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

Gluten Intolerant Vs. Celiac ?


blc40

Recommended Posts

blc40 Newbie

Hi

I was just wondering what is the differnce between being Gluten intolerant and having Celiac ? Are the symptoms different etc ? I have had a stomach biopsy that was negative for Celiac but i went gluten free and most of my symptoms dissapperared ?


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

Welcome to the forum. This is a great place to ask all your questions.

Did you have blood tests run for celiac disease? Which ones? If you post your results here, there are those who are very knowledgable and can explain your test results for you.

There is a lot of debate here about the difference between gluten intolerant and celiac disease. I guess it comes down to what you believe. I don't think medical science agrees on the difference. Some believe an intolerance means you will suffer some symptoms when you ingest gluten which will be uncomfortable but not long term damaging to your body. celiac disease means you have an autoimmune disease where your own body percieves gluten as an enemy and attacks your small intestine when you eat it. This can lead to gluten "leaking" into other organs in your body and all kinds of other diseases and problems.

Some believe that's true but others think that an intolerance to gluten is the beginning stages of celiac disease. If a gluten-free diet is followed at this stage, other long term damage can be stopped in its tracks, if not, the damage to your intestine progresses until you have serious health issues that you may not be able to stop with a gluten-free diet.

It's a heated debate on this forum so I'm sure many will let you know what they believe. Those with more knowledge than I, can give you links to evidence on what they believe. It's good for us to talk about it as we are all learning new information.

Mother of Jibril Enthusiast
I have had a stomach biopsy that was negative for Celiac

By definition, celiac disease is an autoimmune disorder that causes damage to the villi in your intestines. A stomach biopsy can't rule it in or out.

blc40 Newbie
Welcome to the forum. This is a great place to ask all your questions.

Did you have blood tests run for celiac disease? Which ones? If you post your results here, there are those who are very knowledgable and can explain your test results for you.

There is a lot of debate here about the difference between gluten intolerant and celiac disease. I guess it comes down to what you believe. I don't think medical science agrees on the difference. Some believe an intolerance means you will suffer some symptoms when you ingest gluten which will be uncomfortable but not long term damaging to your body. celiac disease means you have an autoimmune disease where your own body percieves gluten as an enemy and attacks your small intestine when you eat it. This can lead to gluten "leaking" into other organs in your body and all kinds of other diseases and problems.

Some believe that's true but others think that an intolerance to gluten is the beginning stages of celiac disease. If a gluten-free diet is followed at this stage, other long term damage can be stopped in its tracks, if not, the damage to your intestine progresses until you have serious health issues that you may not be able to stop with a gluten-free diet.

It's a heated debate on this forum so I'm sure many will let you know what they believe. Those with more knowledge than I, can give you links to evidence on what they believe. It's good for us to talk about it as we are all learning new information.

thanks so much

i have not had blood tests yet i had a Biopsy which came back negative , i went gluten free after my biopsy was taken and it was the best i have felt in months ! so i was again disappointed when results were negative . i have colonoscopy tomoorow and then my follow up appointment . very frustrated but i think if i felt better gluten free i might follow my bodies advice !

what blood tests should i ask to have done for further checking ?

blc40 Newbie
By definition, celiac disease is an autoimmune disorder that causes damage to the villi in your intestines. A stomach biopsy can't rule it in or out.

so why did they take one to see if i had it ?

Jestgar Rising Star
so why did they take one to see if i had it ?

A very good question. And one you should ask your doctor.

happygirl Collaborator

They may have been looking for something else in your stomach. Did they take a biopsy of your intestine? If they didn't, they can't say you do/don't have Celiac. You may want to follow up with your doctor for clarification.

Info on Celiac/gluten intolerance: Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

None of the tests given now will be positive since you've been eating gluten-free. If you are planning further testing for celiac disease, you must eating gluten some say for at least 3 months. Being gluten-free for your testing will result in negatives. Don't worry about the colonoscopy though. It doesn't test for celiac disease and it won't matter if you're gluten-free for that test.

Gfresh404 Enthusiast
so why did they take one to see if i had it ?

Usually when they take a biopsy of the stomach, they also take one of the duodenum (the opening of the small intestine) and sometimes even the esophagus. So they had to have taken one of the small intestine when they were down there.

Fiddle-Faddle Community Regular

Not necessarily, gfresh--I've had 2 endoscopies, and they looked at ONLY stomach and esophagus. In my case, they were looking for Barrett's esophagus, and were not suspecting celiac at all.

gfb1 Rookie
By definition, celiac disease is an autoimmune disorder that causes damage to the villi in your intestines. A stomach biopsy can't rule it in or out.

this is a VERY interesting thread.

so...

has the work on mhc locus completely supplanted the concept of celiac as an inborn error of metabolism??

the nih does not say so directly... i Open Original Shared Link:

Celiac disease is a digestive disease that damages the small intestine and interferes with absorption of nutrients from food. People who have celiac disease cannot tolerate gluten, a protein in wheat, rye, and barley.

however.. later the same article suggests an immune component/causation

When people with celiac disease eat foods or use products containing gluten, their immune system responds by damaging or destroying villi

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    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)

  • Upcoming Events

  • Posts

    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
×
×
  • 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.