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循环单核细胞上尿激酶型纤溶酶原激活物受体表达增加与冠状动脉疾病患者的临床不稳定及长期不良心脏事件相关。

Increased Urokinase-Type Plasminogen Activator Receptor Expression on Circulating Monocytes Is Correlated with Clinical Instability and Long-Term Adverse Cardiac Events in Patients with Coronary Artery Disease.

作者信息

Zhang Yan, Chen Wei, Chen Lian-Feng, Wang Xuan, Hsu Jeffrey, Fang Li-Gang, Fang Quan

机构信息

Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, PR China.

出版信息

Cardiology. 2016;135(2):98-107. doi: 10.1159/000446392. Epub 2016 Jun 15.

Abstract

OBJECTIVES

This study sought to investigate the clinical correlates and prognostic roles of urokinase-type plasminogen activator receptor (uPAR) on circulating monocytes in patients with coronary artery disease (CAD).

METHODS

263 angina patients were included in this study. The percentage of uPAR expressing monocytes (PUEM) and the mean fluorescence intensity (MFI) index of uPAR were measured using flow cytometry. Patient follow-up was on average 604 days. Major adverse cardiac events (MACE) were defined as a composite of cardiac death, reinfarction, acute heart failure and hospitalization for revascularization.

RESULTS

The PUEM and MFI index levels were significantly more elevated in acute coronary syndrome patients than in stable ones. uPAR expressions on circulating monocytes at admission were correlated to inflammatory biomarkers and myocardial necrosis. Logistic regression analysis revealed that PUEM ≥15% (OR 21.96, 95% CI 7.31-65.98, p < 0.001) and uPAR MFI index ≥3.00 (OR 3.54, 95% CI 1.18-10.59, p = 0.024) were independent determinants of clinical instability in patients with CAD. When followed up, a high PUEM level at admission was an independent prognostic parameter for long-term MACE (HR 3.99, 95% CI 1.31-12.11, p = 0.015).

CONCLUSIONS

uPAR expression on circulating monocytes is associated with clinical instability and myocardial necrosis and independently predicts the risk of MACE in patients with CAD.

摘要

目的

本研究旨在探讨冠心病(CAD)患者循环单核细胞上尿激酶型纤溶酶原激活物受体(uPAR)的临床相关性及预后作用。

方法

本研究纳入了263例心绞痛患者。采用流式细胞术检测表达uPAR的单核细胞百分比(PUEM)和uPAR的平均荧光强度(MFI)指数。患者平均随访604天。主要不良心脏事件(MACE)定义为心源性死亡、再梗死、急性心力衰竭和血运重建住院的综合情况。

结果

急性冠状动脉综合征患者的PUEM和MFI指数水平显著高于稳定型患者。入院时循环单核细胞上的uPAR表达与炎症生物标志物和心肌坏死相关。逻辑回归分析显示,PUEM≥15%(OR 21.96,95%CI 7.31 - 65.98,p < 0.001)和uPAR MFI指数≥3.00(OR 3.54,95%CI 1.18 - 10.59,p = 0.024)是CAD患者临床不稳定的独立决定因素。随访时,入院时高PUEM水平是长期MACE的独立预后参数(HR 3.99,95%CI 1.31 - 12.11,p = 0.015)。

结论

循环单核细胞上的uPAR表达与临床不稳定和心肌坏死相关,并独立预测CAD患者发生MACE的风险。

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