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缺血性中风的骨髓单个核细胞治疗:一项系统评价

Bone marrow mononuclear cell therapy in ischaemic stroke: a systematic review.

作者信息

Kumar A, Prasad M, Jali V P, Pandit A K, Misra S, Kumar P, Chakravarty K, Kathuria P, Gulati A

机构信息

Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Acta Neurol Scand. 2017 May;135(5):496-506. doi: 10.1111/ane.12666. Epub 2016 Aug 24.

Abstract

Bone marrow mononuclear cell (BM-MNC) therapy has emerged as a potential therapy for the treatment of stroke. We performed a systematic review of published studies using BM-MNC therapy in patients with ischaemic stroke (IS). Literature was searched using MEDLINE, PubMed, EMBASE, Trip Database, Cochrane library and clinicaltrial.gov to identify studies on BM-MNC therapy in IS till June, 2016. Data were extracted independently by two reviewers. STATA version 13 was used for carrying out meta-analysis. We included non-randomized open-label, single-arm and non-randomized comparative studies or randomized controlled trials (RCTs) if BM-MNCs were used to treat patients with IS in any phase after the index stroke. One randomized trial, two non-randomized comparative trials and four single-arm open-label trials (total seven studies) involving 227 subjects (137 patients and 90 controls) were included in the systematic review and meta-analysis. The pooled proportion for favourable clinical outcome (modified Rankin Scale score ≤2) in six studies involving 122 subjects was 29% (95% CI 0.16-0.43) who were exposed to BM-MNCs and pooled proportion for favourable clinical outcome of 69 subjects (taken from two trials) who did not receive BM-MNCs was 20% (95% CI 0.12-0.32). The pooled difference in the safety outcomes was not significant between both the groups. Our systematic review suggests that BM-MNC therapy is safe up to 1 year post-intervention and is feasible; however, its efficacy in the case of IS patients is debatable. Well-designed randomized controlled trials are required to provide more information on the efficacy of BM-MNC transplantation in patients with IS.

摘要

骨髓单个核细胞(BM-MNC)疗法已成为治疗中风的一种潜在疗法。我们对已发表的使用BM-MNC疗法治疗缺血性中风(IS)患者的研究进行了系统评价。通过检索MEDLINE、PubMed、EMBASE、Trip数据库、Cochrane图书馆和clinicaltrial.gov来查找截至2016年6月关于IS患者BM-MNC疗法的研究。由两名评价员独立提取数据。使用STATA 13版进行荟萃分析。如果在索引中风后的任何阶段使用BM-MNC治疗IS患者,我们纳入非随机开放标签、单臂和非随机对照研究或随机对照试验(RCT)。系统评价和荟萃分析纳入了一项随机试验、两项非随机对照试验和四项单臂开放标签试验(共七项研究),涉及227名受试者(137例患者和90名对照)。在涉及122名受试者的六项研究中,接受BM-MNC治疗的患者获得良好临床结局(改良Rankin量表评分≤2)的合并比例为29%(95%CI 0.16 - 0.43),而未接受BM-MNC治疗的69名受试者(来自两项试验)获得良好临床结局的合并比例为20%(95%CI 0.12 - 0.32)。两组安全性结局的合并差异无统计学意义。我们的系统评价表明,BM-MNC疗法在干预后1年内是安全可行的;然而,其对IS患者的疗效存在争议。需要设计良好的随机对照试验来提供更多关于BM-MNC移植对IS患者疗效的信息。

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