Last updated:
Author(s):
Mehak Gurnani, Konstantinos Patlatzoglou, Joseph Barker, Libor Pastika, Boroumand Zeidaabadi, Ibrahim Antoun, Riyaz Somani, G. Andre Ng, Paolo Inglese, Lara Curran, Declan O'Regan, Nicholas S. Peters, Daniel B. Kramer, Jonathan W. Waks, Arunashis Sau, Fu Siong Ng
Publish date:
4 December 2025
Journal:
npj Digital Medicine
PubMed ID:
41345458

Abstract

Atrial fibrillation (AF) is classically categorised by arrhythmia duration, but these subtypes have limitations in capturing mechanistic and prognostic diversity. A variational autoencoder, trained on >1.1M ECGs, extracted representative features, filtered for an AF cohort of 20,291 unique patients. These features were input into an unsupervised tree-based clustering method to map AF heterogeneity as a tree structure and identify phenogroups. Five phenogroups stratified by future disease risk were identified: (1) higher-risk AF; (2) highest-risk AF with heart failure (HF); (3) average paroxysmal AF; (4) lower-risk paroxysmal AF; and (5) higher-risk paroxysmal AF. The tree trajectory positioned individuals based on shared traits, emphasising explainability. Paroxysmal phenogroups 4 and 5 differed in risk and ventricular structure, with phenogroup 5 exhibiting more adverse features. Mixed AF phenogroup 2 reflected advanced AF with greater HF burden and mortality risk. This AI-ECG framework augments AF subtypes with a risk-based dimension, supporting personalised care.

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Our research has two aims. Firstly, to study the electrical activity of the heart in individuals that have a higher risk of heart rhythm disturbance,…

Institution:
Imperial College London, Great Britain

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