Preservation from left ventricular remodeling by front-integrated Revascularization and stem cell liberation in evolving acute myocardial infarction by use of granulocyte-colony-stimulating factor (FIRSTLINE-AMI)

被引:174
作者
Ince, H
Petzsch, M
Kleine, HD
Schmidt, H
Rehders, T
Körber, T
Schümichen, C
Freund, M
Nienaber, CA
机构
[1] Univ Hosp Rostock, Rostock Sch Med, Div Cardiol, Dept Internal Med, D-18057 Rostock, Germany
[2] Univ Hosp Rostock, Rostock Sch Med, Div Hematol, D-18057 Rostock, Germany
[3] Univ Hosp Rostock, Rostock Sch Med, Dept Nucl Med, D-18057 Rostock, Germany
关键词
myocardial infarction; remodeling; cells; angioplasty; glucose;
D O I
10.1161/CIRCULATIONAHA.105.541433
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Considering experimental evidence that stem cells enhance myocardial regeneration and granulocyte colony - stimulating factor ( G-CSF) mediates mobilization of CD34 + mononuclear blood stem cells ( MNCCD34+), we tested the impact of G-CSF integrated into primary percutaneous coronary intervention ( PCI) management of acute myocardial infarction in man. Methods and Results - Fifty consecutive patients with ST-segment elevation myocardial infarction were subjected to primary PCI stenting with abciximab and followed up for 6 months; 89 +/- 35 minutes after successful PCI, 25 patients were randomly assigned in this pilot study ( PROBE design) to receive subcutaneous G-CSF at 10 mu g/kg body weight for 6 days in addition to standard care, including aspirin, clopidogrel, an ACE inhibitor, beta-blocking agents, and statins. By use of CellQuest software on peripheral blood samples incubated with CD45 and CD34, mobilized MNCCD34+ were quantified on a daily basis. With homogeneous demographics and clinical and infarct-related characteristics, G-CSF stimulation led to mobilization of MNCCD34+ to between 3.17 +/- 2.93 MNCCD34+/mu L at baseline and 64.55 +/- 37.11 MNCCD34+/mu L on day 6 ( P < 0.001 versus control); there was no indication of leukocytoclastic effects, significant pain, impaired rheology, inflammatory reactions, or accelerated restenosis at 6 months. Within 35 days, G-CSF and MNCCD34+ liberation led to enhanced resting wall thickening in the infarct zone of between 0.29 +/- 0.22 and 0.99 +/- 0.32 mm versus 0.49 +/- 0.29 mm in control subjects ( P < 0.001); under inotropic challenge with dobutamine ( 10 mu g (.) kg(-1) (.) min(-1)), wall motion score index showed improvement from 1.66 +/- 0.23 to 1.41 +/- 0.21 ( P < 0.004 versus control) and to 1.35 +/- 0.24 after 4 months ( P < 0.001 versus control), respectively, coupled with sustained recovery of wall thickening to 1.24 +/- 0.31 mm ( P < 0.001 versus control) at 4 months. Accordingly, resting wall motion score index improved with G-CSF to 1.41 +/- 0.25 ( P < 0.001 versus control), left ventricular end-diastolic diameter to 55 +/- 5 mm ( P < 0.002 versus control), and ejection fraction to 54 +/- 8% ( P < 0.001 versus control) after 4 months. Morphological and functional improvement with G-CSF was corroborated by enhanced metabolic activity and F-18-deoxyglucose uptake in the infarct zone ( P < 0.001 versus control). Conclusions - G-CSF and mobilization of MNCCD34+ after reperfusion of infarcted myocardium may offer a pragmatic strategy for preservation of myocardium and prevention of remodeling without evidence of aggravated restenosis.
引用
收藏
页码:3097 / 3106
页数:10
相关论文
共 58 条
[1]   G-CSF treatment increases side population cell infiltration after myocardial infarction in mice [J].
Adachia, Y ;
Imagawa, J ;
Suzuki, Y ;
Yogo, K ;
Fukazawa, M ;
Kuromaru, O ;
Saito, Y .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 36 (05) :707-710
[2]   Assessment of the tissue distribution of transplanted human endothelial progenitor cells by radioactive labeling [J].
Aicher, A ;
Brenner, W ;
Zuhayra, M ;
Badorff, C ;
Massoudi, S ;
Assmus, B ;
Eckey, T ;
Henze, E ;
Zeiher, AM ;
Dimmeler, S .
CIRCULATION, 2003, 107 (16) :2134-2139
[3]   The revised CONSORT statement for reporting randomized trials: Explanation and elaboration [J].
Altman, DG ;
Schulz, KF ;
Moher, D ;
Egger, M ;
Davidoff, F ;
Elbourne, D ;
Gotzsche, PC ;
Lang, T .
ANNALS OF INTERNAL MEDICINE, 2001, 134 (08) :663-694
[4]   Effect of stromal-cell-derived factor 1 on stem-cell homing and tissue regeneration in ischaemic cardiomyopathy [J].
Askari, AT ;
Unzek, S ;
Popovic, ZB ;
Goldman, CK ;
Forudi, F ;
Kiedrowski, M ;
Rovner, A ;
Ellis, SG ;
Thomas, JD ;
DiCorleto, PE ;
Topol, EJ ;
Penn, MS .
LANCET, 2003, 362 (9385) :697-703
[5]   Transdifferentiation of blood-derived human adult endothelial progenitor cells into functionally active cardiomyocytes [J].
Badorff, C ;
Brandes, RP ;
Popp, R ;
Rupp, S ;
Urbich, C ;
Aicher, A ;
Fleming, I ;
Busse, R ;
Zeiher, A ;
Dimmeler, S .
CIRCULATION, 2003, 107 (07) :1024-1032
[6]   Haematopoietic stem cells adopt mature haematopoietic fates in ischaemic myocardium [J].
Balsam, LB ;
Wagers, AJ ;
Christensen, JL ;
Kofidis, T ;
Weissman, IL ;
Robbins, RC .
NATURE, 2004, 428 (6983) :668-673
[7]   Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium - Feasibility, cell migration, and body distribution [J].
Barbash, IM ;
Chouraqui, P ;
Baron, J ;
Feinberg, MS ;
Etzion, S ;
Tessone, A ;
Miller, L ;
Guetta, E ;
Zipori, D ;
Kedes, LH ;
Kloner, RA ;
Leor, J .
CIRCULATION, 2003, 108 (07) :863-868
[8]   Association between white blood cell count, epicardial blood flow, myocardial perfusion, and clinical outcomes in the setting of acute myocardial infarction - A Thrombolysis in Myocardial Infarction 10 substudy [J].
Barron, HV ;
Cannon, CP ;
Murphy, SA ;
Braunwald, E ;
Gibson, CM .
CIRCULATION, 2000, 102 (19) :2329-2334
[9]   Optimal metabolic conditions during fluorine-18 fluorodeoxyglucose imaging; A comparative study using different protocols [J].
Bax, JJ ;
Veening, MA ;
Visser, FC ;
vanLingen, A ;
Heine, RJ ;
Cornel, JH ;
Visser, CA .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1997, 24 (01) :35-41
[10]   Transplantation of allogeneic peripheral blood stem cells mobilized by recombinant human granulocyte colony stimulating factor [J].
Bensinger, WI ;
Clift, RA ;
Anasetti, C ;
Appelbaum, FA ;
Demirer, T ;
Rowley, S ;
Sandmaier, BM ;
TorokStorb, B ;
Storb, R ;
Buckner, CD .
STEM CELLS, 1996, 14 (01) :90-105