Abdelalem Aziz Ahmed Mohamed
School of Advanced Education Research and Accreditation, Universidad Isabel I, Burgos, Spain.
F1000Res. 2019 Dec 10;8:2078. doi: 10.12688/f1000research.21372.1. eCollection 2019.
Safinamide, a recently developed drug with several mechanisms of action has been investigated as an add-on therapy for Parkinson's disease patients suffering from motor complications due to the usage of anti-Parkinson's medications such as levodopa and dopaminergic drugs. The aim of the study is to investigate the efficacy and safety of Safinamide as add-on therapy for Parkinson's disease patients. A computerized literature search was conducted of PubMed, EMBASE, ClinicalTrial.gov and Cochrane Library until August 2019. We selected relevant randomized controlled trials comparing safinamide groups to placebo groups. Relevant outcomes were pooled as mean difference (MD) and risk ratio (RR) using Review Manager 5.3. We found that the overall MD of changes in "off-time" and "on time without troublesome dyskinesia" favored the safinamide group over the placebo group (MD -0.72 h, 95% CI -0.89 to -0.56 and MD 0.71 h, 95% CI 0.52 to 0.90, respectively). Additionally, the overall MD of change in Unified Parkinson's Disease Rating Scale part three (UPDRS III) favored the safinamide group (MD -1.83, 95% CI -2.43 to -1.23). In case of adverse events, the pooled meta-analysis did not favor the safinamide group over the placebo group. In this study, we provide class I evidence about the potential role of safinamide as an add-on therapy for Parkinson's disease patients suffering from motor fluctuations. However, a few included studies did not mention the data of important outcomes. Also, we report high risk of bias in individual studies. Future randomized controlled trials with different doses are recommended to provide more evidence for the efficacy and safety of safinamide as a treatment for motor complications of anti-Parkinson's medications.
沙芬酰胺是一种最近研发出的具有多种作用机制的药物,已被作为附加疗法,用于治疗因使用左旋多巴和多巴胺能药物等抗帕金森药物而出现运动并发症的帕金森病患者。本研究的目的是调查沙芬酰胺作为帕金森病患者附加疗法的疗效和安全性。截至2019年8月,我们在PubMed、EMBASE、ClinicalTrial.gov和Cochrane图书馆进行了计算机化文献检索。我们选择了比较沙芬酰胺组和安慰剂组的相关随机对照试验。使用Review Manager 5.3将相关结果汇总为平均差(MD)和风险比(RR)。我们发现,“关期”和“无麻烦异动症的开期”变化的总体MD有利于沙芬酰胺组而非安慰剂组(MD分别为-0.72小时,95%CI为-0.89至-0.56;MD为0.71小时,95%CI为0.52至0.90)。此外,统一帕金森病评定量表第三部分(UPDRS III)变化的总体MD有利于沙芬酰胺组(MD为-1.83,95%CI为-2.43至-1.23)。在不良事件方面,汇总的荟萃分析并不支持沙芬酰胺组优于安慰剂组。在本研究中,我们提供了I级证据,证明沙芬酰胺作为附加疗法对患有运动波动的帕金森病患者的潜在作用。然而,一些纳入研究未提及重要结果的数据。此外,我们报告了个别研究存在高偏倚风险。建议未来进行不同剂量的随机对照试验,为沙芬酰胺治疗抗帕金森药物运动并发症的疗效和安全性提供更多证据。