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 Being Done At U Of C


Lynayah

Recommended Posts

Lynayah Enthusiast

Interesting new research being done at the University of Chicago:

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Ahorsesoul Enthusiast

I have to laugh, just how in the world do they know that 97% of celiacs are undiagnosed! This is on their website: Open Original Shared Link

How did they come up with this number, a survey? Hello sir, are you an undiagnosed celiac patient? Why yes I am but no one knows it yet.

Updated: I did email them asking how they came up with this number. Maybe they mean that 97% of celiac patients are self-diagnosed which I think is about right.

YoloGx Rookie

Interesting new research being done at the University of Chicago:

Open Original Shared Link

It is always wonderful to hear that more research on celiac is being proposed. Thank you for the link!

I had no idea however that there were mice that were affected by celiac. Are there?? I wonder what is done to either find or create that state in mice. I also wonder why more research concerning celiac and severe gluten intolerance isn't being done with actual humans.

Meanwhile I think the "97% undiagnosed" part is based on the fact that when doctors actually test for people who have celiac, they consistently find that its one in 133 who has it. However not that many people in our country actually have been diagnosed with it since the medical establishment isn't looking and most folks are ignorant or uninformed about the subject.

Even more folks are probably affected by severe gluten intolerance in my opinion. I say this based on the fact so many here on celiac.com cannot tolerate gluten despite having been tested and found not to officially have celiac.

Bea

Lynayah Enthusiast

It is always wonderful to hear that more research on celiac is being proposed. Thank you for the link!

I had no idea however that there were mice that were affected by celiac. Are there?? I wonder what is done to either find or create that state in mice. I also wonder why more research concerning celiac and severe gluten intolerance isn't being done with actual humans.

Meanwhile I think the "97% undiagnosed" part is based on the fact that when doctors actually test for people who have celiac, they consistently find that its one in 133 who has it. However not that many people in our country actually have been diagnosed with it since the medical establishment isn't looking and most folks are ignorant or uninformed about the subject.

Even more folks are probably affected by severe gluten intolerance in my opinion. I say this based on the fact so many here on celiac.com cannot tolerate gluten despite having been tested and found not to officially have celiac.

Bea

Hi, Bea: Yes, I agree that this 97% draws merit from the current stats of 1 out of 133. It's quite an eye opener to see it described with the 97% slant, isn't it? It says the same thing (or almost the same?) yet gives it a whole new perspective.

I'm a little confused about the exact math they use, though. Ahorsesoul: I hope they answer your letter. I'd love to hear what they say. The next time I'm there, I'll ask as well

Bea, I agree with your gluten intolerance thoughts as well. I'm one of those folks who is "lucky" (HA!) enough to be so highly symptomatic (gliadin, gliadin everywhere, and not a drop to eat!) that U of C has asked me to be part of their research.

Seriously though, I do hope they learn a lot from us intolerant folks. :)

YoloGx Rookie

Hi, Bea: Yes, I agree that this 97% draws merit from the current stats of 1 out of 133. It's quite an eye opener to see it described with the 97% slant, isn't it? It says the same thing (or almost the same?) yet gives it a whole new perspective.

I'm a little confused about the exact math they use, though. Ahorsesoul: I hope they answer your letter. I'd love to hear what they say. The next time I'm there, I'll ask as well

Bea, I agree with your gluten intolerance thoughts as well. I'm one of those folks who is "lucky" (HA!) enough to be so highly symptomatic (gliadin, gliadin everywhere, and not a drop to eat!) that U of C has asked me to be part of their research.

Seriously though, I do hope they learn a lot from us intolerant folks. :)

Thankfully celiac is getting more noticed. Am glad to hear that severe gluten intolerance is starting to be too.

I was reading the info below your posts and noticed you also have muscle and joint aches and pains. Its one thing that has stayed with me--fragile joint connections, try as I might old injuries still plaque me if I am not careful. I have to exercise gradually. I walk nearly every day and when am in good shape do push ups and use my Pilates machine, but can't always due to old injuries in my elbow/shoulder area from an old car accident. Its so frustrating! Am too hyper mobile. Seems a family trait. It would be nice to figure out if there was some kind of supplement(s) one could take to counteract this more effectively. I am much better overall being off all trace gluten and taking minerals and co-enzyme B complex and vit. D etc., but still must be careful. Latest discovery for me of late is to increase collagen and silica. Am actually drinking green tea to help with this... Am wondering if the trade off of now having caffeine is worth it...

Meanwhile let us know more about this study if you get a chance!

Bea

GottaSki Mentor

Interesting new research being done at the University of Chicago:

Open Original Shared Link

Great info -- here is a video about their work

Open Original Shared Link

Lynayah Enthusiast

Thankfully celiac is getting more noticed. Am glad to hear that severe gluten intolerance is starting to be too.

