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腹侧前额叶皮层的激活对注意力缺陷多动障碍的遗传易感性敏感。

Activation in ventral prefrontal cortex is sensitive to genetic vulnerability for attention-deficit hyperactivity disorder.

作者信息

Durston Sarah, Mulder Martijn, Casey B J, Ziermans Tim, van Engeland Herman

机构信息

Rudolf Magnus Institute of Neuroscience, Department of Child and Adolescent Psychiatry, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

出版信息

Biol Psychiatry. 2006 Nov 15;60(10):1062-70. doi: 10.1016/j.biopsych.2005.12.020. Epub 2006 May 19.

Abstract

BACKGROUND

Attention-deficit hyperactivity disorder (ADHD) is a heritable neuropsychiatric disorder, associated with atypical patterns of brain activation in functional imaging studies. Neuroimaging measures may serve as an intermediate phenotype in genetic studies of ADHD, as they are putatively more closely linked to gene expression than a clinical diagnosis.

METHODS

We used rapid, mixed-trial, event-related functional magnetic resonance imaging (fMRI) to investigate changes in brain activation during a go no-go task in boys with ADHD, their unaffected siblings, and matched control subjects.

RESULTS

On the hardest inhibitory trials in our task, children and adolescents with ADHD had lower accuracy than control subjects, whereas their unaffected siblings did not. Control subjects activated a network of regions, including ventral prefrontal and inferior parietal cortex. Both children and adolescents with ADHD and their unaffected siblings showed decreased activation in these areas, as well as fewer correlations between performance and activation.

CONCLUSIONS

These findings suggest that the magnitude of activation during successful inhibitions is sensitive to genetic vulnerability for ADHD in a number of regions, including ventral prefrontal cortex. If this can be replicated in future studies, this suggests that neuroimaging measures related to inhibitory control may be suitable as intermediate phenotypes in studies investigating gene effects in ADHD.

摘要

背景

注意力缺陷多动障碍(ADHD)是一种遗传性神经精神疾病,在功能成像研究中与大脑激活的非典型模式相关。神经成像测量可能作为ADHD基因研究中的一种中间表型,因为与临床诊断相比,它们可能与基因表达联系更为紧密。

方法

我们使用快速、混合试验、事件相关功能磁共振成像(fMRI)来研究患有ADHD的男孩、其未受影响的兄弟姐妹以及匹配的对照受试者在执行停止信号任务期间大脑激活的变化。

结果

在我们任务中最难的抑制试验中,患有ADHD的儿童和青少年的准确率低于对照受试者,而他们未受影响的兄弟姐妹则没有。对照受试者激活了包括腹侧前额叶和顶下皮质在内的一系列脑区。患有ADHD的儿童和青少年及其未受影响的兄弟姐妹在这些区域的激活均减少,并且表现与激活之间的相关性也较少。

结论

这些发现表明,在包括腹侧前额叶皮质在内的多个区域,成功抑制期间的激活程度对ADHD的遗传易感性敏感。如果这一点能在未来的研究中得到重复,这表明与抑制控制相关的神经成像测量可能适合作为研究ADHD基因效应的中间表型。

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