Literature DB >> 25414237

Corticosteroid Treatments in Males With Duchenne Muscular Dystrophy: Treatment Duration and Time to Loss of Ambulation.

Sunkyung Kim1, Kimberly A Campbell2, Deborah J Fox2, Dennis J Matthews3, Rodolfo Valdez4.   

Abstract

This population-based study examines the association between corticosteroid treatment and time to loss of ambulation, stratifying by treatment duration (short: 0.25-3 years, long: >3 years), among 477 Duchenne muscular dystrophy cases identified by the Muscular Dystrophy Surveillance Tracking and Research Network (MDSTARnet). Those cases who received short-term corticosteroid treatment had a time to loss of ambulation that was 0.8 years shorter (t test) and an annual risk of losing ambulation 77% higher than the untreated (Cox regression). Conversely, cases who received long-term corticosteroid treatment had a time to loss of ambulation that was 2 years longer and an annual risk of losing ambulation 82% lower than the untreated, up to age 11 years; after which the risks were not statistically different. The relationship of corticosteroids and time to loss of ambulation is more complex than depicted by previous studies limited to treatment responders or subjects who lost ambulation during study follow-up.
© The Author(s) 2014.

Entities:  

Keywords:  Duchenne muscular dystrophy; ambulation; corticosteroid; treatment duration

Mesh:

Substances:

Year:  2014        PMID: 25414237      PMCID: PMC4439376          DOI: 10.1177/0883073814558120

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  31 in total

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4.  The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology.

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4.  Risk Factors for Cardiac and Non-cardiac Causes of Death in Males with Duchenne Muscular Dystrophy.

Authors:  Carol A Wittlieb-Weber; Kenneth R Knecht; Chet R Villa; Chentel Cunningham; Jennifer Conway; Matthew J Bock; Katheryn E Gambetta; Ashwin K Lal; Kurt R Schumacher; Sabrina P Law; Shriprasad R Deshpande; Shawn C West; Joshua M Friedland-Little; Irene D Lytrivi; Michael A McCulloch; Ryan J Butts; David R Weber; Jonathan N Johnson
Journal:  Pediatr Cardiol       Date:  2020-02-03       Impact factor: 1.655

5.  Muscular Dystrophy Surveillance, Tracking, and Research Network pilot: Population-based surveillance of major muscular dystrophies at four U.S. sites, 2007-2011.

Authors:  ThuyQuynh N Do; Natalie Street; Jennifer Donnelly; Melissa M Adams; Christopher Cunniff; Deborah J Fox; Richard O Weinert; Joyce Oleszek; Paul A Romitti; Christina P Westfield; Julie Bolen
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6.  Corticosteroid Treatment and Growth Patterns in Ambulatory Males with Duchenne Muscular Dystrophy.

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Review 7.  A Review of MD STAR net's Research Contributions to Pediatric-Onset Dystrophinopathy in the United States; 2002-2017.

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8.  Use of advanced heart failure therapies in Duchenne muscular dystrophy.

Authors:  Carol A Wittlieb-Weber; Chet R Villa; Jennifer Conway; Matthew J Bock; Katheryn E Gambetta; Jonathan N Johnson; Ashwin K Lal; Kurt R Schumacher; Sabrina P Law; Shriprasad R Deshpande; Shawn C West; Joshua M Friedland-Little; Irene D Lytrivi; Michael A McCulloch; Ryan J Butts; David R Weber; Kenneth R Knecht
Journal:  Prog Pediatr Cardiol       Date:  2019-01-11

9.  Health Care Use of Cardiac Specialty Care in Children With Muscular Dystrophy in the United States.

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10.  Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy.

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Journal:  Muscle Nerve       Date:  2020-11-17       Impact factor: 3.852

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