Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway

Abstract Background Physical activity is associated with positive health effects, but individuals with neuromuscular disease (NMD) may experience constraints being physically active. There is a gap in the literature on the activity level of people with NMDs, and therefore we did a study to determine...

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Main Authors: Aristomo Andries, Marleen R. van Walsem, Jan C. Frich
Format: Article
Language:English
Published: BMC 2020-04-01
Series:BMC Musculoskeletal Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12891-020-03246-w
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spelling doaj-d633b629a88d410c800bca376de865282020-11-25T03:00:27ZengBMCBMC Musculoskeletal Disorders1471-24742020-04-012111910.1186/s12891-020-03246-wSelf-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in NorwayAristomo Andries0Marleen R. van Walsem1Jan C. Frich2Institute of Health and Society, University of OsloDepartment of Neurohabilitation, Oslo University HospitalInstitute of Health and Society, University of OsloAbstract Background Physical activity is associated with positive health effects, but individuals with neuromuscular disease (NMD) may experience constraints being physically active. There is a gap in the literature on the activity level of people with NMDs, and therefore we did a study to determine the physical activity level in people with Limb-Girdle muscular dystrophy (LGMD) and Charcot-Marie-Tooth disease (CMT). Methods This study used a cross-sectional design to obtain self-reported physical activity and sitting time among individuals with LGMD and CMT who were recruited from the Norwegian registry for hereditary and congenital neuromuscular diseases. Results A total of 127 respondents who filled out questionnaires about either physical activity or sitting time were included in the analysis. Seventy (55.1%) had a diagnosis of CMT and 57 (44.9%) had a diagnosis of LGMD. Seventy-three (57.5%) respondents were female and 54 (42.5%) were male. Among the 108 respondents with available physical activity data, 44.4% reported being physically inactive. Among the 109 respondents with available sitting time data, the average sitting time was 8.6 h. Longer sitting time was associated with higher physical inactivity. Conclusion Among people with LGMD and CMT in our study, 55.6% reported being physically active. Respondents with LGMD and CMT reported longer sitting time and less physical activity compared with healthy respondents in other studies. Further research should explore variables and measures that can promote physical activity among people with neuromuscular conditions.http://link.springer.com/article/10.1186/s12891-020-03246-wNeuromuscular diseasePhysical activityLimb-girdle muscular dystrophyCharcot-Marie-Tooth diseaseHereditary motor and sensory neuropathySedentary
collection DOAJ
language English
format Article
sources DOAJ
author Aristomo Andries
Marleen R. van Walsem
Jan C. Frich
spellingShingle Aristomo Andries
Marleen R. van Walsem
Jan C. Frich
Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
BMC Musculoskeletal Disorders
Neuromuscular disease
Physical activity
Limb-girdle muscular dystrophy
Charcot-Marie-Tooth disease
Hereditary motor and sensory neuropathy
Sedentary
author_facet Aristomo Andries
Marleen R. van Walsem
Jan C. Frich
author_sort Aristomo Andries
title Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
title_short Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
title_full Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
title_fullStr Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
title_full_unstemmed Self-reported physical activity in people with limb-girdle muscular dystrophy and Charcot-Marie-Tooth disease in Norway
title_sort self-reported physical activity in people with limb-girdle muscular dystrophy and charcot-marie-tooth disease in norway
publisher BMC
series BMC Musculoskeletal Disorders
issn 1471-2474
publishDate 2020-04-01
description Abstract Background Physical activity is associated with positive health effects, but individuals with neuromuscular disease (NMD) may experience constraints being physically active. There is a gap in the literature on the activity level of people with NMDs, and therefore we did a study to determine the physical activity level in people with Limb-Girdle muscular dystrophy (LGMD) and Charcot-Marie-Tooth disease (CMT). Methods This study used a cross-sectional design to obtain self-reported physical activity and sitting time among individuals with LGMD and CMT who were recruited from the Norwegian registry for hereditary and congenital neuromuscular diseases. Results A total of 127 respondents who filled out questionnaires about either physical activity or sitting time were included in the analysis. Seventy (55.1%) had a diagnosis of CMT and 57 (44.9%) had a diagnosis of LGMD. Seventy-three (57.5%) respondents were female and 54 (42.5%) were male. Among the 108 respondents with available physical activity data, 44.4% reported being physically inactive. Among the 109 respondents with available sitting time data, the average sitting time was 8.6 h. Longer sitting time was associated with higher physical inactivity. Conclusion Among people with LGMD and CMT in our study, 55.6% reported being physically active. Respondents with LGMD and CMT reported longer sitting time and less physical activity compared with healthy respondents in other studies. Further research should explore variables and measures that can promote physical activity among people with neuromuscular conditions.
topic Neuromuscular disease
Physical activity
Limb-girdle muscular dystrophy
Charcot-Marie-Tooth disease
Hereditary motor and sensory neuropathy
Sedentary
url http://link.springer.com/article/10.1186/s12891-020-03246-w
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