Efficacy and safety of adjunctive oral therapy in Parkinson's disease with motor complications: a systematic review and network meta-analysis.

IF 2.1 Q3 CLINICAL NEUROLOGY BMJ Neurology Open Pub Date : 2024-02-10 eCollection Date: 2024-01-01 DOI:10.1136/bmjno-2023-000573
Vibuthi Sisodia, Lars Dubbeld, Rob M A De Bie, Gonçalo S Duarte, João Costa, Joke M Dijk
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Abstract

Background: The aim of this manuscript is to review the evidence and compare the efficacy and safety of catechol-O-methyltransferase inhibitors (COMT-Is), dopamine receptor agonists (DRAs) and monoamine-oxidase B inhibitors (MAOB-Is) as adjunctive treatment to levodopa in patients with Parkinson's disease (PD) experiencing motor complications.

Methods: In this systematic review and network meta-analysis, literature searches were performed in MEDLINE and Embase to identify eligible randomised controlled trials (RCTs) with a minimal follow-up of at least 4 weeks published in English between 1980 and 2021. RCTs were included if either a COMT-I, DRA or MAOB-I was evaluated as an adjunctive therapy to levodopa in patients with PD experiencing motor complications and dyskinesia. The main outcomes included daily off-medication time, motor and non-motor examination scales, and adverse events including dyskinesia.

Results: 74 RCTs reporting on 18 693 patients were included. All three studied drug classes decreased daily off-medication time compared with placebo (COMT-Is mean -0.8 hours (95% CI -1.0 to -0.6), DRAs -1.1 hours (95% CI -1.4 to -0.8), MAOB-Is -0.9 hours (95% CI -1.2 to -0.6)). Safety analysis showed an increased risk of dyskinesia for all three drug classes (COMT-Is OR 3.3 (95% CI 2.7 to 4.0), DRAs 3.0 (95% CI 2.5 to 3.5), MAOB-Is 1.6 (95% CI 1.2 to 2.2)). According to surface under the cumulative ranking curve scores, pramipexole IR was associated with the most favourable benefit-risk profile.

Conclusions: COMT-Is, DRAs and MAOB-Is effectively reduce motor complications and increase incidence of dyskinesia. In the network meta-analysis, adjunctive use of DRAs appeared most effective.

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帕金森病运动并发症辅助口服疗法的疗效和安全性:系统综述和网络荟萃分析。
背景:本稿件旨在回顾证据并比较儿茶酚-O-甲基转移酶抑制剂(COMT-Is)、多巴胺受体激动剂(DRAs)和单胺氧化酶B抑制剂(MAOB-Is)作为左旋多巴辅助治疗出现运动并发症的帕金森病(PD)患者的疗效和安全性:在本系统综述和网络荟萃分析中,我们在 MEDLINE 和 Embase 中进行了文献检索,以确定符合条件的随机对照试验 (RCT),这些试验的最小随访时间至少为 4 周,且均为 1980 年至 2021 年间用英语发表。如果COMT-I、DRA或MAOB-I作为左旋多巴的辅助疗法对出现运动并发症和运动障碍的帕金森病患者进行了评估,则纳入RCT。主要结果包括每日停药时间、运动和非运动检查量表以及包括运动障碍在内的不良反应:结果:共纳入了 74 项研究,报告了 18 693 名患者的情况。与安慰剂相比,所研究的三种药物类别都缩短了每日停药时间(COMT-Is 平均-0.8 小时(95% CI -1.0 至 -0.6),DRAs 平均-1.1 小时(95% CI -1.4 至 -0.8),MAOB-Is 平均-0.9 小时(95% CI -1.2 至 -0.6))。安全性分析表明,所有三类药物的运动障碍风险均有所增加(COMT-Is OR 3.3(95% CI 2.7 至 4.0),DRAs 3.0(95% CI 2.5 至 3.5),MAOB-Is 1.6(95% CI 1.2 至 2.2))。根据累积排名曲线下表面得分,普拉克索IR具有最有利的获益-风险特征:结论:COMT-Is、DRAs和MAOB-Is能有效减少运动并发症并增加运动障碍的发生率。在网络荟萃分析中,DRAs 的辅助使用似乎最为有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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