Association of Waist Circumference with the Risk of Inflammatory Bowel Disease: a Nationwide Cohort Study of 10 Million Individuals in Korea

医学 腰围 危险系数 炎症性肠病 体质指数 队列 内科学 腹部肥胖 肥胖 入射(几何) 溃疡性结肠炎 人口 队列研究 代谢综合征 置信区间 腰高比 疾病 环境卫生 物理 光学
作者
Yeonjin Je,Kyung Do Han,Jaeyoung Chun,Yuna Kim,Joo Hang Kim,Young Hoon Youn,Hyojin Park,Jong Pil Im,Sang Woo Kim
出处
期刊:Journal of Crohn's and Colitis [Oxford University Press]
卷期号:17 (5): 681-692 被引量:2
标识
DOI:10.1093/ecco-jcc/jjac193
摘要

Abstract Background and Aims Metabolic syndrome may share the pathophysiology of adipose tissue dysregulation and inadequate immune response with inflammatory bowel disease [IBD]. We determined the association of abdominal obesity [AO] with the risk of developing IBD. Methods We conducted a nationwide population-based cohort study using the Korean National Health Insurance Services database. A total of 10 082 568 participants of the 2009 national health screening programme were enrolled. Newly diagnosed Crohn’s disease [CD] and ulcerative colitis [UC] were identified using the International Classification of Diseases 10th Revision and specialized national codes for rare intractable diseases. Waist circumference [WC] was classified into six groups and compared with the reference values of 85.0–89.9 cm for men and 80.0–84.9 cm for women. AO was defined as a WC of ≥90 cm for men and ≥85 cm for women. Results During a median follow-up of 9.3 years, the incidence rates of CD and UC were 2.11 and 8.40 per 100 000 person-years, respectively. After adjustment for age, sex, lifestyle behaviours, income and body mass index [BMI], the increase in baseline WC was significantly associated with the risk of developing CD, but not UC, compared to the references. The risk of developing CD in subjects with AO increased significantly compared to those without AO [adjusted hazard ratio, 1.40; 95% confidence interval, 1.21–1.61], regardless of obesity based on BMI. Conclusions Individuals with AO bore an increased risk of developing CD proportional to WC, but not UC, suggesting that visceral adiposity is related to the pathophysiology of CD.

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