    Newest Member
    EBeloved
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Wheatwacked
    • Wheatwacked
      Celiac Disease causes more vitamin D deficiency than the general population because of limited UV sunlight in the winter and the little available from food is not absorbed well in the damaged small intestine.  Taking 10,000 IU a day (250 mcg) a day broke my depression. Taking it for eleven years.  Doctor recently said to not stop.  My 25(OH)D is around 200 nmol/L (80 ng/ml) but it took about six years to get there.  Increasing vitamin D also increases absorption of Calcium. A good start is 100-gram (3.5-ounce) serving of salmon,  vitamin D from 7.5 to 25 mcg (300 to 1,000 IU) but it is going to take additional vitamin D supplement to be effective.  More importantly salmon has an omega-6 to omega-3 ratio 1:10 anti-inflammatory compared to the 15:1 infammatory ratio of the typical Western diet. Vitamin D and Depression: Where is all the Sunshine?
    • Known1
      Thank you for sharing your thoughts.  I respectfully disagree.  You cherry picked a small section from the page.  I will do the same below: The agency is seeking information on adverse reactions due to “ingredients of interest” (i.e., non-wheat gluten containing grains (GCGs) which are rye and barley, and oats due to cross-contact with GCGs) and on labeling issues or concerns with identifying these “ingredients of interest” on packaged food products in the U.S. “People with celiac disease or gluten sensitives have had to tiptoe around food, and are often forced to guess about their food options,” said FDA Commissioner Marty Makary, M.D., M.P.H. “We encourage all stakeholders to share their experiences and data to help us develop policies that will better protect Americans and support healthy food choices.” --- end quote Anyone with celiac disease is clearly a stakeholder.  The FDA is encouraging us to share our experiences along with any data to help develop future "policies that will better protect Americans and support healthy food choices".  I see this as our chance to speak up or forever hold our peace.  Like those that do not participate in elections, they are not allowed to complain.  The way I see it, if we do not participate in this request for public comment/feedback, then we should also not complain when we get ill from something labeled gluten-free. Have a blessed day ahead, Known1
    • Wheatwacked
      Here is a link to the spreadsheet I kept to track my nutrition intakes.  Maybe it will give you ideas. It is not https so browsers may flag a security warning. There is nothing to send or receive. http://doodlesnotes.net/index3.html I tracked everything I ate, used the National Nutrition Database https://www.foodrisk.org/resources/display/41 to add up my daily intake and supplemented appropriately.  It tracks about 30 nutrients at once.
    • Wheatwacked
      Hello @catnapt, That's so true.  Every person with Celiac Disease has different symptoms.  There are over 200 that it mimics.  Too many still believe that it is only a childhood disease you outgrow.  Or it's psychosomatic or simply a fad.  Idiots.  It's easy to get angry at all of them.   You just have to pick at the answers until you find the ones that work for you.  I too suffer from not being able to take the drugs that work for "everyone else".  SSRIs make me twitch ane feel like toothpicks are holding my eye open, ARBs cripple me.  Statins cause me intestinal Psuedo Obstruction.  Espresso puts me to sleep.  I counted 19 different symptoms that improved from GFD and dealing with my nutritional defecits.  I couldn't breath through my mouth until I started GFD at 64 years old.   My son was born with celiac disease, biopsy diagnosed at weaning.   So why are we the one-percenters.  Why, after being silent for so long, does it suddenly flare? There is the possibility that you have both Celiac Disease and Non Celiac Gluten Sensitivity.  NCGS was not established as a diagnosis until 1980.  NCGS is diagnost by first elimating Celiac Disease as the cause, and showing improvement on GFD.  Nothing says you can't have symptoms from both.  Wheatbelly: Total Nutrition by Dr. Davis was helpful to me. We come to the forum to share what we've learned in dealing with our own symptoms.  Maybe this will help someone. Speaking of which if you don't mind; what is your 25(OH)D vitamin D blood level?  You mentioned a mysterious Calcium issue. Vitamin D, Calcium and Iodine are closely interactive. It is not uncommon for postmenopausal women to have insufficient intake of Iodine.   (RDA): Average daily level of intake sufficient to meet the nutrient requirements of nearly all (97%–98%) healthy individuals; often used to plan nutritionally adequate diets for individuals You are a one-percenter.  You may need higher intake of some essential nutrient supplements to speed up repairing the damages.
×
×
  • 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.