Key result
Serum metabolite network shifts, notably creatinine and mannose, are linked to 2-year post-MI mortality.
Why the study?
Metabolic determinants associated with mortality in AMI patients and the molecular mechanisms underlying different clinical risk scores for death prediction remain incompletely understood.
Observational (n=825)
Yes
We present here the differential analysis of metabolite-metabolite association networks constructed from an array of 24 serum metabolites identified and quantified via nuclear magnetic resonance spectroscopy in a cohort of 825 patients of which 123 died within 2 years from acute myocardial infarction (AMI). We investigated differences in metabolite connectivity of patients who survived, at 2 years, the AMI event, and we characterized metabolite-metabolite association networks specific to high and low risks of death according to four different risk parameters, namely, acute coronary syndrome classification, Killip, Global Registry of Acute Coronary Events risk score, and metabolomics NOESY RF risk score. We show significant differences in the connectivity patterns of several low-molecular-weight molecules, implying variations in the regulation of several metabolic pathways regarding branched-chain amino acids, alanine, creatinine, mannose, ketone bodies, and energetic metabolism. Our results demonstrate that the characterization of metabolite-metabolite association networks is a promising and powerful tool to investigate AMI patients according to their outcomes at a molecular level.
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Vignoli et al. (2020) conducted an observational in Acute Myocardial Infarction (n=825). Serum metabolite-metabolite association networks (NMR metabolomics) vs. Survivors vs Deceased at 2 years was evaluated on Metabolite differential connectivity associated with 2-year mortality. Differential connectivity of serum metabolites, notably creatinine and mannose, was significantly associated with 2-year mortality risk in patients following acute myocardial infarction.
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