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Neural mechanisms of attention-deficit/hyperactivity disorder symptoms are stratified by MAOA genotype

机译:注意缺陷/多动障碍症状的神经机制通过MAOA基因型分层

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Background Attention-deficit/hyperactivity disorder (ADHD) is characterized by deficits in reward sensitivity and response inhibition. The relative contribution of these frontostriatal mechanisms to ADHD symptoms and their genetic determinants is largely unexplored. Methods Using functional magnetic resonance imaging and genetic analysis of the monoamine oxidase A (MAOA) gene, we investigated how striatal and inferior frontal activation patterns contribute to ADHD symptoms depending on MAOA genotype in a sample of adolescent boys (n = 190). Results We demonstrate an association of ADHD symptoms with distinct blood oxygen level-dependent (BOLD) responses depending on MAOA genotype. In A hemizygotes of the expression single nucleotide polymorphism rs12843268, which express lower levels of MAOA, ADHD symptoms are associated with lower ventral striatal BOLD response during the monetary incentive delay task and lower inferior frontal gyrus BOLD response during the stop signal task. In G hemizygotes, ADHD symptoms are associated with increased inferior frontal gyrus BOLD response during the stop signal task in the presence of increased ventral striatal BOLD response during the monetary incentive delay task. Conclusions Depending on MAOA genotype, ADHD symptoms in adolescent boys are associated with either reward deficiency or insufficient response inhibition. Apart from its mechanistic interest, our finding may aid in developing pharmacogenetic markers for ADHD.
机译:背景技术注意缺陷多动障碍(ADHD)的特征是奖励敏感性和反应抑制能力不足。这些前额骨机制对ADHD症状及其遗传决定因素的相对贡献在很大程度上尚待探索。方法使用功能性磁共振成像和单胺氧化酶A(MAOA)基因的遗传分析,我们研究了青春期男孩(n = 190)样品中纹状体和下额叶激活模式如何根据MAOA基因型影响ADHD症状。结果我们证明了多动症的症状与依赖于MAOA基因型的独特的血氧水平依赖性(BOLD)反应相关。在表达较低MAOA水平的单核苷酸多态性rs12843268表达的半合子中,ADHD症状与金钱激励延迟任务期间较低的腹侧纹状体BOLD反应和停止信号任务期间较低的额下回BOLD反应相关。在G半合子中,在金钱激励延迟任务期间出现腹侧纹状体BOLD反应增加的情况下,ADHD症状与停止信号任务期间下额额回BOLD反应增加有关。结论取决于MAOA基因型,青春期男孩的ADHD症状与奖励不足或反应抑制不足有关。除了对机械的兴趣外,我们的发现可能有助于开发ADHD的药物遗传学标记。

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