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):
    GliadinX



    Celiac.com Sponsor (A1-M):
    GliadinX


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Gi Doc Said Dont Need To Eat Gluten For Blood Test?


tbradley93

Recommended Posts

tbradley93 Apprentice

I read on this forum that you need to eat wheat (gluten) to get an accurate result for blood panel. My GI doc said that as long as it hasnt been 3 years w no gluten the test would still pick up the antibodies he is looking for.

I guess it really doesn't matter b/c he said either way the results go he will still do the endoscopy and test my intestines (I think I said that right).

Has anyone got a pos blood panel after not eating gluten for a little over a month? I have had an accident on halloween where I took a bite of a candy bar that had gluten in it.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):
Little Northern Bakehouse
Little Northern Bakehouse



Celiac.com Sponsor (A8-M):
GliadinX


dolly Apprentice

I am not a doctor so I don't know for certain, but that doesn't sound correct to me. Hopefully, more knowledgable others on this board will respond. Good Luck!!

Ursa Major Collaborator

Unfortunately, this doctor doesn't have a clue what he is talking about. Three years? By then your intestines will be perfectly healed, and you'd be told you definitely don't have celiac disease, even if you do.

After being gluten-free for a month you will likely get a false negative on your blood tests, possibly even on your endoscopy, unless the damage was very severe to begin with.

Yes, you absolutely have to eat A LOT of gluten to test positive. After being gluten-free for a month, probably four slices of bread for about three to six months might result in an accurate test result.

Your only chance of getting accurate results at this point would be to get tested with Enterolab.

Emily Elizabeth Enthusiast

The endoscopy is the "gold standard" for diagnosis right now (so I'm told) so as long as he does that you should know for sure. I have read that you have to be ingesting gluten for at least 2 months (I think it was) to get accurate, no fail blood test results. I know my doctor told me that 1 year after diagnosis he will order another blood test for me and as long as I am successful with following the diet then the test should be completely normal. So I don't think the 3 years amount is correct. Like Dolly though, I'm not a doctor. I can only share what I have learned over the last six months. Good luck!

I read on this forum that you need to eat wheat (gluten) to get an accurate result for blood panel. My GI doc said that as long as it hasnt been 3 years w no gluten the test would still pick up the antibodies he is looking for.

I guess it really doesn't matter b/c he said either way the results go he will still do the endoscopy and test my intestines (I think I said that right).

Has anyone got a pos blood panel after not eating gluten for a little over a month? I have had an accident on halloween where I took a bite of a candy bar that had gluten in it.

Ursa Major Collaborator
The endoscopy is the "gold standard" for diagnosis right now (so I'm told) so as long as he does that you should know for sure. I have read that you have to be ingesting gluten for at least 2 months (I think it was) to get accurate, no fail blood test results. I know my doctor told me that 1 year after diagnosis he will order another blood test for me and as long as I am successful with following the diet then the test should be completely normal. So I don't think the 3 years amount is correct. Like Dolly though, I'm not a doctor. I can only share what I have learned over the last six months. Good luck!

Well, you don't seem to understand that the blood tests after a year are supposed to tell the doctor if you've followed the diet. If you have been cheating and haven't healed as a result, your blood tests could come back elevated. If, on the other hand, you've been strictly gluten-free, your numbers should be in the normal range.

The three years are garbage. Most people heal perfectly within six months to a year. Only older people with a lot of damage over many years might never heal properly, because of permanent damage. And then of course those unfortunate people who have refractory sprue, who will never heal.

And you can never get 'no fail' blood test results, as they aren't all that reliable. Neither are the biopsies, as the damage is so easily missed.

nora-n Rookie

I think they actually call it refractory celiac disease if there is still damage after three years off gluten...

Sometimes people post on the forums with something like that, but it is rare.

nora

tbradley93 Apprentice

the doc did say that I need to eat wheat the night before the endoscopy procedure. He said that the damage is done right after I eat the wheat product.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):
Tierra Farm
Holidaily Brewing Co.



Celiac.com Sponsor (A8-M):
GliadinX


Ridgewalker Contributor
the doc did say that I need to eat wheat the night before the endoscopy procedure. He said that the damage is done right after I eat the wheat product.

:o Well, now THAT is definitely wacky. . :( So he's saying you don't need to eat gluten for a blood test, but you do for an endoscopy- but just right before the procedure? This is nonsense.

First of all, it takes consistent ingestion of gluten to raise antibody levels and cause intestinal damage.

Secondly, what would that prove? That gluten still causes damage? ie- That you still have Celiac? Of course you do, you have it forever.

:( I am generally hesitant about badmouthing doctors, but this one truly sounds like he doesn't know what he's talking about.

The only point of having further endoscopies would be to see how well you're healing- which, with your level of damage, I don't blame you for wanting to do, for your peace of mind!

Edit-- Actually, I have no idea what level of damage you have, or if this is your 1st endoscopy- got you mixed up with someone else there for a sec ;) Sorry. Doesn't really affect anything else I said above.

nora-n Rookie

Some researchers take biopsies and then expose the biopsies to gluten or lgiadin and then measure the antibodies with immunfluorescence.

Only then would the test be accurate, if you happen to be a subject in one of these studies......

