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去铁酮治疗帕金森病患者的疗效:系统评价和荟萃分析。

Efficacy of the iron-chelating agent, deferiprone, in patients with Parkinson's disease: A systematic review and meta-analysis.

机构信息

Parkinson's and Movement Disorder Center, Virginia Commonwealth University, Richmond, Virginia, USA.

Medical Research Group of Egypt, Negida Academy, Arlington, Massachusetts, USA.

出版信息

CNS Neurosci Ther. 2024 Feb;30(2):e14607. doi: 10.1111/cns.14607.

Abstract

INTRODUCTION

Several studies have reported iron accumulation in the basal ganglia to be associated with the development of Parkinson's Disease (PD). Recently, a few trials have examined the efficacy of using the iron-chelating agent Deferiprone (DFP) for patients with PD. We conducted this meta-analysis to summarize and synthesize evidence from published randomized controlled trials about the efficacy of DFP for PD patients.

METHODS

A comprehensive literature search of four electronic databases was performed, spanning until February 2023. Relevant RCTs were selected, and their data were extracted and analyzed using the RevMan software. The primary outcome was the change in the Unified Parkinson's Disease Rating Scale (UPDRS-III).

RESULTS

Three RCTs with 431 patients were included in this analysis. DFP did not significantly improve UPDRS-III score compared to placebo (Standardized mean difference -0.06, 95% CI [-0.69, 0.58], low certainty evidence). However, it significantly reduced iron accumulation in the substantia nigra, putamen, and caudate as measured by T2*-weighted MRI (with high certainty evidence).

CONCLUSION

Current evidence does not support the use of DFP in PD patients. Future disease-modification trials with better population selection, adjustment for concomitant medications, and long-term follow up are recommended.

摘要

简介

多项研究报道,基底节铁沉积与帕金森病(PD)的发展有关。最近,一些试验研究了使用铁螯合剂地拉罗司(DFP)治疗 PD 患者的疗效。我们进行了这项荟萃分析,以总结和综合已发表的随机对照试验的证据,评估 DFP 治疗 PD 患者的疗效。

方法

对四个电子数据库进行了全面的文献检索,检索时间截至 2023 年 2 月。选择了相关的 RCT,并使用 RevMan 软件提取和分析其数据。主要结局是统一帕金森病评定量表(UPDRS-III)的变化。

结果

这项分析纳入了三项包含 431 名患者的 RCT。与安慰剂相比,DFP 并未显著改善 UPDRS-III 评分(标准化均数差-0.06,95%置信区间[-0.69,0.58],低确定性证据)。然而,它显著降低了 T2*-加权 MRI 测量的黑质、壳核和尾状核的铁沉积(具有高确定性证据)。

结论

目前的证据不支持 DFP 用于 PD 患者。建议未来开展更好的人群选择、调整伴随药物和长期随访的疾病修饰试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9f0/10853946/b7752faf772a/CNS-30-e14607-g004.jpg

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