• Title of article

    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

  • Author/Authors

    Tardif، نويسنده , , Jean-Claude and Tanguay، نويسنده , , Jean-François and Wright، نويسنده , , Scott S. and Duchatelle، نويسنده , , Valérie and Petroni، نويسنده , , Thibaut and Grégoire، نويسنده , , Jean C. and Ibrahim، نويسنده , , Reda and Heinonen، نويسنده , , Therese M. and Robb، نويسنده , , Stephen and Bertrand، نويسنده , , Olivier F. and Cournoyer، نويسنده , , Daniel and Johnson، نويسنده , , Dominique and Mann، نويسنده , , Jessica and Guertin، نويسنده , , Marie-Claude and LʹAllier، نويسنده , , Philippe L.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    8
  • From page
    2048
  • To page
    2055
  • Abstract
    Objectives udy 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. ound ctin 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, antithrombotic, and antiatherogenic properties. s ts (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. s 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. sions umab 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)
  • Keywords
    inclacumab , Myocardial infarction , percutaneous coronary intervention , p-Selectin
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Serial Year
    2013
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Record number

    1756640