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Prophylactic use of cardiac medications for delay of left ventricular dysfunction in Duchenne muscular dystrophy.
Conway, Kristin M; Thomas, Shiny; Ciafaloni, Emma; Khan, Rabia S; Mann, Joshua R; Romitti, Paul A; Mathews, Katherine D.
Afiliação
  • Conway KM; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, Iowa, USA.
  • Thomas S; New York State Department of Health, Albany, New York, USA.
  • Ciafaloni E; Department of Neurology, School of Medicine and Dentistry, University of Rochester Medical Center, Rochester, New York, USA.
  • Khan RS; Department of Pediatrics, UCLA Health Sciences, Los Angeles, California, USA.
  • Mann JR; Department of Pediatrics, Roy J and Lucille A Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA.
  • Romitti PA; Department of Preventive Medicine, School of Medicine and John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Mathews KD; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, Iowa, USA.
Birth Defects Res ; 116(1): e2260, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37850663
ABSTRACT

BACKGROUND:

Epidemiological support for prophylactic treatment of left ventricular dysfunction (LVD) in Duchenne muscular dystrophy is limited. We used retrospective, population-based surveillance data from the Muscular Dystrophy Surveillance, Tracking and Research Network to evaluate whether prophylaxis delays LVD onset.

METHODS:

We analyzed 455 males born during 1982-2009. Age at first abnormal echocardiogram (ejection fraction <55% or shortening fraction <28%) determined LVD onset. Prophylaxis was defined as cardiac medication use at least 1 year prior to LVD. Corticosteroid use was also coded. Kaplan-Meier curve estimation and Cox Proportional Hazard modeling with time-varying covariates describe associations.

RESULTS:

LVD was identified among 40.7%; average onset age was 14.2 years. Prophylaxis was identified for 20.2% and corticosteroids for 57.4%. Prophylaxis showed delayed LVD onset (p < .001) and lower hazard of dysfunction (adjusted hazard ratio [aHR] = 0.39, 95%CL = 0.22, 0.65) compared to untreated. Compared to no treatment, continuous corticosteroids only (aHR = 1.01, 95%CL = 0.66, 1.53) and prophylaxis only (aHR = 0.67, 95%CL = 0.25, 1.50) were not cardioprotective, but prophylaxis plus continuous corticosteroids were associated with lower hazard of dysfunction (aHR = 0.37, 95%CL = 0.15, 0.80).

CONCLUSIONS:

Proactive cardiac treatment and monitoring are critical aspects of managing Duchenne muscular dystrophy. Consistent with clinical care guidelines, this study supports clinical benefit from cardiac medications initiated prior to documented LVD and suggests further benefit when combined with corticosteroids.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Distrofia Muscular de Duchenne Limite: Adolescent / Humans / Male Idioma: En Revista: Birth Defects Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Distrofia Muscular de Duchenne Limite: Adolescent / Humans / Male Idioma: En Revista: Birth Defects Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos