Abstrakti
Chronic heart failure (CHF) is a condition affecting millions worldwide, characterized by the heart’s reduced ability to pump blood efficiently. Conventional diagnostics, such as imaging and ECG assessments, can be time-consuming and expensive, often identifying CHF only after significant progression. Early detection is crucial for improving treatment options and reducing healthcare costs.Heart rate variability (HRV), which measures the variation in time intervals between heartbeats, is emerging as a non-invasive and cost-effective biomarker for CHF detection. HRV reflects the autonomic nervous system’s regulatory functions, often impaired in CHF patients. This study aims to assess advanced HRV measures for earlier CHF detection.The research involved examining CHF patients (N = 934, Age 65 ± 12) compared to healthy controls (N = 274, Age 43 ± 17). Data was sourced from Physionet and the Telemetric and Holter ECG Warehouse, with RR interval (RRI) data extracted from 24-h Holter recordings. The study utilized dynamical detrended fluctuation analysis (DDFA), which considers changes in RRI correlations over time and scale, resulting in scaling exponent (Formula presented). This was further aggregated into scale and heart rate (HR)-dependent forms, (Formula presented), classified using XGBoost ensemble method with 10-fold nested cross-validation.The classifier achieved 97% sensitivity and 90% specificity for distinguishing between CHF and control groups. Sensitivity and specificity remained consistent across subgroup analyses based on beta blocker medication and NYHA class. This method demonstrated high classification accuracy, suggesting potential utility for early CHF detection, independent of CHF severity.
| Alkuperäiskieli | Englanti |
|---|---|
| Artikkeli | 154242 |
| Julkaisu | Journal of Electrocardiology |
| Vuosikerta | 97 |
| DOI - pysyväislinkit | |
| Tila | E-pub ahead of print - 24 maalisk. 2026 |
| OKM-julkaisutyyppi | A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä |
Rahoitus
The authors acknowledge KAUTE foundation, Finland (Grant No. 20240420 ), the Finnish Foundation for Cardiovascular Research, Finland (grant No. 240052 ) and Finnish Doctoral Program Network in Artificial Intelligence (AI-DOC). We are also grateful to Matti Molkkari for supplying us with the computer program used to calculate DDFA and Marjaana Nurmo for her assistance with Fig. 2 .
Julkaisufoorumi-taso
- Jufo-taso 1
!!ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
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