van Beijsterveldt C E, Molenaar P C, de Geus E J, Boomsma D I
Department of Psychophysiology, Vrije Universiteit, Amsterdam, The Netherlands.
Biol Psychol. 1998 Feb;47(2):97-120. doi: 10.1016/s0301-0511(97)00025-2.
Using quantitative genetic research designs, we decomposed phenotypic variance in P300 parameters into genetic and environmental components. The twin method was used to carry out this decomposition. Event related potentials (ERPs) were measured during a visual oddball paradigm in a sample of 213 adolescent twin pairs. The presence of male and female same-sex and opposite-sex twins in the sample enabled us to study sex differences in the contributions of genetic and environmental effects to P300 parameters. For targets and nontargets, half of the variance in the P300 amplitude is attributable to factors shared by the family members. However, it remains unclear whether this resemblance is attributable to shared environmental or genetic influences. The same factors (genetic or shared environmental) were found to contribute to the individual differences in males and females. The contributions do, however, differ across gender. Multivariate genetic analyses investigated the covariance among various brain areas to determine whether the covariance between two or more leads is attributable to the same genetic and/or the same environmental factors. The covariance of the P300 amplitude measured at different locations was attributable both to unshared environmental and to shared factors. Again it was not possible to show that the shared factors where either genetic or shared environmental.
我们采用定量遗传学研究设计,将P300参数中的表型方差分解为遗传和环境成分。运用双胞胎方法进行这种分解。在213对青少年双胞胎样本的视觉Oddball范式中测量事件相关电位(ERP)。样本中存在同性和异性的男性及女性双胞胎,这使我们能够研究遗传和环境效应在P300参数贡献方面的性别差异。对于目标和非目标,P300波幅中一半的方差可归因于家庭成员共有的因素。然而,这种相似性是归因于共享环境还是遗传影响仍不清楚。发现相同的因素(遗传或共享环境)导致男性和女性的个体差异。不过,这些贡献在性别上存在差异。多变量遗传分析研究了不同脑区之间的协方差,以确定两个或多个导联之间的协方差是否归因于相同的遗传和/或相同的环境因素。在不同位置测量的P300波幅的协方差既归因于非共享环境,也归因于共享因素。同样,无法表明共享因素是遗传的还是共享环境的。