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Personalized Research on Diet in Ulcerative Colitis and Crohn's Disease: A Series of N-of-1 Diet Trials.
Kaplan, Heather C; Opipari-Arrigan, Lisa; Yang, Jiabei; Schmid, Christopher H; Schuler, Christine L; Saeed, Shehzad A; Braly, Kimberly L; Chang, Fandi; Murphy, Lauren; Dodds, Cassandra M; Nuding, Mason; Liu, Hao; Pilley, Sheri; Stone, Julie; Woodward, Gisele; Yokois, Nancy; Goyal, Alka; Lee, Dale; Yeh, Ann Ming; Lee, Peter; Gold, Benjamin D; Molle-Rios, Zarela; Zwiener, R Jeff; Ali, Sabina; Chavannes, Mallory; Linville, Tiffany; Patel, Ashish; Ayers, Travis; Bassett, Mikelle; Boyle, Brendan; Palomo, Pablo; Verstraete, Sofia; Dorsey, Jill; Kaplan, Jess L; Steiner, Steven J; Nguyen, Kaylie; Burgis, Jennifer; Suskind, David L.
Affiliation
  • Kaplan HC; Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Opipari-Arrigan L; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Yang J; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Schmid CH; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Schuler CL; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Saeed SA; Division of Behavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Braly KL; Department of Biostatistics and Center for Evidence Synthesis in Health, School of Public Health, Brown University, Providence, Rhode Island, USA.
  • Chang F; Department of Biostatistics and Center for Evidence Synthesis in Health, School of Public Health, Brown University, Providence, Rhode Island, USA.
  • Murphy L; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Dodds CM; Division of Hospital Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Nuding M; Department of Medical Affairs, Dayton Children's Hospital and Boonshoft School of Medicine, Wright State University, Dayton, Ohio, USA.
  • Liu H; Division of Gastroenterology and Hepatology, Seattle Children's Hospital, Seattle, Washington, USA.
  • Pilley S; Department of Biostatistics and Center for Evidence Synthesis in Health, School of Public Health, Brown University, Providence, Rhode Island, USA.
  • Stone J; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Woodward G; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Yokois N; Center for Clinical and Translational Research, Seattle Children's Research Institute, Division of Gastroenterology, Seattle Children's Hospital, Seattle, Washington, USA.
  • Goyal A; Division of Applied Mathematics, Brown University, Providence, Rhode Island, USA.
  • Lee D; Parent Working Group, ImproveCareNow Pediatric IBD Learning Health System.
  • Yeh AM; MUSC Health Shawn Jenkins Children's Hospital, Charleston, South Carolina, USA.
  • Lee P; Parent Working Group, ImproveCareNow Pediatric IBD Learning Health System.
  • Gold BD; The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Molle-Rios Z; Parent Working Group, ImproveCareNow Pediatric IBD Learning Health System.
  • Zwiener RJ; Division of Gastroenterology, GI Care for Kids, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Ali S; Childrens Hospital of the King's Daughters, Division of Pediatric Gastroenterology, Norfolk, Virginia, USA.
  • Chavannes M; Division of Gastroenterology, Hepatology, and Nutrition, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Linville T; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Stanford University, Palo Alto, California, USA.
  • Patel A; Division of Gastroenterology and Hepatology, Seattle Children's Hospital, Seattle, Washington, USA.
  • Ayers T; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Stanford University, Palo Alto, California, USA.
  • Bassett M; Division of Pediatric Gastroenterology, Pediatric Specialists of Virginia, Fairfax, Virginia, USA.
  • Boyle B; Division of Gastroenterology, GI Care for Kids, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Palomo P; Division of Pediatric Gastroenterology, Nemours Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
  • Verstraete S; Dell Children's Medical Group, Pediatric Gastroenterology, Dell Children's Medical Center of Central Texas, Austin, Texas, USA.
  • Dorsey J; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, UCSF Benioff Children's Hospital, Oakland, California, USA.
  • Kaplan JL; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital Los Angeles, Los Angeles, California, USA.
  • Steiner SJ; Department of Pediatrics, University of Southern California, Los Angeles, California, USA.
  • Nguyen K; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Levine Children's Hospital, Charlotte, North Carolina, USA.
  • Burgis J; Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Suskind DL; Pediatric Gastroenterology, Phoenix Children's Hospital, Phoenix, Arizona, USA.
Am J Gastroenterol ; 117(6): 902-917, 2022 06 01.
Article in En | MEDLINE | ID: mdl-35442220
INTRODUCTION: Evidence about specific carbohydrate diet (SCD) for inflammatory bowel disease (IBD) is limited. We conducted 54 single-subject, double-crossover N-of-1 trials comparing SCD with a modified SCD (MSCD) and comparing each with the participant's baseline, usual diet (UD). METHODS: Across 19 sites, we recruited patients aged 7-18 years with IBD and active inflammation. Following a 2-week baseline (UD), patients were randomized to 1 of 2 sequences of 4 alternating 8-week SCD and MSCD periods. Outcomes included fecal calprotectin and patient-reported symptoms. We report posterior probabilities from Bayesian models comparing diets. RESULTS: Twenty-one (39%) participants completed the trial, 9 (17%) completed a single crossover, and 24 (44%) withdrew. Withdrawal or early completion occurred commonly (lack of response [n = 11], adverse events [n = 11], and not desiring to continue [n = 6]). SCD and MSCD performed similarly for most individuals. On average, there was <1% probability of a clinically meaningful difference in IBD symptoms between SCD and MSCD. The average treatment difference was -0.3 (95% credible interval -1.2, 0.75). There was no significant difference in the ratio of fecal calprotectin geometric means comparing SCD and MSCD (0.77, 95% credible interval 0.51, 1.10). Some individuals had improvement in symptoms and fecal calprotectin compared with their UD, whereas others did not. DISCUSSION: SCD and MSCD did not consistently improve symptoms or inflammation, although some individuals may have benefited. However, there are inherent difficulties in examining dietary changes that complicate study design and ultimately conclusions regarding effectiveness.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Colitis, Ulcerative / Crohn Disease / Leukocyte L1 Antigen Complex Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Child / Humans Language: En Journal: Am J Gastroenterol Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Colitis, Ulcerative / Crohn Disease / Leukocyte L1 Antigen Complex Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Child / Humans Language: En Journal: Am J Gastroenterol Year: 2022 Type: Article Affiliation country: United States