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Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis

BACKGROUND: Core sets, while widely adopted for clinical assessment in juvenile dermatomyositis (JDM), have some drawbacks – they are time consuming, were developed primarily for research, and require an experienced multidisciplinary team. We propose the Wingate Anaerobic Test, a 30-s all out test p...

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Autores principales: Dover, Saunya, Stephens, Samantha, Clairman, Hayyah, Abesamis, Andrew, Jazi, Omidali Aghababaei, Babij, Stephanie, Marcuz, Jo-Anne, Naraidoo, Natasha, Pan, Jing, Pullenayegum, Eleanor, Rumsey, Dax, Whitney, Kristi, Feldman, Brian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962236/
https://www.ncbi.nlm.nih.gov/pubmed/35346243
http://dx.doi.org/10.1186/s12969-022-00679-6
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author Dover, Saunya
Stephens, Samantha
Clairman, Hayyah
Abesamis, Andrew
Jazi, Omidali Aghababaei
Babij, Stephanie
Marcuz, Jo-Anne
Naraidoo, Natasha
Pan, Jing
Pullenayegum, Eleanor
Rumsey, Dax
Whitney, Kristi
Feldman, Brian M.
author_facet Dover, Saunya
Stephens, Samantha
Clairman, Hayyah
Abesamis, Andrew
Jazi, Omidali Aghababaei
Babij, Stephanie
Marcuz, Jo-Anne
Naraidoo, Natasha
Pan, Jing
Pullenayegum, Eleanor
Rumsey, Dax
Whitney, Kristi
Feldman, Brian M.
author_sort Dover, Saunya
collection PubMed
description BACKGROUND: Core sets, while widely adopted for clinical assessment in juvenile dermatomyositis (JDM), have some drawbacks – they are time consuming, were developed primarily for research, and require an experienced multidisciplinary team. We propose the Wingate Anaerobic Test, a 30-s all out test performed on a cycle ergometer, as a potential alternative; it is valid and reliable in this patient population. We aimed to determine the feasibility of performing the Wingate test as part of a typical clinic visit, and to determine if it is correlated to current measures of disease activity. METHODS: Patients 5–18 years of age, with JDM, were recruited from the JDM clinic at a large Canadian academic children’s hospital. Participants underwent a standard clinic assessment, then completed a Wingate test at the end of the visit. RESULTS: Twenty-six patients participated in the study, representing a recruitment rate of 81%; of those, 88% were able to complete the Wingate test. Patients liked the Wingate test and felt it should be included as a regular clinic test. Absolute peak power (watts) on the Wingate test was strongly correlated to the manual muscle test (MMT-8) and the timed squat test. Relative peak power (watts/kg) on the Wingate test was strongly correlated to the timed squat test and the Childhood Myositis Assessment Scale (CMAS). Exploratory principal components analysis revealed that Wingate relative average power explained almost 2/3 of the variance of the CMAS, MMT and timed squats combined. CONCLUSION: The Wingate test is a feasible test for children with JDM and correlates well with standard clinical assessments. Given its brevity, it has the potential to replace more standard measures of physical function currently used in clinical assessments for children with JDM. Future work should focus on how best to operationalize Wingate testing in clinic without the use of dedicated personnel.
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spelling pubmed-89622362022-03-30 Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis Dover, Saunya Stephens, Samantha Clairman, Hayyah Abesamis, Andrew Jazi, Omidali Aghababaei Babij, Stephanie Marcuz, Jo-Anne Naraidoo, Natasha Pan, Jing Pullenayegum, Eleanor Rumsey, Dax Whitney, Kristi Feldman, Brian M. Pediatr Rheumatol Online J Research Article BACKGROUND: Core sets, while widely adopted for clinical assessment in juvenile dermatomyositis (JDM), have some drawbacks – they are time consuming, were developed primarily for research, and require an experienced multidisciplinary team. We propose the Wingate Anaerobic Test, a 30-s all out test performed on a cycle ergometer, as a potential alternative; it is valid and reliable in this patient population. We aimed to determine the feasibility of performing the Wingate test as part of a typical clinic visit, and to determine if it is correlated to current measures of disease activity. METHODS: Patients 5–18 years of age, with JDM, were recruited from the JDM clinic at a large Canadian academic children’s hospital. Participants underwent a standard clinic assessment, then completed a Wingate test at the end of the visit. RESULTS: Twenty-six patients participated in the study, representing a recruitment rate of 81%; of those, 88% were able to complete the Wingate test. Patients liked the Wingate test and felt it should be included as a regular clinic test. Absolute peak power (watts) on the Wingate test was strongly correlated to the manual muscle test (MMT-8) and the timed squat test. Relative peak power (watts/kg) on the Wingate test was strongly correlated to the timed squat test and the Childhood Myositis Assessment Scale (CMAS). Exploratory principal components analysis revealed that Wingate relative average power explained almost 2/3 of the variance of the CMAS, MMT and timed squats combined. CONCLUSION: The Wingate test is a feasible test for children with JDM and correlates well with standard clinical assessments. Given its brevity, it has the potential to replace more standard measures of physical function currently used in clinical assessments for children with JDM. Future work should focus on how best to operationalize Wingate testing in clinic without the use of dedicated personnel. BioMed Central 2022-03-28 /pmc/articles/PMC8962236/ /pubmed/35346243 http://dx.doi.org/10.1186/s12969-022-00679-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Dover, Saunya
Stephens, Samantha
Clairman, Hayyah
Abesamis, Andrew
Jazi, Omidali Aghababaei
Babij, Stephanie
Marcuz, Jo-Anne
Naraidoo, Natasha
Pan, Jing
Pullenayegum, Eleanor
Rumsey, Dax
Whitney, Kristi
Feldman, Brian M.
Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title_full Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title_fullStr Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title_full_unstemmed Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title_short Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
title_sort feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962236/
https://www.ncbi.nlm.nih.gov/pubmed/35346243
http://dx.doi.org/10.1186/s12969-022-00679-6
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