Department of Medical Pharmacology, Expert Center for Parkinson, CHU-Lille, Lille Neuroscience & Cognition, Inserm, zUMR-S1172, LICEND, University of Lille, Lille, France.
Institut du Cerveau-ICM, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, Paris, France.
Mov Disord. 2021 Feb;36(2):306-316. doi: 10.1002/mds.28379. Epub 2020 Nov 13.
Parkinson's disease (PD) is a neurodegenerative disorder characterized by loss of dopaminergic neurons in the substantia nigra and accumulation of iron and alpha-synuclein; it follows a characteristic pattern throughout the nervous system. Despite decades of successful preclinical neuroprotective studies, no drug has then shown efficacy in clinical trials. Considering this dilemma, we have reviewed and organized solutions of varying importance that can be exclusive or additive, and we outline approaches to help generate successful development of neuroprotective drugs for PD: (1) select patients in which the targeted mechanism is involved in the pathological process associated with the monitoring of target engagement, (2) combine treatments that target multiple pathways, (3) establish earliest interventions and develop better prodromal biomarkers, (4) adopt rigorous methodology and specific disease-relevant designs for disease-modifying clinical trials, (5) customize drug with better brain biodistribution, (6) prioritize repurposed drugs as a first line approach, and (7) adapt preclinical models to the targeted mechanisms with translational biomarkers to increase their predictive value. © 2020 International Parkinson and Movement Disorder Society.
帕金森病(PD)是一种神经退行性疾病,其特征是黑质中多巴胺能神经元丧失和铁及α-突触核蛋白积累;它在整个神经系统中呈现出特征性的模式。尽管经过了几十年成功的临床前神经保护研究,但没有一种药物在临床试验中显示出疗效。考虑到这一困境,我们已经审查并组织了各种具有不同重要性的解决方案,这些解决方案可以是排他的或附加的,我们概述了有助于成功开发帕金森病神经保护药物的方法:(1)选择目标机制参与与监测目标结合相关的病理过程的患者,(2)结合靶向多种途径的治疗方法,(3)尽早干预并开发更好的前驱生物标志物,(4)采用严格的方法和特定的疾病相关设计进行疾病修饰临床试验,(5)用更好的大脑生物分布定制药物,(6)优先选择重新定位的药物作为一线治疗方法,(7)采用具有转化生物标志物的靶向机制的临床前模型来提高其预测价值。© 2020 国际帕金森病和运动障碍学会。