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

Any Long Term Studies On Gluten/cc & Risks?


2wheels4eyes

Recommended Posts

2wheels4eyes Explorer

Despite my care, I've glutened myself for the second time this week--not even sure on what at this point. I think just CC, either in my house or the pre-made/packaged foods (which are gluten-free--ha ha--but "made in facilities that...")

So tonight I'm sitting for a dinner I had no interest in eating at Outback's, waiting for my latest symptoms to pass (fortunately I don't think it was a lot of gluten--and I hasten to add this wasn't Outback--I glutened myself at home.) Everyone at the table is talking about, y'know, life and stuff and in the back of my head I'm thinking about my gut. And how stupid I am that this happened again. And about the relatives I learned about last week (all my grandmother's generation or before) that were diagnosed with celiac disease too late in life and died of rare intestinal cancers in their 50s or early 60s.

I have no intention of dying in my 50s or 60s of some stupid celiac disease-related thing (I'm 29; dx'd 8 mos. ago.) I'm beginning to think my greater risk with celiac disease isn't cancer & osteo but paranoia.

Does anyone know of any *good* long term studies of morbidity in those following the gluten-free diet? I know they've got some ballpark figures and that lab tests show even minute amounts can damage the villi. But c'mon. Just because they can detect the effects of gluten doesn't mean (necessarily) that my risks for various things has gone up until that damage is severe enough.

I'm guessing that a really good, longitudinal, double-blind trial hasn't been done, first because who would spend the $ on something like that and second because you'd have to put celiacs on gluten diets and then conduct repeated biopsies. But maybe something could be done using non-compliant (non-gluten-free) celiacs and those sticking to the gluten-free diet? Anyone heard of such things? I want hard numbers on risks as correlated to frequency and severity of gluten exposures.


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



Celiac.com Sponsor (A8-M):



happygirl Collaborator

To my knowledge, there are no studies that link exposure/glutenings to morbidity. That would be near impossible to do, as we don't always know when we are glutened (i.e., esp for asymptomatic Celiacs), so the validity/reliability of a study such as this would be highly questionable.

In general, it appears that the higher risk of morbidity and most other serious problems (cancer, etc) increases for those who are not on a gluten free diet but are Celiacs. Going gluten free and maintaining (with, some accidents, of course, but in general, gluten free) the diet lowers this risk (same with fertility numbers/Celiac).

here are some references to some of the studies of morbidity.

https://www.celiac.com/st_prod.html?p_prodi...-25107204802.c9

https://www.celiac.com/st_prod.html?p_prodi...-25107204802.c9

2wheels4eyes Explorer
To my knowledge, there are no studies that link exposure/glutenings to morbidity. That would be near impossible to do, as we don't always know when we are glutened (i.e., esp for asymptomatic Celiacs), so the validity/reliability of a study such as this would be highly questionable.

Right--unless you purposely glutened people occasionally in a lab environment and then marked the effects over a period of years. Which no one would get IRB approval for anyway--hence relying on subjects' self reports, food diaries, etc. as a proxy for lab glutenings. Like for the two above studies you linked, what does it mean to be "gluten-free" exactly? How strictly (or not) are the diets being followed?

Not that I'm a cheater--I just find it maddening not to know what the correlation is between exposure and risk.

Thanks for the links!!!

Celiac Sufferer Newbie
Right--unless you purposely glutened people occasionally in a lab environment and then marked the effects over a period of years. Which no one would get IRB approval for anyway--hence relying on subjects' self reports, food diaries, etc. as a proxy for lab glutenings. Like for the two above studies you linked, what does it mean to be "gluten-free" exactly? How strictly (or not) are the diets being followed?

Not that I'm a cheater--I just find it maddening not to know what the correlation is between exposure and risk.

Thanks for the links!!!

Celiac Disease even following the diet can cause problems. I have been on a gluten-free diet for 4 years and have had 6 surgeries and were all related to Celiac disease. I even have heart problems due to Celiac. The reason for that is because I was diagnosed too late. I am 21 years old and all though my life had horrid symptoms and even bone deformaties and I had a hard time gaining weight because throughout my younger life the doctors told me I had IBS. They didn't do any test. Until I was in High School they noticed that I was weighin in at 88 pounds. The doctor rushed me into a Endo and colonoscopy and found out I had a severe case of Celiac Disease. For 4 years being on the Diet I still run into lots of problems. They come one right after the other. That is because I am Nonresponsive Celiac Disease. That means I not getting the tummy symptoms, but the Celiac is damaging other parts of my body. You know that Celiac Disease is not an allergy it is an Auto Immune Disease. So I will have a lifetime of complications from cancer to getting other auto immune diseases. It is very important to stay on the Gluten-Free diet and try not to contaminate or run into gluten because yes a little tiny bit can trigger the celiac to become more active. My Celiac will be always active due to the fact of having such a severe case and being diagnosed to late.

2wheels4eyes Explorer

Celiac Sufferer... my heart goes out to you... thanks for sharing with me your hard-earned knowledge about celiac disease.

I'm symptomatic after CC but usually not to a debilitating degree (i.e., don't usually have to take time off work or anything.) It's more frustrating when I know I'm in control of what I eat (ha ha) and still end up making mistakes that could jeopardize my health.

However, I think my post was motivated in equal parts by a desire for better research and a desire to simply whine!

Generic Apprentice

From personal experience, I believe it can cause more problems. I have been gluten free for 19 years and have been accidentally glutened more times than I care to remember. I have since developed over the years hypoglycemia, fibromyalgia and something else that they aren't sure of yet. Possibly MS, rheumatoid arthritis or myositis.

Yippee! :angry: I just wonder what other auto-immune disease I will develop as I get older. I try to stay positive but it is hard sometimes. I often wonder if it is going to shorten my life. But so far my grandparents lived into their 80's and I'm pretty sure they were undiagnosed celiac.

Oh and not to mention I have put more money into my mouth than what my jeep is worth.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.