Laboratory of Neurodegenerative Diseases, Centre for Clinical, Experimental Surgery & Translational Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Biomolecules. 2020 Jun 16;10(6):912. doi: 10.3390/biom10060912.
Biomarkers and disease-modifying therapies are both urgent unmet medical needs in the treatment of Parkinson's disease (PD) and must be developed concurrently because of their interdependent relationship: biomarkers for the early detection of disease (i.e., prior to overt neurodegeneration) are necessary in order for patients to receive maximal therapeutic benefit and vice versa; disease-modifying therapies must become available for patients whose potential for disease diagnosis and prognosis can be predicted with biomarkers. This review provides an overview of the milestones achieved to date in the therapeutic strategy development of disease-modifying therapies and biomarkers for PD, with a focus on the most common and advanced genetically linked targets alpha-synuclein (), leucine-rich repeat kinase-2 () and glucocerebrosidase (. Furthermore, we discuss the convergence of the different pathways and the importance of patient stratification and how these advances may apply more broadly to idiopathic PD. The heterogeneity of PD poses a challenge for therapeutic and biomarker development, however, the one gene- one target approach has brought us closer than ever before to an unprecedented number of clinical trials and biomarker advancements.
生物标志物和疾病修饰疗法都是治疗帕金森病(PD)中未满足的迫切医学需求,必须同时开发,因为它们是相互依存的关系:生物标志物可用于早期发现疾病(即在明显神经退行性变之前),以便患者获得最大的治疗效益,反之亦然;对于那些可以用生物标志物预测疾病诊断和预后潜力的患者,必须提供疾病修饰疗法。本综述概述了迄今为止在 PD 的疾病修饰疗法和生物标志物治疗策略开发方面取得的里程碑式进展,重点介绍了最常见和最先进的与遗传相关的靶点:α-突触核蛋白()、富亮氨酸重复激酶 2()和葡萄糖脑苷脂酶(。此外,我们还讨论了不同途径的趋同以及患者分层的重要性,以及这些进展如何更广泛地应用于特发性 PD。PD 的异质性给治疗和生物标志物的发展带来了挑战,然而,一种基因-一种靶标的方法使我们比以往任何时候都更接近前所未有的临床试验和生物标志物进展数量。