Riley Kathryn P, Snowdon David A, Markesbery William R
Sanders-Brown Center on Aging, Department of Preventive Medicine, University of Kentucky, Lexington, KY 40536, USA.
Ann Neurol. 2002 May;51(5):567-77. doi: 10.1002/ana.10161.
The development of interventions designed to delay the onset of dementia highlights the need to determine the neuropathologic characteristics of individuals whose cognitive function ranges from intact to demented, including those with mild cognitive impairments. We used the Braak method of staging Alzheimer's disease pathology in 130 women ages 76-102 years who were participants in the Nun Study, a longitudinal study of aging and Alzheimer's disease. All participants had complete autopsy data and were free from neuropathologic conditions other than Alzheimer's disease lesions that could affect cognitive function. Findings showed a strong relationship between Braak stage and cognitive state. The presence of memory impairment was associated with more severe Alzheimer's disease pathology and higher incidence of conversion to dementia in the groups classified as having mild or global cognitive impairments. In addition to Braak stage, atrophy of the neocortex was significantly related to the presence of dementia. Our data indicate that Alzheimer's neurofibrillary pathology is one of the neuropathologic substrates of mild cognitive impairments. Additional studies are needed to help explain the variability in neuropathologic findings seen in individuals whose cognitive performance falls between intact function and dementia.
旨在延缓痴呆症发病的干预措施的发展凸显了确定认知功能从完好到痴呆的个体(包括轻度认知障碍者)的神经病理学特征的必要性。我们对参与修女研究(一项关于衰老和阿尔茨海默病的纵向研究)的130名76至102岁女性,采用Braak方法对阿尔茨海默病病理进行分期。所有参与者都有完整的尸检数据,且除了可能影响认知功能的阿尔茨海默病病变外,没有其他神经病理学状况。研究结果显示Braak分期与认知状态之间存在密切关系。在被归类为轻度或整体认知障碍的组中,记忆障碍的存在与更严重的阿尔茨海默病病理以及转化为痴呆症的更高发生率相关。除了Braak分期外,新皮质萎缩与痴呆症的存在也显著相关。我们的数据表明,阿尔茨海默病神经原纤维病理是轻度认知障碍的神经病理学基础之一。需要进一步的研究来帮助解释在认知表现介于完好功能和痴呆之间的个体中所见神经病理学发现的变异性。