Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy.


Journal

The international journal of cardiovascular imaging
ISSN: 1875-8312
Titre abrégé: Int J Cardiovasc Imaging
Pays: United States
ID NLM: 100969716

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 09 05 2021
accepted: 27 07 2021
pubmed: 15 12 2021
medline: 9 2 2022
entrez: 14 12 2021
Statut: ppublish

Résumé

Prognosis of Duchenne muscular dystrophy (DMD) is related to cardiac dysfunction. Two dimensional-speckle tracking echocardiography (2D-STE) has recently emerged as a non-invasive functional biomarker for early detection of DMD-related cardiomyopathy. This study aimed to determine, in DMD children, the existence of left ventricle (LV) dyssynchrony using 2D-STE analysis. This prospective controlled study enrolled 25 boys with DMD (mean age 11.0 ± 3.5 years) with normal LV ejection fraction and 50 age-matched controls. Three measures were performed to assess LV mechanical dyssynchrony: the opposing-wall delays (longitudinal and radial analyses), the modified Yu index, and the time-to-peak delays of each segment. Feasibility and reproducibility of 2D-STE dyssynchrony were evaluated. All three mechanical dyssynchrony criteria were significantly higher in the DMD group than in healthy subjects: (1) opposing-wall delays in basal inferoseptal to basal anterolateral segments (61.4 ± 45.3 ms vs. 18.3 ± 50.4 ms, P < 0.001, respectively) and in mid inferoseptal to mid anterolateral segments (58.6 ± 35.3 ms vs. 42.4 ± 36.4 ms, P < 0.05, respectively), (2) modified Yu index (33.3 ± 10.1 ms vs. 28.5 ± 8.1 ms, P < 0.05, respectively), and (3) most of time-to-peak values, especially in basal and mid anterolateral segments. Feasibility was excellent and reliability was moderate to excellent, with ICC values ranging from 0.49 to 0.97. Detection of LV mechanical dyssynchrony using 2D-STE analysis is an easily and reproducible method in paediatric DMD. The existence of an early LV mechanical dyssynchrony visualized using 2D-STE analysis in children with DMD before the onset of cardiomyopathy represents a perspective for future paediatric drug trials in the DMD-related cardiomyopathy prevention.Clinical Trial Registration Clinicaltrials.gov NCT02418338. Post-hoc study, registered on April 16, 2015.

Identifiants

pubmed: 34905152
doi: 10.1007/s10554-021-02369-y
pii: 10.1007/s10554-021-02369-y
doi:

Banques de données

ClinicalTrials.gov
['NCT02418338']

Types de publication

Controlled Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-89

Subventions

Organisme : Centre Hospitalier Régional Universitaire de Montpellier
ID : PHRC-MERRI UF 9458
Organisme : French Muscular Dystrophy Association
ID : AFM 20225

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Nature B.V.

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Auteurs

Nicolas Lanot (N)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.

Marie Vincenti (M)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.
PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Hamouda Abassi (H)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.
PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Charlene Bredy (C)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.

Audrey Agullo (A)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.

Lucie Gamon (L)

Epidemiology and Clinical Research Department, CHU Montpellier, Montpellier, France.

Thibault Mura (T)

Epidemiology and Clinical Research Department, CHU Nimes, Nimes, France.

Kathleen Lavastre (K)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.

Gregoire De La Villeon (G)

Paediatric and Adult Cardiology Department, M3C Regional Reference CHD Center, CHU Montpellier, Montpellier, France.
Paediatric Cardiology and Rehabilitation Unit, Saint-Pierre Institute, Palavas-Les-Flots, France.

Catherine Barrea (C)

Paediatric and Congenital Cardiology Department, Cliniques Universitaires Saint-Luc, UCL University, Brussels, Belgium.

Pierre Meyer (P)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.
Paediatric Neurology, National Reference Center for Neuromuscular Diseases, CHU Montpellier, Montpellier, France.

François Rivier (F)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.
Paediatric Neurology, National Reference Center for Neuromuscular Diseases, CHU Montpellier, Montpellier, France.

Albano C Meli (AC)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Jeremy Fauconnier (J)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Olivier Cazorla (O)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Alain Lacampagne (A)

PhyMedExp, University of Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

Pascal Amedro (P)

Department of Paediatric and Adult Congenital Cardiology, M3C National Reference Centre, Bordeaux University Hospital, Haut Lévêque Hospital, Avenue de Magellan, 33604, Pessac Cedex, France. pascal.amedro@chu-bordeaux.fr.
University of Bordeaux, INSERM, Bordeaux Cardio-Thoracic Research Centre, U1045, Pessac, France. pascal.amedro@chu-bordeaux.fr.
IHU Liryc, Electrophysiology and Heart Modelling Institute, Fondation Bordeaux Université, Pessac, France. pascal.amedro@chu-bordeaux.fr.

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