Why the study?
Understanding mechanisms driving high-risk vulnerable plaque formation and progression to myocardial infarction is a key priority, motivating investigation into associations between circulating lipid metabolites and imaging-defined vulnerable plaque features.
Are specific circulating lipid metabolites associated with imaging-defined features of vulnerable coronary plaque in patients with myocardial infarction?
Population
877 patients with myocardial infarction following revascularization
Comparison
Levels of 424 plasma lipid metabolites vs imaging-defined coronary plaque measures
Design
Substudy with external cohort validation
Key result
Circulating sphingomyelins were negatively associated, and 1-palmitoyl-2-oleoyl-GPE positively associated, with vulnerable coronary plaque features in patients with myocardial infarction (q<0.05).
Authors
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These metabolite-plaque associations require prospective validation; extends metabolomics to vulnerable features post-MI.
Observational (n=877)
Yes
Are specific circulating lipid metabolites associated with imaging-defined features of vulnerable coronary plaque in patients with myocardial infarction?
p-value: p=q<0.05
Specific circulating lipid metabolites, notably sphingomyelins (inversely) and 1-palmitoyl-2-oleoyl-GPE (positively), are associated with vulnerable coronary plaque features, providing potential novel targets for diagnostics and therapeutics.
Sharma et al. (2026) conducted an observational in Myocardial infarction (n=877). Circulating lipid metabolites was evaluated on Pan-coronary lipid, pan-coronary plaque burden, and high-risk vulnerable plaque measures (p=q<0.05). Circulating sphingomyelins were negatively associated, and 1-palmitoyl-2-oleoyl-GPE positively associated, with vulnerable coronary plaque features in patients with myocardial infarction (q<0.05).
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