Translational Psychiatry Research Group and Department of Clinical Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.
Department of Hygiene and Epidemiology, University of Ioannina Medical School, Ioannina, Greece; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
J Psychiatr Res. 2018 Aug;103:189-207. doi: 10.1016/j.jpsychires.2018.05.020. Epub 2018 May 25.
The development of depression may involve a complex interplay of environmental and genetic risk factors. PubMed and PsycInfo databases were searched from inception through August 3, 2017, to identify meta-analyses and Mendelian randomization (MR) studies of environmental risk factors associated with depression. For each eligible meta-analysis, we estimated the summary effect size and its 95% confidence interval (CI) by random-effects modeling, the 95% prediction interval, heterogeneity with I, and evidence of small-study effects and excess significance bias. Seventy meta-analytic reviews met the eligibility criteria and provided 134 meta-analyses for associations from 1283 primary studies. While 109 associations were nominally significant (P < 0.05), only 8 met the criteria for convincing evidence and, when limited to prospective studies, convincing evidence was found in 6 (widowhood, physical abuse during childhood, obesity, having 4-5 metabolic risk factors, sexual dysfunction, job strain). In studies in which depression was assessed through a structured diagnostic interview, only associations with widowhood, job strain, and being a Gulf War veteran were supported by convincing evidence. Additionally, 8 MR studies were included and provided no consistent evidence for the causal effects of obesity, smoking, and alcohol consumption. The proportion of variance explained by genetic risk factors was extremely small (0.1-0.4%), which limited the evidence provided by the MR studies. Our findings suggest that despite the large number of putative risk factors investigated in the literature, few associations were supported by robust evidence. The current findings may have clinical and research implications for the early identification of individuals at risk for depression.
抑郁症的发展可能涉及环境和遗传风险因素的复杂相互作用。我们从 2017 年 8 月 3 日开始在 PubMed 和 PsycInfo 数据库中进行检索,以确定与抑郁症相关的环境风险因素的荟萃分析和孟德尔随机化 (MR) 研究。对于每个合格的荟萃分析,我们通过随机效应模型估计汇总效应大小及其 95%置信区间 (CI)、95%预测区间、I 型异质性和小样本效应及过度显著性偏差的证据。70 项荟萃分析综述符合入选标准,并提供了 134 项来自 1283 项主要研究的荟萃分析。虽然 109 项关联具有名义显著性 (P<0.05),但只有 8 项符合令人信服的证据标准,并且当仅限于前瞻性研究时,仅在 6 项研究中发现了令人信服的证据 (鳏寡、儿童期身体虐待、肥胖、有 4-5 个代谢风险因素、性功能障碍、工作压力)。在使用结构化诊断访谈评估抑郁症的研究中,只有与鳏寡、工作压力和海湾战争老兵身份相关的关联得到了令人信服的证据支持。此外,还纳入了 8 项 MR 研究,但没有提供肥胖、吸烟和饮酒与因果关系的一致证据。遗传风险因素解释的方差比例极小 (0.1-0.4%),这限制了 MR 研究提供的证据。我们的研究结果表明,尽管文献中研究了大量潜在的风险因素,但很少有关联得到了可靠证据的支持。目前的研究结果可能对个体抑郁症风险的早期识别具有临床和研究意义。