Improvement in Left Ventricular Function with Intracoronary Mesenchymal Stem Cell Therapy in a Patient with Anterior Wall ST-Segment Elevation Myocardial Infarction

被引:80
作者
Kim, Su Hyun [1 ]
Cho, Jang Hyun [1 ]
Lee, Yoon Ho [2 ]
Lee, Ji Hye [2 ]
Kim, Soo Sung [2 ]
Kim, Mi Yang [2 ]
Lee, Min Gu [1 ]
Kang, Won Yu [1 ]
Lee, Kyung Sim [3 ]
Ahn, Young Keun [4 ]
Jeong, Myung Ho [4 ]
Kim, Hyun Soo [5 ]
机构
[1] St Carollo Hosp, Cardiovasc Intervent, Suncheon Si, Jeollanam Do, South Korea
[2] St Carollo Hosp, Dept Internal Med, Suncheon Si, Jeollanam Do, South Korea
[3] Gwangyang Hlth Sci Univ, Dept Nursing, Gwangyang Si, Jeollanam Do, South Korea
[4] Chonnam Natl Univ Hosp, Cardiovasc Ctr, Dept Cardiol, Gwangju, South Korea
[5] Dr Kims Stem Cell Clin, Seoul, South Korea
关键词
Acute myocardial infarction; Heart failure; Mesenchymal stem cell; PROGENITOR CELLS; DOUBLE-BLIND; TRANSPLANTATION; REPAIR; HEART; QUANTIFICATION; GUIDELINES;
D O I
10.1007/s10557-018-6804-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The progression and development of congestive heart failure is still considered a large problem despite the existence of revascularization therapies and optimal, state-of-the-art medical services. An acute myocardial infarction (AMI) is a major cause of congestive heart failure, so researchers are investigating techniques to complement primary percutaneous coronary intervention (PCI) or thrombolytic therapy to prevent congestive heart failure after AMI. Twenty-six patients with successful PCI for acute ST-segment elevation anterior wall myocardial infarction were assigned to either a control group (n = 12) or a bone marrow mesenchymal stem cells (BM-MSC) group (n = 14). The control group received optimum post-infarction treatment, and the BMSC group received intracoronary delivery of autologous BMSC at 1 month after PCI with the optimum medical treatment. The primary endpoint was a left ventricular ejection fraction (LVEF) change from baseline to 4-month follow-up, as determined via myocardial single-photon emission computed tomography (SPECT). The global LVEF at baseline (determined 3.5 +/- 1.5 days after PCI) was 35.4 +/- 3.0% in the control group and 33.6 +/- 4.7% in the BM-MSC group. BMSC transfer enhanced left ventricular systolic function primarily in anterior wall myocardial segments adjacent to the LAD infarcted area. Four months later, via SPECT, global LVEF had increased by 4.8 +/- 1.9% in the control group and 8.8 +/- 2.9% in the BM-MSC group (p = 0.031). The cell transfer did not increase the risk of adverse clinical events, in-stent restenosis, or proarrhythmic effects. The echocardiographic evaluation also revealed a significant increase in the LVEF value from baseline to the 4-month (9.0 +/- 4.7 and 5.3 +/- 2.6%, p = 0.023) and 12-month (9.9 +/- 5.2% and 6.5 +/- 2.7%, p = 0.048) follow-up in the BM-MSC group but not in the control group. Intracoronary administration of autologous BM-MSC was tolerable and safe with significant improvement in LVEF at 4-month (SPECT and echocardiography result) and 12-month (echocardiography result only) follow-up in patients with anterior AMI.
引用
收藏
页码:329 / 338
页数:10
相关论文
共 29 条
[1]  
Antman EM, 2008, J AM COLL CARDIOL, V51, P2028, DOI 10.1016/j.jacc.2007.10.001
[2]  
Antman Elliott M, 2004, J Am Coll Cardiol, V44, P671, DOI 10.1016/j.jacc.2004.07.002
[3]   Mesenchymal Stem Cells Provide Better Results Than Hematopoietic Precursors for the Treatment of Myocardial Infarction [J].
Arminan, Ana ;
Gandia, Carolina ;
Manuel Garcia-Verdugo, J. ;
Lledo, Elisa ;
Trigueros, Cesar ;
Ruiz-Sauri, Amparo ;
Dolores Minana, Maria ;
Solves, Pilar ;
Paya, Rafael ;
Anastasio Montero, J. ;
Sepulveda, Pilar .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (20) :2244-2253
[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]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[6]   Restoration of microvascular function in the infarct-related artery by intracoronary transplantation of bone marrow progenitor cells in patients with acute myocardial infarction -: The Doppler substudy of the reinfusion of enriched progenitor cells and infarct remodeling in acute myocardial infarction (REPAIR-AMI) trial [J].
Erbs, Sandra ;
Linke, Axel ;
Schaechinger, Volker ;
Assmus, Birgit ;
Thiele, Holger ;
Diederich, Klaus-Werner ;
Hoffmann, Christina ;
Dimmeler, Stefanie ;
Tonn, Torsten ;
Hambrecht, Rainer ;
Zeiher, Andreas M. ;
Schuler, Gerhard .
CIRCULATION, 2007, 116 (04) :366-374
[7]   Predictive value of the index of microcirculatory resistance in patients with ST-segment elevation myocardial infarction [J].
Fearon, William F. ;
Shah, Maulik ;
Ng, Martin ;
Brinton, Todd ;
Wilson, Andrew ;
Trernmel, Jennifer A. ;
Schnittger, Ingela ;
Lee, David P. ;
Vagelos, Randall H. ;
Fitzgerald, Peter J. ;
Yock, Paul G. ;
Yeung, Alan C. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (05) :560-565
[8]  
Fisher SA, 2015, COCHRANE LIB, P9
[9]  
GERMANO G, 1995, J NUCL MED, V36, P2138
[10]   A Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study of Intravenous Adult Human Mesenchymal Stem Cells (Prochymal) After Acute Myocardial Infarction [J].
Hare, Joshua M. ;
Traverse, Jay H. ;
Henry, Timothy D. ;
Dib, Nabil ;
Strumpf, Robert K. ;
Schulman, Steven P. ;
Gerstenblith, Gary ;
DeMaria, Anthony N. ;
Denktas, Ali E. ;
Gammon, Roger S. ;
Hermiller, James B., Jr. ;
Reisman, Mark A. ;
Schaer, Gary L. ;
Sherman, Warren .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 54 (24) :2277-2286