Galeano-Otero Isabel, Del Toro Raquel, Guisado Agustín, Díaz Ignacio, Mayoral-González Isabel, Guerrero-Márquez Francisco, Gutiérrez-Carretero Encarnación, Casquero-Domínguez Sara, Díaz-de la Llera Luis, Barón-Esquivias Gonzalo, Jiménez-Navarro Manuel, Smani Tarik, Ordóñez-Fernández Antonio
Departamento de Fisiología Médica y Biofísica, Universidad de Sevilla, 41009 Sevilla, Spain.
Grupo de Fisiopatología Cardiovascular, Instituto de Biomedicina de Sevilla-IBiS, Universidad de Sevilla/HUVR/Junta de Andalucía/CSIC, Sevilla 41013, CIBERCV, 28029 Madrid, Spain.
J Clin Med. 2020 Apr 8;9(4):1051. doi: 10.3390/jcm9041051.
Restoration of epicardial coronary blood flow, achieved by early reperfusion with primary percutaneous coronary intervention (PPCI), is the guideline recommended to treat patients with ST-segment-elevation myocardial infarction (STEMI). However, despite successful blood restoration, increasing numbers of patients develop left ventricular adverse remodelling (LVAR) and heart failure. Therefore, reliable prognostic biomarkers for LVAR in STEMI are urgently needed. Our aim was to investigate the role of circulating microRNAs (miRNAs) and their association with LVAR in STEMI patients following the PPCI procedure. We analysed the expression of circulating miRNAs in blood samples of 56 patients collected at admission and after revascularization (at 3, 6, 12 and 24 h). The associations between miRNAs and left ventricular end diastolic volumes at 6 months were estimated to detect LVAR. miRNAs were also analysed in samples isolated from peripheral blood mononuclear cells (PBMCs) and human myocardium of failing hearts. Kinetic analysis of miRNAs showed a fast time-dependent increase in miR-133a, miR-133b, miR-193b, miR-499, and miR-320a in STEMI patients compared to controls. Moreover, the expression of miR-29a, miR-29b, miR-324, miR-208, miR-423, miR-522, and miR-545 was differentially expressed even before PPCI in STEMI. Furthermore, the increase in circulating miR-320a and the decrease in its expression in PBMCs were significantly associated with LVAR and correlated with the expression of miR-320a in human failing myocardium from ischaemic origin. In conclusion, we determined the time course expression of new circulating miRNAs in patients with STEMI treated with PPCI and we showed that miR-320a was positively associated with LVAR.
通过早期进行直接经皮冠状动脉介入治疗(PPCI)实现的心外膜冠状动脉血流恢复,是治疗ST段抬高型心肌梗死(STEMI)患者的指南推荐方法。然而,尽管成功恢复了血流,但越来越多的患者出现左心室不良重塑(LVAR)和心力衰竭。因此,迫切需要用于STEMI患者LVAR的可靠预后生物标志物。我们的目的是研究循环微RNA(miRNA)的作用及其与PPCI术后STEMI患者LVAR的关联。我们分析了56例患者入院时和血运重建后(3、6、12和24小时)采集的血液样本中循环miRNA的表达。估计miRNA与6个月时左心室舒张末期容积之间的关联以检测LVAR。还从外周血单核细胞(PBMC)和衰竭心脏的人心肌中分离的样本中分析了miRNA。与对照组相比,STEMI患者中miR-133a、miR-133b、miR-193b、miR-499和miR-320a的miRNA动力学分析显示其随时间快速增加。此外,即使在STEMI患者进行PPCI之前,miR-29a、miR-29b、miR-324、miR-208、miR-423、miR-522和miR-545的表达也存在差异。此外,循环miR-320a的增加及其在PBMC中表达水平的降低与LVAR显著相关,并且与缺血性来源的人衰竭心肌中miR-320a的表达相关。总之,我们确定了接受PPCI治疗的STEMI患者中新的循环miRNA的时间进程表达,并表明miR-320a与LVAR呈正相关。