Relationship between quantitative strength and functional outcomes in the phase 2 FORTITUDE-ALS trial
dc.contributor.author | Shefner, J.M. | |
dc.contributor.author | Jacobsen, B. | |
dc.contributor.author | Kupfer, S. | |
dc.contributor.author | Malik, F.I. | |
dc.contributor.author | Meng, L. | |
dc.contributor.author | Wei, J. | |
dc.contributor.author | Wolff, A.A. | |
dc.contributor.author | Rudnicki, S.A. | |
dc.date.accessioned | 2024-08-09T00:15:38Z | |
dc.date.available | 2024-08-09T00:15:38Z | |
dc.date.issued | 2023-08-29 | |
dc.identifier.citation | Shefner, 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.issn | 2167-8421 | |
dc.identifier.pmid | 37641579 | |
dc.identifier.doi | 10.1080/21678421.2023.2252468 | |
dc.identifier.uri | http://hdl.handle.net/10150/674028 | |
dc.description.abstract | Objective: 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.iso | en | |
dc.publisher | Taylor 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.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | ALSAQ-5 | |
dc.subject | ALSFRS-R | |
dc.subject | Amyotrophic lateral sclerosis | |
dc.subject | dynamometry | |
dc.subject | reldesemtiv | |
dc.subject | vital capacity | |
dc.title | Relationship between quantitative strength and functional outcomes in the phase 2 FORTITUDE-ALS trial | |
dc.type | Article | |
dc.type | text | |
dc.contributor.department | University of Arizona | |
dc.identifier.journal | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | |
dc.description.note | Open access article | |
dc.description.collectioninformation | This 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.version | Final Published Version | |
dc.source.journaltitle | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | |
refterms.dateFOA | 2024-08-09T00:15:38Z |