白质与帕金森病、帕金森病合并痴呆和阿尔茨海默病的比较研究。

Rodrigo D Perea, Rebecca C Rada, Jessica Wilson, Eric D Vidoni1, Jill K Morris, Kelly E Lyons, Rajesh Pahwa, Jeffrey M Burns, Robyn A Honea
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引用次数: 29

摘要

阿尔茨海默病(AD)和帕金森病(PD)是影响老年人最常见的神经退行性疾病。AD的特点是记忆受损和认知能力下降,而PD的主要症状包括静息性震颤、运动迟缓和僵硬。PD患者经常出现轻度认知改变,并可能发展为痴呆(PD dementia, PDD)。PDD和AD痴呆在病理上不同,但显微结构变化的差异尚不清楚。为了进一步了解这些疾病,有必要了解其微观结构变化的独特机制。我们使用弥散张量成像(DTI)来研究早期AD (n=14)、PD (n=12)、PDD (n=9)和健康非痴呆对照(n=13)之间的白质束差异。我们使用基于全脑束的空间统计(TBSS)和关注黑质(SN)的兴趣区(ROI)分析。我们发现,与PD、AD和CON相比,PDD患者有更广泛的白质变性。AD患者在胼胝体的前后投射区几乎没有区域异常,而PD和CON患者与其他组相比,没有明显的白质变性。ROI分析显示,PDD在SN中的扩散率最高,与CON有显著差异。CON、PD和AD之间的ROI无显著差异。总之,PDD患者整体白质微结构明显恶化,DTI可能为梳理AD和PD痴呆的病理差异提供了一种手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparative White Matter Study with Parkinson's disease, Parkinson's Disease with Dementia and Alzheimer's Disease.
Alzheimer's disease (AD) and Parkinson's disease (PD) are among the most common neurodegenerative disorders affecting older populations. AD is characterized by impaired memory and cognitive decline while the primary symptoms of PD include resting tremor, bradykinesia and rigidity. In PD, mild cognitive changes are frequently present, which could progress to dementia (PD dementia (PDD)). PDD and AD dementias are different in pathology although the difference in microstructural changes remains unknown. To further understand these diseases, it is essential to understand the distinct mechanism of their microstructural changes. We used diffusion tensor imaging (DTI) to investigate white matter tract differences between early stage individuals with AD (n=14), PD (n=12), PDD (n=9), and healthy non-demented controls (CON) (n=13). We used whole brain tract based spatial statistics (TBSS) and a region of interest (ROI) analysis focused on the substantia nigra (SN). We found that individuals with PDD had more widespread white matter degeneration compared to PD, AD, and CON. Individuals with AD had few regional abnormalities in the anterior and posterior projections of the corpus callosum while PD and CON did not appear to have significant white matter degeneration when compared to other groups. ROI analyses showed that PDD had the highest diffusivity in the SN and were significantly different from CON. There were no significant ROI differences between CON, PD, or AD. In conclusion, global white matter microstructural deterioration is evident in individuals with PDD, and DTI may provide a means with which to tease out pathological differences between AD and PD dementias.
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