Perea Rodrigo D, Rada Rebecca C, Wilson Jessica, Vidoni1 Eric D, Morris Jill K, Lyons Kelly E, Pahwa Rajesh, Burns Jeffrey M, Honea Robyn A
Department of Neurology, University of Kansas School of Medicine, Kansas City, KS, USA ; Alzheimer's Research Disease Center, University of Kansas School of Medicine, Kansas City, KS, USA ; Bioengineering Program, Department of Engineering, University of Kansas, Lawrence, KS, USA.
Alzheimer's Research Disease Center, University of Kansas School of Medicine, Kansas City, KS, USA.
J Alzheimers Dis Parkinsonism. 2013 Aug 26;3:123. doi: 10.4172/2161-0460.1000123.
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.
阿尔茨海默病(AD)和帕金森病(PD)是影响老年人群的最常见神经退行性疾病。AD的特征是记忆力受损和认知功能下降,而PD的主要症状包括静止性震颤、运动迟缓及僵硬。在PD中,常出现轻度认知改变,可能进展为痴呆(帕金森病痴呆,PDD)。PDD和AD痴呆在病理学上有所不同,尽管微观结构变化的差异尚不清楚。为了进一步了解这些疾病,了解其微观结构变化的独特机制至关重要。我们使用扩散张量成像(DTI)来研究早期AD患者(n = 14)、PD患者(n = 12)、PDD患者(n = 9)和健康非痴呆对照者(CON)(n = 13)之间的白质束差异。我们使用基于全脑轨迹的空间统计学(TBSS)以及聚焦于黑质(SN)的感兴趣区域(ROI)分析。我们发现,与PD、AD和CON相比,PDD患者的白质变性更为广泛。AD患者在胼胝体前后投射中有一些局部异常,而与其他组相比,PD患者和CON患者似乎没有明显的白质变性。ROI分析显示,PDD患者在SN中的扩散率最高,且与CON有显著差异。CON、PD或AD之间在ROI上没有显著差异。总之,PDD患者存在明显的全脑白质微观结构恶化,DTI可能提供一种区分AD和PD痴呆病理差异的方法。