Sakai Joseph T, Young Susan E, Stallings Michael C, Timberlake David, Smolen Andrew, Stetler Gary L, Crowley Thomas J
Division of Substance Dependence, Department of Psychiatry, University of Colorado School of Medicine, Denver, CO, USA.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):825-32. doi: 10.1002/ajmg.b.30278.
Several lines of research have suggested that serotonin dysfunction is associated with aggression, impulsivity, and antisocial behavior. A functional polymorphism in the promoter region (s, short and l, long allele variant) of the serotonin transporter gene (SLC6A4) that results in decreased transcription of the serotonin transporter gene has been linked with such serotonin dysfunction. To test for an association between 5HTTLPR genotype and conduct disorder diagnosis/aggression. Analysis for association between 5HTTLPR and conduct disorder/aggression using a case-control design and the transmission disequilibrium test. Conduct-disordered adolescents, who were drawn from admissions to a program that treats adolescents with serious substance and behavior problems, and conduct-disordered siblings of these patients (n, 297) were compared with non-conduct-disordered control adolescents and non-conduct-disordered siblings of these controls (n, 93). Second, using patient families where parental DNA was available, transmission disequilibrium tests were conducted for two phenotypes: (1) conduct disorder (74 trios), and (2) conduct disorder with at least one aggressive symptom (57 trios). Case-control analyses suggested a strong association between the ss genotype and conduct disorder (chi2(2) = 14.3; P < 0.01). Within-family analyses for conduct disorder with at least one aggressive symptom significantly favored greater transmission of the s-allele to affected offspring (chi(tdt)(2) = 4.13; P = 0.04); for conduct disorder, without aggressive symptoms, however, results were non-significant (chi(tdt)(2) = 1.61; P = 0.20). These data suggest that the s-allele may confer some risk for aggressive behavior or may be in linkage disequilibrium with such an allele.
多项研究表明,血清素功能障碍与攻击性、冲动性及反社会行为有关。血清素转运体基因(SLC6A4)启动子区域的功能性多态性(s为短等位基因变体,l为长等位基因变体)导致血清素转运体基因转录减少,这与这种血清素功能障碍有关。为了检测5HTTLPR基因型与品行障碍诊断/攻击性之间的关联。采用病例对照设计和传递不平衡检验分析5HTTLPR与品行障碍/攻击性之间的关联。将来自一个治疗有严重物质和行为问题青少年项目的品行障碍青少年及其品行障碍的兄弟姐妹(n = 297)与无品行障碍的对照青少年及其对照的无品行障碍的兄弟姐妹(n = 93)进行比较。其次,在有父母DNA的患者家庭中,对两种表型进行传递不平衡检验:(1)品行障碍(74个三联体),(2)至少有一个攻击症状的品行障碍(57个三联体)。病例对照分析表明,ss基因型与品行障碍之间存在强关联(χ2(2)=14.3;P<0.01)。对至少有一个攻击症状的品行障碍进行的家系内分析显著支持s等位基因向受影响后代的更大传递(χ(tdt)(2)=4.13;P = 0.04);然而,对于无攻击症状的品行障碍,结果不显著(χ(tdt)(2)=1.61;P = 0.20)。这些数据表明,s等位基因可能赋予攻击行为一定风险,或者可能与这样一个等位基因处于连锁不平衡状态。