Elevated FURIN levels in predicting mortality and cardiovascular events in patients with acute myocardial infarction

毛皮 狼牙棒 医学 心肌梗塞 内科学 人口 心脏病学 前蛋白转化酶 经皮冠状动脉介入治疗 生物 脂蛋白 生物化学 低密度脂蛋白受体 环境卫生 胆固醇
作者
Yun Kai Wang,Jia Tang,Lu Han,Xian Dong Liu,Yun Li Shen,Chunyu Zhang,Xue Bo Liu
出处
期刊:Metabolism-clinical and Experimental [Elsevier BV]
卷期号:111: 154323-154323 被引量:18
标识
DOI:10.1016/j.metabol.2020.154323
摘要

Objectives Proprotein convertase subtilisin/kexin (PCSK) family member 3 (FURIN) has been suggested to be involved in the development of atherosclerosis. The aim of this study was to investigate the prognostic implication of FURIN in patients after acute myocardial infarction (AMI). Methods This prospective study analyzed data from a total of 1312 consecutive patients hospitalized with ST-segment elevation myocardial infarction (STEMI) and non-ST-segment elevation myocardial infarction from August 2013 to June 2016. FURIN levels were analyzed in plasma obtained from AMI patients. Results The study included 1312 AMI patients. The patient population was predominantly male (63%) with a median age of 66 years (IQR: 19 years), and 59% were STEMI patients. During a follow-up of 2 years, 117 patients died, and 377 patients reached the combined endpoints of major adverse cardiac events (MACE). Patients with elevated FURIN levels had increased risk of MACE, all-cause mortality, recurrent MI and hospitalization for HF (log-rank test, p < 0.0001). After adjusting for clinical risk factors and established markers, the association of FURIN concentrations with the risk of MACE and its individual components and cardiovascular death was statistically significant in the higher tertile of FURIN concentrations. After the addition of FURIN to the models, FURIN showed additive prognostic significance for 2-year clinical outcomes. Variable importance plots of the models showed that FURIN was of high importance to predict both occurrence of MACE and all-cause mortality. Conclusions We found that FURIN was associated with all-cause mortality and recurrent cardiovascular events in AMI patients independent of conventional risk factors and established markers.
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