首页> 美国卫生研究院文献>Bone Marrow Research >One-Year Safety Analysis of the COMPARE-AMI Trial: Comparison of Intracoronary Injection of CD133+ Bone Marrow Stem Cells to Placebo in Patients after Acute Myocardial Infarction and Left Ventricular Dysfunction
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One-Year Safety Analysis of the COMPARE-AMI Trial: Comparison of Intracoronary Injection of CD133+ Bone Marrow Stem Cells to Placebo in Patients after Acute Myocardial Infarction and Left Ventricular Dysfunction

机译:COMPARE-AMI试验的一年安全性分析:急性心肌梗死和左心室功能不全患者冠状动脉内注射CD133 +骨髓干细胞与安慰剂的比较

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摘要

Bone marrow stem cell therapy has emerged as a promising approach to improve healing of the infarcted myocardium. Despite initial excitement, recent clinical trials using non-homogenous stem cells preparations showed variable and mixed results. Selected CD133+ hematopoietic stem cells are candidate cells with high potential. Herein, we report the one-year safety analysis on the initial 20 patients enrolled in the COMPARE-AMI trial, the first double-blind randomized controlled trial comparing the safety, efficacy, and functional effect of intracoronary injection of selected CD133+ cells to placebo following acute myocardial infarction with persistent left ventricular dysfunction. At one year, there is no protocol-related complication to report such as death, myocardial infarction, stroke, or sustained ventricular arrhythmia. In addition, the left ventricular ejection fraction significantly improved at four months as compared to baseline and remained significantly higher at one year. These data indicate that in the setting of the COMPARE-AMI trial, the intracoronary injection of selected CD133+ stem cells is secure and feasible in patients with left ventricle dysfunction following acute myocardial infarction.
机译:骨髓干细胞疗法已经成为改善梗塞心肌愈合的一种有前途的方法。尽管最初令人兴奋,但最近使用非均质干细胞制备物进行的临床试验显示出可变和混合的结果。所选的CD133 + 造血干细胞是具有高潜力的候选细胞。在此,我们报告了COMPARE-AMI试验中入组的最初20例患者的一年安全性分析,这是首项比较冠状动脉内注射所选CD133 +的安全性,疗效和功能作用的双盲随机对照试验急性心肌梗死后伴持续性左心功能不全的细胞进入安慰剂。一年后,没有死亡,心肌梗塞,中风或持续性室性心律失常等与方案相关的并发症发生。此外,与基线相比,在四个月时左心室射血分数显着改善,在一年时仍显着更高。这些数据表明,在COMPARE-AMI试验的背景下,在急性心肌梗死后左心功能不全的患者中,冠状动脉内注射所选的CD133 + 干细胞是安全可行的。

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