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

被引:34
作者
Mansour, Samer [1 ,2 ]
Roy, Denis-Claude [3 ]
Bouchard, Vincent [4 ]
Stevens, Louis Mathieu [2 ,5 ]
Gobeil, Francois [1 ]
Rivard, Alain [1 ,2 ]
Leclerc, Guy [1 ]
Reeves, Francois [1 ,2 ]
Noiseux, Nicolas [2 ,5 ]
机构
[1] CHUM, Dept Med, Div Cardiol, 3840 Rue St Urbain, Montreal, PQ H2W IT8, Canada
[2] Ctr Rech CHUM CRCHUM, Axe Cardiometabol, Montreal, PQ H2W 1T7, Canada
[3] HMR, Dept Hematol, Montreal, PQ H1T 2M4, Canada
[4] Univ Montreal, Fac Med, Montreal, PQ H3C 3J7, Canada
[5] CHUM, Dept Chirurg, Div Chirurg Cardiaque, Montreal, PQ H2W 1T8, Canada
关键词
D O I
10.1155/2011/385124
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
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.
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