Gerra G, Garofano L, Bosari S, Pellegrini C, Zaimovic A, Moi G, Bussandri M, Moi A, Brambilla F, Mameli A, Pizzamiglio M, Donnini C
Centro Studi Farmaco-tossicodipendenze, Ser T, AUSL, Italy.
J Neural Transm (Vienna). 2004 May;111(5):611-21. doi: 10.1007/s00702-004-0129-8. Epub 2004 Mar 19.
The promoter of the monoamine oxidase A (MAO-A) gene was analysed to test whether length variation of the repeat polymorphism contributes to variation in individual vulnerability to aggressive-criminal behaviour, and liability to heroin dependence. The repeat number of the MAO-A polymorphism was assessed in 199 male subjects of Italian descent, a sample comprising 95 healthy subjects and 104 heroin-dependent subjects including 52 addicted individuals with violent behaviour and antisocial personality disorder. The frequency of the low-activity 3-repeat allele was significantly higher in violent offenders among heroin addicts, compared to addicted individuals without antisocial behaviour (34.6 vs. 15.4%; p<0.03) and controls (18.9%; p<0.05). No significant difference was evidenced in the frequencies of the MAO-A alleles between heroin-dependent subjects in general and control subjects. High activity 4-repeat allele frequency was significantly higher in addicted individuals without antisocial behavior compared to antisocial-aggressive heroin-dependent subjects (76.9 vs. 55.8%; p<0.02). Buss Durkee Hostility Inventory (BDHI) mean total scores were significantly higher in heroin addicts than in controls (p<0.001), and in antisocial-violent heroin addicts in comparison with addicted individuals without antisocial behaviour (p<0.005). Among heroin addicts BDHI irritability, suspiciousness and resentment subscales scores were found significantly higher in low activity 3-repeat allele subjects than in high activity alleles subjects (p<0.001; p<0.05; p<0.05, respectively). No association was found between MAO-A polymorphism and suicide history. Our findings suggest that the low-activity 3-repeat allele of the MAO-A promoter polymorphism confers increased susceptibility to antisocial-violent behavior and aggressiveness, rather than drug dependence per se, in heroin-dependent males.
对单胺氧化酶A(MAO-A)基因的启动子进行分析,以检验重复多态性的长度变异是否会导致个体对攻击性行为和犯罪行为的易感性差异,以及对海洛因依赖的易感性差异。在199名意大利裔男性受试者中评估了MAO-A多态性的重复次数,该样本包括95名健康受试者和104名海洛因依赖受试者,其中包括52名有暴力行为和反社会人格障碍的成瘾个体。与无反社会行为的成瘾个体(34.6%对15.4%;p<0.03)和对照组(18.9%;p<0.05)相比,海洛因成瘾者中暴力犯罪者的低活性3重复等位基因频率显著更高。一般而言,海洛因依赖受试者与对照受试者之间的MAO-A等位基因频率没有显著差异。与有反社会攻击性的海洛因依赖受试者相比,无反社会行为的成瘾个体的高活性4重复等位基因频率显著更高(76.9%对55.8%;p<0.02)。海洛因成瘾者的布斯-杜克敌意量表(BDHI)平均总分显著高于对照组(p<0.001),与无反社会行为的成瘾个体相比,反社会暴力海洛因成瘾者的BDHI总分更高(p<0.005)。在海洛因成瘾者中,低活性3重复等位基因受试者的BDHI易怒、多疑和怨恨子量表得分显著高于高活性等位基因受试者(分别为p<0.001;p<0.05;p<0.05)。未发现MAO-A多态性与自杀史之间存在关联。我们的研究结果表明,MAO-A启动子多态性的低活性3重复等位基因会增加海洛因依赖男性对反社会暴力行为和攻击性的易感性,而不是对药物依赖本身的易感性。