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

How long does it take to get Gluten out of your system


Raptorsgal

Recommended Posts

Raptorsgal Enthusiast

  Does anyone know how long does it take.  After eating gluten for years how long will it take get out of your system 


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



Celiac.com Sponsor (A8-M):



Russ H Community Regular
4 hours ago, Raptorsgal said:

  Does anyone know how long does it take.  After eating gluten for years how long will it take get out of your system 

That is an interesting question.

It is certainly true that fragments of gliadin (one of the proteins present in gluten) can escape the lumen and enter the wall of the gut where the immune response leading to coeliac disease takes place. In classical coeliac disease, a fragment of gliadin binds to an enzyme found in the gut wall called tTG2 and forms a highly immunogenic complex. The body reacts to this complex as if it were an infectious organism and in doing so generates antibodies to both gluten and tTG2. What is curious is that in the closely related conditions dermatitis herpetiformis and gluten ataxia, a similar process occurs but to related enzymes called tTG3 and tTG6 respectively. The antibodies generated against tTG3 and tTG6 are different to those generated against tTG2, and as tTG3 and tTG6 are not found in the gut wall, it suggests that gluten fragments are crossing into the blood stream and migrating to other sites around the body where these enzymes are found (the skin and brain). I haven't seen any research on how long these might remain and cause effects.

Raptorsgal Enthusiast

Thanks for your input I haven’t had gluten since Thursday it not that long that when I find out about my blood test it most likely celiac 

Russ H Community Regular

The symptoms of coeliac come from the body's immune response to gluten rather than gluten itself. As soon as you eliminate gluten from your diet, your symptoms will gradually begin to improve. It can take 2 years for the gut to fully heal. I began to notice improvements within a week or so but it took a year before I was back to normal. I had had coeliac for many years though. You must eliminate every trace of gluten from your diet - even a few breadcrumbs contains enough gluten to make you ill.

Scott Adams Grand Master

I know that some people with DH can have flare ups for weeks after having incredibly tiny amounts of gluten. I think for most people the gluten would pass though your system in a few days, but could trigger an autoimmune response that could go on for a week or even several weeks.

  • 3 weeks later...
CMCM Rising Star
On 2/5/2023 at 11:40 AM, Russ H said:

That is an interesting question.

It is certainly true that fragments of gliadin (one of the proteins present in gluten) can escape the lumen and enter the wall of the gut where the immune response leading to coeliac disease takes place. In classical coeliac disease, a fragment of gliadin binds to an enzyme found in the gut wall called tTG2 and forms a highly immunogenic complex. The body reacts to this complex as if it were an infectious organism and in doing so generates antibodies to both gluten and tTG2. What is curious is that in the closely related conditions dermatitis herpetiformis and gluten ataxia, a similar process occurs but to related enzymes called tTG3 and tTG6 respectively. The antibodies generated against tTG3 and tTG6 are different to those generated against tTG2, and as tTG3 and tTG6 are not found in the gut wall, it suggests that gluten fragments are crossing into the blood stream and migrating to other sites around the body where these enzymes are found (the skin and brain). I haven't seen any research on how long these might remain and cause effects.

Here's what happened with my mother.  This was in 1967 when she was 46 almost no doctor knew about celiac disease.  She was unable to keep food down and her weight had plummeted to 89 when she finally met a doctor who instead of telling her it was all in her head, he asked if she had been tested for celiac disease.  He did an endoscopy and saw the evidence...her villi were totally gone and her intestinal walls were in his words, "smooth as a billiard ball".  They put her on a strict gluten-free diet, which was hard in those days as there were no gluten-free foods.  She just ate meat, eggs, fruits, vegetables.  No grains of any kind.  She started to get better, slowly at first, then faster.  She put back her lost weight, and a year later she had a second endoscopy and her villi had regenerated.  She had to eat gluten-free for the rest of her life, but she lived until 95! 

She was always hyper sensitive to accidental exposure, and for that reason she rarely ate in restaurants.  When she did get accidental gluten, she would get violently sick very quickly and be sick for several days.  We did gene testing at the time I did mine in 2009, and discovered that she had TWO copies of the predisposing celiac gene.  That of course meant that I had at least one celiac gene, although I had already learned that through my own test. 

My son also got the gene from me, and a gluten sensitive one from his dad.  His celiac disease first manifested as dermatitis herpetiformis.  No one could figure it out, but through reading I learned of it and we later got it confirmed.  He had gone to dermatologists, who just couldn't seem to recognize what his rashes were.  He went gluten-free, but in the last few years it has shifted from the DH (which he doesn't get) but with any accidental gluten he gets violently sick for a couple of days.   I find this kind of odd, but maybe the DH version develops when you are eating gluten and don't know about the celiac disease. 

Anyway, both my mom and son got better pretty quickly once they went strictly gluten-free.    I have to be gluten-free as well, but my issues extend to dairy and corn as well.  I keep my diet very very simple, very low carb and keto in  nature and I do fine.

Russ H Community Regular
2 hours ago, CMCM said:

My son also got the gene from me, and a gluten sensitive one from his dad.  His celiac disease first manifested as dermatitis herpetiformis.  No one could figure it out, but through reading I learned of it and we later got it confirmed.  He had gone to dermatologists, who just couldn't seem to recognize what his rashes were.  He went gluten-free, but in the last few years it has shifted from the DH (which he doesn't get) but with any accidental gluten he gets violently sick for a couple of days.   I find this kind of odd, but maybe the DH version develops when you are eating gluten and don't know about the celiac disease. 

 

It does not seem at all well understood but the current idea is that DH develops from coeliac disease. So it is possible to have silent coeliac disease that progresses to DH. On a gluten-free diet, both go into remission but then either or both can flare up on readmission of gluten to the diet.

