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成人及儿童注意力缺陷多动障碍中的遗传风险因素及基因-环境相互作用

Genetic risk factors and gene-environment interactions in adult and childhood attention-deficit/hyperactivity disorder.

作者信息

Palladino Viola S, McNeill Rhiannon, Reif Andreas, Kittel-Schneider Sarah

机构信息

Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.

出版信息

Psychiatr Genet. 2019 Jun;29(3):63-78. doi: 10.1097/YPG.0000000000000220.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a common and highly heritable neurodevelopmental disorder. In recent years, genetic studies have revealed several risk gene variants associated with ADHD; however, these variants could only be partly replicated and are responsible for only a fraction of the whole heritability of ADHD estimated from family and twin studies. One factor that could potentially explain the 'missing heritability' of ADHD is that childhood and adult or persistent ADHD could be genetically distinct subtypes, which therefore need to be analyzed separately. Another approach to identify this missing heritability could be combining the investigation of both common and rare gene risk variants as well as polygenic risk scores. Finally, environmental factors are also thought to play an important role in the etiology of ADHD, acting either independently of the genetic background or more likely in gene-environment interactions. Environmental factors might additionally convey their influence by epigenetic mechanisms, which are relatively underexplored in ADHD. The aforementioned mechanisms might also influence the response of patients with ADHD to stimulant and other ADHD medication. We conducted a selective review with a focus on risk genes of childhood and adult ADHD, gene-environment interactions, and pharmacogenetics studies on medication response in childhood and adult ADHD.

摘要

注意力缺陷多动障碍(ADHD)是一种常见且具有高度遗传性的神经发育障碍。近年来,基因研究已揭示了几种与ADHD相关的风险基因变异;然而,这些变异只能部分被重复验证,且仅占通过家系和双胞胎研究估计的ADHD整体遗传度的一小部分。一个可能解释ADHD“遗传度缺失”的因素是,儿童期和成人期或持续性ADHD可能是基因上不同的亚型,因此需要分别进行分析。另一种识别这种遗传度缺失的方法可能是结合对常见和罕见基因风险变异以及多基因风险评分的研究。最后,环境因素也被认为在ADHD的病因中起重要作用,其作用方式要么独立于遗传背景,要么更可能是在基因-环境相互作用中发挥作用。环境因素还可能通过表观遗传机制传递其影响,而这在ADHD中相对未得到充分研究。上述机制也可能影响ADHD患者对兴奋剂和其他ADHD药物的反应。我们进行了一项选择性综述,重点关注儿童期和成人期ADHD的风险基因、基因-环境相互作用以及儿童期和成人期ADHD药物反应的药物遗传学研究。

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