Social stress and the oxytocin receptor gene interact to predict antisocial behavior in an at-risk cohort

被引:34
|
作者
Smearman, Erica L. [1 ,2 ]
Winiarski, D. Anne [3 ]
Brennan, Patricia A. [3 ]
Najman, Jake [4 ]
Johnson, Katrina C. [2 ]
机构
[1] Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[3] Emory Univ, Atlanta, GA 30322 USA
[4] Univ Queensland, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
LIFE-COURSE-PERSISTENT; CONDUCT PROBLEMS; MISSING HERITABILITY; FOLLOW-UP; DEPRESSION; CHILDREN; OXTR; HUMANS; ADOLESCENCE; POLYMORPHISM;
D O I
10.1017/S0954579414000649
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Polymorphisms in the oxytocin receptor gene are commonly associated with prosocial behaviors in the extant literature, yet their role in antisocial behaviors has rarely been explored, particularly during the transition from adolescence to early adulthood. We examined a prospective cohort (N = 404), collecting youth, mother, and clinician reports of conduct-disordered and antisocial behavior at ages 15 and 20. The oxytocin receptor gene rs53576 polymorphism was hypothesized to interact with social stress to predict antisocial outcomes. Structural equation modeling results revealed a significant main effect at age 15 (p = .025); those with the G allele exhibited higher levels of conduct problems. Structural equation modeling revealed a significant Gene x Environment interaction at age 20 (p = .029); those with the G allele who experienced high social stress exhibited higher levels of antisocial behavior. Heterozygous (AG) grouping models were compared, and parameter estimations supported G dominant groupings. These novel findings suggest that rs53576 polymorphisms may influence social salience and contribute to risk for antisocial outcomes, particularly under conditions of high social stress.
引用
收藏
页码:309 / 318
页数:10
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