Bidirectional associations and a causal mediation analysis between depressive symptoms and chronic digestive diseases: A longitudinal investigation

调解 危险系数 临床心理学 萧条(经济学) 抑郁症状 流行病学研究中心抑郁量表 纵向研究 重性抑郁障碍 入射(几何) 比例危险模型 医学 精神科 内科学 焦虑 置信区间 病理 扁桃形结构 光学 物理 宏观经济学 经济 法学 政治学
作者
Jiali Zheng,Jingmeng Li,Tianduo Pei,Tianren Zhu,Xiaoguang Li,Hui Wang
出处
期刊:Journal of Affective Disorders [Elsevier BV]
卷期号:333: 278-289 被引量:3
标识
DOI:10.1016/j.jad.2023.04.025
摘要

Chronic digestive diseases (CDDs) and depression shared major pathogeneses. We aimed to prospectively examine the bidirectional incidence associations between depressive symptoms and CDDs and explore biologically and behaviorally relevant mediators in the bidirectional associations. Multivariable-adjusted Cox proportional hazard models were used to examine baseline depressive symptoms in relation to incident CDDs among 10,974 adults and the relation of baseline CDDs with new-onset elevated depressive symptoms among 7489 participants in the China Health and Retirement Longitudinal Study of nationally representative middle-aged and older adults. Elevated depressive symptoms were defined as the 10-item Center for Epidemiologic Studies Depression scale (CES-D-10) score at or higher than 10 and CDDs (except for tumor and cancer) were determined by self-reported physician diagnoses. Causal mediation analysis was performed to assess the mediated effects of a priori selected blood biomarkers and lifestyle factors in the bidirectional associations. Prevalence of elevated depressive symptoms and nonmalignant CDDs at baseline was 33.05 % and 17.8 % respectively. During a mean of 5.47 years of follow-up, elevated depressive symptoms significantly increased hazard of CDDs by 1.66 folds (95%CI = 1.49–1.84). Having CDDs at baseline was associated with a 27 % (95%CI = 16 %–39 %) increased hazard of developing elevated depressive symptoms. Shorter sleeping duration at night nominally significantly mediated 8.76 % of the association between depressive symptoms and incident CDDs while no significant mediators were identified in the converse association. Limited mediator information and inadequately long follow-up may reduce chance of identifying significant mediators. Depressive symptoms and CDDs were mutual independent risk factors. Early screening and management of depressive symptoms and sleep disturbance are suggested in the prevention of CDDs and related comorbidities.
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