Knopman D S, Parisi J E, Salviati A, Floriach-Robert M, Boeve B F, Ivnik R J, Smith G E, Dickson D W, Johnson K A, Petersen L E, McDonald W C, Braak H, Petersen R C
Department of Neurology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
J Neuropathol Exp Neurol. 2003 Nov;62(11):1087-95. doi: 10.1093/jnen/62.11.1087.
Despite general agreement about the boundaries of Alzheimer disease (AD), establishing a maximum limit for Alzheimer-type pathology in cognitively intact individuals might aid in defining more precisely the point at which Alzheimer pathology becomes clinically relevant. In this study, we examined the neuropathological changes in the brains of 39 longitudinally followed. cognitively normal elderly individuals (24 women, 15 men; age range 74-95, median 85 years). Neuropathological changes of the Alzheimer type were quantified by determining neurofibrillary tangle (NFT) staging by the method of Braak and Braak and by quantification of the abundance of diffuse, cored, and neuritic plaque burden using the scheme developed by the Consortium to Establish a Registry for Alzheimer Disease (CERAD). Vascular, Lewy body, and argyrophilic grain pathology were also assessed. We found 34 subjects (87%) with a Braak stage <IV; 32 subjects (82%) with less than moderate numbers of cored plaques and 37 subjects (95%) with less than moderate numbers of tau-positive neuritic plaques. Many subjects had moderate or frequent diffuse plaques (n = 19, 49%). By the National Institute on Aging-Reagan Institute (NIA-RI) criteria, none of our cases met criteria for high "likelihood" of AD. Four met NIA-RI criteria for intermediate "likelihood." Seven cases met CERAD criteria for possible AD. Nineteen met Khachaturian criteria for AD. Only 1 subject had neocortical Lewy bodies. Small, old infarcts were common, but no subjects had more than 2 of these and none had a single large infarction. Thus, the majority of individuals who are cognitively normal near the time of their death have minimal amounts of tau-positive neuritic pathology (Braak stage <IV and neuritic plaques <6 per x100 field in the most affected neocortical region). The few subjects with more severe AD pathology can be expected based on incidence rates of AD in the very elderly.
尽管对于阿尔茨海默病(AD)的界限已达成普遍共识,但确定认知功能正常个体中阿尔茨海默型病理变化的最大限度,可能有助于更精确地界定阿尔茨海默病病理在临床上具有相关性的临界点。在本研究中,我们检查了39名纵向随访的认知正常老年人(24名女性,15名男性;年龄范围74 - 95岁,中位数85岁)大脑的神经病理学变化。通过采用Braak和Braak的方法确定神经原纤维缠结(NFT)分期,并使用阿尔茨海默病注册登记协会(CERAD)制定的方案对弥漫性、有核心和神经炎性斑块负荷的丰度进行量化,从而对阿尔茨海默型神经病理学变化进行定量分析。同时也评估了血管、路易体和嗜银颗粒病理。我们发现34名受试者(87%)Braak分期<IV;32名受试者(82%)有核心斑块数量少于中度;37名受试者(95%)tau阳性神经炎性斑块数量少于中度。许多受试者有中度或频繁的弥漫性斑块(n = 19,49%)。按照美国国立衰老研究所 - 里根研究所(NIA - RI)标准,我们的病例均未达到AD高“可能性”标准。4例符合NIA - RI中度“可能性”标准。7例符合CERAD可能AD标准。19例符合哈恰图良AD标准。只有1名受试者有新皮质路易体。小的陈旧性梗死很常见,但没有受试者有超过2个,也没有单个大梗死灶。因此,大多数在接近死亡时认知正常的个体,其tau阳性神经炎性病理变化极少(Braak分期<IV且在最受累新皮质区域每100视野神经炎性斑块<6个)。根据高龄人群中AD的发病率,少数有更严重AD病理变化的受试者是可以预期的。