Metabolomic Approach in STEMI-Patients Undergoing Left Ventricular Remodeling
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Published on: July 14, 2021
Gabriel Garcia1,2,3, Juan Manuel Chao de la Barca1,2,4, Delphine Mirebeau-Prunier1,2,4
1Institut Mitovasc, University of Angers, University Hospital of Angers, 49000 Angers, France.
Insights
A metabolomic approach did not identify new biomarkers for left ventricular remodeling (LVR) after ST-segment elevation myocardial infarction (STEMI). However, infarct size and inflammatory markers effectively distinguished patients with and without LVR.
Area of Science:
- Cardiology
- Metabolomics
- Biomarker Discovery
Background:
- Left ventricular remodeling (LVR) is a frequent and severe complication following ST-segment elevation myocardial infarction (STEMI).
- Identifying reliable biomarkers for post-STEMI LVR is crucial for risk stratification and therapeutic interventions.
Purpose of the Study:
- To investigate the potential of a metabolomic approach in discovering novel biomarkers associated with LVR after STEMI.
- To compare metabolomic profiles between patients with and without LVR post-STEMI.
Main Methods:
- A cohort of 192 STEMI patients with successful revascularization was analyzed.
- Patients were categorized into LVR (n=32) and no-LVR (n=32) groups based on cardiac magnetic resonance imaging over 12 months.
- Blood samples were analyzed using a metabolomic approach, alongside measurements of creatine kinase, inflammatory markers, leukocyte, and neutrophil counts.
Main Results:
- Patients with LVR exhibited significantly higher peak creatine kinase levels, C-reactive protein, leukocyte, and neutrophil counts compared to the no-LVR group.
- While sphingomyelin C20:2 and symmetrical dimethylarginine were elevated in the LVR group, they did not reach statistical significance after correction.
- The metabolomic analysis did not significantly discriminate between patients with and without LVR.
Conclusions:
- The metabolomic approach, in this study, did not identify novel discriminating biomarkers for post-STEMI LVR.
- Traditional markers of infarction severity, including infarct size and inflammatory markers, remain significant indicators differentiating LVR development.
Abstract:
Left ventricular remodeling (LVR) occurring after ST-segment elevation myocardial infarction (STEMI) is frequent and severe. We present a metabolomic approach as an attempt to reveal unknown biomarkers associated with post-STEMI LVR. Out of 192 consecutive patients with successfully revascularized STEMI, 32 presented LVR and were clinically matched with 32 no-LVR patients. They underwent cardiac magnetic resonance at baseline, three months and 12 months. Blood samples were collected during index hospitalization. Creatine kinase (CK) peak and inflammatory markers were higher for LVR patients compared to no-LVR patients (mean 3466 ± 2211 and 2394 ± 1615 UI/L respectively, p = 0.005 for CK peak; mean 35.9 ± 44.3 vs. 21.7 ± 30.4 mg/L respectively, p = 0.020 for C-reactive protein). Leukocyte and neutrophil counts were also higher for LVR patients (mean 12028 ± 2593/mL vs. 10346 ± 3626/mL respectively, p = 0.028 and mean 9035 ± 3036/mL vs. 7596 ± 3822/mL respectively, p < 0.001). For metabolomic analysis, sphingomyelin C20:2 and symmetrical dimethylarginine were higher for LVR patients, but did not reach significance after the correction for the alpha risk. The metabolomic approach did not discriminate patients with and without LVR. However, common parameters that focus on infarction severity, such as infarct size and inflammatory markers, differed between the groups.
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