Dick Danielle M, Aliev Fazil, Wang Jen C, Grucza Richard A, Schuckit Marc, Kuperman Samuel, Kramer John, Hinrichs Anthony, Bertelsen Sarah, Budde John P, Hesselbrock Victor, Porjesz Bernice, Edenberg Howard J, Bierut Laura Jean, Goate Alison
Washington University, St Louis, Missouri, USA.
Arch Gen Psychiatry. 2008 Mar;65(3):310-8. doi: 10.1001/archpsyc.65.3.310.
Twin studies provide compelling evidence that alcohol and drug dependence, childhood conduct disorder, adult antisocial behavior, and disinhibitory personality traits share an underlying genetic liability that contributes to a spectrum of externalizing behaviors. However, this information has not been widely used in gene identification efforts, which have focused on specific disorders diagnosed using traditional psychiatric classification systems.
To test the utility of using a multivariate externalizing phenotype in (1) linkage analyses and (2) association analyses to identify genes that contribute broadly to a spectrum of externalizing disorders.
Data were analyzed from the Collaborative Study on the Genetics of Alcoholism. Linkage analyses were conducted using data from a genome-wide 10-cM microsatellite scan. Association analyses were conducted on 27 single-nucleotide polymorphisms genotyped across a candidate gene, the muscarinic acetylcholine receptor M2 gene (CHRM2).
Six centers across the United States.
Approximately 2300 individuals from 262 families.
Lifetime symptom counts of alcohol dependence, illicit drug dependence, childhood conduct disorder, and adult antisocial personality disorder and novelty seeking, sensation seeking, and general externalizing component scores consisting of a composite of the previous 6 variables.
Principal component analyses indicated that the 6 individual variables loaded on a single externalizing factor. Linkage analyses using the resultant component scores identified a region on chromosome 7 consistent with a gene that broadly predisposes individuals to externalizing behavior. Association analyses of a candidate gene, CHRM2, previously of interest in the Collaborative Study on the Genetics of Alcoholism, suggest that it is involved in a general externalizing phenotype.
Broader conceptualizations of psychiatric disorders, such as studying a spectrum of externalizing psychopathology, may aid in identifying susceptibility genes and understanding the pathways through which genetic factors affect vulnerability for a variety of poor outcomes.
双胞胎研究提供了令人信服的证据,表明酒精和药物依赖、儿童期品行障碍、成人反社会行为以及抑制解除型人格特质具有共同的潜在遗传易感性,这导致了一系列外化行为。然而,这些信息尚未在基因识别研究中得到广泛应用,基因识别研究主要集中在使用传统精神科分类系统诊断的特定疾病上。
测试使用多变量外化表型在(1)连锁分析和(2)关联分析中识别广泛导致一系列外化障碍的基因的效用。
对酒精中毒遗传学合作研究的数据进行分析。使用全基因组10厘摩微卫星扫描的数据进行连锁分析。对候选基因毒蕈碱型乙酰胆碱受体M2基因(CHRM2)上基因分型的27个单核苷酸多态性进行关联分析。
美国的六个中心。
来自262个家庭的约2300名个体。
酒精依赖、非法药物依赖、儿童期品行障碍和成人反社会人格障碍的终生症状计数,以及新奇寻求、感觉寻求和由前6个变量组成的综合一般外化成分得分。
主成分分析表明,这6个个体变量加载在一个单一的外化因子上。使用所得成分得分进行的连锁分析在7号染色体上确定了一个区域,该区域与一个使个体广泛易患外化行为的基因一致。对候选基因CHRM2(该基因先前在酒精中毒遗传学合作研究中受到关注)的关联分析表明,它与一般外化表型有关。
对精神疾病进行更广泛的概念化,例如研究一系列外化精神病理学,可能有助于识别易感基因,并理解遗传因素影响各种不良后果易感性的途径。