Martin Neilson, McDougall Megan, Hay David A
School of Psychology, Curtin University of Technology, Perth, Western Australia.
Curr Opin Psychiatry. 2008 Jul;21(4):356-61. doi: 10.1097/YCO.0b013e328303ba54.
The aim of this review is to describe the considerable advances in consolidating the empirical evidence on several key topics in the genetics of attention deficit hyperactivity disorder, namely the quantitative genetic studies of the nature of attention deficit hyperactivity disorder and its comorbidities, the molecular genetic studies that show modest but consistent effects of specific genotypes, and the growing recognition of genotype by environment interaction. Such interactions are studied to explain what happens when individuals with a susceptible genotype are exposed to a particular environment.
There have been a significant number of twin studies that have examined different models of the symptomatology of attention deficit hyperactivity disorder and how these symptoms are reported. Similarly, molecular genetic research is complicated by very different outcome measures, and study across the whole field is made more problematic by genotype by environment interaction effects. One of the most interesting areas of development is that of psychopharmacogenetics.
Two key developments have been integrative models of the genetics of attention deficit hyperactivity disorder and brain structure, which may have implications for future attention deficit hyperactivity disorder subtyping, and collaboration. This is not just within attention deficit hyperactivity disorder as in the IMAGE study, but also across disciplines.
本综述旨在描述在巩固注意缺陷多动障碍遗传学几个关键主题的实证证据方面取得的重大进展,即注意缺陷多动障碍及其共病本质的定量遗传学研究、显示特定基因型有适度但一致效应的分子遗传学研究,以及对基因与环境相互作用的日益认识。研究这种相互作用是为了解释具有易感基因型的个体暴露于特定环境时会发生什么。
有大量双胞胎研究考察了注意缺陷多动障碍症状学的不同模型以及这些症状的报告方式。同样,分子遗传学研究因结果测量差异很大而变得复杂,基因与环境相互作用效应使整个领域的研究更具问题性。最有趣的发展领域之一是精神神经药理学。
两个关键进展是注意缺陷多动障碍遗传学与脑结构的整合模型,这可能对未来注意缺陷多动障碍的亚型划分及合作有影响。这不仅像在IMAGE研究中那样在注意缺陷多动障碍内部,也跨学科存在。