# Evaluation of artificial intelligence-based electrocardiogram analysis tools in patients with hypertrophic cardiomyopathy

**Authors:** Gamze Babur Guler, Arda Guler, Ozgur Surgit, Irem Turkmen, Sezgin Atmaca, Hasan Sahin, Dilara Pay, Muayad Almasri, Gizemnur Coskun, Utku Yartasi, Dogukan Salduz, Busra Kuru Gorgulu, Sinem Aydin, Nail Guven Serbest, Aysel Turkvatan Cansever, Ibrahim Halil Tanboga

PMC · DOI: 10.1093/ehjdh/ztag026 · 2026-02-26

## TL;DR

AI tools for analyzing ECGs show limited accuracy in patients with hypertrophic cardiomyopathy, suggesting the need for disease-specific validation.

## Contribution

This study evaluates AI ECG tools specifically in patients with hypertrophic cardiomyopathy, revealing their limited performance in this population.

## Key findings

- AI-calculated HCM probabilities were uniformly distributed, with only 41.2% above 50% and 12.5% above 75%.
- HCM probabilities were higher in patients with abnormal ECGs and correlated with disease severity markers.
- SHD probabilities were generally higher, with 51.2% above 50% and 25% above 75%.

## Abstract

Artificial intelligence (AI)-based electrocardiogram (ECG) analysis tools have shown promise in detecting various cardiac conditions. However, their performance in specific patient populations, such as those with hypertrophic cardiomyopathy (HCM), remains incompletely characterized. To evaluate the performance of three AI-based ECG analysis tools in patients with confirmed HCM: (1) a tool calculating HCM probability, (2) a tool calculating structural heart disease (SHD) probability, and (3) a tool providing ECG-based diagnoses across multiple categories.

We analysed digitized 12-lead ECGs from patients with confirmed HCM (n = 681) using three AI tools. We assessed the distribution of AI-calculated probabilities and their associations with clinical parameters and evaluated agreement between AI-based and manually assigned ECG diagnoses using Cohen’s kappa. Despite all patients having confirmed HCM, the AI-calculated HCM probabilities showed a relatively uniform distribution [median 38.8% (IQR: 12.8–63.4%)], with only 41.2% and 12.5% of patients receiving a probability score >50% and >75%. HCM probabilities were significantly higher in patients with abnormal vs. normal ECGs (P < 0.001) and correlated with markers of disease severity. SHD probabilities were generally higher [median 51.4% (IQR: 28.7–74.5%)], with 51.2% and 25% of patients receiving scores >50% and >75%.

AI-based ECG analysis tools demonstrated modest performance in our HCM cohort. These findings highlight the challenges of applying AI tools developed in general populations to specific disease cohorts and underscore the need for disease-specific validation before clinical implementation.

Graphical Abstract

## Linked entities

- **Diseases:** hypertrophic cardiomyopathy (MONDO:0005045)

## Full-text entities

- **Genes:** MYBPC3 (myosin binding protein C3) [NCBI Gene 4607] {aka CMD1MM, CMH4, FHC, LVNC10, MYBP-C, cMyBP-C}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, MYH7 (myosin heavy chain 7) [NCBI Gene 4625] {aka CMD1S, CMH1, CMYO7A, CMYO7B, CMYP7A, CMYP7B}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, MYL3 (myosin light chain 3) [NCBI Gene 4634] {aka CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl}
- **Diseases:** Sinus bradycardia (MESH:D012804), hypertension (MESH:D006973), left ventricular hypertrophy (MESH:D017379), hypertrophy (MESH:D006984), diabetes (MESH:D003920), Right bundle branch block (MESH:D002037), Atrial fibrillation (MESH:D001281), SCD (MESH:C536778), heart abnormalities (MESH:D006330), AV block (MESH:D054537), ST segment depression (MESH:D000072657), heart failure (MESH:D006333), depression (MESH:D003866), tachycardia (MESH:D013610), cardiac structural abnormalities (MESH:C566527), AI (MESH:C538142), coronary artery disease (MESH:D003324), stroke (MESH:D020521), SHD (MESH:D006331), sudden cardiac death (MESH:D016757), hypertropic cardiomyopathy (MESH:D009202), HCM (MESH:D002312), rhythm (MESH:D021081), fibrillation (MESH:D014693), cardiac abnormalities (MESH:D018376), bradycardia (MESH:D001919), MR (MESH:D008944)
- **Chemicals:** alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940111/full.md

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Source: https://tomesphere.com/paper/PMC12940111