Department of Pathology and Division of Neuropathology, University of Kentucky Medical Center, Sanders-Brown Center on Aging and Alzheimer's Disease Center, University of Kentucky, Lexington, KY, USA.
Brain Pathol. 2010 Jan;20(1):66-79. doi: 10.1111/j.1750-3639.2008.00244.x. Epub 2008 Nov 19.
We evaluated the association between mini-mental status examination (MMSE) scores proximal to death and the values of 43 different clinical and pathological parameters. Studies were performed using data from 334 elderly, longitudinally evaluated research subjects who had undergone autopsy and satisfied inclusion criteria from an initial study group of 501. Interindividual variance in MMSE scores was used as a surrogate for the severity of cognitive impairment linked to aging (CILA). A statistical linear regression-based model provided a framework for assessing the parameters with significant, direct impact on CILA severity. Strong association between CILA and Alzheimer's disease (AD) pathology, especially isocortical neurofibrillary tangles, was evident. The pattern of association between AD lesion densities with cognitive impairment severity was biologically informative, with neuritic plaques having more impact in relatively high-functioning individuals. Abundant isocortical Lewy bodies tended to be an additive pathology correlating with final MMSE scores approximately 10 points lower. In a subset of cases we found evidence for association between TDP-43-related pathology and CILA severity, independent of AD or hippocampal sclerosis. There was no support for independent association between CILA severity and most evaluated indices including diffuse plaques, argyrophilic grains, heart disease, education level, apolipoprotein E alleles or diabetes.
我们评估了接近死亡时的简易精神状态检查(MMSE)评分与 43 种不同临床和病理参数值之间的关联。这些研究使用了来自 334 名接受过尸检且符合 501 名初始研究组纳入标准的纵向评估研究对象的数据。MMSE 评分的个体间差异被用作与衰老相关的认知障碍严重程度(CILA)的替代指标。基于统计线性回归的模型为评估对 CILA 严重程度有直接显著影响的参数提供了一个框架。CILA 与阿尔茨海默病(AD)病理学之间存在很强的关联,尤其是皮质神经原纤维缠结。AD 病变密度与认知障碍严重程度之间的关联模式具有生物学意义,神经原纤维缠结在功能相对较高的个体中影响更大。皮质Lewy 体丰富倾向于成为一种附加病理学,与最终的 MMSE 评分相关,约低 10 分。在一部分病例中,我们发现 TDP-43 相关病理学与 CILA 严重程度之间存在关联的证据,与 AD 或海马硬化无关。CILA 严重程度与大多数评估指标之间没有独立关联的证据,包括弥漫性斑块、嗜银颗粒、心脏病、教育程度、载脂蛋白 E 等位基因或糖尿病。