Lee Hyoung-Gon, Castellani Rudy J, Zhu Xiongwei, Perry George, Smith Mark A
Institute of Pathology, Case Western Reserve University, 2085 Adelbert Road, Cleveland, OH 44106, USA.
Int J Exp Pathol. 2005 Jun;86(3):133-8. doi: 10.1111/j.0959-9673.2005.00429.x.
While the pathogenesis of Alzheimer's disease (AD) is unclear, amyloid-beta plaques remain major lesions in the brain of individuals with AD. Likewise, amyloid-beta is one of the best-studied proteins relating to the pathogenesis of AD. Indeed, the pathological diagnosis of AD tends to be congruous with the quantity of amyloid-beta. However, it is important to recognize that pathological diagnosis merely represents the association of a pattern of pathological changes with a clinical phenotype. Therefore, it should be acknowledged that, although amyloid-beta detection and semiquantification have some diagnostic utility, the simple presence of amyloid plaques, as with proteinaceous accumulations in essentially all neurodegenerative diseases, does not presume aetiology. Thus, in this review, we discuss the role of amyloid-beta in the pathogenesis of AD and provide an alternative view to the widely accepted dogma.
虽然阿尔茨海默病(AD)的发病机制尚不清楚,但β-淀粉样蛋白斑块仍然是AD患者大脑中的主要病变。同样,β-淀粉样蛋白是与AD发病机制相关研究最多的蛋白质之一。事实上,AD的病理诊断往往与β-淀粉样蛋白的数量相一致。然而,必须认识到病理诊断仅仅代表了病理变化模式与临床表型之间的关联。因此,应该承认,尽管β-淀粉样蛋白的检测和半定量具有一定的诊断价值,但与基本上所有神经退行性疾病中的蛋白质积聚一样,单纯存在淀粉样斑块并不能推断病因。因此,在本综述中,我们讨论了β-淀粉样蛋白在AD发病机制中的作用,并对广泛接受的教条提出了另一种观点。