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依曲替酯治疗帕金森病的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of istradefylline for Parkinson's disease: A systematic review and meta-analysis.

机构信息

Department of Anatomy, School of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, China.

出版信息

Neurosci Lett. 2022 Mar 23;774:136515. doi: 10.1016/j.neulet.2022.136515. Epub 2022 Feb 8.

Abstract

As an adenosine receptor A2A antagonist, istradefylline is used as an adjunctive agent of levodopa to improve motor symptoms in advanced Parkinson's disease (PD) patients. In this study, we re-evaluated the effects of istradefylline on treating the motor symptoms of PD patients. We performed a literature search up to November 2021 from electronic databases. Eligible studies were synthesized for efficacy, tolerability, OFF time, Unified Parkinson's Disease Rating Scale part III score, ON state with dyskinesia, and the incidence of treatment-emergent adverse events. As a result, nine clinical studies with 2727 subjects on istradefylline treatment for PD patients were included. Our results showed that compared to placebo, istradefylline exhibited a statically significant difference in efficacy (1.39 [1.15 to 1.69]; p = 0.001), decreasing OFF time (-0.58 [-1.01 to - 0.16]; p = 0.007), and improving ON state with dyskinesia (0.69 [0.02 to 1.37]; p = 0.043). For tolerability, UPDRS III, and adverse effects, there was no significant difference between istradefylline and placebo. In conclusion, the results suggest that istradefylline exhibits an efficient and well-tolerated role in treating PD patients. Randomized controlled trials and long-term studies are still required to investigate the effects of istradefylline on motor and non-motor symptoms of PD in future research.

摘要

作为一种腺苷 A2A 受体拮抗剂,伊曲茶碱被用作左旋多巴的辅助药物,以改善晚期帕金森病(PD)患者的运动症状。在这项研究中,我们重新评估了伊曲茶碱治疗 PD 患者运动症状的效果。我们对截至 2021 年 11 月的电子数据库进行了文献检索。对纳入的研究进行了疗效、耐受性、OFF 时间、统一帕金森病评定量表第三部分评分、异动症状态下的 ON 时间和治疗中出现的不良事件发生率的综合评估。结果共纳入了 9 项关于伊曲茶碱治疗 PD 患者的临床研究,共涉及 2727 名受试者。结果显示,与安慰剂相比,伊曲茶碱在疗效(1.39 [1.15 至 1.69];p=0.001)、减少 OFF 时间(-0.58 [-1.01 至 -0.16];p=0.007)和改善异动症状态下的 ON 时间(0.69 [0.02 至 1.37];p=0.043)方面具有统计学意义。在耐受性、UPDRS III 和不良反应方面,伊曲茶碱与安慰剂之间无显著差异。总之,结果表明伊曲茶碱在治疗 PD 患者方面具有高效且耐受性良好的作用。未来的研究仍需要随机对照试验和长期研究来评估伊曲茶碱对 PD 患者运动和非运动症状的影响。

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