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Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
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Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
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Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
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Journal Article
Feasibility of the wingate anaerobic exercise test as a clinical measure in patients with juvenile dermatomyositis
2022
Overview
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.
