MacKillop James, Gray Joshua C, Weafer Jessica, Sanchez-Roige Sandra, Palmer Abraham A, de Wit Harriet
Peter Boris Centre for Addictions Research, McMaster University/St. Joseph's Healthcare Hamilton.
Department of Psychology, University of Georgia.
Exp Clin Psychopharmacol. 2019 Feb;27(1):29-37. doi: 10.1037/pha0000227. Epub 2018 Sep 27.
Delayed reward discounting (DRD) is a behavioral economic measure of impulsivity that has been consistently associated with addiction. It has also been identified as a promising addiction endophenotype, linking specific sources of genetic variation to individual risk. A challenge in the studies to date is that levels of DRD are often confounded with prior drug use, and previous studies have also had limited genomic scope. The current investigation sought to address these issues by studying DRD in healthy young adults with low levels of substance use (N = 986; 62% female, 100% European ancestry) and investigating genetic variation genome-wide. The genome-wide approach used a prioritized subset design, organizing the tests into theoretically and empirically informed categories and apportioning power accordingly. Three subsets were used: (a) a priori loci implicated by previous studies; (b) high-value addiction (HVA) markers from the recently developed SmokeScreen array; and (c) an atheoretical genome-wide scan. Among a priori loci, a nominally significant association was present between DRD and rs521674 in ADRA2A. No significant HVA loci were detected. One statistically significant genome-wide association was detected (rs13395777, p = 2.8 × 10-8), albeit in an intergenic region of unknown function. These findings are generally not supportive of the previous candidate gene studies and suggest that DRD has a complex genetic architecture that will require considerably larger samples to identify genetic associations more definitively. (PsycINFO Database Record (c) 2019 APA, all rights reserved).
延迟奖励折扣(DRD)是一种冲动性的行为经济学测量方法,一直与成瘾相关。它也被确定为一种有前景的成瘾内表型,将特定的遗传变异来源与个体风险联系起来。迄今为止,研究中的一个挑战是DRD水平常常与先前的药物使用相混淆,并且先前的研究基因组范围也有限。当前的调查旨在通过研究物质使用水平较低的健康年轻成年人(N = 986;62%为女性,100%为欧洲血统)的DRD并在全基因组范围内研究遗传变异来解决这些问题。全基因组方法采用了优先子集设计,将测试组织成理论和实证依据的类别并相应地分配效能。使用了三个子集:(a)先前研究涉及的先验基因座;(b)来自最近开发的SmokeScreen阵列的高价值成瘾(HVA)标记;以及(c)一个非理论性的全基因组扫描。在先验基因座中,DRD与ADRA2A中的rs521674之间存在名义上显著的关联。未检测到显著的HVA基因座。检测到一个全基因组关联具有统计学意义(rs13395777,p = 2.8×10 - 8),尽管位于一个功能未知的基因间区域。这些发现总体上不支持先前的候选基因研究,并表明DRD具有复杂的遗传结构,这将需要相当大的样本才能更明确地识别遗传关联。(PsycINFO数据库记录(c)2019美国心理学会,保留所有权利)