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Updated: Nov 28, 2025

Author Spotlight: Advancing the Analysis of Plasma Extracellular Vesicle Proteome for Cardiovascular Biomarker Studies
Published on: January 31, 2025
Plasma Metabolomic Profiles Differentiate Patients With Dilated Cardiomyopathy and Ischemic Cardiomyopathy
Junhan Zhao1, Shengwen Yang1,2, Ran Jing1
1State Key Laboratory of Cardiovascular Disease, Arrhythmia Center, National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Insights
Dilated cardiomyopathy (DCM) and ischemic cardiomyopathy (ICM) have distinct metabolic signatures, though both are common causes of heart failure. A panel of six metabolites may help differentiate between DCM and ICM patients.
Area of Science:
- Cardiovascular disease
- Metabolomics
- Biochemistry
Background:
- Dilated cardiomyopathy (DCM) and ischemic cardiomyopathy (ICM) are leading causes of heart failure (HF).
- Despite shared clinical features, their distinct impacts on cardiovascular metabolomics remain unclear.
- Understanding these differences is crucial for accurate diagnosis and treatment.
Purpose of the Study:
- To investigate the differential metabolomic profiles in patients with DCM and ICM compared to healthy controls.
- To identify common and distinct metabolic pathways associated with each cardiomyopathy type.
- To explore potential metabolite biomarkers for differentiating DCM from ICM.
Main Methods:
- Utilized a comprehensive metabolomics platform on plasma samples.
- Analyzed samples from 38 DCM patients, 18 ICM patients, and 20 healthy controls.
- Performed pathway analysis to identify metabolic signatures.
Main Results:
- Significant differences in metabolomic profiles were observed across all groups.
- Identified 233 dysregulated metabolites in DCM vs. controls and 204 in ICM vs. controls.
- Found 140 common dysregulated metabolites with similar fold-changes, alongside disease-specific signatures.
- A panel of 6 metabolites showed potential for differentiating DCM and ICM.
Conclusions:
- Cardiovascular metabolomics differ significantly between DCM and ICM.
- Metabolomics can reveal both shared and distinct pathways in heart failure etiologies.
- A 6-metabolite panel may serve as a novel diagnostic tool for distinguishing DCM from ICM.
Abstract:
Dilated cardiomyopathy (DCM) and ischemic cardiomyopathy (ICM) are common causes of heart failure (HF). Though they share similar clinical characteristics, their differential effects on cardiovascular metabolomics have yet to be elucidated. In this study, we applied a comprehensive metabolomics platform to plasma samples of HF patients with different etiology (38 patients with DCM and 18 patients with ICM) and 20 healthy controls. Significant differences in metabolomics profiling were shown among two cardiomyopathy groups and healthy controls. Two hundred thirty three dysregulated metabolites were identified between DCM vs. healthy controls, and 204 dysregulated metabolites between ICM patients and healthy controls. They have 140 metabolites in common, with fold-changes in the same direction in both groups. Pathway analysis found the commonalities of HF pathways as well as disease-specific metabolic signatures. In addition, we found that a combination panel of 6 metabolites including 1-pyrroline-2-carboxylate, norvaline, lysophosphatidylinositol (16:0/0:0), phosphatidylglycerol (6:0/8:0), fatty acid esters of hydroxy fatty acid (24:1), and phosphatidylcholine (18:0/18:3) may have the potential to differentiate patients with DCM and ICM.
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