I was reading the info below your posts and noticed you also have muscle and joint aches and pains. Its one thing that has stayed with me--fragile joint connections, try as I might old injuries still plaque me if I am not careful. I have to exercise gradually. I walk nearly every day and when am in good shape do push ups and use my Pilates machine, but can't always due to old injuries in my elbow/shoulder area from an old car accident. Its so frustrating! Am too hyper mobile. Seems a family trait. It would be nice to figure out if there was some kind of supplement(s) one could take to counteract this more effectively. I am much better overall being off all trace gluten and taking minerals and co-enzyme B complex and vit. D etc., but still must be careful. Latest discovery for me of late is to increase collagen and silica. Am actually drinking green tea to help with this... Am wondering if the trade off of now having caffeine is worth it...

Meanwhile let us know more about this study if you get a chance!

Bea

Bea, I feel your pain. Have you tried going without dairy altogether? Also, might you be available to talk privately?


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie

Bea, I feel your pain. Have you tried going without dairy altogether? Also, might you be available to talk privately?

I have previously gone off all dairy. Now seem to do well with yogurt I make myself and ferment for roughly 24-26 hours to get rid of all the lactose. I believe the casein is OK. Maybe though I should go back to no cheese and eggs at all however...The cheese can get addicting, never a good sign. I was off all grains for 10 months and now use brown rice fairly regularly.

Meanwhile, certainly -- let's "talk."

Interestingly enough by the way my mother was part of a celiac sprue study at the University of San Francisco back in the late teens and through the twenties of the previous century. Unfortunately the results of the study were lost however.

Unfortunate for me when I came along doctors still thought one grew out of this condition, so they put me back onto grains when I was 4 years old--since grains no longer made me stop growing (as they had when I was an infant). Of course back then here in the States they didn't know (or should I say "accept"?) that it was the gluten (gliadin) at fault.

The good thing now with the advent of the Internet is that studies such as these are less likely to get "lost." Interestingly many of the things they are discovering now were previously discovered back then (at least according to my mom)! So I guess that has got to say something about the scientific validity of it all, eh??

Lynayah Enthusiast

I have previously gone off all dairy. Now seem to do well with yogurt I make myself and ferment for roughly 24-26 hours to get rid of all the lactose. I believe the casein is OK. Maybe though I should go back to no cheese and eggs at all however...The cheese can get addicting, never a good sign. I was off all grains for 10 months and now use brown rice fairly regularly.

Meanwhile, certainly -- let's "talk."

Interestingly enough by the way my mother was part of a celiac sprue study at the University of San Francisco back in the late teens and through the twenties of the previous century. Unfortunately the results of the study were lost however.

Unfortunate for me when I came along doctors still thought one grew out of this condition, so they put me back onto grains when I was 4 years old--since grains no longer made me stop growing (as they had when I was an infant). Of course back then here in the States they didn't know (or should I say "accept"?) that it was the gluten (gliadin) at fault.

The good thing now with the advent of the Internet is that studies such as these are less likely to get "lost." Interestingly many of the things they are discovering now were previously discovered back then (at least according to my mom)! So I guess that has got to say something about the scientific validity of it all, eh??

I wonder if the research was inconveniently lost . . . or conveniently lost. What a shame that the research disappeared, both for you as well as the celiac community.

GottaSki Mentor

I wonder if the research was inconveniently lost . . . or conveniently lost. What a shame that the research disappeared, both for you as well as the celiac community.

The internet has allowed ordinary individuals to take more control of their medical destiny - we can now circumnavigate the strength of the drug companies to find all the potential ways to improve our health - outside of the prescription drug possibilities.

Please do not misunderstand - for many ailments medical research has produced amazing results - when diagnosed with cancer a person is very fortunate to be living in a day that has seen so much discovery - yet somewhere along the line the focus became selling drugs rather than curing or managing conditions that are curable or manageable with the correct food for each body and exercise!

YoloGx Rookie

I wonder if the research was inconveniently lost . . . or conveniently lost. What a shame that the research disappeared, both for you as well as the celiac community.

I agree. I wonder what the story was about all that. It seems strange that such a long research project should get lost. At the time my mother was considered an oddity since she was intelligent and had energy despite the sprue and a low thyroid--at least that is what she says as to why she was paraded in front of the young interns.

Darissa Contributor

Thanks for the good info! I am excitied about all the new research being done on celiac disease.

Lynayah Enthusiast

Thanks for the good info! I am excitied about all the new research being done on celiac disease.

You are welcome, Darissa! Thank YOU for the thanks.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,975
    • Most Online (within 30 mins)
      7,748

    LRB
    Newest Member
    LRB
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.