MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
Schizophr Bull. 2022 Sep 1;48(5):967-980. doi: 10.1093/schbul/sbac049.
Schizophrenia has been robustly associated with multiple genetic and environmental risk factors. Childhood adversity is one of the most widely replicated environmental risk factors for schizophrenia, but it is unclear if schizophrenia genetic risk alleles contribute to this association.
In this systematic review and meta-analysis, we assessed the evidence for gene-environment correlation (genes influence likelihood of environmental exposure) between schizophrenia polygenic risk score (PRS) and reported childhood adversity. We also assessed the evidence for a gene-environment interaction (genes influence sensitivity to environmental exposure) in relation to the outcome of schizophrenia and/or psychosis. This study was registered on PROSPERO (CRD42020182812). Following PRISMA guidelines, a search for relevant literature was conducted using Cochrane, MEDLINE, PsycINFO, Web of Science, and Scopus databases until February 2022. All studies that examined the association between schizophrenia PRS and childhood adversity were included.
Seventeen of 650 identified studies met the inclusion criteria and were assessed against the Newcastle-Ottawa Scale for quality. The meta-analysis found evidence for gene-environment correlation between schizophrenia PRS and childhood adversity (r = .02; 95% CI = 0.01, 0.03; P = .001), but the effect was small and therefore likely to explain only a small proportion of the association between childhood adversity and psychosis. The 4 studies that investigated a gene-environment interaction between schizophrenia PRS and childhood adversity in increasing risk of psychosis reported inconsistent results.
These findings suggest that a gene-environment correlation could explain a small proportion of the relationship between reported childhood adversity and psychosis.
精神分裂症与多种遗传和环境风险因素密切相关。童年逆境是精神分裂症最广泛复制的环境风险因素之一,但目前尚不清楚精神分裂症遗传风险等位基因是否对此关联有影响。
在这项系统综述和荟萃分析中,我们评估了精神分裂症多基因风险评分(PRS)与报告的童年逆境之间的基因-环境相关性(基因影响环境暴露的可能性)的证据。我们还评估了与精神分裂症和/或精神病结局相关的基因-环境相互作用(基因影响对环境暴露的敏感性)的证据。这项研究已在 PROSPERO(CRD42020182812)上注册。根据 PRISMA 指南,使用 Cochrane、MEDLINE、PsycINFO、Web of Science 和 Scopus 数据库进行了相关文献检索,检索时间截至 2022 年 2 月。所有纳入的研究均检查了精神分裂症 PRS 与童年逆境之间的关联。
在 650 项确定的研究中,有 17 项符合纳入标准,并根据纽卡斯尔-渥太华量表进行了质量评估。荟萃分析发现精神分裂症 PRS 与童年逆境之间存在基因-环境相关性(r =.02;95%CI = 0.01,0.03;P =.001),但效应较小,因此可能仅能解释童年逆境与精神病之间关联的一小部分。有 4 项研究调查了精神分裂症 PRS 与童年逆境之间的基因-环境相互作用在增加精神病风险方面的作用,结果不一致。
这些发现表明,基因-环境相关性可能可以解释报告的童年逆境与精神病之间关系的一小部分。