Childhood quality influences genetic sensitivity to environmental influences across adulthood: A life-course Gene × Environment interaction study

心理学 精神病理学 基因-环境相互作用 发展心理学 年轻人 苦恼 环境富集 母体敏感性 情感(语言学) 幼儿 社会环境 临床心理学 基因 遗传学 生物 神经科学 沟通 政治学 基因型 法学
作者
Robert Keers,Michael Pluess
出处
期刊:Development and Psychopathology [Cambridge University Press]
卷期号:29 (5): 1921-1933 被引量:46
标识
DOI:10.1017/s0954579417001493
摘要

Abstract While environmental adversity has been shown to increase risk for psychopathology, individuals differ in their sensitivity to these effects. Both genes and childhood experiences are thought to influence sensitivity to the environment, and these factors may operate synergistically such that the effects of childhood experiences on later sensitivity are greater in individuals who are more genetically sensitive. In line with this hypothesis, several recent studies have reported a significant three-way interaction (Gene × Environment × Environment) between two candidate genes and childhood and adult environment on adult psychopathology. We aimed to replicate and extend these findings in a large, prospective multiwave longitudinal study using a polygenic score of environmental sensitivity and objectively measured childhood and adult material environmental quality. We found evidence for both Environment × Environment and Gene × Environment × Environment effects on psychological distress. Children with a poor-quality material environment were more sensitive to the negative effects of a poor environment as adults, reporting significantly higher psychological distress scores. These effects were further moderated by a polygenic score of environmental sensitivity. Genetically sensitive children were more vulnerable to adversity as adults, if they had experienced a poor childhood environment but were significantly less vulnerable if their childhood environment was positive. These findings are in line with the differential susceptibility hypothesis and suggest that a life course approach is necessary to elucidate the role of Gene × Environment in the development of mental illnesses.
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