Armstrong R A
Vision Sciences, Aston University, Birmingham, UK.
Curr Aging Sci. 2008 Jul;1(2):122-32. doi: 10.2174/1874609810801020122.
Since the earliest descriptions of Alzheimer's disease (AD), the presence of senile plaques (SP) and neurofibrillary tangles (NFT) have been regarded as the typical pathological hallmarks of the disease. Studies over the last twenty years, however, have reported a considerable degree of heterogeneity within the AD phenotype and as a consequence, an overlap between the pathological features of AD not only with normal aging, but also with disorders related to AD. This review discusses: 1) the degree of heterogeneity within AD, 2) the concept of an 'interface' between disorders, 3) the nature and degree of the interface between AD and normal aging, vascular dementia (VD), the tauopathies, synucleinopathies, and prion disease, and 4) whether the original status of AD should be retained or whether AD, normal aging, and the related disorders should be regarded as representing a 'continuum' of neuropathological change.
自最早对阿尔茨海默病(AD)进行描述以来,老年斑(SP)和神经原纤维缠结(NFT)的存在一直被视为该疾病的典型病理标志。然而,过去二十年的研究报告称,AD表型存在相当程度的异质性,因此,AD的病理特征不仅与正常衰老存在重叠,还与AD相关疾病存在重叠。本综述讨论了:1)AD内部的异质性程度;2)疾病之间“界面”的概念;3)AD与正常衰老、血管性痴呆(VD)、tau蛋白病、α-突触核蛋白病和朊病毒病之间界面的性质和程度;4)AD的原始状态是否应保留,或者AD、正常衰老及相关疾病是否应被视为代表神经病理变化的“连续体”。