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

Anyone Read This Book


confused

Recommended Posts

confused Community Regular

From "Gluten sensitivitiy as a neurological Illness" by M Hadjivassiliou, R A Grunewald, G A B Davies-Jones:

"Within the group of patients with neurological disease and gluten sensitivity (defined by the presence of anti-gliadin antibodies) we have found a similar HLA association to that seen in patients with celiac disease: 70% of patients have the HLA DQ2 (30% in the general population), 9% have the HLA DQ8, and the remainder have HLA DQ1. The finding of an additional HLA marker (DQ1) seen in the remaining 20% of our patients may represent an important difference between the genetic susceptibility of patients with neurological presentation to those with gastrointestinal presentation within the range of gluten sensitivity."

I just wanted to know if anyone read this book, I am really interested in what he has to say about all of this.

So is it possible one day that they will inclute DQ! as a gene for celiac i have found many other articles of people with DQ1 who test positive celiac in blook work or biopsy.

What does eveyone else think?

paula


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



Celiac.com Sponsor (A8-M):



larry mac Enthusiast

deleted/lm

happygirl Collaborator
From "Gluten sensitivitiy as a neurological Illness" by M Hadjivassiliou, R A Grunewald, G A B Davies-Jones:

"Within the group of patients with neurological disease and gluten sensitivity (defined by the presence of anti-gliadin antibodies) we have found a similar HLA association to that seen in patients with celiac disease: 70% of patients have the HLA DQ2 (30% in the general population), 9% have the HLA DQ8, and the remainder have HLA DQ1. The finding of an additional HLA marker (DQ1) seen in the remaining 20% of our patients may represent an important difference between the genetic susceptibility of patients with neurological presentation to those with gastrointestinal presentation within the range of gluten sensitivity."

I just wanted to know if anyone read this book, I am really interested in what he has to say about all of this.

So is it possible one day that they will inclute DQ! as a gene for celiac i have found many other articles of people with DQ1 who test positive celiac in blook work or biopsy.

What does eveyone else think?

paula

Dr. H is one of the (if not THE) leading researcher in terms of gluten/neurological. His work is often cited by the other "big" Celiac researchers. There is evidence that there are gluten problems that don't cause GI damage, but instead 'damage' us neurologically (similar to how DH affects our skin).

Can you post the other articles you have found about DQ1 people? I would apprecaite it.

confused Community Regular
Your confused? I can't even understand the authors name, much less what you said. And what does Dairy Queen have to do with Celiac?

best reagrds, lm

Sorry i meant DQ1 gene, some of my keys on my keyboard are stuck.

I was just saying do u think that someday there will be more genes that show celiac besides dq2 and dq8,

paula

confused Community Regular
Dr. H is one of the (if not THE) leading researcher in terms of gluten/neurological. His work is often cited by the other "big" Celiac researchers. There is evidence that there are gluten problems that don't cause GI damage, but instead 'damage' us neurologically (similar to how DH affects our skin).

Can you post the other articles you have found about DQ1 people? I would apprecaite it.

I will go threw all my articles i have saved tommorow and post them.

So have you read a lot of his work?

paula

Nantzie Collaborator

This is actually not a book (that I know of anyway). It's an article in a medical journal, which you can usually look at a small excerpt of (an abstract) on www.pubmed.gov. Which is a neat site to look at if you're into medical stuff.

This one was published in the Journal of Neurology and Neurosurgery in May 2002. I was actually trying to look at this study a couple months ago on pubmed, but it's one of the ones they don't have an abstract for :rolleyes: .

DQ1 seems to be one of the most common non-celiac genes around here. So that study saying that DQ1 may make up 20% of people with celiac, but just with different symptoms, makes SOOO much sense doesn't it? I have two copies of DQ1, subtype 6. I had GI symptoms for 18 years, and neuro symptoms for about three years.

It's frustrating that a study that came out almost five years ago hasn't seeped into the knowledge of the medical community. But then again, many of them don't know much about what to look for in classic cases either.

I think that's why message boards like this one are so important. Without regular people exchanging information, we'd all be sunk. :blink:

Edited:

I just did a search and found this site, which is by one of our members I believe -

Open Original Shared Link

On there, she has a link to the full text article of the study you mentioned

Open Original Shared Link

Here's the main page of her site - Open Original Shared Link

Very informative. Lots of information. I had come across her page a long time ago, but lost the bookmark.

Nancy

confused Community Regular
This is actually not a book (that I know of anyway). It's an article in a medical journal, which you can usually look at a small excerpt of (an abstract) on www.pubmed.gov. Which is a neat site to look at if you're into medical stuff.

This one was published in the Journal of Neurology and Neurosurgery in May 2002. I was actually trying to look at this study a couple months ago on pubmed, but it's one of the ones they don't have an abstract for :rolleyes: .

DQ1 seems to be one of the most common non-celiac genes around here. So that study saying that DQ1 may make up 20% of people with celiac, but just with different symptoms, makes SOOO much sense doesn't it? I have two copies of DQ1, subtype 6. I had GI symptoms for 18 years, and neuro symptoms for about three years.

It's frustrating that a study that came out almost five years ago hasn't seeped into the knowledge of the medical community. But then again, many of them don't know much about what to look for in classic cases either.

I think that's why message boards like this one are so important. Without regular people exchanging information, we'd all be sunk. :blink:

Edited:

I just did a search and found this site, which is by one of our members I believe -

Open Original Shared Link

On there, she has a link to the full text article of the study you mentioned

Open Original Shared Link

Here's the main page of her site - Open Original Shared Link

Very informative. Lots of information. I had come across her page a long time ago, but lost the bookmark.

Nancy

Nancy thank you so much for all that information. I found it very informative. If you ever find any other articles will you let me know. I want to learn as much on the medical side as I can. I took lots of psychology classes, and how the brain works and so forth in college, and it always fascinated me. It is sad to say i dont remember much from the classes over 10 years ago, and i doubt we even talked about celiac disease anyway. I was going to call one of my old professors today, we still talk from time to time and see if he knows of any articles.'

paula


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,566
    • Most Online (within 30 mins)
      7,748

    Rrenee2990
    Newest Member
    Rrenee2990
    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

    • cristiana
      That's great news, you can do this.  Let us know how things go and don't hesitate to ask if you have any more questions. Cristiana 😊
    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
    • petitojou
      Thank you so much for the information and kind message! Reading this transformed how I’ve been viewing my efforts and progress. Guess there’s still a lot to celebrate and also heal 😌  Yes, I’ve been taking it! Just recently started taking a multivitamin supplement and separated vitamin D! I also took chewable Iron polymaltose for ferritin deficiency 2 months ago but was unable to absorb any of it.  Thank you again! Hearing such gentle words from the community makes my body and heart more patient and excited for the future. 
    • ckeyser88
      I am looking for a roomie in Chicago, Denver or Nashville! 
    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
×
×
  • 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.