Why the study?
Inadequate resolution of acute post-MI inflammation may contribute to adverse remodeling and heart failure, prompting investigation into whether circulating fatty acid metabolites measured early after MI correlate with post-infarction LVEF.
Are circulating fatty acid metabolites measured early after MI associated with post-infarction left ventricular ejection fraction?
Cross-Sectional (n=164)
Are circulating fatty acid metabolites measured early after MI associated with post-infarction left ventricular ejection fraction?
Early after MI, reduced LVEF is associated with an imbalance between pro-inflammatory and pro-resolving lipid mediators, suggesting a role for inflammation resolution in early systolic dysfunction.
Lipid mediator imbalance marks reduced LVEF early post-MI; hypothesis-generating for resolution-targeted interventions.
BACKGROUND: Acute inflammation after myocardial infarction (MI) is required for healing, but inadequate resolution may contribute to adverse remodeling and heart failure. Specialized pro-resolving mediators (SPMs) and eicosanoids derived from polyunsaturated fatty acids regulate the intensity and duration of inflammation. OBJECTIVE: To assess whether circulating fatty acid metabolites measured early after MI are associated with post-infarction left ventricular ejection fraction (LVEF). METHODS: This study included 164 patients with MI (STEMI and NSTEMI) treated with primary percutaneous coronary intervention (PCI). Blood samples were collected 24-48 h after PCI. Fatty acid metabolites were isolated by solid-phase extraction and quantified using HPLC with diode-array detection. Transthoracic echocardiography was performed before discharge; patients were categorized as low-EF (LVEF <40%, n = 31) or preserved-EF (LVEF ≥40%, n = 133). Group differences were tested using t-tests; Pearson correlations were calculated for selected metabolites. RESULTS: Low-EF patients had higher hs-troponin and white blood cell count than preserved-EF patients (p = 0.035 and p = 0.040). Concentrations of leukotriene B4 and 12(S)-HETE were higher in the low-EF group (p = 0.040 and p = 0.020), whereas resolvin E1, maresin 1, and lipoxin A4 were lower (p = 0.0001, p = 0.040, and p = 0.010). No significant differences were observed for resolvin D1, thromboxane B2, or prostaglandin E2. CONCLUSIONS: Early after MI, reduced LVEF is associated with higher pro-inflammatory lipid mediators and lower pro-resolving mediators, suggesting an imbalance between inflammatory activation and resolution in patients with early systolic dysfunction.
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Olędzki et al. (2026) conducted a cross-sectional in Myocardial infarction (n=164). Circulating fatty acid metabolites was evaluated on Post-infarction left ventricular ejection fraction (LVEF).
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