Functional Ability and Physical Activity in Hereditary Neuromuscular Diseases.


Journal

Journal of neuromuscular diseases
ISSN: 2214-3602
Titre abrégé: J Neuromuscul Dis
Pays: Netherlands
ID NLM: 101649948

Informations de publication

Date de publication:
2022
Historique:
pubmed: 19 2 2022
medline: 11 5 2022
entrez: 18 2 2022
Statut: ppublish

Résumé

Physical activity may help to promote health in patients with Limb-girdle muscular dystrophy (LGMD) and Charcot-Marie-Tooth disease (CMT). To investigate associations between functional ability and other variables, with physical activity in people with LGMD and CMT grouped according to the International Classification of Functioning, Disability, and Health (ICF). We did a cross-sectional study, recruiting respondents from the Norwegian registry of inherited neuromuscular disorders. We used the Norwegian version of Barthel index of Activities of Daily Living (ADL) to measure functional ability and the International Physical Activity Questionnaire -short form (IPAQ-sf) to classify physical activity. We used multivariable logistic regression analysis to investigate associations between variables. 145 subjects were recruited (79 with CMT and 66 with LGMD). 55.6% of the subjects met a minimum recommendation of physical activity. Participants with moderate to severe functional ability were more likely to be physically inactive compared to those with normal functional ability (OR 19.7; 95% CI 3.1-127.2). Mildly decreased functional ability also showed higher odds of being physically inactive compared to participants with normal functional ability (OR 4.1; 95% CI 1.1-15.6). Higher education was associated with inactivity. Fatigue, participation in physiotherapy, and participation in adapted physical activity programs were not associated with physical activity. Low functional ability was associated with physical inactivity in both LGMD and CMT. Association between higher education and inactivity might indicate the need to provide more understanding about physical activity benefit in this group.

Sections du résumé

BACKGROUND BACKGROUND
Physical activity may help to promote health in patients with Limb-girdle muscular dystrophy (LGMD) and Charcot-Marie-Tooth disease (CMT).
OBJECTIVE OBJECTIVE
To investigate associations between functional ability and other variables, with physical activity in people with LGMD and CMT grouped according to the International Classification of Functioning, Disability, and Health (ICF).
METHODS METHODS
We did a cross-sectional study, recruiting respondents from the Norwegian registry of inherited neuromuscular disorders. We used the Norwegian version of Barthel index of Activities of Daily Living (ADL) to measure functional ability and the International Physical Activity Questionnaire -short form (IPAQ-sf) to classify physical activity. We used multivariable logistic regression analysis to investigate associations between variables.
RESULTS RESULTS
145 subjects were recruited (79 with CMT and 66 with LGMD). 55.6% of the subjects met a minimum recommendation of physical activity. Participants with moderate to severe functional ability were more likely to be physically inactive compared to those with normal functional ability (OR 19.7; 95% CI 3.1-127.2). Mildly decreased functional ability also showed higher odds of being physically inactive compared to participants with normal functional ability (OR 4.1; 95% CI 1.1-15.6). Higher education was associated with inactivity. Fatigue, participation in physiotherapy, and participation in adapted physical activity programs were not associated with physical activity.
CONCLUSIONS CONCLUSIONS
Low functional ability was associated with physical inactivity in both LGMD and CMT. Association between higher education and inactivity might indicate the need to provide more understanding about physical activity benefit in this group.

Identifiants

pubmed: 35180128
pii: JND210677
doi: 10.3233/JND-210677
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

437-446

Auteurs

Aristomo Andries (A)

Department of Neurology, Oslo University Hospital, Nydalen, Oslo, Norway.
Institute of Health and Society, University of Oslo, Blindern, Oslo, Norway.

Marleen R Van Walsem (MR)

Department of Neurology, Oslo University Hospital, Nydalen, Oslo, Norway.
Department of Neurohabilitation, Oslo University Hospital, Nydalen, Oslo, Norway.
Research Center for Habilitation and Rehabilitation Services and Models, Institute of Health and Society, University of Oslo, Blindern, Oslo, Norway.

Kristin Ørstavik (K)

Department of Neurology, Oslo University Hospital, Nydalen, Oslo, Norway.
European Reference Network Neuromuscular Diseases (ERN EURO-NMD), Paris, France.

Jan C Frich (JC)

Institute of Health and Society, University of Oslo, Blindern, Oslo, Norway.

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Classifications MeSH