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Echocardiographic signs of subclinical cardiac function impairment in Duchenne dystrophy gene carriers.
Kincl, Vladimír; Panovský, Roman; Pesl, Martin; Máchal, Jan; Juríková, Lenka; Haberlová, Jana; Masárová, Lucia.
Afiliación
  • Kincl V; Department of Internal Medicine/Cardiology, Faculty of Medicine, St. Anne's University Hospital, Masaryk University, Brno, Czech Republic. vladimir.kincl@fnusa.cz.
  • Panovský R; International Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic. vladimir.kincl@fnusa.cz.
  • Pesl M; Department of Internal Medicine/Cardiology, Faculty of Medicine, St. Anne's University Hospital, Masaryk University, Brno, Czech Republic.
  • Máchal J; International Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
  • Juríková L; Department of Internal Medicine/Cardiology, Faculty of Medicine, St. Anne's University Hospital, Masaryk University, Brno, Czech Republic.
  • Haberlová J; International Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
  • Masárová L; Department of Biology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Sci Rep ; 10(1): 20794, 2020 11 27.
Article en En | MEDLINE | ID: mdl-33247228
ABSTRACT
To assess subclinical cardiac function impairment in Duchenne dystrophy (DMD) female carriers. Forty-four female subjects proved as DMD carriers underwent echocardiographic examination including tissue Doppler imaging (TDI) of mitral and tricuspid annulus. Seventeen age-matched healthy female subjects served as controls. A significant differences in peak systolic annular velocity (Sa) between carriers and controls were found for lateral and septal part of the mitral annulus and for tricuspid annulus (0.09 vs. 0.11 m/s, p < 0.001, 0.08 vs. 0.09 m/s, p < 0.01 and 0.13 vs. 0.14 m/s, p = 0.02 respectively). There was also difference in early diastolic velocity (Ea) of the septal part of the mitral annulus (0.11 vs. 0.13 m/s, p = 0.03). The subclinical deterioration of systolic function is presented even in asymptomatic DMD female carriers.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne / Heterocigoto Tipo de estudio: Diagnostic_studies / Observational_studies Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: República Checa

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne / Heterocigoto Tipo de estudio: Diagnostic_studies / Observational_studies Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: República Checa