G-CSF treatment for STEMI: final 3-year follow- up of the randomised placebo- controlled STEM- AMI trial

被引:16
作者
Achilli, Felice [1 ]
Malafronte, Cristina [2 ]
Maggiolini, Stefano [3 ]
Lenatti, Laura [2 ]
Squadroni, Lidia [4 ]
Gibelli, Giuseppe [5 ]
Capogrossi, Maurizio C. [6 ]
Dadone, Viola [7 ]
Gentile, Francesco [7 ]
Bassetti, Beatrice [8 ]
Di Gennaro, Filiberto [9 ]
Camisasca, Paola [1 ]
Calchera, Ivan [1 ]
Valagussa, Laura [1 ]
Colombo, Gualtiero I. [10 ]
Pompilio, Giulio [8 ,11 ,12 ]
机构
[1] San Gerardo Hosp, Dept Cardiol, I-20900 Monza, Italy
[2] A Manzoni Hosp, Dept Cardiol, Lecce, Italy
[3] San L Mandic Hosp, Dept Cardiol, Merate, Lecco, Italy
[4] San Carlo Hosp, Dept Cardiol, Milan, Italy
[5] Clin San Carlo, Cardiol Unit, Paderno Dugnano, Italy
[6] Ist Dermopat Immacolata IRCCS, Lab Vasc Pathol, Rome, Italy
[7] Bassini Hosp, Dept Cardiol, Milan, Italy
[8] Univ Milan, Dept Clin & Community Sci, Milan, Italy
[9] San Gerardo Hosp, Dept Radiol, I-20900 Monza, Italy
[10] Ctr Cardiol Monzino IRCCS, Lab Immunol & Funct Genom, Milan, Italy
[11] Ctr Cardiol Monzino IRCCS, Lab Vasc Biol & Regenerat Med, Milan, Italy
[12] Ctr Cardiol Monzino IRCCS, Dept Cardiovasc Surg, Milan, Italy
关键词
ACUTE MYOCARDIAL-INFARCTION; COLONY-STIMULATING FACTOR; CARDIOVASCULAR MAGNETIC-RESONANCE; CELL-BASED THERAPY; BONE-MARROW-CELLS; HEART-FAILURE; SEGMENT ELEVATION; CARDIAC REPAIR; SIZE; TRANSMURALITY;
D O I
10.1136/heartjnl-2013-304955
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To assess whether granulocyte colony-stimulating factor (G-CSF) treatment induces a sustained benefit on adverse remodelling in patients with large anterior ST-elevation myocardial infarction (STEMI) and left ventricular (LV) dysfunction after successful reperfusion. Methods The STEM-AMI Trial was a prospective, placebo-controlled, multicentre study. Sixty consecutive patients with a first anterior STEMI, who underwent primary percutaneous coronary intervention 2-12h after symptom onset, with LV ejection fraction (LVEF) 45% measured by echocardiography within 12h after successful revascularisation (TIMI flow score 2), were randomised 1:1 to G-CSF (5 mu g/Kg body weight b.i.d.) or placebo. Clinical events and Major Adverse Cardiac and Cerebrovascular Event (MACCE) were monitored, and LVEF, LV end-diastolic (LVEDV) and end-systolic (LVESV) volumes, and infarct size were evaluated by MRI at the final 3-year follow-up. Results Fifty-four patients completed the study, of whom 35 with MRI. No significant differences were found in mortality and MACCE between G-CSF and placebo-treated groups. The 3-year infarct size was not different between groups, whereas LVEDV was significantly lower in G-CSF (n=20) than in placebo (n=15) patients (170.18.1 vs 197.2 +/- 8.9mL, respectively; p=0.033 at analysis of covariance). A significant inverse correlation was detected in G-CSF patients between the number of circulating CD34 cells at 30days after reperfusion and the 3-year absolute and indexed LVEDV (=-0.71, 95% CI -0.90 to -0.30, and =-0.62, -0.86 to -0.14, respectively), or their change over time (r=-0.59, -0.85 to -0.11, and r=-0.55, -0.83 to -0.06, respectively). Conclusions G-CSF therapy may be beneficial in attenuating ventricular remodelling subsequent to a large anterior STEMI in the long term. No differences have been detected in clinical outcome.
引用
收藏
页码:574 / 581
页数:8
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