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Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients

INTRODUCTION: Muscle ultrasound is a fast, non-invasive and cost-effective examination that can identify structural muscular changes by assessing muscle thickness and echointensity (EI) with a quantitative analysis (QMUS). To assess applicability and repeatability of QMUS, we evaluated patients with...

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Autores principales: Fionda, Laura, Vanoli, Fiammetta, Di Pasquale, Antonella, Leonardi, Luca, Morino, Stefania, Merlonghi, Gioia, Lauletta, Antonio, Alfieri, Girolamo, Costanzo, Rocco, Tufano, Laura, Rossini, Elena, Bucci, Elisabetta, Grossi, Andrea, Tupler, Rossella, Salvetti, Marco, Garibaldi, Matteo, Antonini, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570177/
https://www.ncbi.nlm.nih.gov/pubmed/37311950
http://dx.doi.org/10.1007/s10072-023-06842-5
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author Fionda, Laura
Vanoli, Fiammetta
Di Pasquale, Antonella
Leonardi, Luca
Morino, Stefania
Merlonghi, Gioia
Lauletta, Antonio
Alfieri, Girolamo
Costanzo, Rocco
Tufano, Laura
Rossini, Elena
Bucci, Elisabetta
Grossi, Andrea
Tupler, Rossella
Salvetti, Marco
Garibaldi, Matteo
Antonini, Giovanni
author_facet Fionda, Laura
Vanoli, Fiammetta
Di Pasquale, Antonella
Leonardi, Luca
Morino, Stefania
Merlonghi, Gioia
Lauletta, Antonio
Alfieri, Girolamo
Costanzo, Rocco
Tufano, Laura
Rossini, Elena
Bucci, Elisabetta
Grossi, Andrea
Tupler, Rossella
Salvetti, Marco
Garibaldi, Matteo
Antonini, Giovanni
author_sort Fionda, Laura
collection PubMed
description INTRODUCTION: Muscle ultrasound is a fast, non-invasive and cost-effective examination that can identify structural muscular changes by assessing muscle thickness and echointensity (EI) with a quantitative analysis (QMUS). To assess applicability and repeatability of QMUS, we evaluated patients with genetically confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1), comparing their muscle ultrasound characteristics with healthy controls and with those detected by MRI. We also evaluated relationships between QMUS and demographic and clinical characteristics. MATERIALS AND METHODS: Thirteen patients were included in the study. Clinical assessment included MRC sum score, FSHD score and The Comprehensive Clinical Evaluation Form (CCEF). QMUS was performed with a linear transducer scanning bilaterally pectoralis major, deltoid, rectus femoris, tibialis anterior and semimembranosus muscles in patients and healthy subjects. For each muscle, we acquired three images, which were analysed calculating muscle EI by computer-assisted grey-scale analysis. QMUS analysis was compared with semiquantitative 1.5 T muscle MRI scale. RESULTS: All muscles in FSHD patients showed a significant increased echogenicity compared to the homologous muscles in healthy subjects. Older subjects and patients with higher FSHD score presented increased muscle EI. Tibialis anterior MRC showed a significant inverse correlation with EI. Higher median EI was found in muscles with more severe MRI fat replacement. CONCLUSIONS: QMUS allows quantitative evaluation of muscle echogenicity, displaying a tight correlation with muscular alterations, clinical and MRI data. Although a confirmation on larger sample is needed, our research suggests a possible future application of QMUS in diagnosis and management of muscular disorders.
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spelling pubmed-105701772023-10-14 Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients Fionda, Laura Vanoli, Fiammetta Di Pasquale, Antonella Leonardi, Luca Morino, Stefania Merlonghi, Gioia Lauletta, Antonio Alfieri, Girolamo Costanzo, Rocco Tufano, Laura Rossini, Elena Bucci, Elisabetta Grossi, Andrea Tupler, Rossella Salvetti, Marco Garibaldi, Matteo Antonini, Giovanni Neurol Sci Original Article INTRODUCTION: Muscle ultrasound is a fast, non-invasive and cost-effective examination that can identify structural muscular changes by assessing muscle thickness and echointensity (EI) with a quantitative analysis (QMUS). To assess applicability and repeatability of QMUS, we evaluated patients with genetically confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1), comparing their muscle ultrasound characteristics with healthy controls and with those detected by MRI. We also evaluated relationships between QMUS and demographic and clinical characteristics. MATERIALS AND METHODS: Thirteen patients were included in the study. Clinical assessment included MRC sum score, FSHD score and The Comprehensive Clinical Evaluation Form (CCEF). QMUS was performed with a linear transducer scanning bilaterally pectoralis major, deltoid, rectus femoris, tibialis anterior and semimembranosus muscles in patients and healthy subjects. For each muscle, we acquired three images, which were analysed calculating muscle EI by computer-assisted grey-scale analysis. QMUS analysis was compared with semiquantitative 1.5 T muscle MRI scale. RESULTS: All muscles in FSHD patients showed a significant increased echogenicity compared to the homologous muscles in healthy subjects. Older subjects and patients with higher FSHD score presented increased muscle EI. Tibialis anterior MRC showed a significant inverse correlation with EI. Higher median EI was found in muscles with more severe MRI fat replacement. CONCLUSIONS: QMUS allows quantitative evaluation of muscle echogenicity, displaying a tight correlation with muscular alterations, clinical and MRI data. Although a confirmation on larger sample is needed, our research suggests a possible future application of QMUS in diagnosis and management of muscular disorders. Springer International Publishing 2023-06-14 2023 /pmc/articles/PMC10570177/ /pubmed/37311950 http://dx.doi.org/10.1007/s10072-023-06842-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Fionda, Laura
Vanoli, Fiammetta
Di Pasquale, Antonella
Leonardi, Luca
Morino, Stefania
Merlonghi, Gioia
Lauletta, Antonio
Alfieri, Girolamo
Costanzo, Rocco
Tufano, Laura
Rossini, Elena
Bucci, Elisabetta
Grossi, Andrea
Tupler, Rossella
Salvetti, Marco
Garibaldi, Matteo
Antonini, Giovanni
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title_full Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title_fullStr Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title_full_unstemmed Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title_short Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients
title_sort comparison of quantitative muscle ultrasound and whole-body muscle mri in facioscapulohumeral muscular dystrophy type 1 patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570177/
https://www.ncbi.nlm.nih.gov/pubmed/37311950
http://dx.doi.org/10.1007/s10072-023-06842-5
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