Abstract
Primary muscle disorders form a group of very heterogeneous diseases in which the diseases’ underlying causes lie in the muscle tissue itself. Whole-body vibration is a novel, promising option of intensive muscle training in a short time. Yet, there are only a few systematic evaluations of the application of whole-body vibration for training purposes in children and adults with primary muscle disorders. It seemed to be well tolerated in subjects with primary muscle disorders. Further studies are needed to evaluate the short- and long-term therapeutic effect on the gross motor function in children and adults with primary muscle disorders.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Zierz S, Jerusalem F, Deschauer M. Muskelerkrankungen, 4. Aufl. Referenz-Reihe Neurologie Klinische Neurologie: Georg Thieme Verlag KG, s.l; 2014.
Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010;9(1):77–93. https://doi.org/10.1016/S1474-4422(09)70271-6.
Lindberg C, Bjerkne F. Prevalence of myotonic dystrophy type 1 in adults in western Sweden. Neuromuscul Disord. 2017;27(2):159–62. https://doi.org/10.1016/j.nmd.2016.12.005.
Roussel M-P, Morin M, Gagnon C, et al. 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. BMC Musculoskelet Disord. 2019;20(1):101. https://doi.org/10.1186/s12891-019-2458-7.
Okkersen K, Jimenez-Moreno C, Wenninger S, et al. Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial. Lancet Neurol. 2018;17(8):671–80. https://doi.org/10.1016/S1474-4422(18)30203-5.
Salmaninejad A, Valilou SF, Bayat H, et al. Duchenne muscular dystrophy: an updated review of common available therapies. Int J Neurosci. 2018;128(9):854–64.
Vry J, Schubert IJ, Semler O, et al. Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophy. Eur J Paediatr Neurol. 2014;18(2):140–9. https://doi.org/10.1016/j.ejpn.2013.09.005.
Söderpalm A-C, Kroksmark A-K, Magnusson P, et al. Whole body vibration therapy in patients with Duchenne muscular dystrophy – a prospective observational study. J Musculoskelet Neuronal Interact. 2013;13(1):13–8.
Myers KA, Ramage B, Khan A, et al. Vibration therapy tolerated in children with Duchenne muscular dystrophy: a pilot study. Pediatr Neurol. 2014;51(1):126–9. https://doi.org/10.1016/j.pediatrneurol.2014.03.005.
Petryk A, Polgreen LE, Grames M, et al. Feasibility and tolerability of whole-body, low-intensity vibration and its effects on muscle function and bone in patients with dystrophinopathies: a pilot study. Muscle Nerve. 2017;55(6):875–83. https://doi.org/10.1002/mus.25431.
Novotny SA, Eckhoff MD, Eby BC, et al. Musculoskeletal response of dystrophic mice to short term, low intensity, high frequency vibration. J Musculoskelet Neuronal Interact. 2013;13(4):418–29.
Novotny SA, Mader TL, Greising AG, et al. Low intensity, high frequency vibration training to improve musculoskeletal function in a mouse model of Duchenne muscular dystrophy. PLoS One. 2014;9(8):e104339. https://doi.org/10.1371/journal.pone.0104339.
Wollersheim T, Haas K, Wolf S, et al. Whole-body vibration to prevent intensive care unit-acquired weakness: safety, feasibility, and metabolic response. Crit Care. 2017;21(1):9. https://doi.org/10.1186/s13054-016-1576-y.
Rogan S, de Bruin ED, Radlinger L, et al. Effects of whole-body vibration on proxies of muscle strength in old adults: a systematic review and meta-analysis on the role of physical capacity level. Eur Rev Aging Phys Act. 2015;12:12. https://doi.org/10.1186/s11556-015-0158-3.
Sievänen H, Karinkanta S, Moisio-Vilenius P, et al. Feasibility of whole-body vibration training in nursing home residents with low physical function: a pilot study. Aging Clin Exp Res. 2014;26(5):511–7. https://doi.org/10.1007/s40520-014-0206-2.
Miokovic T, Armbrecht G, Gast U, et al. Muscle atrophy, pain, and damage in bed rest reduced by resistive (vibration) exercise. Med Sci Sports Exerc. 2014;46(8):1506–16. https://doi.org/10.1249/MSS.0000000000000279.
Belavý DL, Miokovic T, Armbrecht G, et al. Resistive vibration exercise reduces lower limb muscle atrophy during 56-day bed-rest. J Musculoskelet Neuronal Interact. 2009;9(4):225–35.
Belavý DL, Beller G, Armbrecht G, et al. Evidence for an additional effect of whole-body vibration above resistive exercise alone in preventing bone loss during prolonged bed rest. Osteoporos Int. 2011;22(5):1581–91. https://doi.org/10.1007/s00198-010-1371-6.
Ebid AA, Ahmed MT, Mahmoud Eid M, et al. Effect of whole body vibration on leg muscle strength after healed burns: a randomized controlled trial. Burns. 2012;38(7):1019–26. https://doi.org/10.1016/j.burns.2012.02.006.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Duran, I., Stark, C., Schoenau, E. (2020). Primary Muscle Disorders. In: Rittweger, J. (eds) Manual of Vibration Exercise and Vibration Therapy. Springer, Cham. https://doi.org/10.1007/978-3-030-43985-9_24
Download citation
DOI: https://doi.org/10.1007/978-3-030-43985-9_24
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-43984-2
Online ISBN: 978-3-030-43985-9
eBook Packages: MedicineMedicine (R0)