A critical challenge: Dosage-related efficacy and acute complication intracoronary injection of autologous bone marrow mesenchymal stem cells in acute myocardial infarction

被引:109
作者
Gao, Lian R. [1 ]
Pei, Xue T. [2 ]
Ding, Qing A. [1 ]
Chen, Yu [1 ]
Zhang, Ning K. [1 ]
Chen, Hai Y. [1 ]
Wang, Zhi G. [1 ]
Wang, Yun F. [2 ]
Zhu, Zhi M. [1 ]
Li, Tian C. [3 ]
Liu, Hui L. [4 ]
Tong, Zi C. [5 ]
Yang, Yong [4 ]
Nan, Xue [2 ]
Guo, Feng [6 ]
Shen, Jian L. [5 ,7 ]
Shen, Yan H. [8 ]
Zhang, Jian J.
Fei, Yu X. [1 ]
Xu, Hong T. [1 ]
Wang, Li H. [1 ]
Tian, Hai T. [1 ]
Liu, Da Q. [2 ]
Yang, Ye [1 ]
机构
[1] Navy Gen Hosp, Ctr Cardiol, Beijing 100048, Peoples R China
[2] Acad Mil Med Sci, Stem Cell Inst, Beijing 100850, Peoples R China
[3] Beijing Tongren Hosp, Ctr Cardiol, Beijing, Peoples R China
[4] Armed Police Gen Hosp, Dept Cardiol, Beijing, Peoples R China
[5] Beijing Chaoyang Hosp, Ctr Cardiol, Beijing, Peoples R China
[6] Navy Gen Hosp, Dept Diagnost Radiol, Beijing 100048, Peoples R China
[7] Navy Gen Hosp, Dept Hematol, Beijing 100048, Peoples R China
[8] Navy Gen Hosp, Dept Ultrason Diag, Beijing 100048, Peoples R China
关键词
Acute myocardial infarction; Bone marrow mesenchymal stem cells; Intracoronary injection; CARDIOMYOCYTE PHENOTYPE; MONONUCLEAR-CELLS; STROMAL CELLS; IN-VITRO; TRANSPLANTATION; DIFFERENTIATE; AGE; DELIVERY; THERAPY;
D O I
10.1016/j.ijcard.2013.04.112
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Previous studies showed improvement in heart function by injecting bone marrow mesenchymal stem cells (BMSCs) after AMI. Emerging evidence suggested that both the number and function of BMSCs decline with ageing. We designed a randomized, controlled trial to further investigate the safety and efficacy of this treatment. Methods: Patients with ST-elevation AMI undergoing successful reperfusion treatment within 12 hours were randomly assigned to receive an intracoronary infusion of BMSCs (n = 21) or standard medical treatment (n = 22) (the numbers of patients were limited because of the complication of coronary artery obstruction). Results: There is a closely positive correlation of the number and function of BMSCs vs. the cardiac function reflected by LVEF at baseline (r = 0.679, P = 0.001) and at 12-month follow-up (r = 0.477, P = 0.039). Six months after cell administration, myocardial viability within the infarct area by 18-FDG SPECT was improved in both groups compared with baseline, but no significant difference in the BMSCs compared with control groups (4.0 +/- 0.4% 95%CI 3.1-4.9 vs. 3.2 +/- 0.5% 95%CI 2.1-4.3, P = 0.237). 99mTc-sestamibi SPECT demonstrated that myocardial perfusion within the infarct area in the BMSCs did not differ from the control group (4.4 +/- 0.5% 95%CI 3.2-5.5 vs. 3.9 +/- 0.6% 95%CI 2.6-5.2, P = 0.594). Similarly, LVEF after 12 and 24 months follow-up did not show any difference between the two groups. In the BMSCs group, one patient suffered a serious complication of coronary artery occlusion during the BMSCs injection procedure. Conclusions: The clinical benefits of intracoronary injection of autologous BMSCs in acute STEMI patients need further investigation and reevaluation. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:3191 / 3199
页数:9
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