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The IMAGE project: methodological issues for the molecular genetic analysis of ADHD

机译:IMAGE项目:ADHD分子遗传分析的方法论问题

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摘要

The genetic mechanisms involved in attention deficit hyperactivity disorder (ADHD) are being studied with considerable success by several centres worldwide. These studies confirm prior hypotheses about the role of genetic variation within genes involved in the regulation of dopamine, norepinephrine and serotonin neurotransmission in susceptibility to ADHD. Despite the importance of these findings, uncertainties remain due to the very small effects sizes that are observed. We discuss possible reasons for why the true strength of the associations may have been underestimated in research to date, considering the effects of linkage disequilibrium, allelic heterogeneity, population differences and gene by environment interactions.With the identification of genes associated with ADHD, the goal of ADHD genetics is now shifting from gene discovery towards gene functionality – the study of intermediate phenotypes ('endophenotypes'). We discuss methodological issues relating to quantitative genetic data from twin and family studies on candidate endophenotypes and how such data can inform attempts to link molecular genetic data to cognitive, affective and motivational processes in ADHD.The International Multi-centre ADHD Gene (IMAGE) project exemplifies current collaborative research efforts on the genetics of ADHD. This European multi-site project is well placed to take advantage of the resources that are emerging following the sequencing of the human genome and the development of international resources for whole genome association analysis. As a result of IMAGE and other molecular genetic investigations of ADHD, we envisage a rapid increase in the number of identified genetic variants and the promise of identifying novel gene systems that we are not currently investigating, opening further doors in the study of gene functionality.
机译:全球多个中心正在研究与注意力缺陷多动障碍(ADHD)有关的遗传机制。这些研究证实了关于多巴胺,去甲肾上腺素和5-羟色胺神经传递调节基因在多动症易感性中的作用的先前假设。尽管这些发现很重要,但由于观察到的效应很小,因此不确定性仍然存在。考虑到连锁不平衡,等位基因异质性,种群差异和环境相互作用对基因的影响,我们讨论了迄今为止迄今为止在研究中可能低估了关联的真正强度的可能原因。 ADHD遗传学的研究正从基因发现转向基因功能-中间表型(“表型”)的研究。我们讨论与双胞胎和家族研究中有关候选内表型的定量遗传数据有关的方法论问题,以及这些数据如何为将分子遗传数据与ADHD的认知,情感和动机过程联系起来的尝试提供参考。国际多中心ADHD基因(IMAGE)项目举例说明了当前有关多动症遗传学的合作研究成果。这个欧洲多站点项目的位置很好,可以利用人类基因组测序和开发用于全基因组关联分析的国际资源后出现的资源。由于IMAGE和ADHD的其他分子遗传学研究的结果,我们设想已鉴定出的遗传变异数量将迅速增加,并有望鉴定出我们目前尚未研究的新型基因系统,从而为基因功能性研究打开了新的大门。

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