Giannakopoulos P, Hof P R, Mottier S, Michel J P, Bouras C
Geriatric Hospital, University of Geneva School of Medicine, Switzerland.
Acta Neuropathol. 1994;87(5):456-68. doi: 10.1007/BF00294172.
To examine the neuropathological and clinical characteristics of cerebral aging, we evaluated retrospectively a non-selected autopsy population of 1258 patients from the Geriatric Hospital of the University of Geneva School of Medicine. The prevalence of Alzheimer's disease increased with age below 90 years of age. In the nonagenarians and centenarians, there was a decline in the number of affected cases. The distribution with age of neurofibrillary tangles and senile plaques varied among the cortical areas studied. The CA1 field of the hippocampus and the inferior temporal cortex displayed increasing densities of neurofibrillary tangles with age, whereas the superior frontal and the occipital cortex were relatively spared, especially in patients in their tenth and eleventh decade. The percentage of cases presenting with senile plaques in the neocortex and hippocampal structure increased with age with a marked predominance of cases with moderate to high senile plaque densities. Neurofibrillary tangles were often observed in the CA1 field and the inferior temporal cortex of non-demented individuals and were present in most cases with Alzheimer's disease. Conversely, the involvement of the superior frontal and occipital cortex was moderate even in demented patients. The distribution of senile plaques was homogeneous in all of the neocortical areas independently of the clinical diagnosis. Moreover, there was no correlation between the presence of neurofibrillary tangles and senile plaques in the cerebral regions studied. These results indicate a differential topography of neurofibrillary tangles and senile plaques, and suggest that overt clinical signs of Alzheimer's disease are linked to the progression of the neurodegenerative process in neocortical areas.
为研究大脑衰老的神经病理学和临床特征,我们对日内瓦大学医学院老年医院1258例未经过挑选的尸检患者进行了回顾性评估。阿尔茨海默病的患病率在90岁以下随年龄增长而增加。在九旬老人和百岁老人中,患病病例数有所下降。神经原纤维缠结和老年斑的年龄分布在所研究的皮质区域中各不相同。海马体的CA1区和颞下回皮质中神经原纤维缠结的密度随年龄增加,而额上回和枕叶皮质相对较少受累,尤其是在十和十一十年纪的患者中。新皮质和海马结构中出现老年斑的病例百分比随年龄增加,且中度至高度老年斑密度的病例明显占优势。在非痴呆个体的CA1区和颞下回皮质中经常观察到神经原纤维缠结,且在大多数阿尔茨海默病病例中也存在。相反,即使在痴呆患者中,额上回和枕叶皮质的受累程度也较轻。老年斑在所有新皮质区域的分布均一,与临床诊断无关。此外,在所研究的脑区中,神经原纤维缠结和老年斑的存在之间没有相关性。这些结果表明神经原纤维缠结和老年斑的分布存在差异,并提示阿尔茨海默病的明显临床症状与新皮质区域神经退行性过程的进展有关。