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Tissue-specific miRNA Expression Profiling in Mouse Heart Sections Using In Situ Hybridization
Published on: September 15, 2018
Determination of microRNAs associated with adverse left ventricular remodeling after myocardial infarction
Ferhat Eyyupkoca1, Karabekir Ercan2, Emrullah Kiziltunc3
1Department of Cardiology, Dr. Nafiz Korez Sincan State Hospital, Fatih District, Gazi Mustafa Kemal Boulevard, 06930, Ankara, Turkey. eyupkocaferhat@gmail.com.
Abstract:
Increasing evidence indicates that microRNA (miRNA) regulated mechanisms in myocardial healing and ventricular remodeling following acute myocardial infarction (AMI). We aim to comprehensively investigate changes of exosomal miRNA profile during the post-MI period and determine potential miRNAs associated to adverse left ventricular remodeling (ALVR). We prospectively evaluated ST-elevated MI patients with cardiac magnetic resonance imaging at the 2 weeks and 6 months after AMI (n = 10). ALVR was defined as an increase in LV end-diastolic and end-systolic volume > 13%. The blood samples were taken for miRNA measurements at the baseline, 2 and 6 weeks after AMI. In the miRNA profile assessment, 8 miRNAs were identified that were associated ALVR (miR-199a-5p, miR-23b-3p, miR-26b-5p, miR-301a-3p, miR-374a-5p, miR-423-5p, miR-483-5p and miR-652-3p). Three of them (miR-301a-3p, miR-374a-5p and miR-423-5p) differed significantly between patients with and without ALVR during follow-up period and the rest of them during the acute phase of AMI. The detection of these miRNAs, which have different role in various pathways, necessitate future mechanistic studies unravel the complex remodeling process after AMI.
Insights
Changes in exosomal microRNAs (miRNAs) after acute myocardial infarction (AMI) may predict adverse left ventricular remodeling (ALVR). Specific miRNAs like miR-301a-3p, miR-374a-5p, and miR-423-5p show potential as biomarkers for ALVR post-AMI.
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Biomarker Discovery
Background:
- MicroRNA (miRNA) regulation is increasingly implicated in myocardial healing and ventricular remodeling post-acute myocardial infarction (AMI).
- Understanding exosomal miRNA profiles offers insights into the complex post-MI cardiac repair and remodeling processes.
Purpose of the Study:
- To comprehensively investigate exosomal miRNA profile changes following AMI.
- To identify specific miRNAs associated with adverse left ventricular remodeling (ALVR).
Main Methods:
- Prospective evaluation of ST-elevated MI patients (n=10) using cardiac magnetic resonance imaging at 2 weeks and 6 months post-AMI.
- ALVR defined as >13% increase in left ventricular (LV) end-diastolic and end-systolic volumes.
- Exosomal miRNA measurements from blood samples at baseline, 2 weeks, and 6 weeks post-AMI.
Main Results:
- Eight miRNAs (miR-199a-5p, miR-23b-3p, miR-26b-5p, miR-301a-3p, miR-374a-5p, miR-423-5p, miR-483-5p, miR-652-3p) were associated with ALVR.
- Three miRNAs (miR-301a-3p, miR-374a-5p, miR-423-5p) showed significant differences between ALVR and non-ALVR groups during follow-up.
- Other identified miRNAs differed during the acute phase of AMI.
Conclusions:
- Specific exosomal miRNAs are associated with adverse left ventricular remodeling following acute myocardial infarction.
- MiRNAs such as miR-301a-3p, miR-374a-5p, and miR-423-5p may serve as potential biomarkers for ALVR.
- Further mechanistic studies are needed to elucidate the role of these miRNAs in post-AMI cardiac remodeling.
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