Minshew Nancy J, Williams Diane L
Webster Hall, Suite 300, 3811 O'Hara St, Pittsburgh, PA 15213, USA.
Arch Neurol. 2007 Jul;64(7):945-50. doi: 10.1001/archneur.64.7.945.
This review covers a fraction of the new research developments in autism but establishes the basic elements of the new neurobiologic understanding of autism. Autism is a polygenetic developmental neurobiologic disorder with multiorgan system involvement, though it predominantly involves central nervous system dysfunction. The evidence supports autism as a disorder of the association cortex, both its neurons and their projections. In particular, it is a disorder of connectivity, which appears, from current evidence, to primarily involve intrahemispheric connectivity. The focus of connectivity studies thus far has been on white matter, but alterations in functional magnetic resonance imaging activation suggest that intracortical connectivity is also likely to be disturbed. Furthermore, the disorder has a broad impact on cognitive and neurologic functioning. Deficits in high-functioning individuals occur in processing that places high demands on integration of information and coordination of multiple neural systems. Intact or enhanced abilities share a dependence on low information-processing demands and local neural connections. This multidomain model with shared characteristics predicts an underlying pathophysiologic mechanism that impacts the brain broadly, according to a common neurobiologic principle. The multiorgan system involvement and diversity of central nervous system findings suggest an epigenetic mechanism.
本综述涵盖了自闭症新研究进展的一部分内容,但确立了对自闭症神经生物学新认识的基本要素。自闭症是一种多基因发育性神经生物学障碍,涉及多器官系统,不过主要累及中枢神经系统功能障碍。有证据表明,自闭症是联合皮质及其神经元和投射的一种障碍。特别是,它是一种连接障碍,从目前的证据来看,主要涉及半球内连接。迄今为止,连接性研究的重点一直是白质,但功能磁共振成像激活的改变表明皮质内连接也可能受到干扰。此外,该障碍对认知和神经功能有广泛影响。高功能个体在对信息整合和多个神经系统协调有高要求的加工过程中存在缺陷。完好或增强的能力都依赖于低信息加工需求和局部神经连接。这种具有共同特征的多领域模型预测了一种根据共同神经生物学原理对大脑产生广泛影响的潜在病理生理机制。多器官系统受累以及中枢神经系统发现的多样性提示存在一种表观遗传机制。