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

New To Celiac, Can I Have Oats?


kaygato

Recommended Posts

kaygato Explorer

I most likely don't have celiac, but testing says I'm sensitive to it so I started an elimination diet 4 days ago. I also was sensitive to a lot of other foods, most notably yeast, dairy, soy, egg yolk, and a couple veggies, nuts, and most seafood.

Anyway, I've been lurking around the forums for the past couple months, and I've seen conflicting opinions on oats. A lot of people said there was high risk of cross contamination with wheat, but that certified gluten free oats should be ok. Since I'm just starting to go gluten free and really want to see if it makes me feel better, I'd like to avoid gluten as much as possible. I feel like it would be best to stop eating oats, because I'm scared of cross-contamination and the effect it could have on the results.

Anyway, most of you have more experience than me, so what do you think about oats? Also, what are the main causes of cross-contamination, and what products should make me suspicious?

And one last question, can cross contamination interfere with the results of an elimination diet and keep me from feeling improvement on the diet?


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

I'd suggest eliminating oats for now. There is not only a CC issue, but some folks with celiac are sensitive to them because they're so closely related to wheat and barley. You can always try certified gluten-free oats like Bob's Red Mill after you're feeling better.

AVR1962 Collaborator

I would only eat oats labled as gluten-free. Problem is not so much in the oat itself, we all have our sensativities, but unless labeled gluten-free you are at risk of oats being processed in the same machine as other foods containing gluten.

Ellie84 Apprentice

Oats are only safe to eat if they were grown and processed in a wheat/rye/barley-free environment. Always look for a gluten-free logo on oats.

My personal experience with oats is very good: I eat oat-products on a daily basis. A Dutch company has a product line of oat bread (which is very soft and tasty) and I often have oat flakes for breakfast. To me it's a great source of fiber and low-GI carbs.

There are coeliacs who react to other grains as well, I know people on the Dutch coeliac forum who are sensitive to oats, teff or buckwheat as well. Eating these products causes no damage to them, but brings discomfort like indigestion.

Roda Rising Star

I agree with waiting on trying the oats for awhile. When you are ready to introduce them I would only get certified gluten free oats. I waited until i was 7 months gluten free to try them. OH BOY, I was not happy. I reacted horrible to them, just as bad as wheat, barley and rye. Unfortunately I was unaware of gluten free oat cross contamination(CC) so I continued to eat other products that were CC'd with them. I eventually became sick and had symptoms for 8 months straight. I did a further elimination and that's when I realized I was reacting to even the Oat cross contamination. So for me this eliminates a lot of gluten free products even.

irish daveyboy Community Regular

I agree with waiting on trying the oats for awhile. When you are ready to introduce them I would only get certified gluten free oats. I waited until i was 7 months gluten free to try them. OH BOY, I was not happy. I reacted horrible to them, just as bad as wheat, barley and rye. Unfortunately I was unaware of gluten free oat cross contamination(CC) so I continued to eat other products that were CC'd with them. I eventually became sick and had symptoms for 8 months straight. I did a further elimination and that's when I realized I was reacting to even the Oat cross contamination. So for me this eliminates a lot of gluten free products even.

As a general rule Celiacs are advised to avoid Gluten Free Oats until their Villi have healed, this can take anything up to 2 yrs to complete.

If the villi are healed (no longer flattened) then it's suggested to initially restrict yourself to 50g per week. (this includes oatmeal, cookies that may contain Gluten Free Oat Flour, or Oat Cakes).

3 heaped Tablespoons of Gluten Free oats = approx 25g.

50g of Gluten Free Oats would convert to 2 hearty bowls of Oatmeal per week.

You can then gradually increase the amount and see if you still tolerate larger amounts.

My Villi have benefited from a strict Gluten Free Diet over 7yrs and I can tolerate oatmeal 4-5 times a week + cookies and oatcakes.

I've had additional Colonoscopies and my Villi are normal, but this may not hold true for everyone.

That's a matter for you, your dietician and Celiac consultant.

Skylark Collaborator

I would only eat oats labled as gluten-free. Problem is not so much in the oat itself, we all have our sensativities, but unless labeled gluten-free you are at risk of oats being processed in the same machine as other foods containing gluten.

No, for some celiacs like Roda the problem is the oat itself. There are studies where celiacs eating pure oats with no gluten CC had antibodies and villous atrophy.


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



Celiac.com Sponsor (A8-M):



Roda Rising Star

No, for some celiacs like Roda the problem is the oat itself. There are studies where celiacs eating pure oats with no gluten CC had antibodies and villous atrophy.

It will be interesting when I have my blood work redone in Feb. My tTG has been normal since 6 months gltuen free but I have had continued elevated IgG gliadin. They kept telling me gluten was getting into my diet. I'm hoping it will be normal now that I have eliminated all gluten free oat CC(It has been 1 year 4 months now since I eliminated it and had blood work) The unfortunate thing about not realizing the CC for so long is that I think I have some permanant deficiencies, mainly pancreatic enzymes.

