Giannakopoulos P, Hof P R, Giannakopoulos A S, Herrmann F R, Michel J P, Bouras C
Department of Psychiatry, University of Geneva School of Medicine, Switzerland.
Arch Neurol. 1995 Dec;52(12):1150-9. doi: 10.1001/archneur.1995.00540360028012.
To examine the correlations between senile lesion densities and development of dementia symptoms in very old people. To perform a quantitative neuropathologic evaluation of several cortical and subcortical areas in a series of 29 nonagenarians and centenarians.
Ten patients with no cognitive impairment and 19 patients with clinically overt Alzheimer's disease.
Neuropathologic case series. Severity of Alzheimer's disease was assessed with the Mini-Mental State examination and by postmortem chart review using the extended Clinical Dementia Rating Scale. Comparisons between neurofibrillary tangle and senile plaque densities in demented and nondemented individuals were performed by analysis of covariance controlling for age at the time of death.
Studies were conducted at the Psychiatric and Geriatric hospitals of the University of Geneva School of Medicine in Geneva, Switzerland.
Correlations between clinical diagnosis and severity of Alzheimer's disease and neuropathologic change densities.
Statistically significant differences were found in neurofibrillary tangle densities in the superior parietal, superior temporal, anterior and posterior cingulate cortex, and nucleus basalis of Meynert between nondemented and Alzheimer's disease cases. The superior parietal and posterior cingulate cortex contained significantly higher senile plaque counts in demented compared with nondemented cases. In contrast to younger demented cases, the number of senile plaques in the neocortex was correlated with the severity of dementia in centenarians.
These results indicate that the neuronal degeneration in very old demented patients involves cortical areas usually preserved at the early stages of the dementing process. Senile plaque formation in certain neocortical areas may be a pathologic hallmark of the severity of dementia in this particular age group.
研究高龄老人衰老病变密度与痴呆症状发展之间的相关性。对29例九旬老人和百岁老人的多个皮质和皮质下区域进行定量神经病理学评估。
10例无认知障碍患者和19例临床确诊为阿尔茨海默病的患者。
神经病理学病例系列研究。采用简易精神状态检查表评估阿尔茨海默病的严重程度,并使用扩展临床痴呆评定量表通过尸检图表回顾进行评估。通过协方差分析对死亡时的年龄进行控制,比较痴呆患者和非痴呆患者神经原纤维缠结和老年斑密度。
研究在瑞士日内瓦大学医学院的精神病医院和老年病医院进行。
临床诊断与阿尔茨海默病严重程度及神经病理学变化密度之间的相关性。
在非痴呆患者和阿尔茨海默病患者之间,顶叶上部、颞叶上部、前扣带回和后扣带回皮质以及迈内特基底核的神经原纤维缠结密度存在统计学显著差异。与非痴呆患者相比,痴呆患者的顶叶上部和后扣带回皮质老年斑计数明显更高。与年轻痴呆患者不同,百岁老人新皮质中的老年斑数量与痴呆严重程度相关。
这些结果表明,高龄痴呆患者的神经元变性涉及通常在痴呆过程早期得以保留的皮质区域。某些新皮质区域的老年斑形成可能是该特定年龄组痴呆严重程度的病理标志。