Genetic Basis and Neural Mechanism of Autism Spectrum Disorder

Pub Date : 2012-10-01 DOI:10.3724/sp.j.1206.2011.00519
Li Jing, Lin Zhu-mei, Zhu Li-qi
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Abstract

Autism spectrum disorder (ASD) is a defective mental disease and its core impairments are social function defect, communication defect, restrictive and stereotyped behavior pattern. The paper introduces the genetic basis and neural mechanism of ASD. ASD has high genetic rate, and 5-HT and testosterone of ASD individual are both higher. Neuroimaging studies find that there are some differences between ASD and normal individuals in the structure and function of amygdala, cingulate gyrus, the fusiform gyrus, mirror neurons, prefrontal lobe and other brain areas, but it is inconsistent in the discrepancy direction of some areas' activation patterns. In addition, the results of functional connectivity studies also confirm the hypothesis that the ASD individuals are under-connection. Future research should focus more on how to use the basic research outcomes to put forward effective treatment and training for clinical research.
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自闭症谱系障碍的遗传基础和神经机制
自闭症谱系障碍(Autism spectrum disorder, ASD)是一种缺陷性精神疾病,其核心缺陷是社会功能缺陷、沟通缺陷、限制性刻板行为模式。本文介绍了自闭症谱系障碍的遗传基础和神经机制。ASD遗传率高,个体5-HT和睾酮水平均较高。神经影像学研究发现,ASD与正常人在杏仁核、扣带回、梭状回、镜像神经元、前额叶等脑区结构和功能上存在一定差异,但在部分区域激活模式的差异方向上并不一致。此外,功能连接研究的结果也证实了ASD个体连接不足的假设。未来的研究应更多关注如何利用基础研究成果为临床研究提出有效的治疗和培训。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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