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Updated: Jul 25, 2025

Oxygenation-sensitive Cardiac MRI with Vasoactive Breathing Maneuvers for the Non-invasive Assessment of Coronary Microvascular Dysfunction
Published on: August 17, 2022
Trans-myocardial omega-3 fatty acid gradient in coronary microvascular dysfunction
Ellen C Keeley1, Eileen M Handberg1, C Noel Bairey Merz2
1Department of Medicine, Division of Cardiovascular Medicine, University of Florida, Gainesville, FL, United States of America.
18-hydroxyeicosapentaenoic acid (HEPE), an omega-3 fatty acid metabolite, is lower in heart venous plasma than aortic plasma. This suggests HEPE is synthesized outside the heart and used within the heart muscle.
Area of Science:
- Cardiovascular Science
- Metabolomics
- Omega-3 Fatty Acids
Background:
- Cardiac remodeling involves 18-hydroxyeicosapentaenoic acid (HEPE), a metabolite of eicosapentaenoic acid (EPA).
- Heart failure with preserved ejection fraction (HFpEF) pathophysiology may be informed by trans-myocardial 18-HEPE levels.
Purpose of the Study:
- To investigate the trans-myocardial concentrations of 18-HEPE and EPA.
- To explore the relationship between 18-HEPE and EPA levels in the myocardial bed.
Main Methods:
- Trans-myocardial plasma samples were collected from 10 subjects in the WISE Mechanisms of Coronary Microvascular Dysfunction Leading to Pre-HFpEF project.
- Concentrations of 18-HEPE and EPA were measured.
Main Results:
- 18-HEPE concentrations were significantly lower in coronary venous plasma compared to aortic plasma (p = 0.0039).
- Significant correlations were found between coronary venous EPA and aortic 18-HEPE (r = 0.94, p = 0.0002), and aortic EPA and aortic 18-HEPE (r = 0.82, p = 0.0058).
Conclusions:
- This pilot study suggests 18-HEPE is synthesized outside the heart.
- Evidence indicates 18-HEPE is utilized within the myocardial bed.
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