Systematic assessment of heart valves and cardiac function by echocardiography in axial spondyloarthritis: A systematic review and meta-analysis.


Journal

Joint bone spine
ISSN: 1778-7254
Titre abrégé: Joint Bone Spine
Pays: France
ID NLM: 100938016

Informations de publication

Date de publication:
07 2022
Historique:
received: 22 12 2021
revised: 17 02 2022
accepted: 22 02 2022
pubmed: 9 3 2022
medline: 7 7 2022
entrez: 8 3 2022
Statut: ppublish

Résumé

Axial Spondyloarthritis (ax-SpA) is associated with increased risk of cardiovascular disease (CVD)-specific deaths. We aimed to assess the prevalence of left ventricular (LV) systolic and diastolic dysfunction and valvular heart disease (VHD) by transthoracic echocardiography (TTE) in ax-SpA patients without history of CVD. A systematic literature review was performed in PUBMED, Embase, Cochrane Library databases published before April 2020. We included all controlled studies assessing myocardial function and heart valve by TTE in ax-SpA without history of CVD. A meta-analysis was performed with random or fixed effects model estimating mean differences (MD) and odds ratio (OR). Literature search selected 189 abstracts and 28 articles were included (1471 ax-SpA and 1115 controls). ax-SpA had a statistically slight alteration of LV ejection fraction (MD=0.64%, 95%CI: 0.14-1.14). ax-SpA had more frequently LV diastolic dysfunction (OR=3.43, 95%CI: 1.78-6.59) and an alteration of E/A ratio (MD=0.15, 95%CI: 0.08-0.21), deceleration time (MD=13.07ms, 95%CI: 7.75-18.40), isovolumetric relaxation time (MD=7.90ms, 95%CI: 4.50-11.30), left-ventricular end diastolic (MD=0.57mm, 95%CI: 0.19-0.95) and systolic (MD=0.77mm, 95%CI: 0.36-1.17) diameters. Three studies (15%) used a combination of TTE parameters to diagnose LV diastolic dysfunction. Prevalence of mitral regurgitation and aortic regurgitation were similar in ax-SpA patients and healthy individuals. ax-SpA have a non-clinically relevant alteration of LV ejection fraction and similar prevalence of VHD compared to healthy individuals. LV diastolic TTE parameters are altered in ax-SpA. However, most studies do not combine set of parameters to recognize diastolic dysfunction. The clinical relevance of diastolic dysfunction observed by TTE remains to be determined in future longitudinal studies.

Identifiants

pubmed: 35259478
pii: S1297-319X(22)00034-3
doi: 10.1016/j.jbspin.2022.105375
pii:
doi:

Types de publication

Journal Article Meta-Analysis Systematic Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105375

Informations de copyright

Copyright © 2022 Société française de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Xavier Romand (X)

University Grenoble Alpes, T-RAIG, TIMC-IMAG, CNRS UMR 5525, Grenoble, France; Department of Rheumatology, Grenoble Alpes University Hospital, 38130 Échirolles, Grenoble, France. Electronic address: xromand@chu-grenoble.fr.

Fanny Adeline (F)

Department of Rheumatology, Grenoble Alpes University Hospital, 38130 Échirolles, Grenoble, France.

Mickael Dalecky (M)

University Grenoble Alpes, T-RAIG, TIMC-IMAG, CNRS UMR 5525, Grenoble, France; Department of Rheumatology, Grenoble Alpes University Hospital, 38130 Échirolles, Grenoble, France.

Arnaud Pflimlin (A)

Department of Rheumatology, Lille University Hospital, Lille, France.

Alexandre Bellier (A)

Quality of Care Unit, Grenoble Alpes University Hospital, Grenoble, France.

Gilles Barone-Rochette (G)

University Grenoble Alpes, INSERM, U1039, RadiopharmaceutiquesBiocliniques, Grenoble, France; Department of Cardiology, Grenoble Alpes University Hospital, Grenoble, France; French Alliance Clinical Trial, French Clinical Research Infrastructure Network, Toulouse, France.

Daniel Wendling (D)

Department of Rheumatology, CHRU Besançon and Université Bourgogne Franche-Comté (EA 4266), Besançon, France.

Philippe Gaudin (P)

University Grenoble Alpes, T-RAIG, TIMC-IMAG, CNRS UMR 5525, Grenoble, France; Department of Rheumatology, Grenoble Alpes University Hospital, 38130 Échirolles, Grenoble, France.

Pascal Claudepierre (P)

Department of Rheumatology, University Paris Est Créteil, Henri Mondor Hospital, Creteil, France.

Maxime Dougados (M)

Université de Paris, Department of Rheumatology - Hôpital Cochin, Assistance Publique - Hôpitaux de Paris INSERM (U1153): Clinical epidemiology and biostatistics, PRES Sorbonne Paris-Cité, Paris, France.

Athan Baillet (A)

University Grenoble Alpes, T-RAIG, TIMC-IMAG, CNRS UMR 5525, Grenoble, France; Department of Rheumatology, Grenoble Alpes University Hospital, 38130 Échirolles, Grenoble, France.

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