Henri Begleiter Neurodynamics Laboratory, Department of Psychiatry and Behavioral Sciences, SUNY Downstate Medical Center, 450 Clarkson Ave., Brooklyn, NY, USA.
Behav Genet. 2013 Sep;43(5):386-401. doi: 10.1007/s10519-013-9604-z. Epub 2013 Aug 21.
Discrete time survival analysis was used to assess the age-specific association of event-related oscillations (EROs) and CHRM2 gene variants on the onset of regular alcohol use and alcohol dependence. The subjects were 2,938 adolescents and young adults ages 12-25. Results showed that the CHRM2 gene variants and ERO risk factors had hazards which varied considerably with age. The bulk of the significant age-specific associations occurred in those whose age of onset was under 16. These associations were concentrated in those subjects who at some time took an illicit drug. These results are consistent with studies which associate greater rates of alcohol dependence among those who begin drinking at an early age. The age specificity of the genetic and neurophysiological factors is consistent with recent studies of adolescent brain development, which locate an interval of heightened vulnerability to substance use disorders in the early to mid teens.
采用离散时间生存分析评估与事件相关振荡(EROs)和 CHRM2 基因变异相关的年龄特异性,以评估其与规律饮酒和酒精依赖的发病相关。研究对象为 12-25 岁的 2938 名青少年和年轻人。结果表明,CHRM2 基因变异和 ERO 风险因素的危害随年龄变化相当大。大部分具有显著年龄特异性的关联发生在发病年龄在 16 岁以下的人群中。这些关联集中在那些曾经使用过非法药物的人群中。这些结果与那些在早期开始饮酒的人群中酒精依赖发生率较高的研究一致。遗传和神经生理学因素的年龄特异性与最近的青少年大脑发育研究一致,该研究发现,在青少年早期到中期,物质使用障碍的易感性增加。