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脆性X前突变携带者小脑和脑干体积的异常轨迹。

Abnormal trajectories in cerebellum and brainstem volumes in carriers of the fragile X premutation.

作者信息

Wang Jun Yi, Hessl David, Hagerman Randi J, Simon Tony J, Tassone Flora, Ferrer Emilio, Rivera Susan M

机构信息

Center for Mind and Brain, University of California-Davis, Davis, CA, USA.

Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California-Davis Medical Center, Sacramento, CA, USA; Department of Psychiatry and Behavioral Sciences, University of California-Davis, School of Medicine, Sacramento, CA, USA.

出版信息

Neurobiol Aging. 2017 Jul;55:11-19. doi: 10.1016/j.neurobiolaging.2017.03.018. Epub 2017 Mar 18.

Abstract

Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder typically affecting male premutation carriers with 55-200 CGG trinucleotide repeat expansions in the FMR1 gene after age 50. The aim of this study was to examine whether cerebellar and brainstem changes emerge during development or aging in late life. We retrospectively analyzed magnetic resonance imaging scans from 322 males (age 8-81 years). Volume changes in the cerebellum and brainstem were contrasted with those in the ventricles and whole brain. Compared to the controls, premutation carriers without FXTAS showed significantly accelerated volume decrease in the cerebellum and whole brain, flatter inverted U-shaped trajectory of the brainstem, and larger ventricles. Compared to both older controls and premutation carriers without FXTAS, carriers with FXTAS exhibited significant volume decrease in the cerebellum and whole brain and accelerated volume decrease in the brainstem. We therefore conclude that cerebellar and brainstem volumes were likely affected during both development and progression of neurodegeneration in premutation carriers, suggesting that interventions may need to start early in adulthood to be most effective.

摘要

脆性X相关震颤/共济失调综合征(FXTAS)是一种迟发性神经退行性疾病,通常影响携带前突变的男性,这些男性在50岁以后FMR1基因中出现55 - 200个CGG三核苷酸重复扩增。本研究的目的是检查小脑和脑干的变化是在发育过程中还是在晚年衰老过程中出现。我们回顾性分析了322名男性(年龄8 - 81岁)的磁共振成像扫描结果。将小脑和脑干的体积变化与脑室和全脑的体积变化进行对比。与对照组相比,未患FXTAS的前突变携带者小脑和全脑体积显著加速减小,脑干的倒U形轨迹更平缓,脑室更大。与老年对照组和未患FXTAS的前突变携带者相比,患FXTAS的携带者小脑和全脑体积显著减小,脑干体积加速减小。因此,我们得出结论,前突变携带者在神经退行性变的发育和进展过程中,小脑和脑干体积可能均受到影响,这表明干预可能需要在成年早期开始才最有效。

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