Ecker Christine
University Hospital Frankfurt am Main, Germany
Autism. 2017 Jan;21(1):18-28. doi: 10.1177/1362361315627136. Epub 2016 Mar 14.
Autism spectrum disorder is a complex neurodevelopmental disorder, which is accompanied by differences in brain anatomy, functioning and brain connectivity. Due to its neurodevelopmental character, and the large phenotypic heterogeneity among individuals on the autism spectrum, the neurobiology of autism spectrum disorder is inherently difficult to describe. Nevertheless, significant progress has been made in characterizing the neuroanatomical underpinnings of autism spectrum disorder across the human life span, and in identifying the molecular pathways that may be affected in autism spectrum disorder. Moreover, novel methodological frameworks for analyzing neuroimaging data are emerging that make it possible to characterize the neuroanatomy of autism spectrum disorder on the case level, and to stratify individuals based on their individual phenotypic make up. While these approaches are increasingly more often employed in the research setting, their applicability in the clinical setting remains a vision for the future. The aim of the current review is to (1) provide a general overview of recent structural neuroimaging findings examining the neuroanatomy of autism spectrum disorder across the human life span, and in males and females with the condition, (2) highlight potential neuroimaging (bio)markers that may in the future be used for the stratification of autism spectrum disorder individuals into biologically homogeneous subgroups and (3) inform treatment and intervention strategies.
自闭症谱系障碍是一种复杂的神经发育障碍,伴有大脑解剖结构、功能及脑连接性方面的差异。由于其神经发育特性,以及自闭症谱系个体间巨大的表型异质性,自闭症谱系障碍的神经生物学本质上难以描述。尽管如此,在描述自闭症谱系障碍在人类整个生命周期中的神经解剖学基础,以及识别自闭症谱系障碍中可能受影响的分子途径方面,已经取得了显著进展。此外,用于分析神经影像数据的新方法框架正在出现,这使得在个体层面上描述自闭症谱系障碍的神经解剖结构,并根据个体的表型构成对个体进行分层成为可能。虽然这些方法在研究环境中越来越多地被采用,但其在临床环境中的适用性仍是未来的愿景。本综述的目的是:(1)对近期结构神经影像研究结果进行总体概述,这些研究考察了自闭症谱系障碍在人类整个生命周期中的神经解剖结构,以及患有该疾病的男性和女性的神经解剖结构;(2)强调潜在的神经影像(生物)标志物,这些标志物未来可能用于将自闭症谱系障碍个体分层为生物学上同质的亚组;(3)为治疗和干预策略提供信息。