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首页> 外文期刊>Journal of the American College of Cardiology >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
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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

机译:P-选择素拮抗剂Heldacumab对非ST段抬高后经皮冠状动脉介入后心肌损伤的影响:选择 - ACS试验的结果

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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, antithrombotic, 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)
机译:目的:该研究旨在评估Went-ST-Segment excation心肌梗死患者经皮冠状动脉干预(PCI)期间对心肌损伤的减少。背景:P-SELETIN是涉及内皮细胞,血小板和白细胞之间的相互作用的粘附分子。 Contracumab是针对p-选择素的重组单克隆抗体,具有潜在的抗炎,抗炎,抗抗细胞组织和抗真菌性质。方法:患者(n = 544)与冠状动脉血管造影和可能的ad hoc pCI调度的非ST段抬高心肌梗死,随机化以获得1个Prentacumab 5或20mg / kg或安慰剂的预程序输注。在接受PCI,接受研究药物的患者中评估的主要终点,并具有可用的疗效数据(n = 322),是PCI后16和24小时的肌钙蛋白I从基线的变化。结果:LetaCumab 5 mg / kg没有效果。放置调整后的几何平均百分比肌钙蛋白I的变化20mg / kg为-24.4%在24小时(p = 0.05),16小时,p = 0.07)。峰肌钙蛋白I降低23.8%(p = 0.05),曲线下的面积超过24小时,达33.9%(P = 0.08)。肌酸激酶 - 心肌带产生类似的结果,结果为-17.4%,在24小时(p = 0.06),16小时,p = 0.09)。肌酸激酶 - 心肌带的发病率增加> 24小时内正常的上限的3倍分别在安慰剂和包含含量20-mg / kg基团中的18.3%和8.9%(P = 0.05)。可溶性P-选择素水平的安慰剂调节的变化为-9.5%(p = 0.25)和-22.0%(P <0.01),包含含有胞残米和20mg / kg。组之间的不良事件没有显着差异。结论:在非ST段升高心肌梗死患者患者中,葡萄干似乎减少了PCI后的心肌损伤。 (研究非ST-EXTIVATION心肌梗死患者RO4905417 [非STEMI]经皮冠状动脉介入的患者; NCT01327183)

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  • 作者单位

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Mayo Clinic Rochester MN United States;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

    Montreal Heart Institute Coordinating Center (MHICC) Montreal QC Canada;

    Hoffmann-La Roche Basel Switzerland;

    Institut Universitaire de Cardiologie et de Pneumologie de Québec Quebec City QC Canada;

    Montreal Heart Institute Coordinating Center (MHICC) Montreal QC Canada;

    Montreal Heart Institute Coordinating Center (MHICC) Montreal QC Canada;

    Hoffmann-La Roche Basel Switzerland;

    Montreal Heart Institute Coordinating Center (MHICC) Montreal QC Canada;

    Montreal Heart Institute Université de Montréal 5000 Belanger Street Montreal QC H1T 1C8 Canada;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 心脏、血管(循环系)疾病;
  • 关键词

    inclacumab; myocardial infarction; P-selectin; percutaneous coronary intervention;

    机译:Heldacumab;心肌梗死;p-selectin;经皮冠状动脉介入;

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