Psychological Resilience and Mental Wellbeing Mitigate the Risk of Irritable Bowel Syndrome

医学 心理健康 临床心理学 肠易激综合征 孟德尔随机化 精神科 神经质 应对(心理学) 前瞻性队列研究 危险系数 心理弹性 调解 精神病理学 心理干预 队列 共病 队列研究 处于危险心理状态 混淆 人格 焦虑 萧条(经济学) 置信区间 疾病
作者
M. Zhang,Judith Wellens,Jianhui Zhao,Haosen Ji,Jing Sun,Xinxuan Li,Rahul Kalla,Yuan Chun Ding,Evropi Τheodoratou,Jack Satsangi,Xue Li
出处
期刊:The American Journal of Gastroenterology [American College of Gastroenterology]
标识
DOI:10.14309/ajg.0000000000003833
摘要

INTRODUCTION: Comorbidities between mental disorders and irritable bowel syndrome (IBS) have been widely reported, yet associations between mental wellbeing and IBS, particularly regarding underlying genetic modification and proteomic signatures, remain underexplored. METHODS: This prospective cohort study analyzed 75,842 IBS-free participants aiming to investigate the prospective association between mental wellbeing and the risk of IBS in UK Biobank. Mental wellbeing was assessed through life satisfaction, positive affect, neuroticism, and depressive/anxiety symptoms. Cox models evaluate the hazard ratio (HR) for mental wellbeing and plasma proteome in relation to incident IBS during follow-up. Proteomic profiling identified mental wellbeing-associated proteins, with pathway enrichment analysis revealing biological mechanisms. Mediation and Mendelian randomization analyses further examine intermediate pathways and causality. RESULTS: With a 12.4-year follow-up period, 1,400 cases of incident IBS were documented. Better mental wellbeing mitigated IBS risk dose-dependently (low risk group: HR, 0.37; 95% confidence interval [CI]: 0.31–0.43). Higher life satisfaction (HR, 0.41; 95% CI: 0.30–0.56) and positive affect (HR, 0.50; 95% CI: 0.41–0.62) were inversely associated with IBS risk, whereas neuroticism (HR, 2.35; 95% CI: 1.92–2.88) and depressive/anxiety symptoms (HR, 3.09; 95% CI: 2.17–4.42) increased the risk. Findings remained consistent in across prevalent IBS and IBS subtypes. Mental wellbeing effects were independent of genetic predisposition. Mediation analyses revealed about 27% of protective effect of mental wellbeing were mediated through reduced depression and anxiety. Mendelian randomization supports causal protective effects of positive mental wellbeing on IBS. Proteomic profiling identified mental wellbeing-associated proteins mainly enriched in cytokine-cytokine receptor interactions. Chromogranin A and gastrin emerged as key protein biomarkers, showing significant associations with both mental wellbeing components and IBS risk. DISCUSSION: Our study demonstrates that enhanced mental wellbeing confers substantial protection against IBS development, highlighting psychological interventions as potential primary prevention strategies.
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