%0 Journal Article
%T Metabolic health and genetic predisposition in inflammatory bowel disease: Insights from a prospective cohort study.
%A Mi N
%A He Q
%A Liu Y
%A Li Y
%A Li Y
%A Wu Y
%A Yang M
%A Zhao Y
%A Xie P
%A Li W
%A Wu S
%A Li Z
%A Wang D
%A Qin X
%A Yuan J
%A Lei P
%A Qi J
%A Xia B
%J Eur J Intern Med
%V 0
%N 0
%D 2024 Jul 2
%M 38955589
%F 7.749
%R 10.1016/j.ejim.2024.06.020
%X BACKGROUND: Metabolic disorders exhibit strong inflammatory underpinnings and vice versa. This study aimed to investigate the association between metabolic health status, genetic predisposition, and the risk of inflammatory bowel disease (IBD), and to explore the potential benefits of maintaining ideal metabolic status for individuals with a predetermined genetic risk of IBD.
METHODS: This population-based prospective study included 385,820 unrelated European descent participants from the UK Biobank. Using multivariable Cox regression, we assessed the relationship of metabolic phenotypes with risk of IBD and its subtypes. We also developed a polygenic risk score to examine how metabolic health status interacted with genetic risk in relation to IBD risk.
RESULTS: During the follow-up period of 4,328,895 person-years, 2,044 newly-diagnosed IBD cases were identified. Higher genetic risk and an increasing number of abnormal metabolic phenotypes were associated with elevated IBD risk (p-trend <0.001). Individuals with high genetic risk and poor metabolic health had a significantly higher risk of IBD (HR=4.56, 95 % CI=3.27-6.36) compared to those with low genetic risk and ideal metabolic health. These results remained consistent for IBD subtypes. Maintaining ideal metabolic status reduced IBD risk within each genetic risk category and jointly decreased subsequent risk by 40 % in high genetic risk individuals.
CONCLUSIONS: Our study reveals a combined impact of poor metabolic health and genetic risk on IBD incidence. Those with low genetic risk and optimal metabolic health exhibit the lowest IBD risk, offering insights into potential management strategies for individuals at predefined genetic risk.