1. Quantitative electromyography in ambulatory boys with Duchenne muscular dystrophy.
- Author
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Verma S, Lin J, Travers C, McCracken C, and Shah D
- Subjects
- Adolescent, Child, Child, Preschool, Follow-Up Studies, Humans, Male, Electromyography trends, Muscle, Skeletal physiopathology, Muscular Dystrophy, Duchenne diagnosis, Muscular Dystrophy, Duchenne physiopathology, Walking physiology
- Abstract
Introduction: This study's objective was to evaluate quantitative electromyography (QEMG) using multiple-motor-unit (multi-MUP) analysis in Duchenne muscular dystrophy (DMD)., Methods: Ambulatory DMD boys, aged 5-15 years, were evaluated with QEMG at 6-month intervals over 14 months. EMG was performed in the right biceps brachii (BB) and tibialis anterior (TA) muscles. Normative QEMG data were obtained from age-matched healthy boys. Wilcoxon signed-rank tests were performed., Results: Eighteen DMD subjects were enrolled, with a median age of 7 (interquartile range 7-10) years. Six-month evaluations were performed on 14 subjects. QEMG showed significantly abnormal mean MUP duration in BB and TA muscles, with no significant change over 6 months., Conclusions: QEMG is a sensitive electrophysiological marker of myopathy in DMD. Preliminary data do not reflect a significant change in MUP parameters over a 6-month interval; long-term follow-up QEMG studies are needed to understand its role as a biomarker for disease progression. Muscle Nerve 56: 1361-1364, 2017., (© 2017 Wiley Periodicals, Inc.)
- Published
- 2017
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