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EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS

OBJECTIVE: To evaluate the effects and safety of exercise training, and to determine the most effective exercise intervention for people with Duchenne muscular dystrophy. Exercise training was compared with no training, placebo or alternative exercise training. Primary outcomes were functioning and...

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Autores principales: HAMMER, Stian, TOUSSAINT, Michel, VOLLSÆTER, Maria, NESBJØRG, Marianne, DRANGE RØKSUND, Ola, REYCHLER, Gregory, LUND, Hans, ANDERSEN, Tiina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Foundation for Rehabilitation Information 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862644/
https://www.ncbi.nlm.nih.gov/pubmed/35642324
http://dx.doi.org/10.2340/jrm.v53.985
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author HAMMER, Stian
TOUSSAINT, Michel
VOLLSÆTER, Maria
NESBJØRG, Marianne
DRANGE RØKSUND, Ola
REYCHLER, Gregory
LUND, Hans
ANDERSEN, Tiina
author_facet HAMMER, Stian
TOUSSAINT, Michel
VOLLSÆTER, Maria
NESBJØRG, Marianne
DRANGE RØKSUND, Ola
REYCHLER, Gregory
LUND, Hans
ANDERSEN, Tiina
author_sort HAMMER, Stian
collection PubMed
description OBJECTIVE: To evaluate the effects and safety of exercise training, and to determine the most effective exercise intervention for people with Duchenne muscular dystrophy. Exercise training was compared with no training, placebo or alternative exercise training. Primary outcomes were functioning and health-related quality of life. Secondary outcomes were muscular strength, endurance and lung function. DATA SOURCES: A systematic literature search was conducted in Medline, EMBASE, CINAHL, Cochrane Central, PEDro and Scopus. STUDY SELECTION AND DATA EXTRACTION: Screening, data extraction, risk of bias and quality assessment were carried out. Risk of bias was assessed using the Cochrane Collaborations risk of bias tools. The certainty of evidence was assessed using Grading of Recommendations Assessment, Development and Evaluation. DATA SYNTHESIS: Twelve studies with 282 participants were included. A narrative synthesis showed limited or no improvements in functioning compared with controls. Health-related quality of life was assessed in only one study. A meta-analysis showed a significant difference in muscular strength and endurance in favour of exercise training compared with no training and placebo. However, the certainty of evidence was very low. CONCLUSION: Exercise training may be beneficial in Duchenne muscular dystrophy, but the evidence remains uncertain. Further research is needed on exercise training to promote functioning and health-related quality of life in Duchenne muscular dystrophy.
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spelling pubmed-88626442022-03-08 EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS HAMMER, Stian TOUSSAINT, Michel VOLLSÆTER, Maria NESBJØRG, Marianne DRANGE RØKSUND, Ola REYCHLER, Gregory LUND, Hans ANDERSEN, Tiina J Rehabil Med Review Article OBJECTIVE: To evaluate the effects and safety of exercise training, and to determine the most effective exercise intervention for people with Duchenne muscular dystrophy. Exercise training was compared with no training, placebo or alternative exercise training. Primary outcomes were functioning and health-related quality of life. Secondary outcomes were muscular strength, endurance and lung function. DATA SOURCES: A systematic literature search was conducted in Medline, EMBASE, CINAHL, Cochrane Central, PEDro and Scopus. STUDY SELECTION AND DATA EXTRACTION: Screening, data extraction, risk of bias and quality assessment were carried out. Risk of bias was assessed using the Cochrane Collaborations risk of bias tools. The certainty of evidence was assessed using Grading of Recommendations Assessment, Development and Evaluation. DATA SYNTHESIS: Twelve studies with 282 participants were included. A narrative synthesis showed limited or no improvements in functioning compared with controls. Health-related quality of life was assessed in only one study. A meta-analysis showed a significant difference in muscular strength and endurance in favour of exercise training compared with no training and placebo. However, the certainty of evidence was very low. CONCLUSION: Exercise training may be beneficial in Duchenne muscular dystrophy, but the evidence remains uncertain. Further research is needed on exercise training to promote functioning and health-related quality of life in Duchenne muscular dystrophy. Foundation for Rehabilitation Information 2021-12-14 /pmc/articles/PMC8862644/ /pubmed/35642324 http://dx.doi.org/10.2340/jrm.v53.985 Text en © 2022 Journal of Rehabilitation Medicine https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Review Article
HAMMER, Stian
TOUSSAINT, Michel
VOLLSÆTER, Maria
NESBJØRG, Marianne
DRANGE RØKSUND, Ola
REYCHLER, Gregory
LUND, Hans
ANDERSEN, Tiina
EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title_full EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title_fullStr EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title_full_unstemmed EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title_short EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
title_sort exercise training in duchenne muscular dystrophy: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862644/
https://www.ncbi.nlm.nih.gov/pubmed/35642324
http://dx.doi.org/10.2340/jrm.v53.985
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