Inflammatory Potential of the Diet and Risk of Crohn's Disease and Ulcerative Colitis

医学 溃疡性结肠炎 克罗恩病 胃肠病学 疾病 炎症性肠病 克罗恩病 结肠炎 内科学 炎症性肠病
作者
Antoine Meyer,Simon S. M. Chan,Mathilde Touvier,Chantal Julia,Anne Tjønneland,Cecilie Kyrø,Christina C. Dahm,Verena Katzke,Matthias B. Schulze,­Rosario ­Tumino,Carlotta Sacerdote,Giovanna Masala,Bas Oldenburg,Marcela Guevara,Luis Bujanda,Nelly Castro,Tammy Y. N. Tong,Alicia K. Heath,Mélanie Deschasaux,Serge Herçberg,Pilar Galán,Yahya Mahamat‐Saleh,Gianluca Severi,Franck Carbonnel,Aurélien Amiot
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
标识
DOI:10.1111/apt.18497
摘要

Association between dietary factors and the risk of developing inflammatory bowel disease (IBD) has been studied extensively. However, identification of deleterious dietary patterns merits further study. To investigate the risk of developing Crohn's disease (CD) and ulcerative colitis (UC) according to the inflammatory score of the diet (ISD) in the multinational European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. We used validated food frequency questionnaires collected at baseline to compute ISD scores. We estimated the association between ISD score and risks of CD and UC risks using Cox models stratified by centre, sex and age. We adjusted for smoking status, BMI, physical activity, energy intake, educational level and alcohol intake. We included 394,255 individuals including 184 incident cases of CD and 459 of UC after median follow-up of 13.6 years (4,889,910 person-years). High ISD scores were associated with a higher risk of CD (fourth vs. first quartile-adjusted HR: 1.88, 95% CI: 1.14-3.10; p-trend < 0.01) but not of UC (adjusted HR: 0.85, 95% CI: 0.63-1.15; p-trend 0.21). For CD, this association was mainly observed for women (adjusted HR: 2.14, 95% CI: 1.17-3.91; p-trend < 0.01). On subgroup analyses, those differences were mainly driven by low intakes of fibre, mono-unsaturated fatty acids, vitamin C, magnesium, onion and alcohol. A high ISD score is associated with a higher risk of developing CD but not UC. These results should be taken into account in high-risk populations.
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