Abstract

Coronary collateral circulation (CCC), an alternative blood supply for ischemic myocardium, improves survival rates among patients with coronary artery disease (CAD). However, there remains a lack of biomarkers to discriminate between patients with poor or good CCC. In this study, we aimed to observe the relationship between plasma microRNA-146a (miR-146a) levels and the coronary collateral circulation (CCC). Additionally, we aimed to explore whether the plasma miR-146a level could serve as a blood-based biomarker for CCC in patients with CAD. We measured the plasma levels of vascular endothelial growth factor A (VEGF-A) and miR-146a in patients with CCC by ELISA and real-time PCR, respectively, according to the Rentrop grades. The results showed that the plasma miR-146a level is significantly increased in CAD patients with good CCC and significantly decreased in those with poor CCC. In contrast, although VEGFA expression in patients followed a similar trend as the CCC, the differences between the groups were not statistically significant. There was a positive correlation between plasma miR-146a levels and the Rentrop grading. In addition, receiver operator characteristic analysis showed that miR-146a could be a potent biomarker for identifying patients with poor CCC.

Highlights

  • Coronary collateral circulation (CCC), an alternative blood supply for ischemic myocardium, improves survival rates among patients with coronary artery disease (CAD) [1]

  • Relative to the control group, the level of plasma miR-146a was higher in patients with good CCC (1.67-fold, P < 0.05), whereas it was lower in patients with poor CCC 0.17-fold, (P < 0.01)

  • We found that levels of plasma miR-146a were significantly lower in the poor CCC group and significantly higher in the good CCC group, as compared with that in the control group

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Summary

Introduction

Coronary collateral circulation (CCC), an alternative blood supply for ischemic myocardium, improves survival rates among patients with coronary artery disease (CAD) [1]. There are many established determinants of coronary angiogenesis, including chronic inflammation and vascular endothelial growth factor (VEGF) [4], there remains a lack of biomarkers to discriminate between patients with poor or good CCC. It has been reported that there is a close relationship between angiogenesis and several miRNAs: miR21, miR-146a, miR-155, miR-221, and miR-222 [7]. All of these have been shown to exert antiangiogenic effects, apart from miR-146a [7]. Angiogenesis plays an important role in CCC formation [8], the correlation between miR-146a and the CCC has not been substantially investigated

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