Cardiac Remodeling and Diastolic Dysfunction in Paroxysmal Atrial Fibrillation.

atrial fibrillation diastolic dysfunction echocardiography heart failure left atrial remodeling

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
30 Aug 2021
Historique:
received: 05 08 2021
revised: 18 08 2021
accepted: 25 08 2021
entrez: 10 9 2021
pubmed: 11 9 2021
medline: 11 9 2021
Statut: epublish

Résumé

Atrial fibrillation (AF) leads to the development of cardiac remodeling/diastolic dysfunction and vice versa. We intended to determine whether cardiac remodeling/diastolic dysfunction is present at early stages of AF. We studied 175 patients with paroxysmal AF, compared with 175 matched control subjects, who had available echocardiography data to investigate the association between echocardiographic variables and AF from the STANISLAS cohort. In this study (mean age 55 years; 70.3% male), patients with paroxysmal AF had greater left ventricular mass compared to matched controls ( Left ventricular mass and left atrial enlargement rather than diastolic dysfunction (as evaluated by echocardiography) were associated with paroxysmal AF irrespective of body mass index, blood pressure and renal function. These findings suggest that cardiac remodeling may occur very early in the natural history of AF.

Sections du résumé

BACKGROUND BACKGROUND
Atrial fibrillation (AF) leads to the development of cardiac remodeling/diastolic dysfunction and vice versa. We intended to determine whether cardiac remodeling/diastolic dysfunction is present at early stages of AF.
METHODS METHODS
We studied 175 patients with paroxysmal AF, compared with 175 matched control subjects, who had available echocardiography data to investigate the association between echocardiographic variables and AF from the STANISLAS cohort.
RESULTS RESULTS
In this study (mean age 55 years; 70.3% male), patients with paroxysmal AF had greater left ventricular mass compared to matched controls (
CONCLUSIONS CONCLUSIONS
Left ventricular mass and left atrial enlargement rather than diastolic dysfunction (as evaluated by echocardiography) were associated with paroxysmal AF irrespective of body mass index, blood pressure and renal function. These findings suggest that cardiac remodeling may occur very early in the natural history of AF.

Identifiants

pubmed: 34501342
pii: jcm10173894
doi: 10.3390/jcm10173894
pmc: PMC8432208
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Int J Cardiol. 2018 May 1;258:262-268
pubmed: 29452989
Eur Heart J Cardiovasc Imaging. 2020 Oct 20;21(11):1237-1245
pubmed: 32577743
PLoS One. 2015 Apr 08;10(4):e0122336
pubmed: 25853818
J Am Coll Cardiol. 2017 Jun 27;69(25):3119-3121
pubmed: 28641802
Curr Med Chem. 2019;26(5):780-802
pubmed: 28925871
Circ Cardiovasc Imaging. 2017 Jan;10(1):
pubmed: 28073806
Europace. 2021 Aug 11;:
pubmed: 34379753
Circulation. 2016 Feb 2;133(5):484-92
pubmed: 26746177
Eur Heart J Cardiovasc Imaging. 2014 Jun;15(6):680-90
pubmed: 24451180
Int J Mol Sci. 2015 Jan 30;16(2):3133-47
pubmed: 25647414
Sci Rep. 2018 Apr 23;8(1):6366
pubmed: 29686287

Auteurs

Nathalie Noirclerc (N)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Olivier Huttin (O)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Christian de Chillou (C)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Christine Selton-Suty (C)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Laura Fillipetti (L)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Jean Marc Sellal (JM)

Department of Cardiology, University Hospital of Nancy, 54000 Nancy, France.

Erwan Bozec (E)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

Erwan Donal (E)

Département de Cardiologie & CIC-IT U 804, Centre Hospitalier Universitaire de Rennes, 35033 Rennes, France.

Zohra Lamiral (Z)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

Masatake Kobayashi (M)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

João Pedro Ferreira (JP)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

Patrick Rossignol (P)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

Nicolas Girerd (N)

Université de Lorraine, Inserm, Centre d'Investigations Cliniques-1433 and Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT, 54000 Nancy, France.

Classifications MeSH