High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.

Détails

Ressource 1Télécharger: BIB_DC240AF4B1D3.P001.pdf (482.65 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_DC240AF4B1D3
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
Périodique
Neuromuscular Disorders : NMD
Auteur⸱e⸱s
Wahbi K., Béhin A., Charron P., Dunand M., Richard P., Meune C., Vicart P., Laforêt P., Stojkovic T., Bécane H.M., Kuntzer T., Duboc D.
ISSN
1873-2364 (Electronic)
ISSN-L
0960-8966
Statut éditorial
Publié
Date de publication
2012
Peer-reviewed
Oui
Volume
22
Numéro
3
Pages
211-218
Langue
anglais
Notes
Publication types: Journal Article
Résumé
To determine incidence and type of major cardiac adverse events in patients with mutated desmin (DES) gene, we retrospectively reviewed baseline medical information, and examined the long-term outcomes of 28 DES patients (17 men, baseline mean age=37.7±14.4 years [min=9, max=71]) from 19 families. Baseline studies revealed skeletal muscle involvement in 21 patients and cardiac abnormalities in all but one patient. Over a mean follow-up of 10.4±9.4 years [min=1, max=35], cardiac death occurred in three patients, death due to cardiac comorbidities in two, one or more major cardiac adverse events in 13 patients. Among the 19 patients with mild conduction defects at baseline, eight developed high-degree conduction blocks requiring permanent pacing. Cardiac involvement was neither correlated with the type of DES mutation nor with the severity of skeletal muscle involvement. Our study underscores that in DES patients in-depth cardiac investigations are needed to prevent cardiac conduction system disease.
Pubmed
Web of science
Open Access
Oui
Création de la notice
05/05/2012 16:56
Dernière modification de la notice
20/08/2019 17:01
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