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  • Jefferson Adams
    Jefferson Adams

    How Refining the Gluten Challenge May Help Improve Diagnostics for Celiac Disease

    Reviewed and edited by a celiac disease expert.

    Now, a new study sheds light on new biomarkers that could help to rapidly improve the way celiac disease is diagnosed and researched. Here's what it revealed.

    How Refining the Gluten Challenge May Help Improve Diagnostics for Celiac Disease - Vision of Transformation. Image: CC BY-ND 2.0--h.koppdelaney
    Caption: Vision of Transformation. Image: CC BY-ND 2.0--h.koppdelaney

    Celiac.com 06/08/2023 - For people who suspect they have celiac disease, an accurate diagnosis is crucial for managing health and making informed dietary choices. Traditionally, the gold standard for celiac diagnosis has involved a gluten challenge, where individuals are required to consume gluten-containing foods to induce disease activity. 

    However, this approach can be burdensome and time-consuming. Now, a new study conducted at two US centers has shed light on new biomarkers that could help to rapidly improve the way celiac disease is diagnosed and researched.

    The Research Team

    Celiac.com Sponsor (A12):
    The research team included Maureen M. Leonard, Jocelyn A. Silvester, Daniel Leffler, Alessio Fasano, Ciarán P. Kelly, Suzanne K. Lewis, Jeffrey D. Goldsmith, Elliot Greenblatt, William W. Kwok, William J. McAuliffe, Kevin Galinsky, Jenifer Siegelman, I-Ting Chow, John A. Wagner, Anna Sapone, and Glennda Smithson.

    They are variously affiliated with the Center for Celiac Research and Treatment, Massachusetts General Hospital, Boston, Massachusetts; the Celiac Disease Research Program, Harvard Medical School, Boston, Massachusetts; the Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Boston Children’s Hospital, Boston, Massachusetts; the Celiac Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts; Takeda Pharmaceuticals Inc. Co., Cambridge, Massachusetts; the Department of Medicine, Columbia University Medical Center, New York, New York; the Department of Pathology, Boston Children’s Hospital, Boston, Massachusetts; Invicro, A Konica Minolta Company, Boston, Massachusetts; and the Benaroya Research Institute at Virginia Mason, Seattle, Washington.

    A Randomized Double-blind Trial

    In a randomized, double-blind trial, the team enrolled 14 adults with biopsy-proven celiac disease. The participants were divided into two groups and assigned to consume either 3 grams or 10 grams of gluten per day for a period of 14 days. 

    The primary objective was to assess the changes in villous height: crypt depth (Vh:celiac disease), a key histological marker of celiac disease activity. However, the study also aimed to explore other biomarkers that could potentially supplement or even replace histology as a diagnostic tool.

    The results of the study were largely encouraging. All of the biomarkers assessed showed changes in response to gluten challenge, demonstrating their potential for evaluating disease activity. However, the time to reach maximal change, the magnitude of change, and the gluten dose-response relationship varied across different biomarkers. 

    Notably, Vh:celiac disease, a measure of the structural integrity of the small intestine, VCE enteropathy score as assessed by video capsule endoscopy, enzyme-linked immune absorbent spot (ELISpot), gut-homing CD8 T cells, intraepithelial leukocytes, and gluten-specific CD4 T cells, all demonstrated significant changes only at the higher gluten dose of 10 grams. 

    However, symptoms reported by the participants, and plasma interleukin-2 (IL-2) levels, increased significantly or near significantly at both gluten doses. Interestingly, IL-2 appeared to be the earliest and most sensitive marker of acute gluten exposure.

    Conclusions

    These findings can help to improve celiac disease diagnostics, by identifying modern biomarkers that are sensitive and responsive to gluten exposure, this study offers the possibility of less invasive and shorter-duration gluten challenges. This would not only ease the burden on individuals undergoing diagnostic testing but also streamline celiac disease research, enabling more efficient and precise investigations.

    The potential benefits of these novel biomarkers extend beyond diagnostics. They could also play a crucial role in monitoring disease activity, assessing treatment responses, and even exploring the effects of gluten on individuals who are at risk of developing celiac disease.

    While this study represents a significant step forward, further research is needed to validate and refine the biomarkers. Future studies may investigate their utility in larger populations and explore their correlation with long-term clinical outcomes.

    This study shows the potential for modern biomarkers to improve celiac disease diagnostics. By providing a preliminary framework for the rational design of gluten challenge protocols, this work brings us one step closer to more efficient and patient-friendly diagnostic approaches for celiac disease.

