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

Interesting New Research On Corn


Skylark

Recommended Posts

Skylark Collaborator

There is a really interesting new paper on corn and celiac.

Open Original Shared Link

This paper carefully identifies fragments of corn gluten (zein) that could potentially bind to HLA-DQ2 and HLA-DQ8 in a subset of people with celiac disease. They removed all the gluten IgA antibodies from sera of some celiac volunteers and found some antibodies to corn zein were still present. They carefully tracked down what the antibodies were binding to, using mass spectrometry, and found the antibodies were recognizing poorly digested peptides from corn zein. This is similar to gluten, where the most immunogenic peptides are the ones that are not fully digested. Some computer work supported that the peptides would bind best to DQ2.5, and that they are similar but not identical to wheat gluten fragments.

The reaction is NOT a cross-reaction to corn. Let me repeat that lest there is any confusion. THIS IS NOT A CROSS-REACTION TO CORN. It is a completely separate set of anti-zein antibodies in some teens and adults with celiac disease. Interestingly, two of the five corn-sensitive people were still sick gluten-free. They don't mention in the paper if they got well off corn.

First, if you're feeling OK, don't freak out about corn. Corn is still safe for most celiacs. Only 5 out of 24 people they tested had the antibodies. Also, the corn antibodies don't tend to show up in kids suggesting that corn is not inflammatory like wheat. There is no evidence for corn causing celiac in someone who grows up without wheat. The authors suggest that a person needs to be untreated celiac for a while for the corn antibodies to show up.

There have been flaws in little bit of other corn research that has been done (like the one with 80 ppm gluten in their cornmeal), but this seems to be really solid study. It does raise a lot of questions though. Did the people who were still sick recover off corn? Is corn processed by TTG, triggering autoimmunity? Do the corn epitopes the authors identified stimulate T-cells? Can corn cause TTG antibodies to stay elevated in people with anti-zein IgA? If so, can corn trigger villous atrophy in people who have the anti-zein IgA?

This is extremely important for those of you who are gluten-free and still not well, or potentially being diagnosed with refractory celiac disease. We always tell people to eliminate casein. It's looking like we should also be suggesting people try a period of time eliminating corn (which is unfortunately even harder than eliminating gluten or casein).


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



Celiac.com Sponsor (A8-M):



AriesEmber Newbie

Thanks for posting this Skylark. :) I have been gluten and casein free for a couple months now. I have had a huge relief of crippling symptoms that went far beyond GI troubles. However, I was still experiencing intermittent digestive upsets, and abdominal bloating with tenderness. Four days ago, I tossed corn to the curb. (It's scary how many ingredients have corn hidden in them.) I'm happy to report that the upsets, bloating, and tenderness are all gone. (I realize that I am fortunate to see results as quickly as I do. Everyone is different.) Since the end of January, I have been gaining strength and muscle back, and dropping weight from being ill for so long. Knowledge is power. Keep it coming. Thanks again. Cheers :)

Bubba's Mom Enthusiast

I started reacting to gluten-free corn based granola and fritos. I've dropped corn for now..but it seems like corn is in most medicines and supplements? I haven't stopped those. Isn't dextrose and caramel color made from corn too? :o

jess-gf Explorer

I started reacting to corn a few months ago. Honestly I have no idea if it's a separate intolerance or if it has something to do with the GMO freakshow in corn. I just know, a year ago I could eat it just fine. Then over time if I ate "too much" popcorn I would get a slight stomach ache. Then a couple months ago if I even had a handful of popcorn or any corn-containing snack my upper stomach would erupt in pain so intense that it would wrap around to my back (behind my ribs). I don't usually get back pain from glutening. I've quit corn as best I can since then.

Skylark I read the abstract, it looks very interesting. I just wish I understood it :P I need to take a class to learn how to read that stuff!

GFinDC Veteran

Thanks Skylark, very interesting stuff! Might explain a few mild reactions for me. Guess we are still learning every day. :)

mushroom Proficient

Well, that was why I was so confuzzled when I first started reacting to foods. It was after my introduction to Mexican cuisine, so I initially didn't know what to think, then I thought it was the beans, but no, so I thought, gee, I've only ever eaten corn on the cob before and that was okay, but corn became a question mark??? Then I ate corn on the cob in New Zealand and I was fine. Then I definitely reacted to corn in the U.S. I reacted to corn chips when we went out, or pretzels when we snacked when we were out, and every time I went to a Mexican restaurant, whether I had corn or flour tortillas (with or without beans). Hey, this was over 30 years ago when we didn't know much about food intolerances, okay? And I just thought I had a weird stomach and nervous system.

So this pattern continued for a long while, reacting (in retrospect) to both corn and gluten, and not figuring out where it was coming from :rolleyes: By the time I gave up gluten in hopes of curing my psoriatic arthritis I had already given up 99% of corn (including the non-GMO New Zealand corn) - I only ever ate popcorn. Then I had one of my infamous fainting/syncope spells at a party after eating popcorn so I had to quit that too (plus a lot of other things). I will not be at all surprised (if I live long enough to be surprised) if they do not found other zeins or similar proteins (like the lectins I am sure I react to) that are messing us up.

