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This single-center prospective observational study aims to evaluate differences in metabolomic pathways between patients with ischemic and non-ischemic cardiomyopathy with reduced left ventricular ejection fraction and documented ventricular tachycardia. Patients followed at Istanbul University-Cerrahpasa Cardiology Institute Hospital will be included if they meet predefined eligibility criteria. Participants will be categorized into two cohorts according to the etiology of cardiomyopathy: ischemic and non-ischemic. Biospecimens will be collected for metabolomic analyses to identify alterations in metabolic pathways and individual metabolites. The study also aims to explore associations between metabolomic profiles and clinical characteristics, including arrhythmia burden and cardiac function parameters. The findings may provide insights into the underlying pathophysiological mechanisms of ventricular arrhythmias in heart failure and contribute to improved risk stratification and personalized management strategies.
Heart failure with reduced ejection fraction (HFrEF) is associated with significant metabolic remodeling, reflecting alterations in energy substrate utilization, mitochondrial function, and systemic metabolic pathways. Ventricular tachycardia (VT) remains a major cause of morbidity and mortality in this population. Despite advances in clinical management, the underlying metabolic mechanisms contributing to arrhythmogenesis in ischemic and non-ischemic cardiomyopathy are not fully elucidated.
Metabolomics has emerged as a powerful tool to characterize global metabolic changes and identify disease-specific biochemical signatures. However, comparative metabolomic data between ischemic and non-ischemic cardiomyopathy patients with documented ventricular tachycardia remain limited.
This prospective, single-center observational study aims to compare metabolomic pathways in patients with ischemic and non-ischemic cardiomyopathy with left ventricular ejection fraction below 40% and documented ventricular tachycardia detected by Holter monitoring or implantable cardiac devices. Patients will be recruited from Istanbul University-Cerrahpasa Cardiology Institute Hospital and categorized into two cohorts based on the etiology of cardiomyopathy.
Biological samples will be collected and analyzed using metabolomic approaches to identify differences in metabolic pathways and individual metabolite profiles between the two groups. The primary objective is to determine pathway-level alterations associated with ischemic versus non-ischemic cardiomyopathy in the presence of ventricular tachycardia. Secondary analyses will include evaluation of individual metabolites and their associations with clinical variables such as arrhythmia burden, left ventricular function, and relevant laboratory parameters.
This study is expected to provide novel insights into the metabolic basis of ventricular arrhythmias in heart failure and may contribute to improved risk stratification and the development of personalized therapeutic strategies.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ischemic cardiomyopathy | Patients with ischemic cardiomyopathy, left ventricular ejection fraction below 40%, and documented ventricular tachycardia. | ||
| Non-ischemic cardiomyopathy | Patients with non-ischemic cardiomyopathy, left ventricular ejection fraction below 40%, and documented ventricular tachycardia. |
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| Measure | Description | Time Frame |
|---|---|---|
| Differences in metabolomic pathways between ischemic and non-ischemic cardiomyopathy | Comparison of metabolomic pathway profiles derived from biospecimen analyses between patients with ischemic and non-ischemic cardiomyopathy with reduced ejection fraction and documented ventricular tachycardia. | Baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Differences in individual metabolite levels between groups | Quantitative comparison of individual metabolite concentrations between ischemic and non-ischemic cardiomyopathy patients using metabolomic analysis techniques. | Baseline |
| Association between metabolomic profiles and clinical parameters |
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Inclusion Criteria:
Age ≥18 years Diagnosis of ischemic or non-ischemic cardiomyopathy Left ventricular ejection fraction <40% Documented ventricular tachycardia detected by Holter monitoring, implantable cardioverter-defibrillator (ICD), pacemaker, or other implantable rhythm monitoring devices Availability of metabolomic sample collection Ability and willingness to provide informed consent
Exclusion Criteria:
History of cardiotoxic chemotherapy or radiotherapy Cirrhosis or advanced hepatic failure Active malignancy Acute decompensated heart failure at presentation Active infection or acute inflammatory disease End-stage renal disease requiring dialysis Absence of Holter monitoring or implantable rhythm monitoring data No documented ventricular tachycardia despite rhythm monitoring Inability to provide informed consent
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Adult patients (≥18 years) with ischemic or non-ischemic cardiomyopathy and reduced left ventricular ejection fraction (<40%) who have documented ventricular tachycardia and are followed at Istanbul University-Cerrahpasa Cardiology Institute Hospital.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Istanbul University-Cerrahpasa Cardiology Institute | Istanbul | 34098 | Turkey (Türkiye) |
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Peripheral blood samples will be collected from all participants and processed to obtain serum and plasma for metabolomic analyses. Samples will be stored under appropriate conditions and used to evaluate metabolic pathways and individual metabolite profiles.
Evaluation of correlations between metabolomic findings and clinical variables including left ventricular ejection fraction, arrhythmia burden, and relevant laboratory parameters. |
| Baseline |
| ID | Term |
|---|---|
| D017180 | Tachycardia, Ventricular |
| D001145 | Arrhythmias, Cardiac |
| D006333 | Heart Failure |
| ID | Term |
|---|---|
| D013610 | Tachycardia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D000075224 | Cardiac Conduction System Disease |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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