Karimi Mohammad Amin, Ghajari Alireza, Khademi Reza, Etemadi Mohammad Hossein, Firouz Narges Safar, Mohammadvand Behnaz, Janeshin Kimia, Darvishi Afra, Asgarzadeh Shafagh, Sadat-Madani Sayedeh-Fatemeh, Abbasalizadeh Mohammad, Shendi Zahra Jafari, Kohnehshahri Ata Akhtari, Deravi Niloofar, Mazhari Seyed Amirhossein, Aziz Mahsa, Bidares Matin, Belbasi Mohaddeseh, Naziri Mahdyieh, Motlagh Hossein Ashkpour
School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
School of pharmacy Mashhad University of medical science, Mashhad, Iran.
IBRO Neurosci Rep. 2024 Jul 21;17:207-219. doi: 10.1016/j.ibneur.2024.07.005. eCollection 2024 Dec.
Parkinson's disease (PD) is a complex neurodegenerative disorder characterized by dopamine depletion and severe motor impairments. Preladenant, an adenosine A2 receptor antagonist, is an investigational treatment for PD. This systematic review and meta-analysis aimed to critically evaluate the efficacy of Preladenant in improving motor symptoms in patients with PD.
A comprehensive literature search was conducted in PubMed, Embase, and Cochrane Central Register of Controlled Trials from inception to March 2023, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Randomized controlled trials (RCTs) comparing Preladenant with placebo in PD patients were included. The primary outcome was the change in daily ON time without troublesome dyskinesia. Secondary outcomes included the change in daily OFF time and adverse events. The risk of bias was assessed using the Cochrane Risk of Bias tool.
Four RCTs with a total of 2097 PD patients were included. Pooled analysis showed that Preladenant could generally increase daily ON time (pooled effect 0.15 and 95 % CI: -0.19-0.48) and reduce daily OFF time (pooled effect -0.04 and 95 % CI: -0.43-0.36) compared to placebo, however it was not significant. The included studies had moderate to high heterogeneity. No significant differences in adverse events were observed between Preladenant and placebo.
This meta-analysis suggests that Preladenant may improve motor fluctuations in PD patients by increasing ON time and reducing OFF time. However, the high heterogeneity among studies warrants further large-scale, high-quality RCTs to confirm these findings and establish the long-term safety and efficacy of Preladenant in PD management.
帕金森病(PD)是一种复杂的神经退行性疾病,其特征为多巴胺耗竭和严重的运动障碍。普雷拉登特是一种腺苷A2受体拮抗剂,是一种用于治疗帕金森病的研究性药物。本系统评价和荟萃分析旨在严格评估普雷拉登特改善帕金森病患者运动症状的疗效。
按照系统评价和荟萃分析的首选报告项目(PRISMA)指南,在PubMed、Embase和Cochrane对照试验中央注册库中进行了全面的文献检索,检索时间从建库至2023年3月。纳入了比较普雷拉登特与安慰剂治疗帕金森病患者的随机对照试验(RCT)。主要结局是无麻烦异动症的每日“开”期时间变化。次要结局包括每日“关”期时间变化和不良事件。使用Cochrane偏倚风险工具评估偏倚风险。
纳入了4项RCT,共2097例帕金森病患者。汇总分析显示,与安慰剂相比,普雷拉登特通常可增加每日“开”期时间(汇总效应0.15,95%CI:-0.19-0.48)并减少每日“关”期时间(汇总效应-0.04,95%CI:-0.43-0.36),但差异无统计学意义。纳入的研究具有中度至高度异质性。普雷拉登特与安慰剂之间在不良事件方面未观察到显著差异。
本荟萃分析表明,普雷拉登特可能通过增加“开”期时间和减少“关”期时间来改善帕金森病患者的运动波动。然而,研究之间的高度异质性需要进一步开展大规模、高质量的RCT来证实这些发现,并确定普雷拉登特在帕金森病管理中的长期安全性和疗效。