Zhang Yao, Li Hai-Hong, Yang Rui, Yang Bai-Jing, Gao Zhao-Yu
a Department of Intensive Medicine , Hongqi Hospital, Mudanjiang Medical University , Mudanjiang , China.
b Department of Digestive Diseases , Hongqi Hospital, Mudanjiang Medical University , Mudanjiang , China.
Scand J Clin Lab Invest. 2017 Sep;77(5):379-384. doi: 10.1080/00365513.2017.1328740. Epub 2017 May 30.
Circulating microRNA (miR)-208a is specifically expressed in the heart muscle, which is involved in the regulation of myosin during cardiac development. Previous studies reported that cardiac-specific miR-208a level is significantly higher in plasma of coronary heart disease (CHD) patients. However, whether it correlates with severity of CHD, has never been elucidated before. The aim of this study was to explore the association between miR-208a and the presence and severity of CHD. Samples were collected from 290 CHD patients and 110 subjects with angiographic exclusion of CHD. Circulating miRNA-208a expression was detected using quantitative real-time PCR. The Gensini score was used to evaluate the severity of coronary stenotic lesions. Expression of miRNA-208a was identified on the basis of the quartiles of the Gensini score, and association between the miRNA-208a levels and CHD was analyzed. Diagnostic potential of miR-208a of CHD was performed by ROC analysis. CHD patients had higher miRNA-208a expression (1.61, 0.45-3.86 vs. 0.66, 0.11-1.42, p < .001), and the biomarker level significantly increased following an increasing the Gensini score (p < .001). Gensini score was significantly associated with miRNA-208a expression (r = 0.8525, p < .001). The optimal cut-off value of the relative level of miR-208a was with a specificity of 93.6% and a sensitivity of 75.5%. The AUC of miR-208a was 0.919 (95% CI, 0.893-0.945; p < .001). These preliminary results suggest that the expression of miR-208a may be associated with atherogenesis. The level of circulating miR-208a in predicting the severity of coronary atherosclerosis may have a relatively certain value.
循环微RNA(miR)-208a在心肌中特异性表达,其在心脏发育过程中参与肌球蛋白的调节。既往研究报道,冠心病(CHD)患者血浆中心脏特异性miR-208a水平显著升高。然而,其是否与CHD严重程度相关此前从未阐明。本研究旨在探讨miR-208a与CHD的存在及严重程度之间的关联。从290例CHD患者和110例经血管造影排除CHD的受试者中采集样本。采用定量实时PCR检测循环miRNA-208a表达。使用Gensini评分评估冠状动脉狭窄病变的严重程度。根据Gensini评分的四分位数确定miRNA-208a的表达,并分析miRNA-208a水平与CHD之间的关联。通过ROC分析评估miR-208a对CHD的诊断潜力。CHD患者miRNA-208a表达较高(1.61,0.45 - 3.86对0.66,0.11 - 1.42,p <.001),且随着Gensini评分增加,生物标志物水平显著升高(p <.001)。Gensini评分与miRNA-208a表达显著相关(r = 0.8525,p <.001)。miR-208a相对水平的最佳截断值的特异性为93.6%,敏感性为75.5%。miR-208a的AUC为0.919(95%CI,0.893 - 0.945;p <.001)。这些初步结果表明,miR-208a的表达可能与动脉粥样硬化形成有关。循环miR-208a水平在预测冠状动脉粥样硬化严重程度方面可能具有相对确定的价值。