Mansouri Fatemeh, Seyed Mohammadzad Mir Hosein
Department of Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran.
Asian Pac J Cancer Prev. 2020 Apr 1;21(4):975-982. doi: 10.31557/APJCP.2020.21.4.975.
Due to the increasing annual incidence rate of disability and mortality in patients with acute myocardial infarction (AMI), the need for an appropriate diagnostic tool has become a crucial urgent issue. An increase in biomarkers and protein levels in response to AMI can be used as a predictive biomarker with different sensitivities and specificities. This study aimed at investigating the role of miR-19a as a biomarker with acceptable sensitivity and specificity for early diagnosis of AMI.
We studied 175 patients with AMI admitted within 12 h of symptom onset and 90 healthy subjects as control group. Patients were divided into two groups, including group I (normal vessels and no significant artery stenosis) and primary percutaneous coronary intervention (PCI) group II (patients with more than 50% stenosis in vessels and severe atherosclerosis) diagnosed by angiography. The expression level of miR-19a was evaluated by the real-time polymerase chain reaction and other serum chemistries were also analyzed.
The results demonstrated that circulating miR-19a levels were significantly increased in patient groups compared to the control group (2.88 ± 1.06 vs. 5.93 ± 1.28, P<0.0001). We also found that miR-19a levels were higher in group II (134.62-fold) than group I (15.42-fold). The upper levels of miR-19a were significantly correlated with the increased serum levels of CK-MB (ρ=0.29, P<0.0001), CTn I (ρ=0.4, P<0.0001) and creatinine (ρ=0.27, P<0.0001). In addition, Receiver Operating Characteristic (ROC) analysis revealed that circulating miR-19a had considerable diagnostic accuracy for the patients with normal vessel with an AUC of 0.930 (95% CI: 0.697-0.765) and for PCI patients with an AUC of 0.966 (95% CI: 0.748-0.784).
Circulating miR-19a possibly has prognostic value to be used as a promising molecular target for early diagnosis and prognosis of AMI.
由于急性心肌梗死(AMI)患者的残疾和死亡率年发生率不断上升,因此需要一种合适的诊断工具已成为一个至关重要的紧迫问题。AMI发生后生物标志物和蛋白质水平的升高可作为具有不同敏感性和特异性的预测生物标志物。本研究旨在探讨miR-19a作为一种生物标志物在AMI早期诊断中具有可接受的敏感性和特异性方面的作用。
我们研究了175例症状发作后12小时内入院的AMI患者,并将90名健康受试者作为对照组。患者分为两组,包括通过血管造影诊断的I组(血管正常且无明显动脉狭窄)和II组原发性经皮冠状动脉介入治疗(PCI)组(血管狭窄超过50%且患有严重动脉粥样硬化的患者)。通过实时聚合酶链反应评估miR-19a的表达水平,并分析其他血清化学指标。
结果表明,与对照组相比,患者组循环miR-19a水平显著升高(2.88±1.06对5.93±1.28,P<0.0001)。我们还发现,II组的miR-19a水平(134.62倍)高于I组(15.42倍)。miR-19a的升高水平与血清CK-MB水平升高(ρ=0.29,P<0.0001)、CTn I水平升高(ρ=0.4,P<0.0001)和肌酐水平升高(ρ=0.27,P<0.0001)显著相关。此外,受试者工作特征(ROC)分析显示,循环miR-19a对血管正常的患者具有相当高的诊断准确性,AUC为0.930(95%CI:0.697-0.765),对PCI患者的AUC为0.966(95%CI:0.748-0.784)。
循环miR-19a可能具有预后价值,有望作为AMI早期诊断和预后的分子靶点。