Derringer Jaime, Corley Robin P, Haberstick Brett C, Young Susan E, Demmitt Brittany A, Howrigan Daniel P, Kirkpatrick Robert M, Iacono William G, McGue Matt, Keller Matthew C, Brown Sandra, Tapert Susan, Hopfer Christian J, Stallings Michael C, Crowley Thomas J, Rhee Soo Hyun, Krauter Ken, Hewitt John K, McQueen Matthew B
Department of Psychology, University of Illinois Urbana-Champaign, Champaign, IL, 61820, USA,
Behav Genet. 2015 Jul;45(4):375-81. doi: 10.1007/s10519-015-9705-y. Epub 2015 Jan 31.
Behavioral disinhibition (BD) is a quantitative measure designed to capture the heritable variation encompassing risky and impulsive behaviors. As a result, BD represents an ideal target for discovering genetic loci that predispose individuals to a wide range of antisocial behaviors and substance misuse that together represent a large cost to society as a whole. Published genome-wide association studies (GWAS) have examined specific phenotypes that fall under the umbrella of BD (e.g. alcohol dependence, conduct disorder); however no GWAS has specifically examined the overall BD construct. We conducted a GWAS of BD using a sample of 1,901 adolescents over-selected for characteristics that define high BD, such as substance and antisocial behavior problems, finding no individual locus that surpassed genome-wide significance. Although no single SNP was significantly associated with BD, restricted maximum likelihood analysis estimated that 49.3 % of the variance in BD within the Caucasian sub-sample was accounted for by the genotyped SNPs (p = 0.06). Gene-based tests identified seven genes associated with BD (p ≤ 2.0 × 10(-6)). Although the current study was unable to identify specific SNPs or pathways with replicable effects on BD, the substantial sample variance that could be explained by all genotyped SNPs suggests that larger studies could successfully identify common variants associated with BD.
行为抑制解除(BD)是一种定量测量方法,旨在捕捉包括冒险和冲动行为在内的可遗传变异。因此,BD是发现基因位点的理想目标,这些基因位点使个体易患广泛的反社会行为和药物滥用,而这些行为加起来给整个社会带来了巨大成本。已发表的全基因组关联研究(GWAS)研究了属于BD范畴的特定表型(如酒精依赖、品行障碍);然而,尚无GWAS专门研究整体BD结构。我们对1901名青少年样本进行了BD的GWAS研究,这些青少年因定义高BD的特征(如物质和反社会行为问题)而被过度选择,未发现任何超过全基因组显著性的单个基因位点。尽管没有单个单核苷酸多态性(SNP)与BD显著相关,但限制最大似然分析估计,在白种人子样本中,BD方差的49.3%由基因分型的SNP解释(p = 0.06)。基于基因的测试确定了七个与BD相关的基因(p≤2.0×10^(-6))。尽管当前研究未能识别出对BD有可重复效应的特定SNP或途径,但所有基因分型的SNP能够解释的大量样本方差表明,更大规模的研究可能成功识别出与BD相关的常见变异。