Prophylactic use of cardiac medications for delay of left ventricular dysfunction in Duchenne muscular dystrophy

Author:

Conway Kristin M.1,Thomas Shiny2ORCID,Ciafaloni Emma3,Khan Rabia S.45,Mann Joshua R.6,Romitti Paul A.1ORCID,Mathews Katherine D.5,

Affiliation:

1. Department of Epidemiology College of Public Health, The University of Iowa Iowa City Iowa USA

2. New York State Department of Health Albany New York USA

3. Department of Neurology School of Medicine and Dentistry, University of Rochester Medical Center Rochester New York USA

4. Department of Pediatrics UCLA Health Sciences Los Angeles California USA

5. Department of Pediatrics Roy J and Lucille A Carver College of Medicine, The University of Iowa Iowa City Iowa USA

6. Department of Preventive Medicine School of Medicine and John D. Bower School of Population Health, University of Mississippi Medical Center Jackson Mississippi USA

Abstract

AbstractBackgroundEpidemiological 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.MethodsWe 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.ResultsLVD 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).ConclusionsProactive 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.

Funder

Centers for Disease Control and Prevention

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

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