University of Rochester Mt. Hope Family Center.
Dev Psychopathol. 2017 Dec;29(5):1807-1821. doi: 10.1017/S0954579417001419.
The present study tested the role of FKBP5 binding protein 5 (FKBP5) genetic variation in an internalizing pathway from child maltreatment to emerging adult problem drinking among a sample of African American youth (N = 280) followed prospectively from ages 11 to 20. Specifically, whether childhood internalizing symptoms and emerging adult tension reduction alcohol expectancies sequentially mediate the effect of child maltreatment on emerging adult problem drinking and whether FKBP5 moderates these associations were investigated. The results indicate that individuals with at least one copy of the FKBP5 CATT haplotype (minor alleles) are more vulnerable to traversing the hypothesized internalizing pathway of risk than individuals without this genotypic profile. Taken together our findings highlight the importance of FKBP5 genetic variation in the context of early adversity; support the role of two prospective sequential mediators of an internalizing pathway to problematic drinking, namely, childhood internalizing symptoms and emerging adult tension reduction alcohol expectancies; and identify a subgroup of maltreated children most susceptible to progressing along this less common pathway of risk.
本研究测试了 FKBP5 结合蛋白 5(FKBP5)遗传变异在一个内化途径中的作用,该途径将儿童期虐待与一个前瞻性的非裔美国青年样本(N=280)从 11 岁到 20 岁的成年初期问题饮酒联系起来。具体来说,儿童期内化症状和成年初期的紧张缓解酒精期望是否依次介导儿童期虐待对成年初期问题饮酒的影响,以及 FKBP5 是否调节这些关联。结果表明,至少有一个 FKBP5 CATT 单倍型(次要等位基因)拷贝的个体比没有这种基因型特征的个体更容易经历假设的风险内化途径。总的来说,我们的研究结果强调了 FKBP5 遗传变异在早期逆境中的重要性;支持内化途径向问题饮酒的两个前瞻性连续中介的作用,即儿童期内化症状和成年初期紧张缓解酒精期望;并确定了一组最容易沿着这条不太常见的风险途径发展的受虐待儿童。