Epicardial adipose tissue is associated with left atrial volume and fibrosis in patients with atrial fibrillation.

Dixon sequence atrial fibrillation cardiac magnetic resonance imaging epicardial adipose tissue fibrosis late gadolinium enhancement (LGE) MRI

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 16 09 2022
accepted: 17 10 2022
entrez: 17 11 2022
pubmed: 18 11 2022
medline: 18 11 2022
Statut: epublish

Résumé

Obesity is a risk factor for atrial fibrillation (AF) and strongly influences the response to treatment. Atrial fibrosis shows similar associations. Epicardial adipose tissue (EAT) may be a link between these associations. We sought to assess whether EAT is associated with body mass index (BMI), left atrial (LA) fibrosis and volume. LA fibrosis and EAT were assessed using late gadolinium enhancement, and Dixon MRI sequences, respectively. We derived 3D models incorporating fibrosis and EAT, then measured the distance of fibrotic and non-fibrotic areas to the nearest EAT to assess spatial colocalization. One hundred and three AF patients (64% paroxysmal, 27% female) were analyzed. LA volume index was 54.9 (41.2, 69.7) mL/m LA EAT is associated with obesity (BMI) as well as LA volume and fibrosis. Regions of LA EAT did not colocalize with fibrotic areas, suggesting a systemic or paracrine mechanism rather than EAT infiltration of fibrotic areas.

Sections du résumé

Background UNASSIGNED
Obesity is a risk factor for atrial fibrillation (AF) and strongly influences the response to treatment. Atrial fibrosis shows similar associations. Epicardial adipose tissue (EAT) may be a link between these associations. We sought to assess whether EAT is associated with body mass index (BMI), left atrial (LA) fibrosis and volume.
Methods UNASSIGNED
LA fibrosis and EAT were assessed using late gadolinium enhancement, and Dixon MRI sequences, respectively. We derived 3D models incorporating fibrosis and EAT, then measured the distance of fibrotic and non-fibrotic areas to the nearest EAT to assess spatial colocalization.
Results UNASSIGNED
One hundred and three AF patients (64% paroxysmal, 27% female) were analyzed. LA volume index was 54.9 (41.2, 69.7) mL/m
Conclusion UNASSIGNED
LA EAT is associated with obesity (BMI) as well as LA volume and fibrosis. Regions of LA EAT did not colocalize with fibrotic areas, suggesting a systemic or paracrine mechanism rather than EAT infiltration of fibrotic areas.

Identifiants

pubmed: 36386377
doi: 10.3389/fcvm.2022.1045730
pmc: PMC9664066
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1045730

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL158667
Pays : United States

Informations de copyright

Copyright © 2022 Chahine, Askari-Atapour, Kwan, Anderson, Macheret, Afroze, Bifulco, Cham, Ordovas, Boyle and Akoum.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Yaacoub Chahine (Y)

Division of Cardiology, University of Washington, Seattle, WA, United States.

Bahareh Askari-Atapour (B)

Division of Cardiology, University of Washington, Seattle, WA, United States.

Kirsten T Kwan (KT)

Department of Bioengineering, University of Washington, Seattle, WA, United States.

Carter A Anderson (CA)

Department of Bioengineering, University of Washington, Seattle, WA, United States.

Fima Macheret (F)

Division of Cardiology, University of Washington, Seattle, WA, United States.

Tanzina Afroze (T)

Division of Cardiology, University of Washington, Seattle, WA, United States.

Savannah F Bifulco (SF)

Department of Bioengineering, University of Washington, Seattle, WA, United States.

Matthew D Cham (MD)

Department of Radiology, University of Washington, Seattle, WA, United States.

Karen Ordovas (K)

Department of Radiology, University of Washington, Seattle, WA, United States.

Patrick M Boyle (PM)

Department of Bioengineering, University of Washington, Seattle, WA, United States.
Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, United States.
Center for Cardiovascular Biology, University of Washington, Seattle, WA, United States.

Nazem Akoum (N)

Division of Cardiology, University of Washington, Seattle, WA, United States.
Department of Bioengineering, University of Washington, Seattle, WA, United States.

Classifications MeSH