Zhang Xingyu, Fu Zhihui, Meng Lanxia, He Mingyang, Zhang Zhentao
Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, China.
Front Aging Neurosci. 2018 Nov 13;10:359. doi: 10.3389/fnagi.2018.00359. eCollection 2018.
Alzheimer's disease (AD) is characterized by the development of amyloid plaques and neurofibrillary tangles (NFTs) consisting of aggregated β-amyloid (Aβ) and tau, respectively. The amyloid hypothesis has been the predominant framework for research in AD for over two decades. According to this hypothesis, the accumulation of Aβ in the brain is the primary factor initiating the pathogenesis of AD. However, it remains elusive what factors initiate Aβ aggregation. Studies demonstrate that AD has multiple causes, including genetic and environmental factors. Furthermore, genetic factors, many age-related events and pathological conditions such as diabetes, traumatic brain injury (TBI) and aberrant microbiota also affect the aggregation of Aβ. Here we provide an overview of the age-related early events and other pathological processes that precede Aβ aggregation.
阿尔茨海默病(AD)的特征是分别由聚集的β-淀粉样蛋白(Aβ)和tau组成的淀粉样斑块和神经原纤维缠结(NFTs)的形成。淀粉样蛋白假说在二十多年来一直是AD研究的主要框架。根据这一假说,大脑中Aβ的积累是引发AD发病机制的主要因素。然而,启动Aβ聚集的因素仍然不明。研究表明,AD有多种病因,包括遗传和环境因素。此外,遗传因素、许多与年龄相关的事件以及诸如糖尿病、创伤性脑损伤(TBI)和异常微生物群等病理状况也会影响Aβ的聚集。在这里,我们概述了在Aβ聚集之前与年龄相关的早期事件和其他病理过程。