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与额前叶执行功能相关的耦合与亨廷顿病的阶段有关。

Prefrontal executive function associated coupling relates to Huntington's disease stage.

机构信息

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Division of Psychiatry Research and Psychogeriatric Medicine, University of Zürich, Zürich, Switzerland.

出版信息

Cortex. 2013 Nov-Dec;49(10):2661-73. doi: 10.1016/j.cortex.2013.05.015. Epub 2013 Jun 26.

Abstract

Huntington's disease (HD) is a neurodegenerative disease caused by cytosine-adenine-guanine (CAG)-repeat expansion in the huntingtin (HTT) gene. Early changes that may precede clinical manifestation of movement disorder include executive dysfunction. The aim of this study was to identify functional network correlates of impaired higher cognitive functioning in relation to HD stage. Blood-oxygenation-level-dependent (BOLD) functional-magnetic resonance imaging (fMRI) and structural-MRI were performed in 53 subjects with the HD-mutation (41 prodromals, 12 early affected) and 52 controls. Disease stage was estimated for each subject with HD-mutation based on age, length of the CAG-repeat expansion mutation and also putaminal atrophy. The Tower of London test was administered with three levels of complexity during fMRI as a challenge of executive function. Functional brain networks of interest were identified based on cortical gray matter voxel-clusters with significantly enhanced task-related functional coupling to the medial prefrontal cortex (MPFC) area. While prodromal HD-subjects showed similar performance levels as controls, multivariate analysis of task-related functional coupling to the MPFC identified reduced connectivity in prodromal and early manifest HD-subjects for a cluster including mainly parts of the left premotor area. Secondary testing indicated a significant moderator effect for task complexity on group differences and on the degree of correlation to measures of HD stage. Our data suggest that impaired premotor-MPFC coupling reflects HD stage related dysfunction of cognitive systems involved in executive function and may be present in prodromal HD-subjects that are still cognitively normal. Additional longitudinal studies may reveal temporal relationships between impaired task-related premotor-MPFC coupling and other brain changes in HD.

摘要

亨廷顿病(HD)是一种神经退行性疾病,由亨廷顿(HTT)基因中的胞嘧啶-腺嘌呤-鸟嘌呤(CAG)重复扩展引起。可能先于运动障碍临床表现的早期变化包括执行功能障碍。本研究的目的是确定与 HD 阶段相关的认知功能障碍的功能网络相关性。对 53 名携带 HD 基因突变的受试者(41 名前驱期,12 名早期受影响)和 52 名对照进行了血氧水平依赖(BOLD)功能磁共振成像(fMRI)和结构磁共振成像。根据每个携带 HD 基因突变的受试者的年龄、CAG 重复扩展突变的长度以及壳核萎缩,估计疾病阶段。伦敦塔测验在 fMRI 期间进行了三个复杂程度的测试,作为执行功能的挑战。基于与内侧前额叶皮层(MPFC)区域显著增强的任务相关功能耦合的皮质灰质体素聚类,确定了感兴趣的功能脑网络。虽然前驱期 HD 受试者的表现水平与对照组相似,但对与 MPFC 相关的任务相关功能耦合的多变量分析确定了前驱期和早期显性 HD 受试者的连通性降低,涉及主要部分的聚类左运动前区。二次测试表明,任务复杂性对组间差异和与 HD 阶段测量的相关性具有显著的调节作用。我们的数据表明,运动前皮层-MPFC 耦合受损反映了与认知系统相关的认知功能障碍,这些认知系统涉及执行功能,并且可能存在于仍然认知正常的前驱期 HD 受试者中。额外的纵向研究可能会揭示 HD 中与任务相关的运动前皮层-MPFC 耦合受损与其他大脑变化之间的时间关系。

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