Monash Centre of Cardiovascular Research & Education in Therapeutics, Department of Epidemiology & Preventive Medicine, School of Public Health & Preventive Medicine, Monash University, 99 Commercial Rd., Melbourne, VIC 3004, Australia.
Eur J Heart Fail. 2012 Jan;14(1):91-105. doi: 10.1093/eurjhf/hfr148. Epub 2011 Nov 6.
Bone marrow stem cell (BMSC) treatment of ST-segment elevation myocardial infarction (STEMI) has been primarily via the intracoronary route or via endogenous mobilization using granulocyte colony-stimulating factor (G-CSF). Studies have provided conflicting results. We therefore performed a meta-analysis of these treatments, examining short- and long-term efficacy and safety.
Randomized controlled trials (RCTs) of BMSC-based therapy for STEMI, delivered within 9 days of reperfusion, were identified by systematic search. Random effects models were used to calculate pooled effects of clinical outcomes, with meta-regression to assess dependence of the magnitude of effect sizes on study characteristics. Twenty-nine RCTs enrolling 1830 patients were included. Intracoronary BMSC therapy resulted in an overall improvement in left ventricular ejection fraction (LVEF) of 2.70% [95% confidence interval (CI) 1.48-3.92; P < 0.001] in the short term and 3.31% (95% CI 1.87-4.75; P < 0.001) longer term. Meta-regression suggested a dose-response relationship between quantity of CD34(+) cells delivered and increase in LVEF (P = 0.007). G-CSF treatment resulted in a trend towards similar benefits (P = 0.20). No significant differences were observed in pooled adverse outcome rates between intervention and control groups of either treatment approach, except for lower revascularization rates with intracoronary BMSC vs. control (odds ratio 0.68, 95% CI 0.47-0.97; P = 0.03).
Intracoronary BMSC therapy post-STEMI improves LVEF beyond standard medical treatment, in both the short and longer term. G-CSF treatment shows positive but non-significant trends. Both treatments demonstrate safety comparable with conventional medical treatment.
骨髓干细胞(BMSC)治疗 ST 段抬高型心肌梗死(STEMI)主要通过冠状动脉内途径或使用粒细胞集落刺激因子(G-CSF)进行内源性动员。研究结果存在矛盾。因此,我们对这些治疗方法进行了荟萃分析,检查短期和长期疗效和安全性。
通过系统搜索确定了在再灌注后 9 天内接受基于 BMSC 的 STEMI 治疗的随机对照试验(RCT)。使用随机效应模型计算临床结局的汇总效应,采用元回归评估效应大小的幅度对研究特征的依赖性。共纳入 29 项 RCT,纳入 1830 例患者。冠状动脉内 BMSC 治疗可使左心室射血分数(LVEF)在短期内总体改善 2.70%[95%置信区间(CI)1.48-3.92;P<0.001],在长期内改善 3.31%(95% CI 1.87-4.75;P<0.001)。元回归提示输送的 CD34+细胞数量与 LVEF 增加之间存在剂量反应关系(P=0.007)。G-CSF 治疗也显示出类似的获益趋势(P=0.20)。两种治疗方法的干预组和对照组的不良结局发生率没有显著差异,但冠状动脉内 BMSC 治疗组的再血管化率低于对照组(比值比 0.68,95% CI 0.47-0.97;P=0.03)。
STEMI 后冠状动脉内 BMSC 治疗可改善 LVEF,优于标准药物治疗,无论是短期还是长期。G-CSF 治疗显示出积极但非显著的趋势。两种治疗方法均显示出与常规药物治疗相当的安全性。