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Cardiogenic Shock Integrated PHenotyping for Event Reduction: A Pilot Metabolomics Analysis
Nuccia Morici1, Gianfranco Frigerio2,3, Jonica Campolo4
1Dipartimento Cardio-Respiratorio, IRCCS Fondazione Don Carlo Gnocchi ONLUS, 20100 Milan, Italy.
Cardiogenic shock (CS) patients show distinct metabolic changes. Survivors had reduced inflammation markers, but increased amino acids and lipids, suggesting potential therapeutic targets for heart failure with CS.
Area of Science:
- Biochemistry
- Cardiology
- Metabolomics
Background:
- Cardiogenic shock (CS) is a severe condition with high mortality.
- Hypoperfusion in CS can lead to uncontrolled inflammation and metabolic issues.
- Understanding metabolic shifts is crucial for improving outcomes in heart failure with CS (HF-CS).
Purpose of the Study:
- To investigate metabolomic profiles in patients with HF-CS.
- To analyze temporal changes in specific biomarkers (IL-6, Ang-2, glycocalyx markers) from admission to discharge.
- To identify metabolic signatures associated with survival or mortality in HF-CS.
Main Methods:
- Studied 18 consecutive HF-CS patients.
- Collected biological samples at admission (T0), 48 hours (T1), and discharge (T2).
- Utilized ELISA and targeted metabolomics for analysis.
Main Results:
- In-hospital mortality was 44% (7 out of 18 patients).
- Survivors showed significant reductions in IL-6 and kynurenine by discharge.
- Survivors exhibited significant increases in amino acids (arginine, threonine, glycine, lysine, asparagine), putrescine, sphingolipids, and glycerophospholipids.
Conclusions:
- HF-CS patients display a unique metabolomic profile.
- Metabolic fingerprints may guide personalized treatment strategies for HF-CS.
- Temporal metabolic changes in survivors indicate shifts in metabolic pathways during recovery.
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