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MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study

机译:一项稳定的研究表明,MiR-423在稳定和不稳定的冠状动脉疾病患者中差异表达

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摘要

Coronary artery disease (CAD) and acute myocardial infarction (AMI) are the leading causes of death worldwide. Since only a subset of CAD patients develops myocardial infarction, it is likely that unique factors predispose to AMI. Circulating microRNAs represent diagnostic powerful biomarkers for detection of heart injuries and patients’ risk stratification. Using an array-based approach, the expression of 84 circulating miRNAs was analyzed in plasma of pooled stable CAD patients (CAD; n = 5) and unstable CAD patients (AMI_T0; n = 5) enrolled within 24 hours from an AMI event. The array experiments showed 27 miRNAs differentially expressed with a two-fold up- or down-regulation (10 up- and 17 down-regulated miRNAs). Among them, miR-423-5p dis-regulation was confirmed in a larger case study (n = 99). Circulating miR-423-5p resulted to be significantly down-regulated within 24 hours from the AMI event (FC = -2, p≤0.05). Interestingly, miR-423-5p expression resulted to be increased (FC = +2; p≤0.005) in a subgroup of the same AMI patients (AMI_T1; n = 11) analyzed after 6 months from the acute event. We extended miR-423-5p expression study on PBMCs (peripheral blood mononuclear cells), confirming also in this tissue its up-regulation at 6 months post-AMI. Receiver operating characteristic analyses (ROC) were performed to detect the power of miR-423-5p to discriminate stable and unstable CAD. In plasma, miR-423-5p expression accurately distinguishes stable and unstable CAD patients (AUC = 0.7143, p≤0.005). Interestingly, the highest discriminatory value (AUC = 0.8529 p≤0.0005) was identified in blood cells, where miR-423-5p expression is able to differentiate unstable CAD patients during an acute event (AMI_T0) from those at six months post-AMI (AMI_T1). Furthermore, cellular miR-423-5p may discriminate also stable CAD patients from unstable CAD patients after six months post-AMI (AUC = 0.7355 p≤0.05). The results of this pilot-study suggest that miR-423-5p expression level both in plasma and blood cells, could represent a new promising biomarker for risk stratification of CAD patients.
机译:冠状动脉疾病(CAD)和急性心肌梗塞(AMI)是全球范围内的主要死亡原因。由于只有一部分CAD患者发展为心肌梗塞,因此独特因素很可能是AMI的诱因。循环中的microRNA代表着诊断功能强大的生物标志物,可用于检测心脏损伤和患者的风险分层。使用基于阵列的方法,分析了AMI事件发生后24小时内入组的稳定CAD患者(CAD; n = 5)和不稳定CAD患者(AMI_T0; n = 5)的血浆中84种循环miRNA的表达。阵列实验显示27种miRNA差异表达,并具有两倍的上调或下调(10种上调和17种下调的miRNA)。其中,在更大的案例研究中证实了miR-423-5p失调(n = 99)。循环发生的miR-423-5p在AMI事件发生后的24小时内被显着下调(FC = -2,p≤0.05)。有趣的是,在急性事件发生6个月后进行分析的同一AMI患者(AMI_T1; n = 11)的亚组中,miR-423-5p表达增加(FC = +2;p≤0.005)。我们扩展了对PBMC(外周血单个核细胞)的miR-423-5p表达研究,也证实了该组织在AMI后6个月的表达上调。进行接收器工作特性分析(ROC)以检测miR-423-5p区分稳定和不稳定CAD的能力。在血浆中,miR-423-5p表达可准确区分稳定和不稳定的CAD患者(AUC = 0.7143,p≤0.005)。有趣的是,在血细胞中鉴定出最高的判别值(AUC = 0.8529p≤0.0005),其中miR-423-5p表达能够将急性事件(AMI_T0)期间不稳定的CAD患者与AMI后六个月的患者区别开来( AMI_T1)。此外,AMI后六个月后,细胞miR-423-5p还可将稳定的CAD患者与不稳定的CAD患者区分开(AUC = 0.7355p≤0.05)。这项初步研究的结果表明,血浆和血细胞中miR-423-5p的表达水平可能代表了CAD患者风险分层的一种新的有前途的生物标志物。

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