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伴有和不伴有脆性X相关震颤/共济失调综合征的脆性X前突变携带者的认知特征。

Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome.

作者信息

Grigsby Jim, Brega Angela G, Engle Karen, Leehey Maureen A, Hagerman Randi J, Tassone Flora, Hessl David, Hagerman Paul J, Cogswell Jennifer B, Bennett Rachael E, Cook Kylee, Hall Deborah A, Bounds Lanee S, Paulich Marsha J, Reynolds Ann

机构信息

Department of Medicine, University of Colorado.

Department of Neurology, University of Colorado.

出版信息

Neuropsychology. 2008 Jan;22(1):48-60. doi: 10.1037/0894-4105.22.1.48.

DOI:10.1037/0894-4105.22.1.48
PMID:18211155
Abstract

Fragile X-associated tremor/ataxia syndrome (FXTAS) develops in a subset of fragile X premutation carriers and involves gait ataxia, action tremor, Parkinsonism, peripheral neuropathy, autonomic disorders, and cognitive impairment. The study was designed to define the nature of cognitive deficits affecting male premutation carriers with and without FXTAS. A sample of 109 men underwent motor, cognitive, genetic, and neurologic testing, as well as brain magnetic resonance imaging. Subjects were classified into 3 groups: (a) asymptomatic premutation carriers, (b) premutation carriers with FXTAS, and (c) normal controls. Men with FXTAS performed worse than controls on mental status, intelligence, executive cognitive functioning (ECF), working memory, remote recall of information, declarative learning and memory, information processing speed, and temporal sequencing, as well as 1 measure of visuospatial functioning. Language and verbal comprehension were spared. Asymptomatic carriers performed worse than controls on ECF and declarative learning and memory. This comprehensive examination of cognitive impairment in male premutation carriers suggests that FXTAS involves substantial executive impairment and diffuse deficits in other cognitive functions. Longitudinal research currently underway will provide insight into the progression of the disorder.

摘要

脆性X染色体相关震颤/共济失调综合征(FXTAS)在一部分脆性X染色体前突变携带者中发病,其症状包括步态共济失调、动作性震颤、帕金森综合征、周围神经病变、自主神经功能障碍以及认知障碍。本研究旨在明确影响患有和未患有FXTAS的男性前突变携带者认知缺陷的本质。109名男性样本接受了运动、认知、基因和神经学检测,以及脑部磁共振成像检查。受试者被分为三组:(a)无症状前突变携带者,(b)患有FXTAS的前突变携带者,(c)正常对照组。患有FXTAS的男性在精神状态、智力、执行认知功能(ECF)、工作记忆、信息的远期回忆、陈述性学习和记忆、信息处理速度、时间序列以及一项视觉空间功能测量方面的表现均不如对照组。语言和言语理解功能未受影响。无症状携带者在ECF以及陈述性学习和记忆方面的表现也不如对照组。对男性前突变携带者认知障碍的这项全面检查表明,FXTAS涉及严重的执行功能障碍以及其他认知功能的弥漫性缺陷。目前正在进行的纵向研究将为该疾病的进展提供深入了解。

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