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A continuous repetitive task to detect fatigability in spinal muscular atrophy

BACKGROUND: To determine the value of a continuous repetitive task to detect and quantify fatigability as additional dimension of impaired motor function in patients with hereditary proximal spinal muscular atrophy (SMA). RESULTS: In this repeated measure case-control study 52 patients with SMA type...

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Autores principales: Stam, Marloes, Wadman, Renske I., Bartels, Bart, Leeuw, Maureen, Westeneng, Henk-Jan, Wijngaarde, Camiel A., van den Berg, Leonard H., van der Pol, W. Ludo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134509/
https://www.ncbi.nlm.nih.gov/pubmed/30208915
http://dx.doi.org/10.1186/s13023-018-0904-5
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author Stam, Marloes
Wadman, Renske I.
Bartels, Bart
Leeuw, Maureen
Westeneng, Henk-Jan
Wijngaarde, Camiel A.
van den Berg, Leonard H.
van der Pol, W. Ludo
author_facet Stam, Marloes
Wadman, Renske I.
Bartels, Bart
Leeuw, Maureen
Westeneng, Henk-Jan
Wijngaarde, Camiel A.
van den Berg, Leonard H.
van der Pol, W. Ludo
author_sort Stam, Marloes
collection PubMed
description BACKGROUND: To determine the value of a continuous repetitive task to detect and quantify fatigability as additional dimension of impaired motor function in patients with hereditary proximal spinal muscular atrophy (SMA). RESULTS: In this repeated measure case-control study 52 patients with SMA types 2–4, 17 healthy and 29 disease controls performed five consecutive rounds of the Nine-Hole Peg test to determine the presence of fatigability. We analysed differences in test performance and associations with disease characteristics. Five patients with SMA type 2 (22%) and 1 disease control (3%) could not finish five rounds due to fatigue (p = 0.01). Patients with SMA type 2 performed the test significantly more slowly than all other groups (p < 0.005) and disease controls were slower than healthy controls (p < 0.05). Patients with SMA type 2 performed round five 27% slower than round one, while healthy controls performed round five 14% faster than round one (p = 0.005). There was no difference between SMA type 3a, type 3b/4 or disease controls and healthy controls (p > 0.4). Time needed to complete each round during the five-round task increased in 15 patients with SMA type 2 (65%), 4 with type 3a (36%), 4 with type 3b/4 (22%), 9 disease controls (31%) and 1 healthy control (6%). There was no effect of age at disease onset or disease duration in SMA type 2 (p = 0.39). Test-retest reliability was high. CONCLUSION: Fatigability of remaining arm function is a feature of SMA type 2 and can be determined with continuous repetitive tasks.
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spelling pubmed-61345092018-09-13 A continuous repetitive task to detect fatigability in spinal muscular atrophy Stam, Marloes Wadman, Renske I. Bartels, Bart Leeuw, Maureen Westeneng, Henk-Jan Wijngaarde, Camiel A. van den Berg, Leonard H. van der Pol, W. Ludo Orphanet J Rare Dis Research BACKGROUND: To determine the value of a continuous repetitive task to detect and quantify fatigability as additional dimension of impaired motor function in patients with hereditary proximal spinal muscular atrophy (SMA). RESULTS: In this repeated measure case-control study 52 patients with SMA types 2–4, 17 healthy and 29 disease controls performed five consecutive rounds of the Nine-Hole Peg test to determine the presence of fatigability. We analysed differences in test performance and associations with disease characteristics. Five patients with SMA type 2 (22%) and 1 disease control (3%) could not finish five rounds due to fatigue (p = 0.01). Patients with SMA type 2 performed the test significantly more slowly than all other groups (p < 0.005) and disease controls were slower than healthy controls (p < 0.05). Patients with SMA type 2 performed round five 27% slower than round one, while healthy controls performed round five 14% faster than round one (p = 0.005). There was no difference between SMA type 3a, type 3b/4 or disease controls and healthy controls (p > 0.4). Time needed to complete each round during the five-round task increased in 15 patients with SMA type 2 (65%), 4 with type 3a (36%), 4 with type 3b/4 (22%), 9 disease controls (31%) and 1 healthy control (6%). There was no effect of age at disease onset or disease duration in SMA type 2 (p = 0.39). Test-retest reliability was high. CONCLUSION: Fatigability of remaining arm function is a feature of SMA type 2 and can be determined with continuous repetitive tasks. BioMed Central 2018-09-12 /pmc/articles/PMC6134509/ /pubmed/30208915 http://dx.doi.org/10.1186/s13023-018-0904-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Stam, Marloes
Wadman, Renske I.
Bartels, Bart
Leeuw, Maureen
Westeneng, Henk-Jan
Wijngaarde, Camiel A.
van den Berg, Leonard H.
van der Pol, W. Ludo
A continuous repetitive task to detect fatigability in spinal muscular atrophy
title A continuous repetitive task to detect fatigability in spinal muscular atrophy
title_full A continuous repetitive task to detect fatigability in spinal muscular atrophy
title_fullStr A continuous repetitive task to detect fatigability in spinal muscular atrophy
title_full_unstemmed A continuous repetitive task to detect fatigability in spinal muscular atrophy
title_short A continuous repetitive task to detect fatigability in spinal muscular atrophy
title_sort continuous repetitive task to detect fatigability in spinal muscular atrophy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134509/
https://www.ncbi.nlm.nih.gov/pubmed/30208915
http://dx.doi.org/10.1186/s13023-018-0904-5
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