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脆性X综合征与自闭症之间区域灰质的基于体素的形态测量学比较。

A voxel-based morphometry comparison of regional gray matter between fragile X syndrome and autism.

作者信息

Wilson Lisa B, Tregellas Jason R, Hagerman Randi J, Rogers Sally J, Rojas Donald C

机构信息

Department of Psychiatry, University of Colorado at Denver, Denver, CO, 80045, USA.

出版信息

Psychiatry Res. 2009 Nov 30;174(2):138-45. doi: 10.1016/j.pscychresns.2009.04.013. Epub 2009 Oct 22.

Abstract

The phenotypic association between fragile X syndrome (FXS) and autism is well established, but no studies have directly compared whole-brain anatomy between the two disorders. We performed voxel-based morphometry analyses of magnetic resonance imaging (MRI) scans on 10 individuals with FXS, 10 individuals with autism, and 10 healthy comparison subjects to identify volumetric changes in each disorder. Regional gray matter volumes within frontal, parietal, temporal, and cingulate gyri, as well as in the caudate nuclei and cerebellum, were larger in the FXS group relative to the autism group. In addition, volume increases in FXS were observed in frontal gyri and caudate nuclei compared to controls. The autism group exhibited volume increases in frontal and temporal gyri relative to the FXS group, and no volume increases relative to controls. Volumetric deficits relative to controls were observed in regions of the cerebellum for both groups, with additional deficits in parietal and temporal gyri for the FXS group. Our caudate nuclei and frontal gyri results may implicate dysfunction of frontostriatal circuitry in FXS. Cerebellar deficits suggest atypical development of the cerebellum contributing to the phenotype of both disorders, but further imply that unique cerebellar regions contribute to the phenotype of each disorder.

摘要

脆性X综合征(FXS)与自闭症之间的表型关联已得到充分证实,但尚无研究直接比较这两种疾病的全脑解剖结构。我们对10名FXS患者、10名自闭症患者和10名健康对照者的磁共振成像(MRI)扫描进行了基于体素的形态学分析,以确定每种疾病中的体积变化。与自闭症组相比,FXS组额叶、顶叶、颞叶和扣带回以及尾状核和小脑中的区域灰质体积更大。此外,与对照组相比,FXS组的额叶回和尾状核体积增加。自闭症组相对于FXS组在额叶和颞叶回中表现出体积增加,相对于对照组则没有体积增加。两组在小脑区域均观察到相对于对照组的体积缺陷,FXS组在顶叶和颞叶回中还有额外的缺陷。我们关于尾状核和额叶回的结果可能暗示了FXS中额叶纹状体回路的功能障碍。小脑缺陷表明小脑的非典型发育导致了这两种疾病的表型,但进一步表明独特的小脑区域导致了每种疾病的表型。

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