Impact of intracoronary bone marrow cell therapy on left ventricular function in the setting of ST-segment elevation myocardial infarction: a collaborative meta-analysis

被引:110
|
作者
Delewi, Ronak [1 ]
Hirsch, Alexander [1 ,2 ]
Tijssen, Jan G. [1 ]
Schaechinger, Volker
Wojakowski, Wojciech [3 ]
Roncalli, Jerome [4 ,5 ]
Aakhus, Svend
Erbs, Sandra [6 ]
Assmus, Birgit [2 ]
Tendera, Michal [3 ]
Turan, R. Goekmen [7 ]
Corti, Roberto [8 ]
Henry, Tim [9 ]
Lemarchand, Patricia [10 ]
Lunde, Ketil [5 ]
Cao, Feng [11 ]
Huikuri, Heikki V. [12 ]
Suerder, Daniel [13 ]
Simari, Robert D. [14 ]
Janssens, Stefan [15 ]
Wollert, Kai C. [16 ]
Plewka, Michal [17 ]
Grajek, Stefan [18 ]
Traverse, Jay H. [9 ]
Zijlstra, Felix [19 ]
Piek, Jan J. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
[2] Goethe Univ Frankfurt, Div Cardiol, Dept Med 3, D-60054 Frankfurt, Germany
[3] Med Univ Silesia, Div Cardiol 3, Katowice, Poland
[4] CHU Rangueil, Serv Cardiol, F-31054 Toulouse, France
[5] Oslo Univ Hosp, Dept Cardiol, Rikshosp, Oslo, Norway
[6] Univ Leipzig, Ctr Heart, Dept Internal Med Cardiol, D-04109 Leipzig, Germany
[7] Univ Hosp Rostock, Div Cardiol, Dept Internal Med, Rostock, Germany
[8] Univ Zurich Hosp, Dept Cardiol, Ctr Cardiovasc, CH-8091 Zurich, Switzerland
[9] Univ Minnesota, Abbott NW Hosp, Minneapolis Heart Inst, Minneapolis, MN USA
[10] Univ Nantes, INSERM, CNRS, UMR1087,UMR6291, Nantes, France
[11] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiol, Xian 710032, Peoples R China
[12] Univ Oulu, Dept Internal Med, Univ Hosp Oulu, SF-90220 Oulu, Finland
[13] Fdn Cardioctr Ticino, Lugano, Switzerland
[14] Mayo Clin, Mayo Grad Sch Med, Rochester, MN USA
[15] Univ Hosp Gasthuisberg, Dept Cardiol, B-3000 Louvain, Belgium
[16] Hannover Med Sch, Dept Cardiol & Angiol, Div Mol & Translat Cardiol, Hannover, Germany
[17] Med Univ Lodz, Dept Cardiol, Lodz, Poland
[18] Poznan Univ, Sch Med Sci, Dept Cardiol 1, Poznan, Poland
[19] Erasmus MC, Dept Cardiol, Ctr Thorax, Rotterdam, Netherlands
关键词
ST-segment elevation myocardial infarction; Bone marrow cells; Ventricular function; Meta-analysis; ENDOTHELIAL PROGENITOR CELLS; MONONUCLEAR-CELLS; VASCULAR COMPLICATIONS; EJECTION FRACTION; DOUBLE-BLIND; FOLLOW-UP; TRANSPLANTATION; INJECTION; INFUSION; IMPROVEMENT;
D O I
10.1093/eurheartj/eht372
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The objective of the present analysis was to systematically examine the effect of intracoronary bone marrow cell (BMC) therapy on left ventricular (LV) function after ST-segment elevation myocardial infarction in various subgroups of patients by performing a collaborative meta-analysis of randomized controlled trials. Methods and results We identified all randomized controlled trials comparing intracoronary BMC infusion as treatment for ST-segment elevation myocardial infarction. We contacted the principal investigator for each participating trial to provide summary data with regard to different pre-specified subgroups [age, diabetes mellitus, time from symptoms to percutaneous coronary intervention, infarct-related artery, LV end-diastolic volume index (EDVI), LV ejection fraction (EF), infarct size, presence of microvascular obstruction, timing of cell infusion, and injected cell number] and three different endpoints [change in LVEF, LVEDVI, and LV end-systolic volume index (ESVI)]. Data from 16 studies were combined including 1641 patients (984 cell therapy, 657 controls). The absolute improvement in LVEF was greater among BMC-treated patients compared with controls: [2.55% increase, 95% confidence interval (CI) 1.83-3.26, P < 0.001]. Cell therapy significantly reduced LVEDVI and LVESVI (-3.17 mL/m(2), 95% CI: -4.86 to -1.47, P < 0.001; -2.60 mL/m(2), 95% CI -3.84 to -1.35, P < 0.001, respectively). Treatment benefit in terms of LVEF improvement was more pronounced in younger patients (age < 55, 3.38%, 95% CI: 2.36-4.39) compared with older patients (age >= 55 years, 1.77%, 95% CI: 0.80-2.74, P 0.03). This heterogeneity in treatment effect was also observed with respect to the reduction in LVEDVI and LVESVI. Moreover, patients with baseline LVEF, < 40% derived more benefit from intracoronary BMC therapy. LVEF improvement was 5.30%, 95% CI: 4.27-6.33 in patients with LVEF,40% compared with 1.45%, 95% CI: 0.60 to 2.31 in LVEF >= 40%, P < 0.001. Noclear interaction was observed between other subgroups and outcomes. Conclusion Intracoronary BMC infusion is associated with improvement of LV function and remodelling in patients after ST-segment elevation myocardial infarction. Younger patients and patients with a more severely depressed LVEF at baseline derived most benefit from this adjunctive therapy.
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收藏
页码:989 / 998
页数:10
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