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The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy

Muscle weakness is a common clinical symptom in children with spastic cerebral palsy (SCP). It is caused by impaired neural ability and altered intrinsic capacity of the muscles. To define the contribution of decreased muscle size to muscle weakness, two cohorts were recruited in this cross-sectiona...

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Autores principales: Hanssen, Britta, Peeters, Nicky, Vandekerckhove, Ines, De Beukelaer, Nathalie, Bar-On, Lynn, Molenaers, Guy, Van Campenhout, Anja, Degelaen, Marc, Van den Broeck, Christine, Calders, Patrick, Desloovere, Kaat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350776/
https://www.ncbi.nlm.nih.gov/pubmed/34381414
http://dx.doi.org/10.3389/fneur.2021.692582
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author Hanssen, Britta
Peeters, Nicky
Vandekerckhove, Ines
De Beukelaer, Nathalie
Bar-On, Lynn
Molenaers, Guy
Van Campenhout, Anja
Degelaen, Marc
Van den Broeck, Christine
Calders, Patrick
Desloovere, Kaat
author_facet Hanssen, Britta
Peeters, Nicky
Vandekerckhove, Ines
De Beukelaer, Nathalie
Bar-On, Lynn
Molenaers, Guy
Van Campenhout, Anja
Degelaen, Marc
Van den Broeck, Christine
Calders, Patrick
Desloovere, Kaat
author_sort Hanssen, Britta
collection PubMed
description Muscle weakness is a common clinical symptom in children with spastic cerebral palsy (SCP). It is caused by impaired neural ability and altered intrinsic capacity of the muscles. To define the contribution of decreased muscle size to muscle weakness, two cohorts were recruited in this cross-sectional investigation: 53 children with SCP [median age, 8.2 (IQR, 4.1) years, 19/34 uni/bilateral] and 31 children with a typical development (TD) [median age, 9.7 (IQR, 2.9) years]. Muscle volume (MV) and muscle belly length for m. rectus femoris, semitendinosus, gastrocnemius medialis, and tibialis anterior were defined from three-dimensional freehand ultrasound acquisitions. A fixed dynamometer was used to assess maximal voluntary isometric contractions for knee extension, knee flexion, plantar flexion, and dorsiflexion from which maximal joint torque (MJT) was calculated. Selective motor control (SMC) was assessed on a 5-point scale for the children with SCP. First, the anthropometrics, strength, and muscle size parameters were compared between the cohorts. Significant differences for all muscle size and strength parameters were found (p ≤ 0.003), except for joint torque per MV for the plantar flexors. Secondly, the associations of anthropometrics, muscle size, gross motor function classification system (GMFCS) level, and SMC with MJT were investigated using univariate and stepwise multiple linear regressions. The associations of MJT with growth-related parameters like age, weight, and height appeared strongest in the TD cohort, whereas for the SCP cohort, these associations were accompanied by associations with SMC and GMFCS. The stepwise regression models resulted in ranges of explained variance in MJT from 29.3 to 66.3% in the TD cohort and from 16.8 to 60.1% in the SCP cohort. Finally, the MJT deficit observed in the SCP cohort was further investigated using the TD regression equations to estimate norm MJT based on height and potential MJT based on MV. From the total MJT deficit, 22.6–57.3% could be explained by deficits in MV. This investigation confirmed the disproportional decrease in muscle size and muscle strength around the knee and ankle joint in children with SCP, but also highlighted the large variability in the contribution of muscle size to muscle weakness.
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spelling pubmed-83507762021-08-10 The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy Hanssen, Britta Peeters, Nicky Vandekerckhove, Ines De Beukelaer, Nathalie Bar-On, Lynn Molenaers, Guy Van Campenhout, Anja Degelaen, Marc Van den Broeck, Christine Calders, Patrick Desloovere, Kaat Front Neurol Neurology Muscle weakness is a common clinical symptom in children with spastic cerebral palsy (SCP). It is caused by impaired neural ability and altered intrinsic capacity of the muscles. To define the contribution of decreased muscle size to muscle weakness, two cohorts were recruited in this cross-sectional investigation: 53 children with SCP [median age, 8.2 (IQR, 4.1) years, 19/34 uni/bilateral] and 31 children with a typical development (TD) [median age, 9.7 (IQR, 2.9) years]. Muscle volume (MV) and muscle belly length for m. rectus femoris, semitendinosus, gastrocnemius medialis, and tibialis anterior were defined from three-dimensional freehand ultrasound acquisitions. A fixed dynamometer was used to assess maximal voluntary isometric contractions for knee extension, knee flexion, plantar flexion, and dorsiflexion from which maximal joint torque (MJT) was calculated. Selective motor control (SMC) was assessed on a 5-point scale for the children with SCP. First, the anthropometrics, strength, and muscle size parameters were compared between the cohorts. Significant differences for all muscle size and strength parameters were found (p ≤ 0.003), except for joint torque per MV for the plantar flexors. Secondly, the associations of anthropometrics, muscle size, gross motor function classification system (GMFCS) level, and SMC with MJT were investigated using univariate and stepwise multiple linear regressions. The associations of MJT with growth-related parameters like age, weight, and height appeared strongest in the TD cohort, whereas for the SCP cohort, these associations were accompanied by associations with SMC and GMFCS. The stepwise regression models resulted in ranges of explained variance in MJT from 29.3 to 66.3% in the TD cohort and from 16.8 to 60.1% in the SCP cohort. Finally, the MJT deficit observed in the SCP cohort was further investigated using the TD regression equations to estimate norm MJT based on height and potential MJT based on MV. From the total MJT deficit, 22.6–57.3% could be explained by deficits in MV. This investigation confirmed the disproportional decrease in muscle size and muscle strength around the knee and ankle joint in children with SCP, but also highlighted the large variability in the contribution of muscle size to muscle weakness. Frontiers Media S.A. 2021-07-26 /pmc/articles/PMC8350776/ /pubmed/34381414 http://dx.doi.org/10.3389/fneur.2021.692582 Text en Copyright © 2021 Hanssen, Peeters, Vandekerckhove, De Beukelaer, Bar-On, Molenaers, Van Campenhout, Degelaen, Van den Broeck, Calders and Desloovere. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Hanssen, Britta
Peeters, Nicky
Vandekerckhove, Ines
De Beukelaer, Nathalie
Bar-On, Lynn
Molenaers, Guy
Van Campenhout, Anja
Degelaen, Marc
Van den Broeck, Christine
Calders, Patrick
Desloovere, Kaat
The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title_full The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title_fullStr The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title_full_unstemmed The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title_short The Contribution of Decreased Muscle Size to Muscle Weakness in Children With Spastic Cerebral Palsy
title_sort contribution of decreased muscle size to muscle weakness in children with spastic cerebral palsy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350776/
https://www.ncbi.nlm.nih.gov/pubmed/34381414
http://dx.doi.org/10.3389/fneur.2021.692582
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