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Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies

INTRODUCTION/AIMS: Duchenne and Becker muscular dystrophies (DMD and BMD, respectively) are characterized by fat replacement of different skeletal muscles in a specific temporal order. Given the structural role of dystrophin in skeletal muscle mechanics, muscle architecture could be important in the...

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Autores principales: Veeger, Thom T. J., van Zwet, Erik W., al Mohamad, Diaa, Naarding, Karin J., van de Velde, Nienke M., Hooijmans, Melissa T., Webb, Andrew G., Niks, Erik H., de Groot, Jurriaan H., Kan, Hermien E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290788/
https://www.ncbi.nlm.nih.gov/pubmed/34383334
http://dx.doi.org/10.1002/mus.27399
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author Veeger, Thom T. J.
van Zwet, Erik W.
al Mohamad, Diaa
Naarding, Karin J.
van de Velde, Nienke M.
Hooijmans, Melissa T.
Webb, Andrew G.
Niks, Erik H.
de Groot, Jurriaan H.
Kan, Hermien E.
author_facet Veeger, Thom T. J.
van Zwet, Erik W.
al Mohamad, Diaa
Naarding, Karin J.
van de Velde, Nienke M.
Hooijmans, Melissa T.
Webb, Andrew G.
Niks, Erik H.
de Groot, Jurriaan H.
Kan, Hermien E.
author_sort Veeger, Thom T. J.
collection PubMed
description INTRODUCTION/AIMS: Duchenne and Becker muscular dystrophies (DMD and BMD, respectively) are characterized by fat replacement of different skeletal muscles in a specific temporal order. Given the structural role of dystrophin in skeletal muscle mechanics, muscle architecture could be important in the progressive pathophysiology of muscle degeneration. Therefore, the aim of this study was to assess the role of muscle architecture in the progression of fat replacement in DMD and BMD. METHODS: We assessed the association between literature‐based leg muscle architectural characteristics and muscle fat fraction from 22 DMD and 24 BMD patients. Dixon‐based magnetic resonance imaging estimates of fat fractions at baseline and 12 (only DMD) and 24 months were related to fiber length and physiological cross‐sectional area (PCSA) using age‐controlled linear mixed modeling. RESULTS: DMD and BMD muscles with long fibers and BMD muscles with large PCSAs were associated with increased fat fraction. The effect of fiber length was stronger in muscles with larger PCSA. DISCUSSION: Muscle architecture may explain the pathophysiology of muscle degeneration in dystrophinopathies, in which proximal muscles with a larger mass (fiber length × PCSA) are more susceptible, confirming the clinical observation of a temporal proximal‐to‐distal progression. These results give more insight into the mechanical role in the pathophysiology of muscular dystrophies. Ultimately, this new information can be used to help support the selection of current and the development of future therapies.
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spelling pubmed-92907882022-07-20 Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies Veeger, Thom T. J. van Zwet, Erik W. al Mohamad, Diaa Naarding, Karin J. van de Velde, Nienke M. Hooijmans, Melissa T. Webb, Andrew G. Niks, Erik H. de Groot, Jurriaan H. Kan, Hermien E. Muscle Nerve Clinical Research Articles INTRODUCTION/AIMS: Duchenne and Becker muscular dystrophies (DMD and BMD, respectively) are characterized by fat replacement of different skeletal muscles in a specific temporal order. Given the structural role of dystrophin in skeletal muscle mechanics, muscle architecture could be important in the progressive pathophysiology of muscle degeneration. Therefore, the aim of this study was to assess the role of muscle architecture in the progression of fat replacement in DMD and BMD. METHODS: We assessed the association between literature‐based leg muscle architectural characteristics and muscle fat fraction from 22 DMD and 24 BMD patients. Dixon‐based magnetic resonance imaging estimates of fat fractions at baseline and 12 (only DMD) and 24 months were related to fiber length and physiological cross‐sectional area (PCSA) using age‐controlled linear mixed modeling. RESULTS: DMD and BMD muscles with long fibers and BMD muscles with large PCSAs were associated with increased fat fraction. The effect of fiber length was stronger in muscles with larger PCSA. DISCUSSION: Muscle architecture may explain the pathophysiology of muscle degeneration in dystrophinopathies, in which proximal muscles with a larger mass (fiber length × PCSA) are more susceptible, confirming the clinical observation of a temporal proximal‐to‐distal progression. These results give more insight into the mechanical role in the pathophysiology of muscular dystrophies. Ultimately, this new information can be used to help support the selection of current and the development of future therapies. John Wiley & Sons, Inc. 2021-08-25 2021-11 /pmc/articles/PMC9290788/ /pubmed/34383334 http://dx.doi.org/10.1002/mus.27399 Text en © 2021 The Authors. Muscle & Nerve published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Clinical Research Articles
Veeger, Thom T. J.
van Zwet, Erik W.
al Mohamad, Diaa
Naarding, Karin J.
van de Velde, Nienke M.
Hooijmans, Melissa T.
Webb, Andrew G.
Niks, Erik H.
de Groot, Jurriaan H.
Kan, Hermien E.
Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title_full Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title_fullStr Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title_full_unstemmed Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title_short Muscle architecture is associated with muscle fat replacement in Duchenne and Becker muscular dystrophies
title_sort muscle architecture is associated with muscle fat replacement in duchenne and becker muscular dystrophies
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290788/
https://www.ncbi.nlm.nih.gov/pubmed/34383334
http://dx.doi.org/10.1002/mus.27399
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