Autologous bone marrow stem cells to treat acute myocardial infarction: a systematic review

被引:383
作者
Martin-Rendon, Enca [1 ,2 ]
Brunskill, Susan J. [3 ]
Hyde, Chris J. [3 ]
Stanworth, Simon J. [3 ]
Mathur, Anthony [4 ]
Watt, Suzanne M. [1 ,2 ]
机构
[1] John Radcliffe Hosp, NHS Blood & Transplant, Stem Cell Res Lab, Oxford OX3 9BQ, England
[2] Univ Oxford, Nuffield Dept Clin Lab Sci, Oxford, England
[3] John Radcliffe Hosp, NHSBT Oxford, Clin Res Grp, Oxford OX3 9BQ, England
[4] William Harvey Res Inst, Dept Clin Pharmacol, London, England
关键词
stem cells; myocardial infarction; bone marrow; systematic review; randomized clinical trials;
D O I
10.1093/eurheartj/ehn220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To provide systematic assessment of the safety and efficacy of autologous bone marrow-derived stem cell (BMSC) transplantation in acute myocardial infarction (AMI) based on clinical evidence. Methods and results The search strategy included MEDLINE, EMBASE, the Cochrane Library, and Current Controlled Trials Register through to August 2007 for randomized controlled trials of BMSC treatment for AMI. Thirteen trials (14 comparisons) with a total of 811 participants were included. Data were analysed using a random effects model. Overall, stem cell therapy improved left ventricular ejection fraction (LVEF) by 2.99% [95% confidence interval (CI), 1.26-4.72%, P = 0.0007], significantly reduced left ventricular end-systolic volume (LVESV) by 4.74 mL (95% CI, -7.84 to -1.64 mL, P = 0.003), and myocardial lesion area by 3.51% (95% CI, -5.91 to -1.11%, P = 0.004) compared with controls. Subgroup analysis revealed that there was statistical significant difference in LEVF in favour of BMSCs when cells were infused within 7 days following AMI and when the BMSC dose administered was higher than 10(8) BMSCs. In addition, there were trends in favour of benefit for most clinical outcomes examined, although it should be acknowledged that the 95%CI included no significant difference. Conclusion Stem cell treatment for AMI still holds promise. Clinically, these data suggest that improvement over conventional therapy can be achieved. Further, adequately powered trials using optimal dosing, longer term outcome assessments, more reliable, and more patient-centred outcomes are required.
引用
收藏
页码:1807 / 1818
页数:12
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