Efficacy of emergent transcatheter transplantation of stem cells for treatment of acute myocardial infarction (TCT-STAMI)

被引:124
作者
Ge, J. [1 ]
Li, Y. [1 ]
Qian, J. [1 ]
Shi, J. [1 ]
Wang, Q. [1 ]
Niu, Y. [1 ]
Fan, B. [1 ]
Liu, X. [1 ]
Zhang, S. [1 ]
Sun, A. [1 ]
Zou, Y. [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Dept Cardiol, Shanghai 200032, Peoples R China
关键词
D O I
10.1136/hrt.2005.085431
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To study whether emergent intracoronary autologous bone marrow cell transplantation (BMT) is applicable for the treatment of acute myocardial infarction (AMI). Methods: 20 patients admitted within 24 h after the onset of a first AMI were randomly allocated to receive intracoronary autologous BMT (n = 10) or bone marrow supernatant (controls, n = 10) immediately after primary percutaneous coronary intervention. Left ventricular ejection fraction (LVEF), left ventricular end diastolic internal diameter (LVDd) and myocardial perfusion defect scores were examined respectively by echocardiography and single-photon emission computed tomography at one week and six months after AMI. Results: From one week to six months after AMI, LVEF was enhanced from mean 53.8 (SD 9.2)% to 58.6 (9.9)% (p < 0.05) in the BMT group but was unchanged in the control group (58.2 (7.5)% v 56.3 (3.5)%, p > 0.05); LVDd remained unchanged (52.5 (2.8) v 52.1 (3.2) mm, p > 0.05) in the BMT group but was significantly enlarged in the control group (50.4 (6.0) v 55.2 (7.1) mm, p < 0.05). Additionally, myocardial perfusion defect scores decreased from 21 (11) to 13 (10) (p < 0.01) in the BMT group but were unchanged in the control group (20 (14) v 17 (15), p > 0.05). Conclusion: Emergent intracoronary transplantation of bone marrow mononuclear cells after AMI is practicable, and it improved cardiac function, prevented myocardial remodelling and increased myocardial perfusion at six months' follow up.
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收藏
页码:1764 / 1767
页数:4
相关论文
共 12 条
[1]   Infarct remodeling after intracoronary progenitor cell treatment in patients with acute myocardial infarction (TOPCARE-AMI) -: Mechanistic insights from serial contrast-enhanced magnetic resonance imaging [J].
Britten, MB ;
Abolmaali, ND ;
Assmus, B ;
Lehmann, R ;
Honold, J ;
Schmitt, J ;
Vogl, TJ ;
Martin, H ;
Schächinger, V ;
Dimmeler, S ;
Zeiher, AM .
CIRCULATION, 2003, 108 (18) :2212-2218
[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]   Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo [J].
Goodell, MA ;
Brose, K ;
Paradis, G ;
Conner, AS ;
Mulligan, RC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1797-1806
[4]   The time course of tumor necrosis factor-α, inducible nitric oxide synthase and vascular endothelial growth factor expression in an experimental model of chronic myocardial infarction in rats [J].
Heba, G ;
Krzeminski, T ;
Porc, M ;
Grzyb, J ;
Ratajska, A ;
Dembinska-Kiec, A .
JOURNAL OF VASCULAR RESEARCH, 2001, 38 (03) :288-300
[5]   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
[6]   Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function [J].
Kocher, AA ;
Schuster, MD ;
Szabolcs, MJ ;
Takuma, S ;
Burkhoff, D ;
Wang, J ;
Homma, S ;
Edwards, NM ;
Itescu, S .
NATURE MEDICINE, 2001, 7 (04) :430-436
[7]  
Matsumoto N, 2001, J NUCL MED, V42, P687
[8]   Bone marrow cells regenerate infarcted myocardium [J].
Orlic, D ;
Kajstura, J ;
Chimenti, S ;
Jakoniuk, I ;
Anderson, SM ;
Li, BS ;
Pickel, J ;
McKay, R ;
Nadal-Ginard, B ;
Bodine, DM ;
Leri, A ;
Anversa, P .
NATURE, 2001, 410 (6829) :701-705
[9]   Autologous mesenchymal stem cell transplantation induce VEGF and neovascularization in ischemic myocardium [J].
Tang, YL ;
Zhao, Q ;
Zhang, YC ;
Cheng, LL ;
Liu, MY ;
Shi, JH ;
Yang, YZ ;
Pan, CZ ;
Ge, JB ;
Phillips, MI .
REGULATORY PEPTIDES, 2004, 117 (01) :3-10
[10]   Improved heart function with myogenesis and angiogenesis after autologous porcine bone marrow stromal cell transplantation [J].
Tomita, S ;
Mickle, DAG ;
Weisel, RD ;
Jia, ZC ;
Tumiati, LC ;
Allidina, Y ;
Liu, P ;
Li, RK .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2002, 123 (06) :1132-1140