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dc.contributor.authorShefner, J.M.
dc.contributor.authorJacobsen, B.
dc.contributor.authorKupfer, S.
dc.contributor.authorMalik, F.I.
dc.contributor.authorMeng, L.
dc.contributor.authorWei, J.
dc.contributor.authorWolff, A.A.
dc.contributor.authorRudnicki, S.A.
dc.date.accessioned2024-08-09T00:15:38Z
dc.date.available2024-08-09T00:15:38Z
dc.date.issued2023-08-29
dc.identifier.citationShefner, J. M., Jacobsen, B., Kupfer, S., Malik, F. I., Meng, L., Wei, J., … Rudnicki, S. A. (2023). Relationship between quantitative strength and functional outcomes in the phase 2 FORTITUDE-ALS trial. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 25(1–2), 162–169. https://doi.org/10.1080/21678421.2023.2252468
dc.identifier.issn2167-8421
dc.identifier.pmid37641579
dc.identifier.doi10.1080/21678421.2023.2252468
dc.identifier.urihttp://hdl.handle.net/10150/674028
dc.description.abstractObjective: To assess the relationship among measurements of strength, function, and quality of life in an amyotrophic lateral sclerosis (ALS) clinical trial. Methods: In the FORTITUDE-ALS clinical trial (NCT03160898), 456 participants in the full-analysis set were treated with either reldesemtiv or placebo for 12 weeks; this post hoc analysis included all participants regardless of treatment assignments. Assessments included slow vital capacity (SVC), the ALS Functional Rating Scale-Revised (ALSFRS-R), and the 5-item ALS Assessment Questionnaire (ALSAQ-5). Muscle strength was measured quantitatively with hand-held dynamometry, and grip strength with a dedicated dynamometer. The relationship between strength and ALSFRS-R fine and gross motor domain scores, or responses to ALSAQ-5 questions on hand function and walking, was assessed with Spearman’s rank correlation. The relationship between mean upper- or lower-extremity muscle strength and specific ALSFRS-R domains was modeled using principal-components analysis. Results: Upper-extremity muscle strength and hand grip were highly correlated with ALSFRS-R fine motor scores and the ALSAQ-5 hand function question. Similarly, lower-extremity strength correlated well with ALSFRS-R gross motor domain and the ALSAQ-5 walking question. For SVC, correlation was poor with the ALSFRS-R respiratory domain, but stronger with the total score, potentially reflecting the insensitivity of the respiratory questions in the scale. Upper- and lower-extremity strength were both strong predictors of ALSFRS-R domain scores. Conclusions: In this analysis of data from an ALS clinical trial, muscle strength quantified by dynamometry was strongly correlated with functional capacity. These results suggest that muscle strength directly relates to specific functions of importance to people with ALS. © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.rights© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (https:// creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectALSAQ-5
dc.subjectALSFRS-R
dc.subjectAmyotrophic lateral sclerosis
dc.subjectdynamometry
dc.subjectreldesemtiv
dc.subjectvital capacity
dc.titleRelationship between quantitative strength and functional outcomes in the phase 2 FORTITUDE-ALS trial
dc.typeArticle
dc.typetext
dc.contributor.departmentUniversity of Arizona
dc.identifier.journalAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration
dc.description.noteOpen access article
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration
refterms.dateFOA2024-08-09T00:15:38Z


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© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (https:// creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (https:// creativecommons.org/licenses/by-nc-nd/4.0/).