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Updated: Jun 10, 2025

Identification and Quantification of Deranged Metabolites in Critically Ill Patients Using NMR-Based Metabolomics
Published on: November 29, 2024
Targeted metabolomic profiling of acute ST-segment elevation myocardial infarction.
Sergey S Markin1, E A Ponomarenko2, Yu A Romashova2
1Institute of Biomedical Chemistry, Moscow, 119121, Russia. phospholipovit@ibmc.msk.ru.
This study reveals altered metabolite levels in ST-segment elevation myocardial infarction (STEMI) patients, identifying key metabolic pathways and ratios for improved diagnosis and understanding of heart attack pathogenesis.
Area of Science:
- Cardiovascular Medicine
- Metabolomics
- Biochemistry
Background:
- Myocardial infarction (MI) is a leading global cause of death.
- Metabolomics offers potential insights into the complex pathogenesis of ST-segment elevation myocardial infarction (STEMI).
Purpose of the Study:
- To conduct targeted metabolomic profiling in STEMI patients.
- To identify significantly altered metabolites and metabolite ratios associated with STEMI pathogenesis.
- To explore the role of tryptophan metabolism in STEMI.
Main Methods:
- Targeted metabolomic profiling of 87 endogenous metabolites in plasma.
- Analysis of 195 subjects: 68 STEMI patients, 84 stable angina pectoris (SAP) patients, and 43 non-cardiovascular disease (non-CVD) controls.
- Machine learning and weighted correlation network analysis were employed.
Main Results:
- Identified 36 significantly altered metabolites in STEMI patients, including amino acids, acylcarnitines, and NO-urea cycle metabolites.
- Observed significant changes in tryptophan metabolism, with increased anthranilic acid and tryptophol, and decreased xanthurenic acid and 3-OH-kynurenine.
- Discovered 22 significantly altered metabolite ratios, with seven common between STEMI vs. non-CVD and STEMI vs. SAP comparisons.
Conclusions:
- Targeted metabolomic profiling provides novel insights into STEMI pathogenesis.
- Specific metabolite ratios, such as anthranilic acid to aspartic acid and GSG, may serve as diagnostic biomarkers.
- Understanding metabolic alterations in STEMI can inform future diagnostic and therapeutic strategies.
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