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首页> 外文期刊>Psychiatric genetics >Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.
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Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.

机译:青春期男性青少年中儿茶酚-O-甲基转移酶Val 158 Met多态性与行为障碍和ADHD症状相关。

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OBJECTIVE: Variation in the catechol-O-methyltransferase gene (COMT) has been associated with antisocial behavior in populations with attention deficit/hyperactivity disorder (ADHD). This study examined whether COMT would predict antisocial behavior in a sample with high levels of behavior problems, not necessarily ADHD. In addition, because previous research suggests that COMT may be associated with ADHD in males, association between COMT and ADHD symptoms was examined. METHOD: This study tested whether variation in three polymorphisms of the COMT gene was predictive of symptoms of conduct disorder and ADHD, in a sample of 174 incarcerated Russian adolescent male delinquents. RESULTS: The Val allele of the ValMet polymorphism was significantly associated with conduct disorder diagnosis and symptoms, whereas the Met allele was associated with ADHD symptoms. CONCLUSION: The ValMet polymorphism of the COMT gene shows a complex relation to behavior problems, influencing conduct disorder and ADHD symptoms in opposite directions in a high-risk population.
机译:目的:儿茶酚-O-甲基转移酶基因(COMT)的变异与注意力缺陷/多动症(ADHD)人群的反社会行为有关。这项研究检验了COMT是否可以预测行为问题水平较高(不一定为ADHD)的样本中的反社会行为。此外,由于先前的研究表明男性COMT可能与ADHD相关,因此检查了COMT与ADHD症状之间的关联。方法:本研究测试了174名被监禁的俄罗斯青少年男性犯罪者的样本中,COMT基因的三种多态性变异是否可预测行为障碍和ADHD症状。结果:ValMet多态性的Val等位基因与行为障碍诊断和症状显着相关,而Met等位基因与ADHD症状相关。结论:COMT基因的ValMet多态性与行为问题有着复杂的关系,在高风险人群中行为行为和ADHD症状的影响方向相反。

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