Journal Article FZJ-2025-05023

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Integrating ECG-derived features with conventional CVD risk models

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2025
Springer Nature [London]

Scientific reports 15(1), 39128 () [10.1038/s41598-025-26471-6]

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Abstract: Non-communicable diseases (NCDs), particularly cardiovascular diseases (CVDs), have becomethe leading cause of mortality worldwide, with Iran exhibiting higher-than-average incidence andmortality rates. Early detection of high-risk individuals is critical, as CVD often progresses silently.Electrocardiogram (ECG) signals may enhance risk prediction beyond Framingham risk score (FRS).This study aimed to evaluate the predictive performance of ECG signal features for incident CVD usingsignal processing in a large population-based cohort from the Tehran Lipid and Glucose Study (TLGS). Atotal of 4,637 adults aged 40 years devoid of past CVD at baseline (2006–2008) were followed up until2018. Baseline characteristics, laboratory measurements, and ECG signal features were collected. CVDevents were defined as coronary heart disease (CHD) or stroke. A recalibrated FRS (baseline) modelassessed the association between ECG features and incident CVD, with model performance evaluatedusing Harrell’s C-index, Net Reclassification Index (NRI), and Integrated Discrimination Improvement(IDI). Over a 10-year follow-up, 483 participants (10.4%) developed CVD. The introduction of ECGsignal features improved risk prediction in women, increasing the Harrell’s C-index from 0.84 to 0.85and demonstrating significant reclassification improvement (NRI: 55.7%, IDI: 2.8%). However, nomeaningful improvement was observed in men. ECG-based modeling outperformed FRS, particularlyfor intermediate-risk categories among women. Incorporating ECG signal features into risk modelssignificantly enhanced CVD prediction performance in women, suggesting potential utility forimproving individualized preventive strategies. Further research is warranted to refine ECG-based riskstratification tools for broader clinical application.

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Contributing Institute(s):
  1. Molekular- und Zellphysiologie (IBI-1)
Research Program(s):
  1. 5243 - Information Processing in Distributed Systems (POF4-524) (POF4-524)
  2. GRK 2610 - GRK 2610: Innovative Schnittstellen zur Retina für optimiertes künstliches Sehen - InnoRetVision (424556709) (424556709)

Appears in the scientific report 2025
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 Record created 2025-12-08, last modified 2026-02-03


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