AnyECG-Echo: Wearable Single-Lead ECG Detects Fine-Grained Structural Heart Disease Through Echo-Report Supervision
Activity counts measure attention, not model quality. Missing counts are unknown. Publication status follows the linked source; a listed venue alone does not confirm peer review.
AnyECG-Echo uses contrastive pretraining between single-lead ECGs and echocardiography reports to screen for structural heart disease, extending earlier single-health-system work toward clinical translation. The authors evaluate it in a geographically independent external cohort (n = 16,621), cover 13 fine-grained structural heart disease subtypes spanning myocardial, chamber, valvular and great-vessel pathologies, and add Shapley-based interpretability. Across validation cohorts totalling 25,222 patients it reached AUROC 0.866-0.924 for reduced left-ventricular systolic function, 0.877-0.931 for global heart enlargement and 0.836-0.906 for mitral stenosis.
- Venue: Research Square preprint (posted 2026-10-14; CC BY)
- Signals: ECG
- Form factor: other
- Venue
- Research Square preprint (posted 2026-10-14; CC BY)
- Published
- 2026
- arXiv
- Not reported
- PMID
- Not reported
- Licence
- Not reported
- Signals
- ECG
- Form factor
- Other
- Subjects
- Not reported
- Code
- Not reported
- Added
- Oct 15, 2026
Abstract
Structural heart disease (SHD) is a primary driver of heart failure and cardiovascular mortality, yet early detection remains constrained by the limited accessibility of echocardiography. While single-lead electrocardiogram (ECG) is ubiquitous through wearables, existing AI screening models often depend on 12-lead inputs, generalize poorly across institutions, or require massive, condition-specific labeled datasets. Recent work has demonstrated the feasibility of contrastive pre-training between single-lead ECGs and echocardiography reports within a single health system. Here, we present AnyECG-Echo, a framework that advance this paradigm toward clinical translation through three key developments: (1) evaluation in a geographically independent external cohort (n = 16,621); (2) diagnostic coverage of 13 fine-grained SHD subtypes spanning myocardial, chamber, valvular, and great-vessel pathologies; and (3) dual-axis mechanistic interpretability combining electrophysiology-grounded Shapley attribution with emergent correlations to quantitative measurements. Across validation cohorts totaling n = 25,222, the model demonstrated high AUROC for high-impact subtypes, including reduced left ventricular systolic functon(AUROC 0.866–0.924), global heart enlargement (0.877–0.931), and mitral stenosis (0.836–0.906). Furthermore, we successfully validated the alignment of model outputs with established medical physiological traits, thereby enhancing interpretability. Notably, we discovered that AnyECG-Echo’s outputs function as physiologically grounded digital biomarkers that accurately track objective metrics such as LVEF and myocardial wall thickness. These findings prove that wearable single-lead ECGs can effectively detect fine-grained structural heart disease, offering a practical solution for population-scale screening.
Verbatim fromthe publisher's DOI record· Publisher licence: https://creativecommons.org/licenses/by/4.0/

Key results
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Cite
@article{anyecgechowearablesingle2026,
title = {{AnyECG-Echo: Wearable Single-Lead ECG Detects Fine-Grained Structural Heart Disease Through Echo-Report Supervision}},
author = {Shenda Hong and Chenyang He and Qinghao Zhao and Shun Huang and Jun Li and Gongzheng Tang and Hao Zhang and Tong Liu and Zhengkai Xue and Jian Liu and Kangyin Chen and Cheng Ding (Research Square record)},
year = {2026},
journal = {Research Square preprint (posted 2026-10-14; CC BY)},
doi = {10.21203/rs.3.rs-11313095/v1}
}History
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