Literature DB >> 10597050

Progressive resistance training in neuromuscular patients. Effects on force and surface EMG.

E Lindeman1, F Spaans, J Reulen, P Leffers, J Drukker.   

Abstract

In a randomized clinical trial the efficacy of strength training was studied in patients with myotonic dystrophy (n = 33) and in patients with Charcot-Marie-Tooth disease (n = 29). Measurements were performed at the start and after 8, 16 and 24 weeks of progressive resistance training. Surface electromyography (SEMG) of proximal leg muscles was recorded during isometric knee extension at maximum voluntary contraction (MVC) and at 20, 40, 60 and 80% of MVC. Changes in MVC, maximum electrical activity and torque-EMG ratios (TER) were calculated. Fatigue was studied by determining the changes in endurance and in the decline of the median frequency (Fmed) of the SEMG during a sustained contraction at 80% MVC. These parameters showed no significant changes after the training in either of the diagnostic groups. Only the Charcot-Marie-Tooth training group showed a gradual significant increase in mean MVC over the whole training period (21%). After 24 weeks, the increase in mean RMS was similar (25%), but this was mainly due to a sharp rise during the first 8 weeks of training (20%). The findings indicate that the initial strength increase was due to a neural factor, while the subsequent increase was mainly due to muscle hypertrophy.

Entities:  

Mesh:

Year:  1999        PMID: 10597050     DOI: 10.1016/s1050-6411(99)00003-6

Source DB:  PubMed          Journal:  J Electromyogr Kinesiol        ISSN: 1050-6411            Impact factor:   2.368


  10 in total

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Authors:  Ruth Nancy Barker; Sandra Brauer; Richard Carson
Journal:  Exp Brain Res       Date:  2009-06-06       Impact factor: 1.972

Review 2.  The muscular dystrophies: from genes to therapies.

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Review 3.  Activity-based therapies.

Authors:  Alexander W Dromerick; Peter S Lum; Joseph Hidler
Journal:  NeuroRx       Date:  2006-10

Review 4.  Strength training and aerobic exercise training for muscle disease.

Authors:  Nicoline Bm Voet; Elly L van der Kooi; Baziel Gm van Engelen; Alexander Ch Geurts
Journal:  Cochrane Database Syst Rev       Date:  2019-12-06

5.  The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period.

Authors:  Shin Kikuchi; Naoki Kozuka; Eiji Uchida; Takafumi Ninomiya; Haruyuki Tatsumi; Hidekatsu Takeda; Nobutada Tachi
Journal:  J Jpn Phys Ther Assoc       Date:  2008

6.  Charcot-Marie-Tooth disease.

Authors:  Kinga Szigeti; James R Lupski
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

Review 7.  What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review.

Authors:  Marie-Pier Roussel; Marika Morin; Cynthia Gagnon; Elise Duchesne
Journal:  BMC Musculoskelet Disord       Date:  2019-03-05       Impact factor: 2.362

Review 8.  Exercise therapy for muscle and lower motor neuron diseases.

Authors:  Aisha Munawar Sheikh; John Vissing
Journal:  Acta Myol       Date:  2019-12-01

Review 9.  Efficacy of muscle exercise in patients with muscular dystrophy: a systematic review showing a missed opportunity to improve outcomes.

Authors:  Silvia Gianola; Valentina Pecoraro; Simone Lambiase; Roberto Gatti; Giuseppe Banfi; Lorenzo Moja
Journal:  PLoS One       Date:  2013-06-12       Impact factor: 3.240

Review 10.  Rehabilitation Management of the Charcot-Marie-Tooth Syndrome: A Systematic Review of the Literature.

Authors:  Bruno Corrado; Gianluca Ciardi; Chiara Bargigli
Journal:  Medicine (Baltimore)       Date:  2016-04       Impact factor: 1.889

  10 in total

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