    Stay tuned for more on this and related stories.

    Read more in Gastroenterology


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    knitty kitty

    Celiac Disease is genetic.  Certain HLA genes are associated with the potential of developing Celiac Disease.  If one doesn't have any of the known Celiac genes, then Celiac Disease can be ruled out.  The most common Celiac genes are HLA DQ 2 and 8.  There are others but they occur less frequently, DQ 7, 4, and 9.  

    Celiac Disease genes can be latent for years.  A triggering event such as an illness, a physical trauma or an emotional trauma can trigger the Celiac genes to switch on.  Low thiamine is also a trigger.  After the triggering event, Celiac Disease develops.  

    If one doesn't have any of the known Celiac Disease genes, it's unlikely one would develop Celiac Disease, and other medical reasons for symptoms should be investigated.  

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    Beverley Ann Johnson

    I would in up in ER if I ate gluten for a whole week!  I drained myself just eating it twice.  The amount of bread, 1 slice the first day, ended with headache and feeling off.  The second day 2 slices of wheat bread and it attacked me big time.  I was having gas, bloating and then vomiting, I emptied my stomach out completely and my muscles were attacked, my legs give out and I have this awful feeling all over.  It takes a couple of days to recover from this, to start over and heal my stomach and intestine.

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    Ginger38
    On 5/3/2024 at 11:54 AM, knitty kitty said:

    Celiac Disease is genetic.  Certain HLA genes are associated with the potential of developing Celiac Disease.  If one doesn't have any of the known Celiac genes, then Celiac Disease can be ruled out.  The most common Celiac genes are HLA DQ 2 and 8.  There are others but they occur less frequently, DQ 7, 4, and 9.  

    Celiac Disease genes can be latent for years.  A triggering event such as an illness, a physical trauma or an emotional trauma can trigger the Celiac genes to switch on.  Low thiamine is also a trigger.  After the triggering event, Celiac Disease develops.  

    If one doesn't have any of the known Celiac Disease genes, it's unlikely one would develop Celiac Disease, and other medical reasons for symptoms should be investigated.  

    Thank you, our lab only tests for the 2 most common genes. 

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    Ginger38
    On 5/7/2024 at 2:44 PM, Beverley Ann Johnson said:

    I would in up in ER if I ate gluten for a whole week!  I drained myself just eating it twice.  The amount of bread, 1 slice the first day, ended with headache and feeling off.  The second day 2 slices of wheat bread and it attacked me big time.  I was having gas, bloating and then vomiting, I emptied my stomach out completely and my muscles were attacked, my legs give out and I have this awful feeling all over.  It takes a couple of days to recover from this, to start over and heal my stomach and intestine.

    Me too! I can’t make it past a few days. The fatigue and brain fog as well as just weakness and gastrointestinal issues 

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    SunshineFace

    Great convo! I’m new here… I’m doing a gluten challenge and eating one full-size croissant per day (with a full meal). I am two weeks in and interestingly, the first two days were the worst, and after that my body seemed to ‘adapt’ somehow. I am operating at pretty diminished levels for sure. But nothing like the first couple of days. Do we have a chart here to look up the gluten content of foods, or is that a resource out on the interwebs somewhere? One croissant ‘seems’ like 2 slices of bread, so I’m wondering if I need to increase the gluten content. Thanks! 

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    trents

    @SunshineFace, the latest guidelines for the gluten challenge are 10g of gluten daily for at least 2 weeks. 10g is the amount of gluten in about 4-6 slices of bread. So, I would say you need to at least one more croissant daily.

    Edited by trents
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    SunshineFace

    Thanks, @trents, appreciate it! I was afraid that might be the answer! 😩 

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    Jefferson Adams

    Jefferson Adams is Celiac.com's senior writer and Digital Content Director. He earned his B.A. and M.F.A. at Arizona State University. His articles, essays, poems, stories and book reviews have appeared in numerous magazines, journals, and websites, including North American Project, Antioch Review, Caliban, Mississippi Review, Slate, and more. He is the author of more than 2,500 articles on celiac disease. His university coursework includes studies in science, scientific methodology, biology, anatomy, physiology, medicine, logic, and advanced research. He previously devised health and medical content for Colgate, Dove, Pfizer, Sharecare, Walgreens, and more. Jefferson has spoken about celiac disease to the media, including an appearance on the KQED radio show Forum, and is the editor of numerous books, including "Cereal Killers" by Scott Adams and Ron Hoggan, Ed.D.

    >VIEW ALL ARTICLES BY JEFFERSON ADAMS

     


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