Literature DB >> 28692198

Longitudinal community walking activity in Duchenne muscular dystrophy.

Eileen G Fowler1, Loretta A Staudt1, Kent R Heberer1, Susan E Sienko2, Cathleen E Buckon2, Anita M Bagley3, Michael D Sussman2, Craig M McDonald3,4.   

Abstract

INTRODUCTION: Natural history studies for Duchenne muscular dystrophy (DMD) have not included measures of community ambulation.
METHODS: Step activity (SA) monitors quantified community ambulation in 42 boys (ages 4-16 years) with DMD with serial enrollment up to 5 years by using a repeated-measures mixed model. Additionally, data were compared with 10-meter walk/run (10mWR) speed to determine validity and sensitivity.
RESULTS: There were significant declines in average strides/day and percent strides at moderate, high and pediatric high rates as a function of age (P < 0.05). Significant correlations for 10mWR versus high and low stride rates were found at baseline (P < 0.05). SA outcomes were sensitive to change over 1 year, but the direction and parameter differed by age group (younger vs. older). Changes in strides/day and percentages of high frequency and low frequency strides correlated significantly with changes in 10mWR speed (P < 0.05). DISCUSSION: Community ambulation data provide valid and sensitive real-world measures that may inform clinical trials. Muscle Nerve 57: 401-406, 2018.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  Duchenne muscular dystrophy; accelerometry; community walking; gait; natural history; physical activity

Mesh:

Year:  2017        PMID: 28692198     DOI: 10.1002/mus.25743

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  11 in total

Review 1.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; David Brumbaugh; Laura E Case; Paula R Clemens; Stasia Hadjiyannakis; Shree Pandya; Natalie Street; Jean Tomezsko; Kathryn R Wagner; Leanne M Ward; David R Weber
Journal:  Lancet Neurol       Date:  2018-02-03       Impact factor: 44.182

2.  Walking activity in a large cohort of boys with Duchenne muscular dystrophy.

Authors:  Donovan J Lott; Tanja Taivassalo; Claudia R Senesac; Rebecca J Willcocks; Ann M Harrington; Kirsten Zilke; Hilary Cunkle; Catherine Powers; Erika L Finanger; William D Rooney; Gihan I Tennekoon; Krista Vandenborne
Journal:  Muscle Nerve       Date:  2020-11-27       Impact factor: 3.217

3.  Leveraging cardiac magnetic resonance imaging to assess skeletal muscle progression in Duchenne muscular dystrophy.

Authors:  Jacob A Kaslow; Andrew G Sokolow; Thomas Donnelly; Maciej S Buchowski; Bruce M Damon; Larry W Markham; W Bryan Burnette; Jonathan H Soslow
Journal:  Neuromuscul Disord       Date:  2022-02-04       Impact factor: 3.538

4.  Step Activity Monitoring in Boys with Duchenne Muscular Dystrophy and its Correlation with Magnetic Resonance Measures and Functional Performance.

Authors:  Kavya S Nair; Donovan J Lott; Sean C Forbes; Alison M Barnard; Rebecca J Willcocks; Claudia R Senesac; Michael J Daniels; Ann T Harrington; Gihan I Tennekoon; Kirsten Zilke; Erika L Finanger; Richard S Finkel; William D Rooney; Glenn A Walter; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2022

Review 5.  First Regulatory Qualification of a Novel Digital Endpoint in Duchenne Muscular Dystrophy: A Multi-Stakeholder Perspective on the Impact for Patients and for Drug Development in Neuromuscular Diseases.

Authors:  Laurent Servais; Eric Camino; Aude Clement; Craig M McDonald; Jacek Lukawy; Linda P Lowes; Damien Eggenspieler; Francesca Cerreta; Paul Strijbos
Journal:  Digit Biomark       Date:  2021-08-05

6.  miR-486 is essential for muscle function and suppresses a dystrophic transcriptome.

Authors:  Adrienne Samani; Rylie M Hightower; Andrea L Reid; Katherine G English; Michael A Lopez; J Scott Doyle; Michael J Conklin; David A Schneider; Marcas M Bamman; Jeffrey J Widrick; David K Crossman; Min Xie; David Jee; Eric C Lai; Matthew S Alexander
Journal:  Life Sci Alliance       Date:  2022-05-05

7.  Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy.

Authors:  Aaron S Zelikovich; Mattia Quattrocelli; Isabella M Salamone; Nancy L Kuntz; Elizabeth M McNally
Journal:  Sci Rep       Date:  2019-04-08       Impact factor: 4.379

Review 8.  Walking and weakness in children: a narrative review of gait and functional ambulation in paediatric neuromuscular disease.

Authors:  Rachel A Kennedy; Kate Carroll; Jennifer L McGinley; Kade L Paterson
Journal:  J Foot Ankle Res       Date:  2020-03-02       Impact factor: 2.303

9.  Assessing Physical Activity Using Accelerometers in Youth with Duchenne Muscular Dystrophy.

Authors:  David Arteaga; Thomas Donnelly; Kimberly Crum; Larry Markham; Mary Killian; W Bryan Burnette; Jonathan Soslow; Maciej S Buchowski
Journal:  J Neuromuscul Dis       Date:  2020

10.  Relationships between muscle size, strength, and physical activity in adults with muscular dystrophy.

Authors:  Matthew F Jacques; Gladys L Onambele-Pearson; Neil D Reeves; Georgina K Stebbings; Jonathon Smith; Christopher I Morse
Journal:  J Cachexia Sarcopenia Muscle       Date:  2018-10-19       Impact factor: 12.910

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