Cambridge Cognition Ltd., Tunbridge Court, Tunbridge Lane, Bottisham, Cambridge CB25 9TU, UK; Faculty of Psychology & Neurosciences, Maastricht University, The Netherlands; Department of Psychiatry, University of Cambridge, Cambridge, UK.
Curr Opin Pharmacol. 2014 Feb;14:18-22. doi: 10.1016/j.coph.2013.10.002. Epub 2013 Nov 13.
Alzheimer's disease (AD) is a chronic neurodegenerative disease leading to cognitive decline, dementia, and ultimately death. Despite extensive R&D efforts, there are no diseases modifying treatments for AD available. The stage in which patients receive a clinical diagnosis of probable AD may be too late for disease modifying pharmacotherapy. Prevention strategies may be required to successfully tackle AD. Preclinical AD applies to over half of all healthy elderly subjects and manifests by signs of amyloid deposition and/or neuronal injury in the brain, preceding the stage in which symptoms of dementia, cognitive and functional impairment become observable. Prevention trials in preclinical AD require longer and larger clinical trials using biomarkers and cognitive endpoints, which requires collaboration across academia, government and industry.
阿尔茨海默病(AD)是一种慢性神经退行性疾病,可导致认知能力下降、痴呆,最终导致死亡。尽管进行了广泛的研发努力,但目前尚无针对 AD 的疾病修饰治疗方法。患者接受可能的 AD 临床诊断的阶段可能为时已晚,无法进行疾病修饰的药物治疗。可能需要预防策略来成功解决 AD 问题。临床前 AD 适用于超过一半的所有健康老年人,其表现为大脑中淀粉样蛋白沉积和/或神经元损伤的迹象,早于痴呆、认知和功能障碍症状可观察到的阶段。临床前 AD 的预防试验需要使用生物标志物和认知终点进行更长时间和更大规模的临床试验,这需要学术界、政府和行业之间的合作。