Greyzone myocardial fibrosis and ventricular arrhythmias in patients with a left ventricular ejection fraction >35.


Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
04 01 2022
Historique:
received: 08 02 2021
pubmed: 12 8 2021
medline: 31 3 2022
entrez: 11 8 2021
Statut: ppublish

Résumé

To determine whether myocardial fibrosis and greyzone fibrosis (GZF) on cardiovascular magnetic resonance (CMR) is associated with ventricular arrhythmias in patients with coronary artery disease (CAD) and a left ventricular ejection fraction (LVEF) >35%. In this retrospective study of CAD patients, GZF mass using the 3SD method (GZF3SD) and total fibrosis mass using the 2SD method (TF2SD) on CMR were assessed in relation to the primary, combined endpoint of sudden cardiac death, ventricular tachycardia, ventricular fibrillation, or resuscitated cardiac arrest. Among 701 patients [age: 65.8 ± 12.3 years (mean ± SD)], 28 (3.99%) patients met the primary endpoint over 5.91 years (median; interquartile range 4.42-7.64). In competing risks analysis, a GZF3SD mass ≥5.0 g was strongly associated with the primary endpoint [subdistribution hazard ratio (sHR): 17.4 (95% confidence interval, CI 6.64-45.5); area under receiver operator characteristic curve (AUC): 0.85, P < 0.001]. A weaker association was observed for TF2SD mass ≥23 g [sHR 10.4 (95% CI 4.22-25.8); AUC: 0.80, P < 0.001]. The range of sHRs for GZF3SD mass (1-527) was wider than for TF2SD mass (1-37.6). In CAD patients with an LVEF >35%, GZF3SD mass was strongly associated with the arrhythmic endpoint. These findings hold promise for its use in identifying patients with CAD and an LVEF >35% at risk of arrhythmic events.

Identifiants

pubmed: 34379762
pii: 6348056
doi: 10.1093/europace/euab167
pmc: PMC8742629
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

31-39

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.

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Auteurs

Abbasin Zegard (A)

Aston Medical School, Aston University, Birmingham, UK.
Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Osita Okafor (O)

Aston Medical School, Aston University, Birmingham, UK.
Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Joseph de Bono (J)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Manish Kalla (M)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Mauro Lencioni (M)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Howard Marshall (H)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Lucy Hudsmith (L)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Tian Qiu (T)

Aston Medical School, Aston University, Birmingham, UK.

Richard Steeds (R)

Department of Cardiology, University Hospitals Birmingham, Queen Elizabeth, Birmingham, UK.

Berthold Stegemann (B)

Aston Medical School, Aston University, Birmingham, UK.

Francisco Leyva (F)

Aston Medical School, Aston University, Birmingham, UK.

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