They do not do that in us ordinary patients (yet)

The researchers are also in the middel of studies for a new test, where you must have been gluten-free for at least a week and then they measure freshly activated T cells in resposne to gluten:

Open Original Shared Link

nora

Joss Rookie

Your GI man must have gone to school with my idiot doctor because he told me that if I am truly gluten intolerant, there are always detectable traces of gluten anitbodies. I tokld him he was an idiot, nicely of course.

ravenwoodglass Mentor
The endoscopy is the "gold standard" for diagnosis right now (so I'm told) so as long as he does that you should know for sure.

The endo may be the gold standard for diagnosis but it is not as accurate as you think. The endo and blood tests can tell you that you definately have full blown celiac but they can not rule it out if they are negative. Also many GI do not recognize the many forms of damage that are seen before you get to the point where you are almost dead. I have actually heard a GI tell a family member that they were not celiac...yet. The guy said if they wanted they could keep eating the gluten until the biopsies showed positive. Celaic has to be one of the few disease in the world where doctors want us to be almost ready to die before they will confirm we have it.

The best diagnostic tool, IMHO, is your bodies reaction to being gluten free and then perhaps a SHORT gluten challenge (until you react) after your problems have resolved a bit. Enterolab is also another valid route to diagnosis, and you don't have to be poisoning yourself to do the tests.

Tequila Newbie

I was symptomatic for a week before i got the blood tests. My mother has celiac so I knew what to look for, didn't even see the dr. Just called her and told her to order the tests. They were all positive. I'll never know if they would have been positive the week before, but I had sudden onset of digestive symptoms. So hard to know how long they had been building up. Anyway, I went gluten-free right away. It was pretty easy since I knew what to do. Not that its that easy getting used to eating rice bread :D . Three months later all blood tests negative, and biopsy was negative also after three months. Hope that helps. I have also heard varying ideas on how long you must ingest gluten. I've heard that the damage can appear immediately. Not sure about that, but sure feels like it does. For sure the blood tests would take longer, it takes a while for the immune response to build up. How long that is I'm not sure, I have not read a study on that. I would have offered to be a guinea pig but the GI docs don't seem to be interested in learning anything new.

Archived

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


  • Celiac.com Sponsor (A19):
    Food for Life



  • Member Statistics

    • Total Members
      130,885
    • Most Online (within 30 mins)
      7,748

    fabian.bornhorst
    Newest Member
    fabian.bornhorst
    Joined

  • Celiac.com Sponsor (A20):
    Holidaily Brewing Co.


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):
    GliadinX




  • Celiac.com Sponsor (A21):
    Food for Life



  • Upcoming Events

  • Posts

    • trents
      It can be almost anything for the individual but I would suggest getting in the habit of reading labels to see if there are patterns. The form of magnesium is very important. Go for magnesium glycinate. A lot of over the counter stuff puts the emphasis on shelf-life as opposed to bio-availability. Magnesium glycinate is very bioavailable, very absorbable and isn't likely to have a laxative effect like some of the high shelf-life stuff which isn't absorbed well and draws water into the colon. Oats and dairy also cause effects a lot like being glutened for many celiacs. 
    • annamarie6655
      Hi everyone,  I don’t mean to use you all as my personal dumping ground, but the support I’ve seen on this forum is unlike anything I’ve ever experienced.    So, my mother and I have always had a rocky relationship, but when I got diagnosed w celiacs, I thought we were now on the same team together. She started off saying things like “ We’re gonna figure this out together” or “I will always make sure you never have to worry about food with me” to telling my siblings that I’m not grateful enough and I don’t have a right to be upset when I get glutened bc I do so “purposefully”…   .. so I’m brand new to celiac and just learned I can’t just trust gluten-free labels unless it’s certified. I’ve been trying my best, and thanking everyone for being accommodating and trying to make things as painless as possible, so I just don’t understand. Should I be bending over backwards for people who accommodate me? Or just general gratefulness?    This whole diagnosis has further ostracized me from my family and friends, and it’s really hard not to feel completely alone. I seriously appreciate any advice you have to share!
    • annamarie6655
      @trents i am only taking collagen powder and Vitamin D, but I can definitely look into Magnesium, thank you!    @Scott Adams  thank you so much for your input! I will watch closer to how I’m reacting to xanthan/guar gum from now on. Are there any other common ingredients to be on the look out for?
    • annamarie6655
      @trents thank you so much for your response!  When i was diagnosed, I was exhibiting mainly joint pain, hair loss, bloating, and allodynia (painful feeling from non painful stimuli). The muscle spasms only started after diagnosis, and it seems to only happen when I am severely glutened. It’s only happened twice, but it definitely makes me nervous when it happens.    In regard to the pizza, thats what i saw after i got sick from it. I’m still trying to figure out how to switch to ALL certified gluten-free goods.    for the dressing, here is the ingredient list:  WATER, VEGETABLE OIL, VINEGAR, SUGAR, GARLIC, SALT, RED BELL PEPPER, ONION, CONCENTRATED LEMON JUICE, XANTHAN GUM, POTASSIUM SORBATE, HERBS, CALCIUM DISODIUM EDTA, MONOACETIN, SPICES. and the link: https://www.kraftheinz.com/en-CA/kraft/products/00068100903577-zesty-italian-salad-dressing  
    • Scott Adams
      This older article makes me wonder about the GFCO and its protocols:  
×
×
  • Create New...