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Updated: Apr 22, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
The association between circulating microRNA levels and coronary endothelial function
R Jay Widmer1, Woo-Young Chung1, Joerg Herrmann1
1Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic and College of Medicine, Rochester, Minnesota, United States of America.
Abstract:
Human microRNAs (miRs) have been implicated in human diseases presumably through the downregulation and silencing of targeted genes via post-translational modifications. However, their role in the early stage of coronary atherosclerosis is not known. The aim of this study was to test the hypothesis that patients with early atherosclerosis and coronary endothelial dysfunction (CED) have alterations in transcoronary miR gradients. Patients underwent coronary angiography and endothelial function testing in the cardiac catheterization laboratory. Patients were divided into abnormal (n = 26) and normal (n = 22) microvascular coronary endothelial function based on intracoronary response to infused acetylcholine measured as a percent change in coronary blood flow (CBF) and arterial diameter. Blood samples were obtained simultaneously from the aorta and coronary sinus at the time of catheterization for RNA isolation, and miR subsequently assessed. Baseline characteristics were similar in both groups. Patients with microvascular CED displayed transcoronary gradients significantly elevated in miR-92a and miR-133 normalized to C-elegans-39 miR. Percent change in CBF and the transcoronary gradient of miR-133 displayed a significant inverse correlation (r2 = 0.11, p = 0.03). Thus, we present novel data whereupon selected miRs demonstrate elevated transcoronary gradients in patients with microvascular CED. The current findings support further studies on the mechanistic role of miRs in coronary atherosclerosis and in humans.
Insights
Patients with early coronary endothelial dysfunction show elevated transcoronary gradients of specific microRNAs (miRs), suggesting their involvement in early atherosclerosis. Further research is needed to understand the mechanistic role of these miRs.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Genetics
Background:
- Human microRNAs (miRs) regulate gene expression and are linked to various diseases.
- The role of miRs in the early stages of coronary atherosclerosis and coronary endothelial dysfunction (CED) remains largely unknown.
- Investigating transcoronary miR gradients may offer insights into early cardiovascular disease mechanisms.
Purpose of the Study:
- To determine if patients with early atherosclerosis and CED exhibit altered transcoronary microRNA gradients.
- To test the hypothesis that microvascular CED is associated with specific changes in circulating miRs across the coronary vasculature.
Main Methods:
- Coronary angiography and endothelial function testing were performed on patients.
- Patients were categorized into groups with normal and abnormal microvascular endothelial function based on acetylcholine infusion response.
- Blood samples were collected simultaneously from the aorta and coronary sinus for microRNA analysis.
Main Results:
- Patients with microvascular CED showed significantly elevated transcoronary gradients for miR-92a and miR-133.
- A significant inverse correlation was observed between the percent change in coronary blood flow (CBF) and the transcoronary gradient of miR-133.
- No significant differences in baseline characteristics were noted between the groups.
Conclusions:
- Selected microRNAs, specifically miR-92a and miR-133, demonstrate elevated transcoronary gradients in patients with microvascular coronary endothelial dysfunction.
- These findings highlight a potential role for specific miRs in the early pathogenesis of coronary atherosclerosis.
- Further investigation into the mechanistic involvement of miRs in human coronary atherosclerosis is warranted.
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