Prichard Zoë M, Jorm Anthony F, Mackinnon Andrew, Easteal Simon
Predictive Medicine Group, John Curtin School of Medical Research, University of Melbourne, Australia.
Psychiatr Genet. 2007 Oct;17(5):299-303. doi: 10.1097/YPG.0b013e32816ebc9e.
This study sought to test 15 simple sequence repeat polymorphisms within 10 candidate genes for association with antisocial behavioural traits. Genes included were those known to regulate dopamine synthesis and transmission in the brain (DBH, DRD2, MAOA, TFAP2B, NR4A2, LMX1B) and those involved in the differentiation of social and sexual behaviour in men and women (AR, ESR1, OXTR, AVPR1A). Participants were Caucasians (men=1007, women=1089) aged 20-24 years who were assessed for indicators of antisocial traits such as pseudo-maturity, substance misuse and unstable lifestyle. Significant associations for antisocial traits were found with AR and ESR1 polymorphisms in men, and with polymorphisms within NR4A2 and TFAP2B in women. The association with TFAP2B remained significant after correction for multiple testing. This pattern of associations suggests that genetic variation within transcription factors may in part explain the variation observed in the population for antisocial behavioural phenotypes.
本研究旨在检测10个候选基因中的15个简单序列重复多态性,以确定其与反社会行为特征的关联。所涉及的基因包括已知在大脑中调节多巴胺合成和传递的基因(DBH、DRD2、MAOA、TFAP2B、NR4A2、LMX1B)以及参与男性和女性社会与性行为分化的基因(AR、ESR1、OXTR、AVPR1A)。参与者为20至24岁的白种人(男性 = 1007人,女性 = 1089人),他们接受了反社会特征指标的评估,如假性成熟、药物滥用和不稳定的生活方式。在男性中,发现反社会特征与AR和ESR1多态性存在显著关联,在女性中则与NR4A2和TFAP2B内的多态性存在显著关联。经过多重检验校正后,与TFAP2B的关联仍然显著。这种关联模式表明,转录因子内的基因变异可能在一定程度上解释了人群中反社会行为表型所观察到的变异。