Department of Cardiology, Charles University, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic.
Faculty of Science, Charles University, Prague, Czech Republic.
Sci Rep. 2020 Apr 3;10(1):5845. doi: 10.1038/s41598-020-62835-w.
We sought to analyse plasma levels of peripheral blood microRNAs (miRs) as biomarkers of ST-segment-elevation myocardial infarction (STEMI) due to type-1 myocardial infarction as a model situation of vulnerable plaque (VP) rupture. Samples of 20 patients with STEMI were compared both with a group of patients without angina pectoris in whom coronary angiogram did not reveal coronary atherosclerotic disease (no coronary atherosclerosis-NCA) and a group of patients with stable angina pectoris and at least one significant coronary artery stenosis (stable coronary artery disease-SCAD). This study design allowed us to identify miRs deregulated in the setting of acute coronary artery occlusion due to VP rupture. Based on an initial large scale miR assay screening, we selected a total of 12 miRs (three study miRs and nine controls) that were tested in the study. Two of the study miRs (miR-331 and miR-151-3p) significantly distinguished STEMI patients from the control groups, while ROC analysis confirmed their suitability as biomarkers. Importantly, this was observed in patients presenting early with STEMI, even before the markers of myocardial necrosis (cardiac troponin I, miR-208 and miR-499) were elevated, which suggests that the origin of miR-331 and miR-151-3p might be in the VP. In conclusion, the study provides two novel biomarkers observed in STEMI, which may be associated with plaque rupture.
我们试图分析外周血 microRNAs (miRs) 的血浆水平,作为 1 型心肌梗死(不稳定斑块破裂的模型情况)所致 ST 段抬高型心肌梗死 (STEMI) 的生物标志物。将 20 例 STEMI 患者的样本与无胸痛的患者组(冠状动脉造影未发现冠状动脉粥样硬化性疾病,无冠状动脉粥样硬化性疾病-NCA)和稳定型心绞痛且至少有一处显著冠状动脉狭窄的患者组(稳定型冠状动脉疾病-SCAD)进行比较。这种研究设计使我们能够识别因 VP 破裂导致的急性冠状动脉闭塞时失调的 miR。基于初始的大规模 miR 检测筛选,我们选择了总共 12 个 miR(三个研究 miR 和九个对照)在研究中进行测试。两个研究 miR(miR-331 和 miR-151-3p)可显著区分 STEMI 患者与对照组,而 ROC 分析证实它们适合作为生物标志物。重要的是,这在 STEMI 患者早期表现出来,甚至在心肌坏死标志物(肌钙蛋白 I、miR-208 和 miR-499)升高之前就观察到了,这表明 miR-331 和 miR-151-3p 的来源可能是在 VP 中。总之,该研究提供了在 STEMI 中观察到的两个新的生物标志物,它们可能与斑块破裂有关。