  • 2 weeks later...
bstassart Newbie

I get sick from oats if they aren't gluten-free Oats.

I really like the Glutenfreeda Instant Oatmeal that Whole Foods and some Safeway's carry. They say it is made in a gluten-free facility with certified gluten-free oats.

As to your question of whether oats are safe for you, it depends on what you are sensitive to. The following is my understanding although I am not an expert at this.

Prolamins:

gliadin - wheat

hordein - barley

secalin - rye

zein - corn

kafirin - sorghum

avenin - oats

Glutelins

glutenin - wheat

hordeum - barley

secale - rye

The combination of prolamin plus glutelin in wheat, barley, and rye is what is classically called gluten. However, sometimes prolamins are referred to as gluten like referring to corn zein as corn gluten.

Some people are only sensitive to glutelins or a combination of glutelin plus prolamin. Other people seem sensitive to all glutelins and prolamins. People with wheat allergies are sometimes also allergic to the albumin and globulin proteins in wheat and other triticeae grasses.

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. - lil-oly replied to Jmartes71's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Gluten tester

    2. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    3. - JudyLou replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    4. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

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

    • Total Members
      133,155
    • Most Online (within 30 mins)
      7,748

    Beccad611
    Newest Member
    Beccad611
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • lil-oly
      Hey there, have you been tested for allergies? You may not only have celiac disease but be allergic. I have celiac disease and am allergic to Barley, wheat and rye. 
    • JudyLou
    • knitty kitty
      I have osteopenia and have cracked three vertebrae.  Niacin is connected to osteoporosis! Do talk to your nutritionist and doctor about supplementing with B vitamins.  Blood tests don't reveal the amount of vitamins stored inside cells.  The blood is a transportation system and can reflect vitamins absorbed from food eaten in the previous twenty-four to forty-eight hours.  Those "normal limits" are based on minimum amounts required to prevent disease, not levels for optimal health.   Keep us posted on your progress.   B Vitamins: Functions and Uses in Medicine https://pmc.ncbi.nlm.nih.gov/articles/PMC9662251/ Association of dietary niacin intake with osteoporosis in the postmenopausal women in the US: NHANES 2007–2018 https://pmc.ncbi.nlm.nih.gov/articles/PMC11835798/ Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/   Nutritional Imbalances in Adult Celiac Patients Following a Gluten-Free Diet https://pmc.ncbi.nlm.nih.gov/articles/PMC8398893/ Nutritional Consequences of Celiac Disease and Gluten-Free Diet https://www.mdpi.com/2036-7422/15/4/61 Simplifying the B Complex: How Vitamins B6 and B9 Modulate One Carbon Metabolism in Cancer and Beyond https://pmc.ncbi.nlm.nih.gov/articles/PMC9609401/
    • JudyLou
      Thank you so much for the clarification! Yes to these questions: Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, or vitamins? I’m within healthy range for nutritional tests, thyroid and am not anemic. I do have osteopenia. I don’t take any medications, and the dietician was actually a nutritionist (not sure if that is the same thing) recommended by my physician at the time to better understand gluten free eating.    I almost wish the gluten exposure had triggered something, so at least I’d know what’s going on. So confusing!    Many thanks! 
    • knitty kitty
      @JudyLou,  I have dermatitis herpetiformis, too!  And...big drum roll... Niacin improves dermatitis herpetiformis!   Niacin is very important to skin health and intestinal health.   You're correct.  dermatitis herpetiformis usually occurs on extensor muscles, but dermatitis herpetiformis is also pressure sensitive, so blisters can form where clothing puts pressure on the skin. Elastic waist bands, bulky seams on clothing, watch bands, hats.  Rolled up sleeves or my purse hanging on my arm would make me break out on the insides of my elbows.  I have had a blister on my finger where my pen rested as I write.  Foods high in Iodine can cause an outbreak and exacerbate dermatitis herpetiformis. You've been on the gluten free diet for a long time.  Our gluten free diet can be low in vitamins and minerals, especially if processed gluten free foods are consumed.  Those aren't fortified with vitamins like gluten containing products are.  Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, medicine, or vitamins? Niacin deficiency is connected to anemia.  Anemia can cause false negatives on tTg IgA tests.  A person can be on that borderline where symptoms wax and wane for years, surviving, but not thriving.  We have a higher metabolic need for more nutrients when we're sick or emotionally stressed which can deplete the small amount of vitamins we can store in our bodies and symptoms reappear.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards. The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.    Some people in remission report being able to consume gluten again without consequence.   However, another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.   I recommend getting checked for vitamin and mineral deficiencies.  More than just Vitamin D and B12.  A gluten challenge would definitely be a stressor capable of precipitating further vitamin deficiencies and health consequences.   Best wishes!    
×
×
  • 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.