Key result
A high EPA/AA ratio (≥0.41) was independently associated with a higher prevalence of layered plaques (OR 5.98) and calcified plaques (OR 3.15) in patients with acute coronary syndrome caused by plaque rupture.
Why the study?
EPA stabilizes coronary plaques, but its association with healed plaques, thrombus size, and plaque rupture characteristics remained unclarified.
Does a high EPA/AA ratio associate with the development of layered and calcified plaques in patients with acute coronary syndrome caused by plaque rupture?
Cross-Sectional (n=95)
No
Does a high EPA/AA ratio associate with the development of layered and calcified plaques in patients with acute coronary syndrome caused by plaque rupture?
Odds Ratio: 5.98 (95% CI 2.04–17.51)
Absolute Event Rate: 75.9% vs 39.4%
p-value: p=<0.01
A high EPA/AA ratio is independently associated with the presence of layered and calcified plaques in patients with ACS caused by plaque rupture, suggesting a potential role of EPA in plaque stabilization and healing.
High EPA/AA ratio associated with layered/calcified plaques in ACS rupture; hypothesis-generating for stabilization, needs prospective confirmation before practice implications.
AIMS: Eicosapentaenoic acid (EPA) has shown beneficial effects on coronary plaque stabilization. Based on our previous study, we speculated that EPA might be associated with the development of healed plaques and might limit thrombus size. This study aimed to elucidate the association between EPA and arachidonic acid (AA) ratios and various plaque characteristics in patients with plaque rupture. METHODS: A total of 95 patients with acute coronary syndrome (ACS) caused by plaque rupture who did not take lipid-lowering drugs and underwent percutaneous coronary intervention using optical coherence tomography (OCT) were included. Clinical characteristics, lipid profiles, and OCT findings were compared between patients with lower and higher EPA/AA ratios (0.41) according to the levels in the Japanese general population. RESULTS: In the high EPA/AA (n=29, 30.5%) and low EPA/AA (n=66, 69.5 %) groups, the high EPA/AA group was significantly older (76.1 vs. 66.1 years, P<0.01) and had lower peak creatine kinase (556 vs. 1651 U/L, P=0.03) than those with low EPA/AA. Similarly, patients with high EPA/AA had higher prevalence of layered and calcified plaque (75.9 vs. 39.4 %, P<0.01; 79.3 vs. 50.0 %, P<0.01, respectively) than low EPA/AA group. Multivariate logistic regression analysis demonstrated that a high EPA/AA ratio was an independent factor in determining the development of layered and calcified plaques. CONCLUSION: A high EPA/AA ratio may be associated with the development of layered and calcified plaques in patients with plaque rupture.
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Sekimoto et al. (2023) conducted a cross-sectional in Acute coronary syndrome caused by plaque rupture (n=95). High EPA/AA ratio (≥0.41) vs. Low EPA/AA ratio (<0.41) was evaluated on Development of layered plaques (OR 5.98, 95% CI 2.04-17.51, p=<0.01). A high EPA/AA ratio (≥0.41) was independently associated with a higher prevalence of layered plaques (OR 5.98) and calcified plaques (OR 3.15) in patients with acute coronary syndrome caused by plaque rupture.
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