SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

Fibrosis Entropy Is Associated With Life‐Threatening Arrhythmia in Nonischemic Cardiomyopathy

Hammersley, DJ; Zaidi, HA; Jones, RE; Hatipoglu, S; Androulakis, E; Balaban, G; Mach, L; Lota, AS; Khalique, Z; De Marvao, A; et al. Hammersley, DJ; Zaidi, HA; Jones, RE; Hatipoglu, S; Androulakis, E; Balaban, G; Mach, L; Lota, AS; Khalique, Z; De Marvao, A; Lopuszko, A; Lazzari, L; Ravendren, A; Gulati, A; Baruah, R; Guha, K; Tayal, U; Leyva, F; Baksi, AJ; Ware, JS; Lamata, P; Pennell, DJ; Halliday, BP; Bishop, MJ; Prasad, SK (2025) Fibrosis Entropy Is Associated With Life‐Threatening Arrhythmia in Nonischemic Cardiomyopathy. Journal of the American Heart Association, 14 (18). e040517. ISSN 2047-9980 https://doi.org/10.1161/jaha.124.040517
SGUL Authors: Androulakis, Emmanouil

[img] PDF Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (685kB)
[img] PDF (Data S1, Tables S1–S17, Figures S1–S4) Supporting information
Download (433kB)

Abstract

Background Greater precision is required for arrhythmic risk stratification of patients with nonischemic cardiomyopathy (NICM). We sought to evaluate whether fibrosis entropy, a measure of scar texture heterogeneity derived from late gadolinium enhancement cardiovascular magnetic resonance, has incremental utility to fibrosis presence for arrhythmic risk prediction in NICM. Methods In this prospective observational cohort study, fibrosis entropy was calculated for patients with NICM and fibrosis (late gadolinium enhancement positive, LGE+), including regions of core fibrosis, gray zone fibrosis and combined core and gray zone fibrosis. Patients with NICM and no fibrosis (LGE‐) were included as a comparator group. Adjudicated follow‐up for life‐threatening arrhythmia included sudden cardiac death, aborted sudden cardiac death, or sustained ventricular tachycardia. Results Of 291 patients with LGE+ NICM, 38 (13.1%) experienced life‐threatening arrhythmia over a median follow‐up of 6.3 years. Core fibrosis entropy (per‐SD hazard ratio [HR], 1.77 [95% CI, 1.25–2.52]; P=0.001), gray zone fibrosis entropy (HR, 1.97 [95% CI, 1.20–2.54]; P=0.004), and combined fibrosis entropy (HR, 1.98 [95% CI, 1.30–3.02]; P=0.004) were each associated with life‐threatening arrhythmia after adjustment for variables used to determine implantable cardioverter‐defibrillator candidacy in clinical practice (left ventricular ejection fraction ≤35% and New York Heart Association class >1) and remained associated after accounting for core and gray zone fibrosis mass. Left ventricular ejection fraction ≤35% was not associated with life‐threatening arrhythmia (HR, 1.45 [95% CI, 0.77–2.74]; P=0.250). Integration of fibrosis presence with fibrosis entropy classified patients into low‐, intermediate‐, and high‐arrhythmic‐risk groups. Conclusions Deeper phenotypic characterization of scar using fibrosis entropy offers incremental utility to left ventricular ejection fraction and fibrosis presence for arrhythmic risk stratification in NICM.

Item Type: Article
Additional Information: © 2025 The Author(s). Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
Keywords: arrhythmic risk stratification, entropy, fibrosis, nonischemic cardiomyopathy, Humans, Male, Female, Cardiomyopathies, Middle Aged, Fibrosis, Prospective Studies, Aged, Risk Assessment, Arrhythmias, Cardiac, Magnetic Resonance Imaging, Cine, Entropy, Myocardium, Risk Factors
SGUL Research Institute / Research Centre: Academic Structure > Cardiovascular & Genomics Research Institute
Academic Structure > Cardiovascular & Genomics Research Institute > Clinical Cardiology
Journal or Publication Title: Journal of the American Heart Association
ISSN: 2047-9980
Language: en
Media of Output: Print-Electronic
Related URLs:
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
WT088641/Z/09/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
FS/ICRF/21/26019British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
RE/18/4/34215British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
SP/17/11/32885British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
EP/R513064/1Engineering and Physical Sciences Research Councilhttps://doi.org/10.13039/501100000266
21JTASir Jules Thorn Charitable Trusthttp://dx.doi.org/10.13039/501100000282
209450/Z/17/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
DTP‐EP/R513064/1Engineering and Physical Sciences Research Councilhttp://dx.doi.org/10.13039/501100000266
PG/22/11159British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
Dates:
Date Event
2025-09-16 Published
2025-09-11 Published Online
2025-05-28 Accepted
URI: https://openaccess.sgul.ac.uk/id/eprint/118453
Publisher's version: https://doi.org/10.1161/jaha.124.040517

Actions (login required)

Edit Item Edit Item