Myocardial blood flow and infarct size after CD133+ cell injection in large myocardial infarction with good recanalization and poor reperfusion: results from a randomized controlled trial

被引:43
作者
Colombo, Alessandro [1 ]
Castellani, Massimo [3 ]
Piccaluga, Emanuela
Pusineri, Enrico [4 ]
Palatresi, Simone [4 ]
Longari, Virgilio [3 ]
Canzi, Cristina [3 ]
Sacchi, Elisabetta
Rossi, Edoardo
Rech, Roberto [5 ]
Gerundini, Paolo [3 ]
Viecca, Maurizio
Deliliers, Giorgio Lambertenghi [6 ,7 ]
Rebulla, Paolo [2 ]
Soligo, Davide [6 ,7 ]
Giordano, Rosaria [2 ]
机构
[1] Luigi Sacco Hosp, Dept Cardiol, Catheterizat Lab, I-20157 Milan, Italy
[2] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Ctr Transfus Med Cellular Therapy & Cryobiol, Cell Factory F Calori, Milan, Italy
[3] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Dept Nucl Med, Milan, Italy
[4] IRCCS Policlin San Donato, Clin Cardiol Unit, San Donato Milanese, Italy
[5] Luigi Sacco Hosp, Emergency Med Unit, Milan, Italy
[6] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Hematol & Bone Marrow Transplantat Ctr, Milan, Italy
[7] Univ Milan, Milan, Italy
关键词
myocardial infarction; PET; stem cells; COLONY-STIMULATING FACTOR; BONE-MARROW-CELLS; ENDOTHELIAL PROGENITOR CELLS; STEM-CELLS; INTRAMYOCARDIAL DELIVERY; INTRACORONARY INJECTION; PRIMARY ANGIOPLASTY; DOUBLE-BLIND; IN-VITRO; HEART;
D O I
10.2459/JCM.0b013e328343d708
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective Large acute ST-elevation myocardial infarction (STEMI) sometimes leaves extensive ischemic damage despite timely and successful primary angioplasty. This clinical picture of good recanalization with incomplete reperfusion represents a good model to assess the reparative potential of locally administered cell therapy. Thus, we conducted a randomized controlled trial aimed at evaluating the effect of intracoronary administration of CD133(+) stem cells on myocardial blood flow and function in this setting. Methods Fifteen patients with large anterior STEMI, myocardial blush grade 0-1 and more than 50% ST-elevation recovery after optimal coronary recanalization (TIMI 3 flow) with stenting were randomly assigned to receive CD133(+) cells from either bone marrow (group A) or peripheral blood (group B), or to stay on drug therapy alone (group C). The cells were intracoronary injected within 10-14 days of STEMI. Infarct-related myocardial blood flow (MBF) was evaluated by NH3 positron emission tomography 2-5 days before cell administration and after 1 year. Results MBF increased in the infarct area from 0.419 (0.390-0.623) to 0.544 (0.371-0.729) ml/min per g in group A, decreased from 0.547 (0.505-0.683) to 0.295 (0.237-0.472) ml/min per g in group B and only slightly changed from 0.554 (0.413-0.662) to 0.491 (0.453-0.717) ml/min per g in group C (A vs. C: P = 0.023; B vs. C: P = 0.066). Left ventricular volume tended to increase more in groups B and C than in group A, ejection fraction and wall motion score index remained stable in the three groups. Conclusion These findings support the hypothesis that intracoronary administration of bone marrow-derived, but not peripheral blood-derived CD133(+) cells 10-14 days after STEMI may improve long-term perfusion. J Cardiovasc Med 12:239-248 (C) 2011 Italian Federation of Cardiology.
引用
收藏
页码:239 / 248
页数:10
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