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Published on: January 28, 2020
Plasma miR-502-5p and coronary artery vasospasm: An exploratory study
Lucía Matute-Blanco1, Miguel Sánchez-Rodríguez2, Juan Casanova-Sandoval1
1Department of Cardiology, Hospital Universitari Arnau de Vilanova, Institut Català de la Salut, Lleida, Spain; Cardiac Physiology and Pathology Group, Institut de Recerca Biomèdica de Lleida Fundació Dr. Pifarré, IRBLleida, Lleida, Spain.
Insights
Plasma miR-502-5p shows potential as a biomarker for coronary artery vasospasm (CAV), a condition causing ischemia without obstructive coronary disease. Further validation is needed for this promising diagnostic marker.
Area of Science:
- Cardiology
- Molecular Biology
- Biomarker Discovery
Background:
- Coronary artery vasospasm (CAV) causes myocardial ischemia in patients lacking obstructive coronary disease.
- Current detection methods for CAV are limited by a lack of specific biomarkers.
- MicroRNAs (miRNAs) are investigated as potential circulating biomarkers for CAV.
Purpose of the Study:
- To investigate circulating microRNAs (miRNAs) as potential biomarkers for coronary artery vasospasm (CAV).
- To assess the diagnostic and prognostic value of plasma miR-502-5p in patients with suspected CAV.
Main Methods:
- Prospective, multicenter cohort study (ANFIBIO) including 70 patients undergoing coronary vasospasm testing.
- Circulating miRNA profiling using RT-qPCR.
- Statistical analysis including AUC, NRI, and IDI to evaluate miR-502-5p's clinical utility.
Main Results:
- A significant association was found between undetectable plasma levels of miR-502-5p and the presence of CAV (60% of patients).
- Plasma miR-502-5p demonstrated exploratory incremental value when added to a clinical model, improving AUC (0.74-0.81) and reclassification metrics (NRI=0.533; IDI=0.079).
- Patients with CAV showed higher use of oral nitrates.
Conclusions:
- Plasma miR-502-5p is associated with CAV in this cohort.
- miR-502-5p shows exploratory potential to enhance clinical models for CAV detection.
- Findings are hypothesis-generating and require validation in larger, independent cohorts.
Background:
Coronary artery vasospasm (CAV) is a major cause of myocardial ischemia in patients without obstructive coronary disease. Its detection remains challenging due to the lack of biomarkers. We investigated circulating microRNAs (miRNAs) as potential biomarkers for CAV.
Methods:
The ANFIBIO study is a prospective, multicenter cohort study that enrolled consecutive patients presenting with chest pain of presumed coronary origin (ClinicalTrials.gov identifier: NCT05374694). Patients were referred for invasive physiological evaluation. For this substudy, only those who underwent a coronary vasospasm test were included (n=70). Circulating miRNA profiling was performed using RT-qPCR.
Results:
The mean age of participants was 66.5 years and 40.0% were women. The prevalence of hypertension, dyslipidemia, and diabetes mellitus was 72.9%, 61.4% and 20.0%, respectively. Patients with CAV showed a higher use of oral nitrates. Notably, most individuals with undetectable plasma levels of miR-502-5p exhibited CAV (60%). Accordingly, detectability was used as the primary representation of miR-502-5p in further analyses. Adding miR-502-5p to a clinical model (age, sex, smoking status, nitrate use and transferrin concentration) was associated with a numerically higher AUC (0.74-0.81) and improved reclassification metrics (NRI=0.533; IDI=0.079).
Conclusions:
In this cohort, plasma miR-502-5p was associated with CAV and showed exploratory incremental value when added to a clinical model. These findings should be considered hypothesis-generating and require further validation in larger and independent cohorts.
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