Efficacy of preladenant in improving motor symptoms in Parkinson's disease: A systematic review and meta-analysis

IF 2 Q3 NEUROSCIENCES IBRO Neuroscience Reports Pub Date : 2024-07-21 DOI:10.1016/j.ibneur.2024.07.005
Mohammad Amin Karimi , Alireza Ghajari , Reza Khademi , Mohammad Hossein Etemadi , Narges Safar Firouz , Behnaz Mohammadvand , Kimia Janeshin , Afra Darvishi , Shafagh Asgarzadeh , Sayedeh-Fatemeh Sadat-Madani , Mohammad Abbasalizadeh , Zahra Jafari Shendi , Ata Akhtari Kohnehshahri , Niloofar Deravi , Seyed Amirhossein Mazhari , Mahsa Aziz , Matin Bidares , Mohaddeseh Belbasi , Mahdyieh Naziri , Hossein Ashkpour Motlagh
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Abstract

Background

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.

Methods

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.

Results

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.

Conclusion

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.

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前列腺素对改善帕金森病患者运动症状的疗效:系统回顾与元分析
背景帕金森病(PD)是一种复杂的神经退行性疾病,以多巴胺耗竭和严重运动障碍为特征。Preladenant是一种腺苷A2受体拮抗剂,是一种正在研究的帕金森病治疗方法。本系统综述和荟萃分析旨在严格评估Preladenant在改善帕金森病患者运动症状方面的疗效。方法按照系统综述和荟萃分析首选报告项目(PRISMA)指南,在PubMed、Embase和Cochrane对照试验中央注册中心进行了全面的文献检索,检索时间从开始到2023年3月。纳入的随机对照试验(RCT)对帕金森病患者进行了普瑞拉登坦与安慰剂的比较。主要研究结果是无运动障碍的每日ON时间的变化。次要结果包括每日关机时间的变化和不良事件。采用 Cochrane 偏倚风险工具对偏倚风险进行了评估。结果共纳入了 4 项 RCT,共 2097 名 PD 患者。汇总分析表明,与安慰剂相比,普瑞拉登坦一般可增加每日开机时间(汇总效应为0.15,95% CI:-0.19-0.48),减少每日关机时间(汇总效应为-0.04,95% CI:-0.43-0.36),但差异不显著。纳入的研究具有中度到高度异质性。结论这项荟萃分析表明,Preladenant可通过增加ON时间和减少OFF时间来改善帕金森病患者的运动波动。然而,由于各研究之间存在高度异质性,因此需要进一步开展大规模、高质量的 RCT 研究,以证实这些研究结果,并确定 Preladenant 在帕金森病治疗中的长期安全性和有效性。
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来源期刊
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
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