Attems Johannes, Lintner Felix, Jellinger Kurt A
Institute of Pathology, O. Wagner Hospital, Vienna, Austria.
J Alzheimers Dis. 2005 Apr;7(2):149-57; discussion 173-80. doi: 10.3233/jad-2005-7208.
Olfactory dysfunction and tau pathology in the olfactory bulb increase with the severity of Alzheimer's disease. We report data of a postmortem study in the aged. 130 autopsy cases (81 female, 49 male, aged 61-102, mean 82.48 +/- 4.35 SD) years, underwent a standardized neuropathological assessment with immunohistochemical study of tau pathology in the olfactory bulb and nerve and of Alzheimer's disease using established criteria including Braak staging. All cases of definite Alzheimer's disease (Braak stages 5 and 6) (n = 40) showed large numbers of neuropil threads and neurofibrillary tangles, with amyloid deposits in 32.5% and neuritic plaques in one single case in the olfactory system. Braak stage 4 (n = 27) was associated with mild to moderate tau pathology in 85.2%, and amyloid plaques in 1.1%, Braak stage 3 (n = 28) with olfactory tau lesions in 37.0% and amyloid deposits in one single case, Braak stages 3 and 4 with olfactory tau lesions in 61.1%. Braak stage 2 (n = 15) showed olfactory tau pathology in 31.2%, whereas Braak stages 0 and 1 (n = 15) were all negative. The olfactory system tau score showed highly significant correlations with neuritic Braak stages in the brain, while both scores showed significant but low correlations with age. These data confirm previous studies demonstrating abundant tau pathology in the olfactory system in all definite Alzheimer's disease cases, in two-thirds of limbic Alzheimer's disease, and in almost one-third of non-demented elderly persons with Braak stage 2. There are strong correlations between tau pathology in the olfactory and limbic systems, both with similar increase in severity. Clinical dementia correlated with both Braak and olfactory system tau scores. Since the involvement of both systems is associated with a high risk of cognitive decline, future studies should validate the sensitivity of olfactory mucosa biopsies in the diagnosis of Alzheimer's disease.
嗅球中的嗅觉功能障碍和tau病理改变随阿尔茨海默病的严重程度而增加。我们报告了一项针对老年人的尸检研究数据。130例尸检病例(81例女性,49例男性,年龄61 - 102岁,平均82.48±4.35标准差),接受了标准化神经病理学评估,包括使用既定标准(包括Braak分期)对嗅球和神经中的tau病理以及阿尔茨海默病进行免疫组织化学研究。所有确诊的阿尔茨海默病病例(Braak分期5和6)(n = 40)显示大量神经纤维丝和神经原纤维缠结,嗅系统中32.5%有淀粉样沉积,1例有神经炎斑块。Braak分期4(n = 27)中85.2%有轻度至中度tau病理改变,1.1%有淀粉样斑块;Braak分期3(n = 28)中37.0%有嗅球tau病变,1例有淀粉样沉积;Braak分期3和4中有61.1%有嗅球tau病变。Braak分期2(n = 15)中31.2%有嗅球tau病理改变,而Braak分期0和1(n = 15)均为阴性。嗅系统tau评分与大脑中的神经炎Braak分期高度相关,而这两个评分与年龄均呈显著但较弱的相关性。这些数据证实了先前的研究,即在所有确诊的阿尔茨海默病病例、三分之二的边缘型阿尔茨海默病以及近三分之一Braak分期为2的非痴呆老年人中,嗅系统存在大量tau病理改变。嗅系统和边缘系统中的tau病理改变之间存在很强的相关性,两者严重程度的增加相似。临床痴呆与Braak评分和嗅系统tau评分均相关。由于这两个系统的受累与认知衰退的高风险相关,未来的研究应验证嗅黏膜活检在阿尔茨海默病诊断中的敏感性。