Sjöberg Rickard L, Nilsson Kent W, Wargelius Hanna-Linn, Leppert Jerzy, Lindström Leif, Oreland Lars
Centre for Clinical Research, Uppsala University, Central Hospital Västerås, Västerås, Sweden.
Am J Med Genet B Neuropsychiatr Genet. 2007 Mar 5;144B(2):159-64. doi: 10.1002/ajmg.b.30360.
Recent findings among boys show that interactions between a polymorphism in the monoamine oxidase A gene promoter region (MAOA-LPR) and psychosocial factors predict criminal activity. The objective of this study was to investigate whether this finding could be extended to adolescent girls. One hundred nineteen female adolescents were recruited among respondents to a cross-sectional study of the total population of 16- and 19-year old girls. These girls constituted a randomly selected sub-sample from groups representing different degrees of risk behavior. The subjects filled in a questionnaire and were interviewed and genotyped with regard to MAOA-LPR. The results indicate that the long, (4-repeat) allele confer an increased risk for criminal behavior in the presence of psychosocial risk. Among girls without social risk, MAOA-LPR genotype was of no importance for criminal behavior. The present results suggest that previous observations on adolescent males, which demonstrate that the short MAOA-LPR genotype and psychosocial adversity interact to predict criminal activity, may not be applicable to females.
最近在男孩中的研究发现表明,单胺氧化酶A基因启动子区域多态性(MAOA-LPR)与心理社会因素之间的相互作用可预测犯罪活动。本研究的目的是调查这一发现是否可扩展至青春期女孩。在一项针对16至19岁女孩总人口的横断面研究的受访者中招募了119名女性青少年。这些女孩构成了一个从代表不同程度风险行为的群体中随机选取的子样本。受试者填写了一份问卷,并就MAOA-LPR接受了访谈和基因分型。结果表明,在存在心理社会风险的情况下,长(4重复)等位基因会增加犯罪行为的风险。在没有社会风险的女孩中,MAOA-LPR基因型对犯罪行为并不重要。目前的结果表明,先前关于青少年男性的观察结果显示短MAOA-LPR基因型与心理社会逆境相互作用以预测犯罪活动,这可能不适用于女性。