Quote

It is noteworthy, however, that while both conditions respond to gluten-free diet (GFD), if gluten is reintroduced to the diet of DH patients, the disease may manifest with either gastrointestinal or skin symptoms.

https://www.mdpi.com/1422-0067/23/6/2910


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



Celiac.com Sponsor (A8-M):



  • 1 month later...
MiriamW Contributor
On 2/23/2023 at 12:19 PM, CMCM said:

Here's what happened with my mother.  This was in 1967 when she was 46 almost no doctor knew about celiac disease.  She was unable to keep food down and her weight had plummeted to 89 when she finally met a doctor who instead of telling her it was all in her head, he asked if she had been tested for celiac disease.  He did an endoscopy and saw the evidence...her villi were totally gone and her intestinal walls were in his words, "smooth as a billiard ball".  They put her on a strict gluten-free diet, which was hard in those days as there were no gluten-free foods.  She just ate meat, eggs, fruits, vegetables.  No grains of any kind.  She started to get better, slowly at first, then faster.  She put back her lost weight, and a year later she had a second endoscopy and her villi had regenerated.  She had to eat gluten-free for the rest of her life, but she lived until 95! 

She was always hyper sensitive to accidental exposure, and for that reason she rarely ate in restaurants.  When she did get accidental gluten, she would get violently sick very quickly and be sick for several days.  We did gene testing at the time I did mine in 2009, and discovered that she had TWO copies of the predisposing celiac gene.  That of course meant that I had at least one celiac gene, although I had already learned that through my own test. 

My son also got the gene from me, and a gluten sensitive one from his dad.  His celiac disease first manifested as dermatitis herpetiformis.  No one could figure it out, but through reading I learned of it and we later got it confirmed.  He had gone to dermatologists, who just couldn't seem to recognize what his rashes were.  He went gluten-free, but in the last few years it has shifted from the DH (which he doesn't get) but with any accidental gluten he gets violently sick for a couple of days.   I find this kind of odd, but maybe the DH version develops when you are eating gluten and don't know about the celiac disease. 

Anyway, both my mom and son got better pretty quickly once they went strictly gluten-free.    I have to be gluten-free as well, but my issues extend to dairy and corn as well.  I keep my diet very very simple, very low carb and keto in  nature and I do fine.

@CMCM please can I ask if your mum ended up eating any grains or nuts after her villi had regenerated? And what type of carbs do you eat? I am on a strict gluten-free diet and don't eat dairy but my duodenum isn't healing. You seem to be very strict and diligent with your diet hence I am very interested to find out what else you are avoiding. How about nuts and coffee? Rice and potatoes? Many thanks.  

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,203
    • Most Online (within 30 mins)
      7,748

    Barbara 1981
    Newest Member
    Barbara 1981
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      For people with celiac disease and corn intolerance, most salts, including table salt with dextrose, are generally safe in small amounts, as the dextrose is typically highly processed and unlikely to contain problematic corn proteins. However, if you’re highly sensitive, you might consider switching to pure kosher or Himalayan salt, which don’t contain additives. While bringing your own salt to restaurants or avoiding seasoned foods can feel overwhelming, it’s a practical step if you’re concerned. Many people with corn intolerance tolerate trace amounts of dextrose in salt without issues, but individual sensitivity varies. If your current salt isn’t causing symptoms, it’s likely fine to continue using it, especially given your financial constraints and the challenges of managing dietary restrictions. Focus on what works for you and prioritize avoiding larger sources of corn, like cornstarch.
    • Scott Adams
      Your daughter’s ongoing stomach pains two weeks into a gluten-free diet could be due to her body still healing after months of gluten exposure, as recovery from celiac disease can take time. Her inconsistent eating habits and possible eating disorder behaviors may also delay healing. While she’s now eating gluten-free snacks, her limited intake and emotional withdrawal complicate the process. It’s positive that she’s trying, but recovery may take weeks to months. Addressing her depression and mental health is crucial, as celiac disease can impact mood, and proper nutrition may help. Patience and support are key, but if symptoms persist, consult her doctor to rule out accidental gluten exposure or other issues. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal.  
    • Scott Adams
      I can testify that Daura does not have a "metallic" taste, or any off taste at all--it's an outstanding beer. I have celiac disease and don't have issues with Daura, but do agree that gluten reduced beers are not for everyone. I also started back in the mid-90's brewing gluten-free beer, so do know a lot about how they do this--AN-PEP enzymes like those in Clarex have been shown in studies to break down gluten (this does not instill any off tastes that I have ever detected), and modern filtration processes further remove remnants of gluten.  There are also studies that show some regular beers have extremely low gluten content, even if they do not use such enzymes. Some of our users with celiac disease have reported drinking regular beers for years without any issues or elevated antibody tests or villi damage, but others have discovered that they cannot tolerate the same beers, or any gluten reduced beers. There are plenty 100% gluten-free beers that use alternative grains for those with celiac disease who prefer to avoid reduced gluten beers.
    • Scott Adams
      At 60, with a family history of celiac disease (mother and sister) and HLA DQ2 positivity, celiac disease is a possibility despite negative tTG antibodies (total IgA was not checked). Your symptoms—abdominal discomfort, gas, brain fog, ataxia, and worsening with gluten or alcohol—could align with celiac disease, though the lack of improvement off gluten is atypical. Normal imaging and fecal elastase reduce the likelihood of pancreatic issues, and a normal hydrogen breath test makes SIBO less likely. The upcoming biopsy will be key for diagnosis; continue eating gluten until then. If celiac disease is ruled out, consider non-celiac gluten sensitivity or a neurological evaluation for symptoms like ataxia and finger numbness.
    • Scott Adams
      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/   
×
×
  • Create New...