Stallings Michael C, Corley Robin P, Hewitt John K, Krauter Kenneth S, Lessem Jeffrey M, Mikulich Susan K, Rhee Soo Hyun, Smolen Andrew, Young Susan E, Crowley Thomas J
Institute for Behavioral Genetics, University of Colorado, Campus Box 447, Boulder, CO 80309-0447, USA.
Drug Alcohol Depend. 2003 Jun 5;70(3):295-307. doi: 10.1016/s0376-8716(03)00031-0.
This study describes results from a genome-wide search for quantitative trait loci (QTL) influencing substance dependence vulnerability in adolescence. We utilized regression-based multipoint (and single-point) QTL mapping procedures designed for selected sibpair samples. Selected sibling pairs included 250 proband-sibling pairs from 192 families. Clinical probands (13-19 years of age) were drawn from consecutive admissions to substance abuse treatment facilities in the Denver metropolitan area; siblings of probands ranged in age from 12 to 25 years. In addition to the selected sample, a community-based sample of 3676 adolescents and young adults were utilized to define a clinically-significant, heritable, age- and sex-normed index of substance dependence vulnerability-a priori and independent of our linkage results. Siblings and their parents were genotyped for 374 STR micro-satellite markers distributed across the 22 autosomes (average inter-marker distance=9.2 cM). Non-parametric single-point linkage results indicated 17 markers on 11 chromosomes with nominally significant tests of linkage; six markers with LOD scores greater than 1.0 and one marker (D3S1614) with a LOD score of 2.2. Multipoint mapping corroborated two locations and provided preliminary evidence for linkage to regions on chromosome 3q24-25 (near markers D3S1279 and D3S1614) and chromosome 9q34 (near markers D9S1826 and D9S1838).
本研究描述了一项全基因组搜索结果,该搜索旨在寻找影响青少年物质依赖易感性的数量性状基因座(QTL)。我们采用了基于回归的多点(和单点)QTL定位程序,这些程序是为选定的同胞对样本设计的。选定的同胞对包括来自192个家庭的250对先证者-同胞对。临床先证者(13 - 19岁)来自丹佛大都市地区物质滥用治疗机构的连续入院患者;先证者的同胞年龄在12至25岁之间。除了选定的样本外,还利用了一个基于社区的3676名青少年和青年成年人样本,以定义一个具有临床意义、可遗传、按年龄和性别标准化的物质依赖易感性指数——该指数先验确定且独立于我们的连锁结果。对同胞及其父母进行了374个STR微卫星标记的基因分型,这些标记分布在22条常染色体上(平均标记间距离 = 9.2 cM)。非参数单点连锁结果表明,11条染色体上有17个标记具有名义上显著的连锁检验;6个标记的LOD得分大于1.0,1个标记(D3S1614)的LOD得分为2.2。多点定位证实了两个位置,并为与3号染色体q24 - 25区域(靠近标记D3S1279和D3S1614)和9号染色体q34区域(靠近标记D9S1826和D9S1838)的连锁提供了初步证据。