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How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?

BACKGROUND: Physical activity (PA) provides many substantial benefits to help reduce risk for cardiometabolic disease, improve cognitive function, and improve quality of life. Individuals with neuromuscular disorders (NMDs), such as spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD)...

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Autores principales: Uher, David, Yoon, Lisa, Garber, Carol Ewing, Montes, Jacqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578218/
https://www.ncbi.nlm.nih.gov/pubmed/37424475
http://dx.doi.org/10.3233/JND-230033
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author Uher, David
Yoon, Lisa
Garber, Carol Ewing
Montes, Jacqueline
author_facet Uher, David
Yoon, Lisa
Garber, Carol Ewing
Montes, Jacqueline
author_sort Uher, David
collection PubMed
description BACKGROUND: Physical activity (PA) provides many substantial benefits to help reduce risk for cardiometabolic disease, improve cognitive function, and improve quality of life. Individuals with neuromuscular disorders (NMDs), such as spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD) are characterized by muscular weakness and fatigue, which limits the capacity to reach the recommended guidelines of PA. Measuring PA in these populations can provide insight to participation in daily activities, track disease progression, and monitor efficacy of drug treatments. OBJECTIVE: The objective of this study was to identify how PA is measured in SMA and DMD using instrumented and self-report methods, and how these methods are employed in ambulatory and non-ambulatory groups. METHODS: A scoping review was performed to identify studies that reported PA in these neuromuscular disorders. Inclusion was determined after a multi-stage review process by several reviewers, followed by an in-depth analysis of metrics reported by each tool that was used. RESULTS: A total of nineteen studies were identified and included in this review. Sixteen studies included instrumented measures and four studies utilized self-reported measures, with eleven studies also reporting PA information from a non-ambulatory group. A variety of metrics have been reported using both classes of measurement tools. CONCLUSION: Although a wide variety of research exists that details both instrumented and self-reported measurement tools, feasibility, cost, and study aims are important factors to consider in addition to testing methodology when selecting which type of tool to use. We recommend using a combination of instrumented and self-report measures to provide context to the PA measured in these populations. Improvements in both instrumented and self-report methodologies will add valuable knowledge about the disease burden and efficacy of treatment and disease management methods in SMA and DMD.
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spelling pubmed-105782182023-10-17 How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy? Uher, David Yoon, Lisa Garber, Carol Ewing Montes, Jacqueline J Neuromuscul Dis Research Report BACKGROUND: Physical activity (PA) provides many substantial benefits to help reduce risk for cardiometabolic disease, improve cognitive function, and improve quality of life. Individuals with neuromuscular disorders (NMDs), such as spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD) are characterized by muscular weakness and fatigue, which limits the capacity to reach the recommended guidelines of PA. Measuring PA in these populations can provide insight to participation in daily activities, track disease progression, and monitor efficacy of drug treatments. OBJECTIVE: The objective of this study was to identify how PA is measured in SMA and DMD using instrumented and self-report methods, and how these methods are employed in ambulatory and non-ambulatory groups. METHODS: A scoping review was performed to identify studies that reported PA in these neuromuscular disorders. Inclusion was determined after a multi-stage review process by several reviewers, followed by an in-depth analysis of metrics reported by each tool that was used. RESULTS: A total of nineteen studies were identified and included in this review. Sixteen studies included instrumented measures and four studies utilized self-reported measures, with eleven studies also reporting PA information from a non-ambulatory group. A variety of metrics have been reported using both classes of measurement tools. CONCLUSION: Although a wide variety of research exists that details both instrumented and self-reported measurement tools, feasibility, cost, and study aims are important factors to consider in addition to testing methodology when selecting which type of tool to use. We recommend using a combination of instrumented and self-report measures to provide context to the PA measured in these populations. Improvements in both instrumented and self-report methodologies will add valuable knowledge about the disease burden and efficacy of treatment and disease management methods in SMA and DMD. IOS Press 2023-09-08 /pmc/articles/PMC10578218/ /pubmed/37424475 http://dx.doi.org/10.3233/JND-230033 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Uher, David
Yoon, Lisa
Garber, Carol Ewing
Montes, Jacqueline
How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title_full How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title_fullStr How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title_full_unstemmed How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title_short How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?
title_sort how is physical activity measured in spinal muscular atrophy and duchenne muscular dystrophy?
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578218/
https://www.ncbi.nlm.nih.gov/pubmed/37424475
http://dx.doi.org/10.3233/JND-230033
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