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Circulating miR-320a as a Predictive Biomarker for Left Ventricular Remodelling in STEMI Patients Undergoing Primary
Isabel Galeano-Otero1,2, Raquel Del Toro1,2, Agustín Guisado3
1Departamento de Fisiología Médica y Biofísica, Universidad de Sevilla, 41009 Sevilla, Spain.
Insights
Circulating microRNAs (miRNAs) can predict adverse heart remodeling after ST-segment-elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (PPCI). Specifically, elevated miR-320a levels are linked to left ventricular adverse remodeling (LVAR) in STEMI patients.
Area of Science:
- Cardiology
- Molecular Biology
- Biomarker Discovery
Background:
- Primary percutaneous coronary intervention (PPCI) restores blood flow in ST-segment-elevation myocardial infarction (STEMI) but doesn't prevent left ventricular adverse remodeling (LVAR) and heart failure.
- Reliable prognostic biomarkers are needed to identify STEMI patients at risk for LVAR post-PPCI.
Purpose of the Study:
- To investigate the role of circulating microRNAs (miRNAs) as potential biomarkers for LVAR in STEMI patients undergoing PPCI.
- To analyze the dynamic changes in miRNA expression following PPCI and their association with LVAR.
Main Methods:
- Blood samples from 56 STEMI patients were collected at admission and at 3, 6, 12, and 24 hours post-PPCI.
- Circulating miRNA expression was analyzed, and associations with left ventricular end-diastolic volumes at 6 months were assessed to detect LVAR.
- miRNA analysis was also performed on peripheral blood mononuclear cells (PBMCs) and human failing myocardium.
Main Results:
- Kinetic analysis revealed rapid increases in miR-133a, miR-133b, miR-193b, miR-499, and miR-320a in STEMI patients compared to controls.
- Differential expression of miR-29a, miR-29b, miR-324, miR-208, miR-423, miR-522, and miR-545 was observed even before PPCI.
- Increased circulating miR-320a and decreased PBMC miR-320a expression were significantly associated with LVAR and correlated with its expression in failing myocardium.
Conclusions:
- The study identified specific circulating miRNAs with time-dependent expression patterns in STEMI patients treated with PPCI.
- Circulating miR-320a emerged as a promising biomarker, positively associated with LVAR in STEMI patients post-PPCI.
Abstract:
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.
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