Effects of the P-Selectin Antagonist Inclacumab on Myocardial Damage After Percutaneous Coronary Intervention for Non-ST-Segment Elevation Myocardial Infarction Results of the SELECT-ACS Trial

被引:164
作者
Tardif, Jean-Claude [1 ]
Tanguay, Jean-Francois [1 ]
Wright, Scott S. [2 ]
Duchatelle, Valerie [1 ]
Petroni, Thibaut [1 ]
Gregoire, Jean C. [1 ]
Ibrahim, Reda [1 ]
Heinonen, Therese M. [3 ]
Robb, Stephen [4 ]
Bertrand, Olivier F. [5 ]
Cournoyer, Daniel [3 ]
Johnson, Dominique [3 ]
Mann, Jessica [4 ]
Guertin, Marie-Claude [3 ]
L'Allier, Philippe L. [1 ]
机构
[1] Univ Montreal, Montreal Heart Inst, Montreal, PQ, Canada
[2] Mayo Clin, Rochester, MN USA
[3] Montreal Heart Inst Coordinating Ctr, Montreal, PQ, Canada
[4] Hoffmann La Roche AG, Basel, Switzerland
[5] Inst Univ Cardiol & Pneumol Quebec, Quebec City, PQ, Canada
关键词
inclacumab; myocardial infarction; percutaneous coronary intervention; P-selectin; RANDOMIZED-TRIAL; BALLOON ANGIOPLASTY; ATORVASTATIN; INJURY; ARTERY; INFLAMMATION; REDUCTION; DISEASE; ACTIVATION; PREVENTION;
D O I
10.1016/j.jacc.2013.03.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The study aimed to evaluate inclacumab for the reduction of myocardial damage during a percutaneous coronary intervention (PCI) in patients with non-ST-segment elevation myocardial infarction. Background P-selectin is an adhesion molecule involved in interactions between endothelial cells, platelets, and leukocytes. Inclacumab is a recombinant monoclonal antibody against P-selectin, with potential anti-inflammatory, anti-thrombotic, and antiatherogenic properties. Methods Patients (N = 544) with non-ST-segment elevation myocardial infarction scheduled for coronary angiography and possible ad hoc PCI were randomized to receive 1 pre-procedural infusion of inclacumab 5 or 20 mg/kg or placebo. The primary endpoint, evaluated in patients who underwent PCI, received study medication, and had available efficacy data (n = 322), was the change in troponin I from baseline at 16 and 24 h after PCI. Results There was no effect of inclacumab 5 mg/kg. Placebo-adjusted geometric mean percent changes in troponin I with inclacumab 20 mg/kg were -24.4% at 24 h (p = 0.05) and -22.4% at 16 h (p = 0.07). Peak troponin I was reduced by 23.8% (p = 0.05) and area under the curve over 24 h by 33.9% (p = 0.08). Creatine kinase-myocardial band yielded similar results, with changes of -17.4% at 24 h (p = 0.06) and -16.3% at 16 h (p = 0.09). The incidence of creatine kinase-myocardial band increases >3 times the upper limit of normal within 24 h was 18.3% and 8.9% in the placebo and inclacumab 20-mg/kg groups, respectively (p = 0.05). Placebo-adjusted changes in soluble P-selectin level were -9.5% (p = 0.25) and -22.0% (p < 0.01) with inclacumab 5 and 20 mg/kg. There was no significant difference in adverse events between groups. Conclusions Inclacumab appears to reduce myocardial damage after PCI in patients with non-ST-segment elevation myocardial infarction. (A Study of RO4905417 in Patients With Non ST-Elevation Myocardial Infarction [Non-STEMI] Undergoing Percutaneous Coronary Intervention; NCT01327183) (C) 2013 by the American College of Cardiology Foundation
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收藏
页码:2048 / 2055
页数:8
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