Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life

dc.contributor
Institut Català de la Salut
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[Karazi W, Coppers J] Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands. [Maas D, Cup E, Voet N] Department of Rehabilitation, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands. [Bloemen B] Department for Health Evidence, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands. [Pinos T, Marti Seves R] Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain. Grup de Recerca de Patologia Neuromuscular i Mitocondrial, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
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Vall d'Hebron Barcelona Hospital Campus
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Karazi, Walaa
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Coppers, Jacqueline
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Maas, Daphne
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Cup, Edith
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Bloemen, Bart
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Voet, Nicole
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Pinós Figueras, Tomas
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Marti, Ramon
dc.date.accessioned
2025-10-24T08:49:18Z
dc.date.available
2025-10-24T08:49:18Z
dc.date.issued
2024-01-24T13:32:52Z
dc.date.issued
2024-01-24T13:32:52Z
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2024
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Karazi W, Coppers J, Maas D, Cup E, Bloemen B, Voet N, et al. Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life. J Neuromuscul Dis. 2024;11(1):103–16.
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2214-3599
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https://hdl.handle.net/11351/10893
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10.3233/JND-230027
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38108358
dc.identifier.uri
http://hdl.handle.net/11351/10893
dc.description.abstract
McArdle disease; International survey; Physical activity
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Enfermedad de McArdle; Encuesta internacional; Actividad física
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Malaltia de McArdle; Enquesta internacional; Activitat física
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Background: Glycogen storage disease type 5 (GSD) is an autosomal recessive inherited metabolic myopathy caused by a deficiency of the enzyme muscle glycogen phosphorylase. Individuals with GSD5 experience physical activity intolerance. Objective: This patient-led study aimed to capture the daily life experiences of GSD5, with a focus on adapting to and coping with their physical activity intolerance. Methods: An online survey was composed in close collaboration with patient organizations. It consisted of customized and validated questionnaires on demographics, general health and comorbidities, physical activity, psychosocial well-being and functioning, pain, fatigue and adapting to and coping with GSD5. Results: One hundred sixty-two participants (16 countries) participated. The majority, n = 86 (69%) were from the Netherlands, USA or UK. We observed a high rate of misdiagnosis prior to GSD5 diagnosis (49%), surprisingly a relatively high proportion had not been diagnosed by DNA testing which is the gold standard. Being diagnosed had a strong impact on emotional status, daily life activities and important life choices. A large proportion had not received any rehabilitation (41%) nor medical treatment (57%) before diagnosis. Engagement in vigorous and moderate physical activity was reduced. Health related quality of life was low, most likely related to low physical health. The median Fatigue Severity Score was 4.3, indicating moderate to severe fatigue. Participants themselves had found various ways to adapt to and cope with their disability. The adaptations concerned all aspect of their life, including household chores, social and physical activities, and work. In addition to lack of support, participants reported limited availability of information sources. Conclusion: Participants have provided guidance for newly diagnosed people, including the advice to accept one’s limited abilities and maintain an active lifestyle. We conclude that adequate counseling on ways of adapting and coping is expected to increase both health-related quality of life and physical activity.
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We are grateful to the Stichting McArdle and Stofwisselkracht for funding this research project. We acknowledge IAMGSD for providing very valuable suggestions to this project.
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application/pdf
dc.language
eng
dc.publisher
IOS Press
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Journal of Neuromuscular Diseases;11(1)
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https://doi.org/10.3233/JND-230027
dc.rights
Attribution-NonCommercial 4.0 International
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http://creativecommons.org/licenses/by-nc/4.0/
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info:eu-repo/semantics/openAccess
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Scientia
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Qualitat de vida
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Fatiga
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Glicogenosi
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Metabolisme - Trastorns
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DISEASES::Nutritional and Metabolic Diseases::Metabolic Diseases::Metabolism, Inborn Errors::Carbohydrate Metabolism, Inborn Errors::Glycogen Storage Disease::Glycogen Storage Disease Type V
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HEALTH CARE::Environment and Public Health::Public Health::Epidemiologic Measurements::Demography::Health Status::Quality of Life
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DISEASES::Pathological Conditions, Signs and Symptoms::Signs and Symptoms::Fatigue
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ENFERMEDADES::enfermedades nutricionales y metabólicas::enfermedades metabólicas::alteraciones congénitas del metabolismo::trastornos congénitos del metabolismo de los carbohidratos::enfermedad por almacenamiento de glucógeno::enfermedad por almacenamiento de glucógeno tipo V
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ATENCIÓN DE SALUD::ambiente y salud pública::salud pública::medidas epidemiológicas::demografía::estado de salud::calidad de vida
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ENFERMEDADES::afecciones patológicas, signos y síntomas::signos y síntomas::fatiga
dc.title
Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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