Polygenic scores for schizophrenia and major depression are associated with psychosocial risk factors in children: evidence of gene-environment correlation

被引:5
作者
Machlitt-Northen, Sandra [1 ]
Keers, Robert [1 ]
Munroe, Patricia B. [2 ]
Howard, David M. [3 ,4 ]
Trubetskoy, Vassily [5 ]
Pluess, Michael [1 ]
机构
[1] Queen Mary Univ London, Dept Biol & Expt Psychol, Mile End Rd, London E1 4NS, England
[2] Queen Mary Univ London, William Harvey Res Inst, Dept Clin Pharmacol, London, England
[3] Kings Coll London, Social Genet & Dev Psychiat Ctr, London, England
[4] Univ Edinburgh, Royal Edinburgh Hosp, Div Psychiat, Edinburgh, Midlothian, Scotland
[5] Univ Med Berlin, Dept Psychiat & Psychotherapy, Campus Charite Mitte, Berlin, Germany
基金
英国惠康基金; 英国经济与社会研究理事会; 英国医学研究理事会;
关键词
Environment; schizophrenia; major depressive disorder; genetics; GENOME-WIDE ASSOCIATION; POPULATION-BASED TWIN; BIRTH; PREGNANCY; COHORT; EPIDEMIOLOGY; METAANALYSIS; INEQUALITY; DISORDER; TRAIT;
D O I
10.1111/jcpp.13657
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Background Whilst genetic and environmental risk factors for schizophrenia (SCZ) and major depressive disorder (MDD) have been established, it is unclear whether exposure to environmental risk factors is genetically confounded by passive, evocative or active gene-environment correlation (rGE). Study Objective This study aims to investigate: (a) whether the genetic risk for SCZ/MDD in children is correlated with established environmental and psychosocial risk factors in two British community samples, the 1958 National Child Development Study (NCDS) and the Millennium Cohort Study (MCS), (b) whether these associations vary between both psychopathologies, and (c) whether findings differ across the two cohorts which were born 42 years apart. Methods Polygenic risk scores (PRS) from existing large genome-wide associations studies (GWAS) were applied to test the correlation between the child genetic risk for SCZ/MDD and known environmental risk factors. In addition, parental and child genetic data from MCS were used to distinguish between passive and evocative rGE. Results The child polygenic risk for SCZ and MDD was correlated with single parenthood in MCS. Moreover, the lack of father's involvement in child care was associated with the genetic risk for SCZ in NCDS. However, we also found associations between several indicators of low socioeconomic status and heightened genetic risk for MDD in children in both cohorts. Further, the genetic risk for MDD was associated with parental lack of interest in the child's education in NCDS as well as more maternal smoking and less maternal alcohol consumption during childhood in MCS. According to sensitivity analyses in MCS (controlling for parental genotype), more than half of our significant correlations reflected passive rGE. Conclusions Findings suggest that several established environmental and psychosocial risk factors for SCZ and MDD are at least partially associated with children's genetic risk for these psychiatric disorders.
引用
收藏
页码:1140 / 1152
页数:13
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