Evidence map›Paper›PMID 42162353›Full record

ArticleNPJ cardiovascular health2026

Optimizing single-lead ECG axis for AI-based detection of myocardial diseases.

Masamitsu Nakayama, Ryuichiro Yagi, Kyohei Daigo, Yoshinori Katsumata, Rahul C Deo, Calum A MacRae, Shinichi Goto

Abstract read
In one paragraph

Article in NPJ cardiovascular health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Masamitsu NakayamaDivision of Cardiovascular Medicine, Department of Medicine, Mass General Brigham, Boston, MA, USA.
Ryuichiro YagiDivision of Cardiovascular Medicine, Department of Medicine, Mass General Brigham, Boston, MA, USA.
Kyohei DaigoDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Yoshinori KatsumataInstitute for Integrated Sports Medicine, Keio University School of Medicine, Tokyo, Japan.
Rahul C DeoDivision of Cardiovascular Medicine, Department of Medicine, Mass General Brigham, Boston, MA, USA.
Calum A MacRaeDivision of Cardiovascular Medicine, Department of Medicine, Mass General Brigham, Boston, MA, USA.
Shinichi GotoDivision of Cardiovascular Medicine, Department of Medicine, Mass General Brigham, Boston, MA, USA. sgoto2.sci@gmail.com.

Funding

American Heart Association AHA's Second Century Early Faculty Independence AwardAmerican Heart Association One Brave Idea AwardAmerican Heart Association postdoctoral fellowship
6 · The paper itself

Abstract

Wearable devices enable electrocardiograms (ECGs) outside traditional healthcare settings. While these devices are usually equipped with single-lead ECGs to monitor rhythm abnormalities, recent studies show utility in detecting myocardial diseases when combined with artificial intelligence (AI). However, the optimal single-lead axis for detecting myocardial diseases beyond rhythm abnormality remains unclear. To address this knowledge gap, we trained models to detect 3 myocardial diseases: left ventricular systolic dysfunction (LVSD), hypertrophic cardiomyopathy (HCM), and cardiac amyloidosis (CA) using single-lead ECGs, systematically synthesized at 10-degree intervals, leveraging the limb leads from 12-lead ECG data. For all 3 diseases, the highest discriminations were observed near the aVR axis and its inverse. The optimal angles were 20° for LVSD (AUROC 0.884 [95% CI: 0.877-0.891]) and HCM (0.911 [0.900-0.922]), and 210° for CA (0.893 [0.888-0.899]). These findings may inform the development of wearable ECG devices with utility beyond rhythm abnormality detection.

Identifiers

PMID42162353
PMCPMC13241514

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.