2016
DOI: 10.1161/jaha.116.004255
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Effects of the P‐Selectin Antagonist Inclacumab on Myocardial Damage After Percutaneous Coronary Intervention According to Timing of Infusion: Insights From the SELECT‐ACS Trial

Abstract: BackgroundThe Effects of the P‐Selectin Antagonist Inclacumab on Myocardial Damage After Percutaneous Coronary Intervention for Non‐ST‐Segment Elevation Myocardial Infarction (SELECT‐ACS) trial suggested beneficial effects of inclacumab, a monoclonal antibody directed against P‐selectin, on periprocedural myocardial damage. This study evaluated the effect of inclacumab on myocardial damage according to varying time intervals between study drug infusion and percutaneous coronary intervention (PCI).Methods and R… Show more

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Cited by 68 publications
(54 citation statements)
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“…Despite advances in the treatment of coronary artery disease, acute myocardial infarction (AMI) remains the leading cause of human mortality worldwide ( 1 ). AMI is characterized by a sudden reduction in blood and oxygen supply to the heart, irreversible muscle damage and cardiomyocyte death, resulting in the formation of an infarct zone containing nonfunctional myocytes, which are remodeled into scar tissue ( 2 ). The limited ability of the damaged heart to regenerate the damaged myocardium leads to the progression of cardiac decompensation and heart failure ( 3 ).…”
Section: Introductionmentioning
confidence: 99%
“…Despite advances in the treatment of coronary artery disease, acute myocardial infarction (AMI) remains the leading cause of human mortality worldwide ( 1 ). AMI is characterized by a sudden reduction in blood and oxygen supply to the heart, irreversible muscle damage and cardiomyocyte death, resulting in the formation of an infarct zone containing nonfunctional myocytes, which are remodeled into scar tissue ( 2 ). The limited ability of the damaged heart to regenerate the damaged myocardium leads to the progression of cardiac decompensation and heart failure ( 3 ).…”
Section: Introductionmentioning
confidence: 99%
“…Table 1 summarizes several trials of agents that modulate a specific pathway, often downstream from the initial insult. Most clinical trials targeting specific downstream targets, such as oxidation of LDL [126], secretory and lipoproteinassociated phospholipase A2 (sPLA2 and LpPLA2) [127e129], Pselectin [130,131] and even the IL-1b inhibitor anakinra [132] failed to meet their primary end-points with respect to a decrease in cardiovascular disease or selected surrogate end-point.…”
Section: Clinical Trials Of Anti-inflammatory Agentsmentioning
confidence: 99%
“…It is evident that the interplay between neutrophil, endothelial and platelet activation cannot be reduced to a single initiator of thrombosis, vessel stenosis or tissue fibrosis. Therefore, while blocking neutrophil-vessel interactions has shown therapeutic promise in reducing neutrophil-mediated vessel damage [81,[88][89][90][91][92], pro-inflammatory neutrophil-platelet interactions are a compelling target for emerging therapeutics [93].…”
Section: Link To the Inflammatory Trianglementioning
confidence: 99%