دورية أكاديمية
أعرض في EDS

Standardizing Randomized Controlled Trials in Celiac Disease: An International Multidisciplinary Appropriateness Study.

التفاصيل البيبلوغرافية
العنوان: Standardizing Randomized Controlled Trials in Celiac Disease: An International Multidisciplinary Appropriateness Study.
المؤلفون: Lebwohl B; Celiac Disease Center, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York; Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York. Electronic address: bl114@cumc.columbia.edu., Ma C; Division of Gastroenterology and Hepatology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada; Alimentiv Inc, London, Ontario, Canada. Electronic address: christopher.ma@ucalgary.ca., Lagana SM; Department of Pathology and Cell Biology, Columbia University, New York, New York., Pai RK; Department of Pathology and Laboratory Medicine, Mayo Clinic Arizona, Scottsdale, Arizona., Baker KA; Alimentiv Inc, London, Ontario, Canada., Zayadi A; Alimentiv Inc, London, Ontario, Canada., Hogan M; Alimentiv Inc, London, Ontario, Canada., Bouma G; Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam, The Netherlands., Cellier C; Department of Gastroenterology, University of Paris-Cité, Georges-Pompidou European Hospital, Assistance Publique des Hôpitaux de Paris, Paris, France., Goldsmith JD; Department of Pathology, Boston Children's Hospital, Boston, Massachusetts., Lundin KEA; Norwegian Coeliac Disease Research Centre, University of Oslo Faculty of Medicine, Oslo, Norway; Department of Gastroenterology, Oslo University Hospital Rikshospitalet, Oslo, Norway., Pinto-Sanchez MI; Department of Medicine, Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada., Robert ME; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut., Rubio-Tapia A; Celiac Disease Program, Division of Gastroenterology, Hepatology, and Nutrition, Digestive Disease and Surgery Institute, Cleveland Clinic, Cleveland, Ohio., Sanders DS; Academic Unit of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom., Schaeffer DF; Department of Pathology and Laboratory Medicine, Vancouver General Hospital, Vancouver, British Columbia, Canada., Semrad CE; Department of Gastroenterology, University of Chicago, Chicago, Illinois., Silvester JA; Harvard Celiac Research Program, Harvard Medical School, Boston, Massachusetts; Division of Gastroenterology, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts; Celiac Disease Center, Division of Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts., Verdú EF; Department of Medicine, Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada., Verma R; Department of Pediatrics, Section of Gastroenterology, Hepatology and Nutrition, The University of Chicago, Chicago, Illinois., Wu TT; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota., Feagan BG; Alimentiv Inc, London, Ontario, Canada; Division of Gastroenterology, Department of Medicine, Western University, London, Ontario, Canada; Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada., Crowley E; Alimentiv Inc, London, Ontario, Canada; Division of Pediatric Gastroenterology, Department of Pediatrics, Children's Hospital Western Ontario, London Health Sciences Centre, Western University, London, Ontario, Canada., Jairath V; Alimentiv Inc, London, Ontario, Canada; Division of Gastroenterology, Department of Medicine, Western University, London, Ontario, Canada; Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada., Murray JA; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
المصدر: Gastroenterology [Gastroenterology] 2024 Jan; Vol. 166 (1), pp. 88-102. Date of Electronic Publication: 2023 Sep 11.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-0012 (Electronic) Linking ISSN: 00165085 NLM ISO Abbreviation: Gastroenterology Subsets: MEDLINE
أسماء مطبوعة: Publication: Philadelphia, PA : W.B. Saunders
Original Publication: Baltimore.
مواضيع طبية MeSH: Celiac Disease*/pathology, Adult ; Humans ; Child ; Neoplasm Recurrence, Local ; Randomized Controlled Trials as Topic ; Glutens/adverse effects ; Diet, Gluten-Free
مستخلص: Background & Aims: There is a need to develop safe and effective pharmacologic options for the treatment of celiac disease (CeD); however, consensus on the appropriate design and configuration of randomized controlled trials (RCTs) in this population is lacking.
Methods: A 2-round modified Research and Development/University of California Los Angeles Appropriateness Method study was conducted. Eighteen gastroenterologists (adult and pediatric) and gastrointestinal pathologists voted on statements pertaining to the configuration of CeD RCTs, inclusion and exclusion criteria, gluten challenge, and trial outcomes. Two RCT designs were considered, representing the following distinct clinical scenarios for which pharmacotherapy may be used: trials incorporating a gluten challenge to simulate exposure; and trials evaluating reversal of histologic changes, despite attempted adherence to a gluten-free diet. Each statement was rated as appropriate, uncertain, or inappropriate, using a 9-point Likert scale.
Results: For trials evaluating prevention of relapse after gluten challenge, participants adherent to a gluten-free diet for 12 months or more with normal or near-normal-sized villi should be enrolled. Gluten challenge should be FODMAPS (fermentable oligosaccharides, disaccharides, monosaccharides, and polyols) free, and efficacy evaluated using histology with a secondary patient-reported outcome measure. For trials evaluating reversal of villus atrophy, the panel voted it appropriate to enroll participants with a baseline villus height to crypt depth ratio ≤2 and measure efficacy using a primary histologic end point. Guidance for measuring histologic, endoscopic, and patient-reported outcomes in adult and pediatric patients with CeD are provided, along with recommendations regarding the merits and limitations of different end points.
Conclusions: We developed standardized recommendations for clinical trial design, eligibility criteria, outcome measures, gluten challenge, and disease evaluations for RCTs in patients with CeD.
(Copyright © 2024 AGA Institute. Published by Elsevier Inc. All rights reserved.)
التعليقات: Comment in: Gastroenterology. 2024 May;166(5):941-942. doi: 10.1053/j.gastro.2024.01.015. (PMID: 38242236)
معلومات مُعتمدة: K23 DK119584 United States DK NIDDK NIH HHS
فهرسة مساهمة: Keywords: Celiac; Gluten; Histology; Patient-Reported Outcomes
المشرفين على المادة: 8002-80-0 (Glutens)
تواريخ الأحداث: Date Created: 20230913 Date Completed: 20231225 Latest Revision: 20240603
رمز التحديث: 20240604
DOI: 10.1053/j.gastro.2023.08.051
PMID: 37704112
قاعدة البيانات: MEDLINE
الوصف
تدمد:1528-0012
DOI:10.1053/j.gastro.2023.08.051