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迈向阿尔茨海默病的临床前试验

[Toward Preclinical Trials for Alzheimer's Disease].

作者信息

Miyagawa Toji, Iwatsubo Takeshi

机构信息

Department of Neurology, The University of Tokyo Hospital.

出版信息

Brain Nerve. 2017 Jul;69(7):711-722. doi: 10.11477/mf.1416200812.

Abstract

A variety of disease-modifying therapies for Alzheimer's disease (AD) have been developed and advanced to late-phase clinical trials in AD dementia patients, but thus far, no single drug has proven its efficacy in a large phase III trial. In 2011, the National Institute on Aging-Alzheimer's Association (NIA-AA) criteria redefined the concept of AD to encompass the earlier amyloid-related pathophysiological changes of the preclinical stage and mild cognitive impairment (MCI). Clinical trials for AD are now moving toward these earlier stages of the disease, targeting MCI due to AD and preclinical AD. Intervention in the earlier stages of the amyloid cascade is believed to have a better chance at changing the natural course of AD and preventing or at least delaying the conversion to dementia. Although conducting a large and prolonged costly clinical trial in the preclinical stage is challenging, the first step in overcoming this challenge has been taken with enthusiasm and commitment.

摘要

针对阿尔茨海默病(AD)的多种疾病修饰疗法已被开发出来,并推进到针对AD痴呆患者的晚期临床试验阶段,但迄今为止,尚无单一药物在大型III期试验中证明其疗效。2011年,美国国立衰老研究所-阿尔茨海默病协会(NIA-AA)标准重新定义了AD的概念,将临床前期和轻度认知障碍(MCI)的早期淀粉样蛋白相关病理生理变化纳入其中。目前,AD的临床试验正朝着疾病的这些早期阶段推进,目标是针对由AD引起的MCI和临床前期AD。人们认为,在淀粉样蛋白级联反应的早期阶段进行干预,更有可能改变AD的自然病程,并预防或至少延缓向痴呆的转化。尽管在临床前期阶段开展大规模、长期且成本高昂的临床试验具有挑战性,但克服这一挑战的第一步已在热情和决心的推动下迈出。

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