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注意缺陷多动障碍的个体内变异性及其对因果关系研究的影响。

Intraindividual variability in ADHD and its implications for research of causal links.

作者信息

Kuntsi Jonna, Klein Christoph

机构信息

King's College London, MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, De Crespigny Park, London, SE5 8AF, UK,

出版信息

Curr Top Behav Neurosci. 2012;9:67-91. doi: 10.1007/7854_2011_145.

Abstract

Intraindividual variability (IIV) - reflecting short-term (within-session), within-person fluctuations in behavioral performance - and, specifically, reaction time (RT) variability, is strongly linked with attention-deficit hyperactivity disorder (ADHD) both at the phenotypic and genetic levels. Phenotypic case-control comparisons show a consistent and robust association between ADHD and RT variability across a broad range of cognitive tasks, samples, and age ranges (from childhood to adulthood). The association does not appear to be a nonspecific effect mediated by lower general cognitive ability. The finding from quantitative genetic studies of the shared genetic etiology between ADHD and RT variability is similarly robust, replicating across tasks, samples, and definitions of ADHD. Molecular genetic studies have produced intriguing initial findings: increasing sample sizes and replications across datasets remain priorities for future efforts. While the field has come a long way from considering increased RT variability in ADHD as the "noise" or "error" that we need to reduce in our data, the investigation of the causal pathways is only beginning. The neural basis of IIV is being investigated, with initial data pointing to a crucial role of fronto-striatal systems in controlling behavioral consistency. Several theories have been put forward to account for the observed IIV in ADHD, including accounts of arousal regulation, temporal processing and the "default-mode network." For the wider implications of the IIV phenomenon to be fully realized, we need to learn further about the underlying processes, their developmental context, and about shared and unique causal pathways across disorders where high RT variability is observed.

摘要

个体内变异性(IIV)——反映行为表现的短期(即单次实验内)、个体内部波动,具体而言是反应时间(RT)变异性——在表型和基因水平上都与注意力缺陷多动障碍(ADHD)密切相关。表型病例对照比较显示,在广泛的认知任务、样本和年龄范围(从儿童期到成年期)内,ADHD与RT变异性之间存在一致且显著的关联。这种关联似乎并非由较低的一般认知能力介导的非特异性效应。ADHD与RT变异性之间共享遗传病因的定量遗传研究结果同样显著,在不同任务、样本和ADHD定义中均得到重复验证。分子遗传研究已得出有趣的初步发现:增加样本量并在不同数据集间进行重复验证仍是未来研究的重点。尽管该领域已取得长足进展,不再将ADHD中增加的RT变异性视为我们需要在数据中减少的“噪声”或“误差”,但因果途径的研究才刚刚开始。IIV的神经基础正在研究中,初步数据表明额纹状体系统在控制行为一致性方面起着关键作用。针对ADHD中观察到的IIV,已提出了几种理论,包括唤醒调节、时间加工以及“默认模式网络”等理论。为了全面认识IIV现象的更广泛影响,我们需要进一步了解其潜在过程、发展背景,以及在观察到高RT变异性的各种疾病中共享和独特的因果途径。

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