Li Hai-Yu, Zhao Xin, Liu Yu-Zhou, Meng Zhe, Wang Dan, Yang Fan, Shi Qiang-Wei
Department of Cardiology, The first Affiliated Hospital, Zhengzhou University, Zhengzhou, China.
Cell Physiol Biochem. 2016;39(3):837-46. doi: 10.1159/000447794. Epub 2016 Aug 9.
Coronary artery disease (CAD) is a major problem worldwide. As an endothelium-enriched microRNA (miRNA), miR-126 has been reported to serve as a potential biomarker of acute myocardial infarction. However, the relationship between miR-126 and the severity of CAD remains unknown. This study was designed to test whether circulating miR-126 levels are associated with the severity of CAD.
The present study enrolled 40 patients who had risk factors for CAD without angiographically significant CAD, and 110 patients presenting with stable angina pectoris, who were validated left main coronary artery disease (LMCA) and/or multi-vessel disease by coronary angiography. The expression levels of plasma miR-126-5p from all enrolled subjects were estimated by quantitative real-time polymerase chain reaction (qRT-PCR). Then, the relationships between plasma miR-126-5p levels, number of diseased vessels and the corresponding Synergy between PCI with Taxus and Cardiac surgery (SYNTAX) score were analyzed.
The expression of circulating miR-126-5p was affected by some CAD risk factors including aging, dyslipidemia and DM. Furthermore, plasma miR-126-5p levels were significantly down-regulated in CAD patients with multi-vessel disease, higher SYNTAX score, rather than isolated LMCA and low SYNTAX score.
Circulating miR-126-5p has emerged as a potential biomarker for complexity and severity of CAD in patients with stable angina pectoris.
冠状动脉疾病(CAD)是全球范围内的一个主要问题。作为一种在内皮细胞中高度富集的微小RNA(miRNA),miR-126已被报道可作为急性心肌梗死的潜在生物标志物。然而,miR-126与CAD严重程度之间的关系仍不清楚。本研究旨在检测循环miR-126水平是否与CAD的严重程度相关。
本研究纳入了40例有CAD危险因素但血管造影显示无显著CAD的患者,以及110例表现为稳定型心绞痛的患者,这些患者经冠状动脉造影证实患有左主干冠状动脉疾病(LMCA)和/或多支血管病变。通过定量实时聚合酶链反应(qRT-PCR)估计所有纳入受试者血浆miR-126-5p的表达水平。然后,分析血浆miR-126-5p水平、病变血管数量与相应的紫杉醇药物洗脱支架与心脏外科手术协同作用(SYNTAX)评分之间的关系。
循环miR-126-5p的表达受到一些CAD危险因素的影响,包括衰老、血脂异常和糖尿病。此外,在患有多支血管病变、SYNTAX评分较高的CAD患者中,血浆miR-126-5p水平显著下调,而在孤立性LMCA和SYNTAX评分较低的患者中则不然。
循环miR-126-5p已成为稳定型心绞痛患者CAD复杂性和严重程度的潜在生物标志物。