Suppr超能文献

基于执行功能测量的内表型对注意力缺陷多动障碍的分子遗传学研究有用吗?

Are endophenotypes based on measures of executive functions useful for molecular genetic studies of ADHD?

作者信息

Doyle Alysa E, Faraone Stephen V, Seidman Larry J, Willcutt Erik G, Nigg Joel T, Waldman Irwin D, Pennington Bruce F, Peart Joanne, Biederman Joseph

机构信息

Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

出版信息

J Child Psychol Psychiatry. 2005 Jul;46(7):774-803. doi: 10.1111/j.1469-7610.2005.01476.x.

Abstract

BACKGROUND

Behavioral genetic studies provide strong evidence that attention-deficit/hyperactivity disorder (ADHD) has a substantial genetic component. Yet, due to the complexity of the ADHD phenotype, questions remain as to the specific genes that contribute to this condition as well as the pathways from genes to behavior. Endophenotypes, or phenotypes that are more closely linked to the neurobiological substrate of a disorder, offer the potential to address these two issues simultaneously (Freedman, Adler, & Leonard, 1999). Thus far, potential endophenotypes for ADHD have not been systematically studied.

METHOD

The current paper reviews evidence supporting the use of deficits on neurocognitive measures of executive functions for this purpose.

RESULTS

Such deficits are a correlate of ADHD and show preliminary evidence of heritability and association with relevant candidate genes. Nonetheless, studies that have assessed the familial and genetic overlap of neurocognitive impairments with ADHD have yielded inconsistent results.

CONCLUSIONS

In order for executive function deficits to be used as an endophenotype for ADHD, we recommend greater attention to the neurocognitive heterogeneity of this disorder and to the precision of measurement of the neuropsychological tests employed. We also discuss empirical strategies that may be necessary to allow such research to progress prior to full resolution of the pathophysiological basis of ADHD.

摘要

背景

行为遗传学研究提供了有力证据,表明注意力缺陷多动障碍(ADHD)具有很大的遗传成分。然而,由于ADHD表型的复杂性,关于导致这种疾病的具体基因以及从基因到行为的途径仍存在疑问。内表型,即与一种疾病的神经生物学底物联系更紧密的表型,有可能同时解决这两个问题(弗里德曼、阿德勒和伦纳德,1999年)。到目前为止,尚未对ADHD的潜在内表型进行系统研究。

方法

本文综述了支持为此目的使用执行功能的神经认知测量缺陷的证据。

结果

此类缺陷与ADHD相关,并显示出遗传力及与相关候选基因关联的初步证据。尽管如此,评估神经认知障碍与ADHD的家族和遗传重叠的研究结果并不一致。

结论

为了将执行功能缺陷用作ADHD的内表型,我们建议更加关注该疾病的神经认知异质性以及所采用神经心理学测试的测量精度。我们还讨论了在ADHD病理生理基础完全解决之前,可能需要采取的实证策略,以使此类研究取得进展。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验