Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Pharmacology, University of Nis School of Medicine, Nis, Serbia.
Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA.
Ageing Res Rev. 2021 Jul;68:101318. doi: 10.1016/j.arr.2021.101318. Epub 2021 Mar 9.
The development of the next generation therapy for Alzheimer's disease (AD) presents a huge challenge given the number of promising treatment candidates that failed in trials, despite recent advancements in understanding of genetic, pathophysiologic and clinical characteristics of the disease. This review reflects some of the most current concepts and controversies in developing disease-modifying and new symptomatic treatments. It elaborates on recent changes in the AD research strategy for broadening drug targets, and potentials of emerging non-pharmacological treatment interventions. Established and novel biomarkers are discussed, including emerging cerebrospinal fluid and plasma biomarkers reflecting tau pathology, neuroinflammation and neurodegeneration. These fluid biomarkers together with neuroimaging findings can provide innovative objective assessments of subtle changes in brain reflecting disease progression. A particular emphasis is given to neurophysiological biomarkers which are well-suited for evaluating the brain overall neural network integrity and function. Combination of multiple biomarkers, including target engagement and outcome biomarkers will empower translational studies and facilitate successful development of effective therapies.
鉴于有大量有前景的治疗候选药物在临床试验中失败,开发阿尔茨海默病(AD)的下一代疗法是一项巨大的挑战,尽管近年来对该疾病的遗传、病理生理和临床特征的理解有了进展。本综述反映了在开发疾病修饰和新症状治疗方法方面的一些最新概念和争议。它详细介绍了为扩大药物靶点而改变 AD 研究策略的最新进展,以及新兴非药物治疗干预措施的潜力。讨论了现有的和新的生物标志物,包括反映 tau 病理学、神经炎症和神经退行性变的新兴脑脊液和血浆生物标志物。这些液体生物标志物与神经影像学发现一起,可以提供反映疾病进展的大脑细微变化的创新客观评估。特别强调了神经生理学生物标志物,它非常适合评估大脑整体神经网络的完整性和功能。多种生物标志物的组合,包括目标参与和结果生物标志物,将为转化研究提供支持,并有助于成功开发有效的治疗方法。