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Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments

INTRODUCTION/AIMS: Becker muscular dystrophy (BMD) is characterized by variable disease severity and progression, prompting the identification of biomarkers for clinical trials. We used data from an ongoing phase II study to provide a comprehensive characterization of a cohort of patients with BMD,...

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Autores principales: Comi, Giacomo P., Niks, Erik H., Cinnante, Claudia M., Kan, Hermien E., Vandenborne, Krista, Willcocks, Rebecca J., Velardo, Daniele, Ripolone, Michela, van Benthem, Jules J., van de Velde, Nienke M., Nava, Simone, Ambrosoli, Laura, Cazzaniga, Sara, Bettica, Paolo U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302983/
https://www.ncbi.nlm.nih.gov/pubmed/34918368
http://dx.doi.org/10.1002/mus.27475
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author Comi, Giacomo P.
Niks, Erik H.
Cinnante, Claudia M.
Kan, Hermien E.
Vandenborne, Krista
Willcocks, Rebecca J.
Velardo, Daniele
Ripolone, Michela
van Benthem, Jules J.
van de Velde, Nienke M.
Nava, Simone
Ambrosoli, Laura
Cazzaniga, Sara
Bettica, Paolo U.
author_facet Comi, Giacomo P.
Niks, Erik H.
Cinnante, Claudia M.
Kan, Hermien E.
Vandenborne, Krista
Willcocks, Rebecca J.
Velardo, Daniele
Ripolone, Michela
van Benthem, Jules J.
van de Velde, Nienke M.
Nava, Simone
Ambrosoli, Laura
Cazzaniga, Sara
Bettica, Paolo U.
author_sort Comi, Giacomo P.
collection PubMed
description INTRODUCTION/AIMS: Becker muscular dystrophy (BMD) is characterized by variable disease severity and progression, prompting the identification of biomarkers for clinical trials. We used data from an ongoing phase II study to provide a comprehensive characterization of a cohort of patients with BMD, and to assess correlations between histological and magnetic resonance imaging (MRI) markers with muscle function and strength. METHODS: Eligible patients were ambulatory males with BMD, aged 18 to 65 years (200 to 450 meters on 6‐minute walk test). The following data were obtained: function test results, strength, fat‐fraction quantification using chemical shift‐encoded MRI (whole thigh and quadriceps), and fibrosis and muscle fiber area (MFA) of the brachial biceps. RESULTS: Of 70 patients screened, 51 entered the study. There was substantial heterogeneity between patients in muscle morphology (histology and MRI), with high fat replacement. Total fibrosis correlated significantly and mostly moderately with all functional endpoints, including both upper arm strength assessments (left and right elbow flexion rho −.574 and −.588, respectively [both P < .0001]), as did MRI fat fraction (whole thigh and quadriceps), for example, with four‐stair‐climb velocity −.554 and −.550, respectively (both P < .0001). Total fibrosis correlated significantly and moderately with both MRI fat fraction assessments (.500 [P = .0003] and .423 [.0024], respectively). DISCUSSION: In this BMD cohort, micro‐ and macroscopic morphological muscle parameters correlated moderately with each other and with functional parameters, potentially supporting the use of MRI fat fraction and histology as surrogate outcome measures in patients with BMD, although additional research is required to validate this.
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spelling pubmed-93029832022-07-22 Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments Comi, Giacomo P. Niks, Erik H. Cinnante, Claudia M. Kan, Hermien E. Vandenborne, Krista Willcocks, Rebecca J. Velardo, Daniele Ripolone, Michela van Benthem, Jules J. van de Velde, Nienke M. Nava, Simone Ambrosoli, Laura Cazzaniga, Sara Bettica, Paolo U. Muscle Nerve Clinical Research Articles INTRODUCTION/AIMS: Becker muscular dystrophy (BMD) is characterized by variable disease severity and progression, prompting the identification of biomarkers for clinical trials. We used data from an ongoing phase II study to provide a comprehensive characterization of a cohort of patients with BMD, and to assess correlations between histological and magnetic resonance imaging (MRI) markers with muscle function and strength. METHODS: Eligible patients were ambulatory males with BMD, aged 18 to 65 years (200 to 450 meters on 6‐minute walk test). The following data were obtained: function test results, strength, fat‐fraction quantification using chemical shift‐encoded MRI (whole thigh and quadriceps), and fibrosis and muscle fiber area (MFA) of the brachial biceps. RESULTS: Of 70 patients screened, 51 entered the study. There was substantial heterogeneity between patients in muscle morphology (histology and MRI), with high fat replacement. Total fibrosis correlated significantly and mostly moderately with all functional endpoints, including both upper arm strength assessments (left and right elbow flexion rho −.574 and −.588, respectively [both P < .0001]), as did MRI fat fraction (whole thigh and quadriceps), for example, with four‐stair‐climb velocity −.554 and −.550, respectively (both P < .0001). Total fibrosis correlated significantly and moderately with both MRI fat fraction assessments (.500 [P = .0003] and .423 [.0024], respectively). DISCUSSION: In this BMD cohort, micro‐ and macroscopic morphological muscle parameters correlated moderately with each other and with functional parameters, potentially supporting the use of MRI fat fraction and histology as surrogate outcome measures in patients with BMD, although additional research is required to validate this. John Wiley & Sons, Inc. 2021-12-30 2022-03 /pmc/articles/PMC9302983/ /pubmed/34918368 http://dx.doi.org/10.1002/mus.27475 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
Comi, Giacomo P.
Niks, Erik H.
Cinnante, Claudia M.
Kan, Hermien E.
Vandenborne, Krista
Willcocks, Rebecca J.
Velardo, Daniele
Ripolone, Michela
van Benthem, Jules J.
van de Velde, Nienke M.
Nava, Simone
Ambrosoli, Laura
Cazzaniga, Sara
Bettica, Paolo U.
Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title_full Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title_fullStr Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title_full_unstemmed Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title_short Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
title_sort characterization of patients with becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302983/
https://www.ncbi.nlm.nih.gov/pubmed/34918368
http://dx.doi.org/10.1002/mus.27475
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