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脆性 X 综合征与自闭症的早期脑容量发育轨迹。

Trajectories of early brain volume development in fragile X syndrome and autism.

机构信息

University of North Carolina at Chapel Hill and the Carolina Institute for Developmental Disabilities, NC 27599-2267, USA.

出版信息

J Am Acad Child Adolesc Psychiatry. 2012 Sep;51(9):921-33. doi: 10.1016/j.jaac.2012.07.003. Epub 2012 Aug 1.

Abstract

OBJECTIVE

To examine patterns of early brain growth in young children with fragile X syndrome (FXS) compared with a comparison group (controls) and a group with idiopathic autism.

METHOD

The study included 53 boys 18 to 42 months of age with FXS, 68 boys with idiopathic autism (autism spectrum disorder), and a comparison group of 50 typically developing and developmentally delayed controls. Structural brain volumes were examined using magnetic resonance imaging across two time points, at 2 to 3 and again at 4 to 5 years of age, and total brain volumes and regional (lobar) tissue volumes were examined. In addition, a selected group of subcortical structures implicated in the behavioral features of FXS (e.g., basal ganglia, hippocampus, amygdala) was studied.

RESULTS

Children with FXS had larger global brain volumes compared with controls but were not different than children with idiopathic autism, and the rate of brain growth from 2 to 5 years of age paralleled that seen in controls. In contrast to children with idiopathic autism who had generalized cortical lobe enlargement, children with FXS showed specific enlargement in the temporal lobe white matter, cerebellar gray matter, and caudate nucleus, but a significantly smaller amygdala.

CONCLUSIONS

This structural longitudinal magnetic resonance imaging study of preschoolers with FXS observed generalized brain overgrowth in children with FXS compared with controls, evident at age 2 and maintained across ages 4 to 5. In addition, different patterns of brain growth that distinguished boys with FXS from boys with idiopathic autism were found.

摘要

目的

研究脆性 X 综合征(FXS)患儿与对照组和特发性自闭症组相比早期大脑生长模式。

方法

该研究纳入了 53 名 18 至 42 个月大的 FXS 男孩、68 名特发性自闭症(自闭症谱系障碍)男孩和 50 名发育正常和发育迟缓的对照组男孩。通过磁共振成像(MRI)在 2 至 3 岁和 4 至 5 岁两个时间点检查脑结构体积,并检查总脑体积和区域(叶)组织体积。此外,还研究了与 FXS 行为特征相关的一组选定的皮质下结构(如基底节、海马体、杏仁核)。

结果

与对照组相比,FXS 患儿的全脑体积较大,但与特发性自闭症患儿无差异,从 2 岁到 5 岁的大脑生长速度与对照组相似。与特发性自闭症患儿的广泛皮质叶增大不同,FXS 患儿的颞叶白质、小脑灰质和尾状核体积增大,但杏仁核体积明显较小。

结论

这项对学龄前 FXS 患儿的结构性纵向磁共振成像研究观察到,与对照组相比,FXS 患儿存在普遍的脑过度生长,这种情况在 2 岁时明显,并在 4 至 5 岁时持续存在。此外,还发现了 FXS 患儿与特发性自闭症患儿之间存在不同的大脑生长模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6a/3428739/0856b8b80449/nihms-393015-f0001.jpg

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