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Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.

Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.

期刊: Open heart 日期: 2026-07-16 PMID: 42463275 DOI: 10.1136/openhrt-2026-004127 浏览: 31
作者: Zhao C, Chan PJ, Dougherty S, Fan Y, Lee APW
C, Z., PJ, C., S, D., Y, F., & APW, L. (2026). Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.. Open heart. https://doi.org/10.1136/openhrt-2026-004127
C Z, PJ C, S D, Y F, APW L. Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.. Open heart. 2026; doi: 10.1136/openhrt-2026-004127
C Z, PJ C, S D, et al. Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.[J]. Open heart. 2026. DOI: 10.1136/openhrt-2026-004127.
@article{c2026,
  author = {Zhao C and Chan PJ and Dougherty S and Fan Y and Lee APW},
  title = {Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.},
  journal = {Open heart},
  year = {2026},
  doi = {10.1136/openhrt-2026-004127},
  note = {PMID: 42463275},
}
TY  - JOUR
AU  - Zhao C
AU  - Chan PJ
AU  - Dougherty S
AU  - Fan Y
AU  - Lee APW
TI  - Differentiating HFmr/rEF from HFpEF using standard 12-lead ECG measurements: an interpretable machine learning study.
T2  - Open heart
PY  - 2026
DO  - 10.1136/openhrt-2026-004127
AN  - PMID:42463275
ER  - 

摘要

BACKGROUND: Differentiating heart failure (HF) with mildly reduced/reduced ejection fraction (HFmr/rEF) from HF with preserved ejection fraction (HFpEF) guides therapy but echocardiography may be delayed or unavailable. We developed and validated machine learning models using routine 12-lead ECG data to classify HF phenotypes. METHODS: In this retrospective cohort of hospitalised patients with HF, predictors available at or before the index ECG were used. HFmrEF was pooled with HFrEF (left ventricular ejection fraction <50%) for model development. Data were split 70/30 into training and held-out test sets. Random forest (RF), Extreme Gradient Boosting and support vector machine models were trained and tuned using fivefold cross-validation in the training set. Boruta was used to select key ECG features. Test-set performance was evaluated by area under the curve (AUC) and accuracy; AUCs were compared using DeLong's test. RESULTS: Overall, 495 patients were included (254 HFmr/rEF; 241 HFpEF). RF consistently performed best. Using ECG features alone, RF achieved an AUC of 0.821 (95% CI 0.752 to 0.890) and accuracy of 75.7%. A parsimonious RF model using 12 Boruta-selected ECG variables achieved an AUC of 0.832 (95% CI 0.766 to 0.899) and accuracy of 76.4%, with no significant AUC difference versus a comprehensive RF model using clinical/laboratory/ECG predictors (AUC 0.804, 95% CI 0.734 to 0.875; p=0.288) or the model using all ECG features (p=0.092). Adding X-ray cardiomegaly did not improve performance. CONCLUSION: A parsimonious RF model based on a small set of standard ECG measurements differentiates HFmr/rEF from HFpEF with good discrimination, supporting ECG as an adjunct for phenotyping when echocardiography is not immediately available.

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