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Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
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Profiling heart failure with preserved or mildly reduced ejection fraction by cluster analysis
Lourdes Vicent1,2,3, Nicolás Rosillo1,2,4, Jorge Vélez2
1Cardiology Department, Hospital Universitario 12 de Octubre, Madrid 28041, Spain.
European Heart Journal. Quality of Care & Clinical Outcomes
|August 9, 2024
Summary
Researchers identified three heart failure (HF) subtypes in patients with preserved or mildly reduced ejection fraction (HFp/mrEF). These HF phenotypes show significant differences in clinical profiles and mortality risk, particularly for women.
Area of Science:
- Cardiology
- Biostatistics
- Internal Medicine
Background:
- Heart failure (HF) patient heterogeneity, especially in preserved or mildly reduced ejection fraction (HFp/mrEF) groups, remains poorly understood.
- Existing knowledge gaps hinder tailored treatment strategies for diverse HF populations.
Purpose of the Study:
- To identify distinct heart failure (HF) subtypes within the HFp/mrEF population.
- To analyze the clinical characteristics and prognostic implications of identified HF phenotypes.
Main Methods:
- Utilized the k-prototypes clustering algorithm on a cohort of 2570 HFp/mrEF patients.
- Applied k-means for quantitative and k-modes for qualitative variables to identify HF phenotypes.
Main Results:
- Identified three distinct HF phenotypes: Cluster A (low comorbidity women), Cluster B (diabetic women with high comorbidity), and Cluster C (men with respiratory comorbidities).
- Observed significant variations in 1-year mortality rates (18% A, 33% B, 26.4% C) and time to death across clusters.
- Found that age, cancer, respiratory failure, and lab parameters predicted mortality.
Conclusions:
- Cluster analysis revealed three unique HFp/mrEF phenotypes with differing clinical profiles and prognoses.
- Women presented two distinct phenotypes: low-risk and high-mortality diabetic groups.
- Men exhibited a more uniform phenotype characterized by a higher prevalence of respiratory disease.
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