Department of Clinical Foundations, Pharmacology Unit, University of Barcelona, Barcelona, Spain.
Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Spain.
Schizophr Bull. 2020 Jul 8;46(4):1019-1025. doi: 10.1093/schbul/sbaa012.
Gene-environment (GxE) interactions have been related to psychosis spectrum disorders, involving multiple common genetic variants in multiple genes with very small effect sizes, and several environmental factors that constitute a dense network of exposures named the exposome. Here, we aimed to analyze GxE in a cohort of 310 first-episode psychotic (FEP) and 236 healthy controls, by using aggregate scores estimated in large populations such as the polygenic risk score for schizophrenia and (PRS-SCZ) and the Maudsley environmental risk score (ERS). In contrast to previous findings, in our study, the PRS-SCZ did not discriminate cases from controls, but the ERS score explained a similar percentage of the variance as in other studies using similar approaches. Our study supports a positive additive interaction, indicating synergy between genetic susceptibility to schizophrenia (PRS-SCZ dichotomized according to the highest quartile distribution of the control population) and the exposome (ERS > 75% of the controls). This additive interaction showed genetic and environmental dose dependence. Our study shows that the use of aggregate scores derived from large and powered studies instead of statistics derived from specific sample characteristics is a powerful tool for the study of the effects of GxE on the risk of psychotic spectrum disorders. In conclusion, by using a genetic risk score and an ERS we have provided further evidence for the role of GxE in psychosis.
基因-环境(GxE)相互作用与精神分裂症谱系障碍有关,涉及多个基因中的多个常见遗传变异,其效应大小非常小,以及构成暴露组学的密集网络的几个环境因素。在这里,我们旨在通过使用聚合分数分析 310 名首发精神病(FEP)和 236 名健康对照者中的 GxE,这些聚合分数是在大人群中估计的,例如精神分裂症的多基因风险评分(PRS-SCZ)和莫兹利环境风险评分(ERS)。与之前的发现相反,在我们的研究中,PRS-SCZ 不能区分病例和对照,但 ERS 评分解释了与使用类似方法的其他研究相似的方差百分比。我们的研究支持积极的加性相互作用,表明精神分裂症遗传易感性(PRS-SCZ 根据对照人群的最高四分位数分布进行二分法)和暴露组学(ERS > 对照组的 75%)之间存在协同作用。这种加性相互作用显示出遗传和环境剂量依赖性。我们的研究表明,使用来自大型和强大研究的聚合分数而不是来自特定样本特征的统计数据是研究 GxE 对精神分裂症谱系障碍风险影响的有力工具。总之,通过使用遗传风险评分和 ERS,我们提供了进一步的证据证明 GxE 在精神病中的作用。