Hey, jess_gf, I was just this morning looking at the topic you started that has been runing all this time, and wondered what had happened to you. Good to see ya!

Skylark Collaborator

Skylark I read the abstract, it looks very interesting. I just wish I understood it :P I need to take a class to learn how to read that stuff!

It took me more than one class. :lol: I do science for a living.

I started reacting to gluten-free corn based granola and fritos. I've dropped corn for now..but it seems like corn is in most medicines and supplements? I haven't stopped those. Isn't dextrose and caramel color made from corn too? :o

Yes, that's why I was saying it would be hard to totally eliminate corn. It's in everything in the US. :unsure:


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



Celiac.com Sponsor (A8-M):



dilettantesteph Collaborator

Thanks for posting that. I have heard about people with severe reactions to corn, so that would explain it.

jess-gf Explorer

Hey, jess_gf, I was just this morning looking at the topic you started that has been runing all this time, and wondered what had happened to you. Good to see ya!

Oh I've been around, mostly lurking. Thanks!

GFreeMO Proficient

I am one of those corn reactive people. Corn is as bad for me as gluten. Makes so much sense. Thanks for posting this. ;)

IrishHeart Veteran

Thanks for taking the time to decipher it all for us, Skylark! I always appreciate your research. :)

I am also glad you made it clear this is not about "cross-reactivity".

I was worried about corn at the beginning of my gluten-free life because nothing seemed to agree with me for many months. I had removed dairy and soy and I still felt lousy. I thought, oh crappers, corn too? :rolleyes: geesh, but it just took me a looooong time to heal my gut. I still have off days, but corn is not the problem.

Corn is one of my favorite summer pleasures and luckily, corn and I seem to be at peace with each other. :)

Di2011 Enthusiast

I had GI and DH flares on corn. I only realised the link, though, when I started getting the nerve shocks in my feet (which had stopped very soon after going gluten free). I knew I hadn't been glutened. I never eat out and rarely eat any processed foods (even gluten-free). GMO sucks. Excuse my language - I rarely swear. There is too much crap on the market and I'm sick of cooking/washing up .. being hungry ..unable to eat enough calories to keep my weight stable/healthy (I was overweight my entire life!!) etc etc <_<

Knoppie Apprentice

some people react ok to wheat starch and is considered gluten free because it obviously contains less gluten, would the same apply to corn? has anybody had experience with reacting to corn but not the starch?

Bubba's Mom Enthusiast

some people react ok to wheat starch and is considered gluten free because it obviously contains less gluten, would the same apply to corn? has anybody had experience with reacting to corn but not the starch?

I react to corn which has been dried and processed..like Fritios..but ate corn on the cob last week with no reaction. :blink:

There's also corn starch in my medications and supplements, which I don't seen to react to?

IrishHeart Veteran

I react to corn which has been dried and processed..like Fritios..but ate corn on the cob last week with no reaction. :blink:

There's also corn starch in my medications and supplements, which I don't seen to react to?

Same here. I can eat plain corn and use corn starch in baking, but sometimes feel "off" after eating a processed product like corn chips. For me, it may be some of the oils.

...which leads me to wonder if the Fritos have something else in them that makes them bothersome for you? maybe? just thinking out loud with you :)

Skylark Collaborator

Aren't corn chips usually made with lime-treated corn? Lime treatment may change the corn enough that your body sees it differently.

mushroom Proficient

Yes, the more highly refined the corn is the more likely that I can eat it. So the starches in pills don't bother me and I can have some starch in baked goods now. It is any corn product that has any of the outer skin covering, like corn chips, masa harina, etc. that get me. Sometimes I don't know where to draw the line. As in sometimes some corn in pasta will get me and other times it won't. I guess I should judge it by its color :huh:

Bubba's Mom Enthusiast

Same here. I can eat plain corn and use corn starch in baking, but sometimes feel "off" after eating a processed product like corn chips. For me, it may be some of the oils.

...which leads me to wonder if the Fritos have something else in them that makes them bothersome for you? maybe? just thinking out loud with you :)

Ingredients in Fritos..Whole corn, corn oil, and salt.

No preservatives.

Makes me wonder about the drying process? :huh:

IrishHeart Veteran

Ingredients in Fritos..Whole corn, corn oil, and salt.

No preservatives.

Makes me wonder about the drying process? :huh:

hmm....maybe.

Skylark is better informed that I am about this...Sky? :)

Skylark Collaborator

I don't even know what the phrase "drying process" means. If you have questions about Fritos you might write Frito-Lay.

  • 3 weeks later...
HoosierMother Newbie

Interesting as I was checking here to see if anyone else has had a reaction to corn flour... I had bought Zatarain's seasoned fish-fri while vacationing in Florida.. I used it on lean pork chops baking them in the oven, plus we had freezer corn and fried potatoes... I knew I was in trouble instantly starting with stomach cramps and diarrhea... This really irked me... We had company and here I am sitting on the toilet... I was in misery as it was because, I had made a homemade apple pie and chocolate chip cookies

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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.