Intimate Relationships and Depression: Searching for Causation in the Sea of Association.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2021-05-07 Epub Date: 2021-02-10 DOI:10.1146/annurev-clinpsy-081219-103323
Mark A Whisman, David A Sbarra, Steven R H Beach
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引用次数: 34

Abstract

This article provides a critical review of existing research on intimate (marriage or marriage-like) relationship distress and risk for depression. Using the meta-framework of research triangulation, we seek to synthesize research evidence across several different methodologies and study designs and to draw the most reliable conclusion regarding a potential causal association between relationship distress and depression. Focusing on existing correlational (i.e., observational), genetically informed, and intervention (i.e., experimental) research on the association between relationship distress and depression, we conclude that the existing body of research evidence supports the claim that relationship distress is a causal risk factor for depression. A secondary aim of the article is to highlight a variety of effective methods that, when viewed from the perspective of triangulation, enhance the pursuit of causal inference, including propensity score matching, target trial emulation, directed acyclic graph approach, and Mendelian randomization.

亲密关系与抑郁:在交往的海洋中寻找因果关系。
这篇文章对现有的关于亲密关系(婚姻或类似婚姻)的困扰和抑郁风险的研究进行了批判性的回顾。使用研究三角测量的元框架,我们试图综合几种不同方法和研究设计的研究证据,并就关系痛苦和抑郁之间的潜在因果关系得出最可靠的结论。通过对关系困扰与抑郁之间关系的相关研究(即观察性研究)、遗传信息研究和干预研究(即实验性研究),我们得出结论,现有的研究证据支持关系困扰是抑郁的因果风险因素这一说法。本文的第二个目的是强调从三角测量的角度来看,增强对因果推理的追求的各种有效方法,包括倾向得分匹配,目标试验模拟,有向无环图方法和孟德尔随机化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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