Intracoronary infusion of autologous bone marrow cells and left ventricular function after acute myocardial infarction: a meta-analysis

被引:69
作者
Hristov, M.
Heussen, Nicole
Schober, A.
Weber, C.
机构
[1] Univ Hosp Aachen, Rhein Westfal TH Aachen, Inst Mol Cardiovasc Res, IMCAR, D-52074 Aachen, Germany
[2] Univ Hosp Aachen, Rhein Westfal TH Aachen, Interdisciplinary Ctr Clin Res BIOMAT, D-52074 Aachen, Germany
[3] Univ Hosp Aachen, Rhein Westfal TH Aachen, Inst Med Stat, D-52074 Aachen, Germany
[4] Univ Munich, Dept Cardiol, Munich, Germany
关键词
myocardial infarction; revascularization; bone marrow; follow-up studies; meta-analysis;
D O I
10.1111/j.1582-4934.2006.tb00432.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent clinical studies have demonstrated that intracoronary infusion of autologous bone marrow cells (BMC) in conjunction with standard treatment may improve left ventricular function after an acute myocardial infarction (AMI). However, the results of these studies remain controversial, as the studies were relatively small in size and partially differed in design. We reviewed primary controlled randomized clinical studies comparing intracoronary transfer of autologous non-mobilized BMC combined with standard therapy versus standard therapy alone in patients with AML We identified five randomized controlled clinical trials, three of which were also placebo- and bone marrow aspiration-controlled. Non-mobilized BMC were infused into the revascularized coronary target artery 6.6 +/- 6.1 days after AML The mean follow-up period of 5.2 +/- 1.1 months was completed by 482 patients, 241 of which received infusion of BMC. The effect of BMC on left ventricular ejection fraction (LVEF) as a major functional parameter was evaluated. Analyzing the overall effect on the change in LVEF between baseline and follow-up value revealed a significant improvement in the BMC-treated group as compared to the control group (P = 0.04). Thus, considering the increase in LVEF during follow-up, transplantation of BMC may be a safe and beneficial procedure to support treatment of AMI. However, the functional improvement observed with this form of therapy was altogether relatively moderate and the studies were heterogeneous in design. Hence, further efforts aiming at large-scale, double-blind, randomized and placebo-controlled multi-center trials in conjunction with better definition of patients, which benefit from BMC infusion, appear to be warranted.
引用
收藏
页码:727 / 733
页数:7
相关论文
共 25 条
[1]   Transplantation of progenitor cells and regeneration enhancement in acute myocardial infarction -: (TOPCARE-AMI) [J].
Assmus, B ;
Schächinger, V ;
Teupe, C ;
Britten, M ;
Lehmann, R ;
Döbert, N ;
Grünwald, F ;
Aicher, A ;
Urbich, C ;
Martin, H ;
Hoelzer, D ;
Dimmeler, S ;
Zeiher, AM .
CIRCULATION, 2002, 106 (24) :3009-3017
[2]   Effect on left ventricular function of intracoronary transplantation of autologous bone marrow mesenchymal stem cell in patients with acute myocardial infarction [J].
Chen, SL ;
Fang, W ;
Ye, F ;
Liu, YH ;
Qian, J ;
Shan, S ;
Zhang, J ;
Zhao, RCH ;
Liao, LM ;
Lin, S ;
Sun, JP .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 94 (01) :92-95
[3]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[4]   Unchain my heart: the scientific foundations of cardiac repair [J].
Dimmeler, S ;
Zeiher, AM ;
Schneider, MD .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (03) :572-583
[5]   Transplantation of blood-derived progenitor cells after recanalization of chronic coronary artery occlusion - First randomized and placebo-controlled study [J].
Erbs, S ;
Linke, A ;
Adams, V ;
Lenk, K ;
Thiele, H ;
Diederich, KW ;
Emmrich, F ;
Kluge, R ;
Kendziorra, K ;
Sabri, O ;
Schuler, G ;
Hambrecht, R .
CIRCULATION RESEARCH, 2005, 97 (08) :756-762
[6]   A different outlook on the role of bone marrow stem cells in vascular growth - Bone marrow delivers software not hardware [J].
Heil, M ;
Ziegelhoeffer, T ;
Mees, B ;
Schaper, W .
CIRCULATION RESEARCH, 2004, 94 (05) :573-574
[7]   The therapeutic potential of progenitor cells in ischemic heart disease - Past, present and future [J].
Hristov, M ;
Weber, C .
BASIC RESEARCH IN CARDIOLOGY, 2006, 101 (01) :1-7
[8]   Endothelial progenitor cells: characterization, pathophysiology, and possible clinical relevance [J].
Hristov, M ;
Weber, C .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (04) :498-508
[9]  
HRISTOV M, 2006, IN PRESS ATHEROSCLER
[10]   Autologous bone marrow-derived stem-cell transfer in patients with ST-segment elevation myocardial infarction: double-blind, randomised controlled trial [J].
Janssens, S ;
Dubois, C ;
Bogaert, J ;
Theunissen, K ;
Deroose, C ;
Desmet, W ;
Kolantzi, M ;
Herbots, L ;
Sinnaeve, P ;
Dens, J ;
Maertens, J ;
Rademakers, F ;
Dymarkowski, S ;
Gheysens, O ;
Van Cleemput, J ;
Bormans, G ;
Nuyts, J ;
Belmans, A ;
Mortelmans, L ;
Boogaerts, M ;
Van de Werf, F .
LANCET, 2006, 367 (9505) :113-121