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Clearing the amyloid in Alzheimer's: progress towards earlier diagnosis and effective treatments - an update for clinicians

机译:清除阿尔茨海默氏病中的淀粉样蛋白:早期诊断和有效治疗的进展-临床医生的最新动态

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摘要

A beta (Ap or (3-amyloid) is a key molecule in Alzheimer's disease (AD) pathogenesis. According to the 'amyloid hypothesis', the gradual accumulation of Ap triggers events which results in neuronal loss in regions of the brain involved with memory and learning. Diverse agents have been developed to reduce brain Ap accumulation or to enhance its clearance. Some have progressed to human trials, however all have failed to improve cognition in patients. This has led researchers to question whether Ap is really the problem. However, the trials have been targeting end stages of AD, by which stage extensive irreversible neuronal damage has already occurred. Intervention is required preclinically, therefore preclinical AD biomarkers are needed. In this regard, amyloid imaging and cerebrospinal fluid biomarkers are leading the way, with plasma biomarkers and eye tests also being investigated. This review covers the current state of knowledge of Ap as an early diagnostic biomarker and as a therapeutic target in AD.
机译:β(Ap或(3-淀粉样蛋白)是阿尔茨海默氏病(AD)发病机理的关键分子。根据“淀粉样蛋白假说”,Ap的逐渐积累会触发事件,导致与记忆有关的大脑区域神经元丢失已经开发出了多种药物来减少脑中AP的积累或提高其清除率;有些药物已经进行了人体试验,但都未能改善患者的认知能力,这引起研究人员质疑Ap的确是问题所在。 ,这些试验针对的是AD的晚期阶段,此阶段已经发生了广泛的不可逆神经元损伤,因此在临床前需要干预,因此需要临床前的AD生物标志物,在这方面,淀粉样蛋白显像和脑脊髓液生物标志物是引领者,血浆生物标志物和眼试验的研究也正在进行中,该综述涵盖了作为早期诊断生物标志物和治疗方法的Ap的最新知识在公元的目标。

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