James J Peters VA Medical Center, Research & Development, Bronx, NY, 10468, USA.
Department of Neurology, Alzheimer Disease Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Mol Neurodegener. 2018 Dec 12;13(1):64. doi: 10.1186/s13024-018-0299-8.
Alzheimer's Disease (AD), the most prevalent neurodegenerative disease of aging, affects one in eight older Americans. Nearly all drug treatments tested for AD today have failed to show any efficacy. There is a great need for therapies to prevent and/or slow the progression of AD. The major challenge in AD drug development is lack of clarity about the mechanisms underlying AD pathogenesis and pathophysiology. Several studies support the notion that AD is a multifactorial disease. While there is abundant evidence that amyloid plays a role in AD pathogenesis, other mechanisms have been implicated in AD such as tangle formation and spread, dysregulated protein degradation pathways, neuroinflammation, and loss of support by neurotrophic factors. Therefore, current paradigms of AD drug design have been shifted from single target approach (primarily amyloid-centric) to developing drugs targeted at multiple disease aspects, and from treating AD at later stages of disease progression to focusing on preventive strategies at early stages of disease development. Here, we summarize current strategies and new trends of AD drug development, including pre-clinical and clinical trials that target different aspects of disease (mechanism-based versus non-mechanism based, e.g. symptomatic treatments, lifestyle modifications and risk factor management).
阿尔茨海默病(AD)是最常见的衰老性神经退行性疾病,影响着每 8 个美国老年人中的 1 个。目前针对 AD 测试的几乎所有药物治疗都未能显示出任何疗效。因此,迫切需要预防和/或减缓 AD 进展的治疗方法。AD 药物开发的主要挑战是对 AD 发病机制和病理生理学的潜在机制缺乏明确认识。有几项研究支持 AD 是一种多因素疾病的观点。虽然有大量证据表明淀粉样蛋白在 AD 发病机制中起作用,但其他机制也与 AD 有关,如缠结的形成和传播、蛋白质降解途径失调、神经炎症以及神经营养因子的丧失。因此,目前 AD 药物设计的范式已从单一靶点方法(主要以淀粉样蛋白为中心)转变为针对多种疾病方面的药物开发,从疾病进展后期的 AD 治疗转变为聚焦于疾病发展早期的预防策略。在这里,我们总结了 AD 药物开发的当前策略和新趋势,包括针对疾病不同方面的临床前和临床试验(基于机制与非基于机制,例如症状治疗、生活方式改变和危险因素管理)。