Prognostic and functional implications of left atrial late gadolinium enhancement cardiovascular magnetic resonance.


Journal

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
ISSN: 1532-429X
Titre abrégé: J Cardiovasc Magn Reson
Pays: England
ID NLM: 9815616

Informations de publication

Date de publication:
03 01 2019
Historique:
received: 07 06 2018
accepted: 04 12 2018
entrez: 4 1 2019
pubmed: 4 1 2019
medline: 20 12 2019
Statut: epublish

Résumé

Left atrial (LA) late gadolinium enhancement (LGE) on cardiovascular magnetic resonance (CMR) imaging is indicative of fibrosis, and has been correlated with reduced LA function, increased LA volume, and poor procedural outcomes in cohorts with atrial fibrillation (AF). However, the role of LGE as a prognostic biomarker for arrhythmia in cardiac disease has not been examined. In this study, we assessed LA LGE using a 3D LGE CMR sequence to examine its relationships with new onset atrial arrhythmia, and LA and left ventricular (LV) mechanical function. LA LGE images were acquired in 111 patients undergoing CMR imaging, including 66 patients with no prior history of an atrial arrhythmia. During the median follow-up of 2.7 years (interquartile range (IQR) 1.8-3.7 years), 15/66 (23%) of patients developed a new atrial arrhythmia. LA LGE ≥10% of LA myocardial volume was significantly associated with an increased rate of new-onset atrial arrhythmia, with a hazard ratio of 3.16 (95% CI 1.14-8.72), p = 0.026. There were significant relationships between LA LGE and both LA ejection fraction (r = - 0.39, p < 0.0005) and echocardiographic LV septal e' (r = - 0.24, p = 0.04) and septal E/e' (r = 0.31, p = 0.007). Elevated LA LGE is associated with reduced LA function and reduced LV diastolic function. LA LGE is associated with new onset atrial arrhythmia during follow-up.

Sections du résumé

BACKGROUND
Left atrial (LA) late gadolinium enhancement (LGE) on cardiovascular magnetic resonance (CMR) imaging is indicative of fibrosis, and has been correlated with reduced LA function, increased LA volume, and poor procedural outcomes in cohorts with atrial fibrillation (AF). However, the role of LGE as a prognostic biomarker for arrhythmia in cardiac disease has not been examined.
METHODS
In this study, we assessed LA LGE using a 3D LGE CMR sequence to examine its relationships with new onset atrial arrhythmia, and LA and left ventricular (LV) mechanical function.
RESULTS
LA LGE images were acquired in 111 patients undergoing CMR imaging, including 66 patients with no prior history of an atrial arrhythmia. During the median follow-up of 2.7 years (interquartile range (IQR) 1.8-3.7 years), 15/66 (23%) of patients developed a new atrial arrhythmia. LA LGE ≥10% of LA myocardial volume was significantly associated with an increased rate of new-onset atrial arrhythmia, with a hazard ratio of 3.16 (95% CI 1.14-8.72), p = 0.026. There were significant relationships between LA LGE and both LA ejection fraction (r = - 0.39, p < 0.0005) and echocardiographic LV septal e' (r = - 0.24, p = 0.04) and septal E/e' (r = 0.31, p = 0.007).
CONCLUSIONS
Elevated LA LGE is associated with reduced LA function and reduced LV diastolic function. LA LGE is associated with new onset atrial arrhythmia during follow-up.

Identifiants

pubmed: 30602395
doi: 10.1186/s12968-018-0514-3
pii: 10.1186/s12968-018-0514-3
pmc: PMC6317232
doi:

Substances chimiques

Contrast Media 0
Organometallic Compounds 0
gadobutrol 1BJ477IO2L

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2

Subventions

Organisme : British Heart Foundation
ID : FS/16/28/32327
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL122560
Pays : United States

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Auteurs

Michael Quail (M)

Department of Internal Medicine (Cardiology), Yale School of Medicine, 300 Cedar St, New Haven, CT, 06520, USA.
Centre for Cardiovascular Imaging, Institute of Cardiovascular Science, University College London, London, UK.

Karl Grunseich (K)

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Lauren A Baldassarre (LA)

Department of Internal Medicine (Cardiology), Yale School of Medicine, 300 Cedar St, New Haven, CT, 06520, USA.
Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Hamid Mojibian (H)

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Mark A Marieb (MA)

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Daniel Cornfeld (D)

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Aaron Soufer (A)

Department of Internal Medicine (Cardiology), Yale School of Medicine, 300 Cedar St, New Haven, CT, 06520, USA.

Albert J Sinusas (AJ)

Department of Internal Medicine (Cardiology), Yale School of Medicine, 300 Cedar St, New Haven, CT, 06520, USA.
Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.

Dana C Peters (DC)

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA. Dana.peters@yale.edu.

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