Literature DB >> 27872178

Childhood Activity on Progression in Limb Girdle Muscular Dystrophy 2I.

Brianna N Brun1, Shelley R H Mockler2, Katie M Laubscher2, Carrie M Stephan1, Julia A Collison1, M Bridget Zimmerman3, Katherine D Mathews1,4.   

Abstract

Limb girdle muscular dystrophy 2I is a slowly progressive muscular dystrophy due to mutations in the Fukutin-related protein ( FKRP) gene. Clinicians are frequently asked if physical activity is harmful for pediatric patients with limb girdle muscular dystrophy 2I. The primary objective of this study was to determine if there is a relationship between self-reported childhood activity level and motor function and respiratory function in older children and adults with limb girdle muscular dystrophy 2I. We compared retrospective self-reported middle school activity level and sport participation with age at onset of weakness, 10-meter walk test, and forced vital capacity later in life in 41 participants with FKRP mutations. We found no relationship between activity level in childhood and disease course later in life, suggesting that self-directed physical activity in children with limb girdle muscular dystrophy 2I does not negatively affect disease progression and outcome.

Entities:  

Keywords:  FKRP; dystroglycanopathy; exercise; muscular dystrophies; α-dystroglycan

Mesh:

Substances:

Year:  2016        PMID: 27872178      PMCID: PMC5464953          DOI: 10.1177/0883073816677680

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


  23 in total

1.  Anti-gravity training improves walking capacity and postural balance in patients with muscular dystrophy.

Authors:  Martin Peter Berthelsen; Edith Husu; Sofie Bouschinger Christensen; Kira Philipsen Prahm; John Vissing; Bente Rona Jensen
Journal:  Neuromuscul Disord       Date:  2014-03-12       Impact factor: 4.296

Review 2.  Response to aerobic exercise training in humans with neuromuscular disease.

Authors:  David D Kilmer
Journal:  Am J Phys Med Rehabil       Date:  2002-11       Impact factor: 2.159

3.  Effect on maximal strength of submaximal exercise in Duchenne muscular dystrophy.

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Journal:  Am J Phys Med       Date:  1979-02

4.  Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

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Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

5.  Progressive deterioration of muscles in mdx mice induced by overload.

Authors:  J Dick; G Vrbová
Journal:  Clin Sci (Lond)       Date:  1993-02       Impact factor: 6.124

6.  Comparison of self-reported versus accelerometer-measured physical activity.

Authors:  Sindre M Dyrstad; Bjørge H Hansen; Ingar M Holme; Sigmund A Anderssen
Journal:  Med Sci Sports Exerc       Date:  2014-01       Impact factor: 5.411

Review 7.  Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

8.  Aerobic walking in slowly progressive neuromuscular disease: effect of a 12-week program.

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Journal:  Arch Phys Med Rehabil       Date:  1996-01       Impact factor: 3.966

9.  Effect of training on the exercise responses of neuromuscular disease patients.

Authors:  J M Florence; J M Hagberg
Journal:  Med Sci Sports Exerc       Date:  1984-10       Impact factor: 5.411

Review 10.  Muscular dystrophies: influence of physical conditioning on the disease evolution.

Authors:  Tor Ansved
Journal:  Curr Opin Clin Nutr Metab Care       Date:  2003-07       Impact factor: 4.294

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