Literature DB >> 10589852

Respiratory muscle training in neuromuscular disease: long-term effects on strength and load perception.

D Gozal1, P Thiriet.   

Abstract

PURPOSE: Deterioration of respiratory muscle function in patients with neuromuscular disorders is primarily responsible for the high morbidity and mortality associated with these diseases.
METHODS: The potential benefit of respiratory muscle training (RMT) on preservation of respiratory muscle strength and respiratory load perception (RLP) was examined in 21 children (mean age: 12.2 +/- 1.8 yr [SD], 16 male) with Duchenne's muscular dystrophy or spinal muscular atrophy type III, and in 20 age-, weight-, and sex-matched controls. Subjects were randomly allocated to undergo incremental RMT with resistive inspiratory and expiratory loads for a period of 6 months (trained group, TR) or to perform similar exercises with no load (NT). Maximal static inspiratory (Pi(max)) and expiratory (Pe(max)) pressures and RLP (modified Borg visual analog scale 0-10) were assessed on two separate occasions before beginning of the training protocol, monthly throughout RMT duration, and every 3-6 months upon cessation of RMT for 1 yr.
RESULTS: In controls, no significant changes in maximal static pressures or load perception occurred during RMT or thereafter. Training in neuromuscular disorder (NMD) patients was associated with improvements in Pi(max) (mean delta max: +19.8 +/- 3.8 cmH2O in TR vs +4.2 +/- 3.6 cmH2O in NT; P < 0.02) and in Pe(max) (mean delta max: +27.1 +/- 4.9 cmH2O in TR vs -1.8 +/- 3.4 cmH2O in NT; P < 0.004). Similarly, RLP significantly decreased during the RMT period in TR (mean delta: 1.9 +/- 0.3; P < 0.01) but did not change in NT (-0.2 +/- 0.2). In addition, with cessation of RMT, static pressures returned to pretraining values in TR within approximately 3 months. However, RLP was still improved after 12 months.
CONCLUSIONS: We conclude that in children with NMD, although RMT-induced increases in expiratory muscle strength are rapidly reversible, long-lasting improvements in RLP occur and could be associated with decreased respiratory symptoms.

Entities:  

Mesh:

Year:  1999        PMID: 10589852     DOI: 10.1097/00005768-199911000-00005

Source DB:  PubMed          Journal:  Med Sci Sports Exerc        ISSN: 0195-9131            Impact factor:   5.411


  14 in total

1.  Safety and efficacy of short- and long-term inspiratory muscle training in late-onset Pompe disease (LOPD): a pilot study.

Authors:  Stephan Wenninger; Eva Greckl; Haris Babačić; Kristina Stahl; Benedikt Schoser
Journal:  J Neurol       Date:  2018-11-14       Impact factor: 4.849

Review 2.  Respiratory involvement in inherited primary muscle conditions.

Authors:  N Shahrizaila; W J M Kinnear; A J Wills
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-10       Impact factor: 10.154

Review 3.  Cardiopulmonary support in duchenne muscular dystrophy.

Authors:  Josef Finsterer
Journal:  Lung       Date:  2006 Jul-Aug       Impact factor: 2.584

Review 4.  Exercise and amyotrophic lateral sclerosis.

Authors:  J P Lopes de Almeida; R Silvestre; A C Pinto; M de Carvalho
Journal:  Neurol Sci       Date:  2012-01-07       Impact factor: 3.307

Review 5.  Pharmacologic and genetic therapy for childhood muscular dystrophies.

Authors:  D M Escolar; C G Scacheri
Journal:  Curr Neurol Neurosci Rep       Date:  2001-03       Impact factor: 5.081

6.  Long-term ventilation of patients with Duchenne muscular dystrophy: experiences at the Neuromuscular Centre Ulm.

Authors:  Kurt H Wollinsky; Bernd Kutter; Peter M Geiger
Journal:  Acta Myol       Date:  2012-12

7.  Respiratory muscle training in children and adults with neuromuscular disease.

Authors:  Ivanizia S Silva; Rafaela Pedrosa; Ingrid G Azevedo; Anne-Marie Forbes; Guilherme Af Fregonezi; Mário Et Dourado Junior; Suzianne Rh Lima; Gardenia Mh Ferreira
Journal:  Cochrane Database Syst Rev       Date:  2019-09-05

8.  Comparison of Experimental Protocols of Physical Exercise for mdx Mice and Duchenne Muscular Dystrophy Patients.

Authors:  Janek Hyzewicz; Urs T Ruegg; Shin'ichi Takeda
Journal:  J Neuromuscul Dis       Date:  2015-11-22

Review 9.  Assessment and management of respiratory function in patients with Duchenne muscular dystrophy: current and emerging options.

Authors:  Antonella LoMauro; Maria Grazia D'Angelo; Andrea Aliverti
Journal:  Ther Clin Risk Manag       Date:  2015-09-28       Impact factor: 2.423

10.  Upper extremity resistance exercise with elastic bands for respiratory function in children with cerebral palsy.

Authors:  Seung-Oh Shin; Nan-Soo Kim
Journal:  J Phys Ther Sci       Date:  2017-12-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.