Cargando…
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy
Becker muscular dystrophy (BMD) is a severe X-linked muscle disease. Age of onset, clinical variability, speed of progression and affected tissues display wide variability, making a clinical trial design for drug development very complex. The histopathological changes in skeletal muscle tissue are c...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994373/ https://www.ncbi.nlm.nih.gov/pubmed/35395784 http://dx.doi.org/10.1186/s40478-022-01354-3 |
_version_ | 1784684094570889216 |
---|---|
author | Ripolone, Michela Velardo, Daniele Mondello, Stefania Zanotti, Simona Magri, Francesca Minuti, Elisa Cazzaniga, Sara Fortunato, Francesco Ciscato, Patrizia Tiberio, Francesca Sciacco, Monica Moggio, Maurizio Bettica, Paolo Comi, Giacomo P. |
author_facet | Ripolone, Michela Velardo, Daniele Mondello, Stefania Zanotti, Simona Magri, Francesca Minuti, Elisa Cazzaniga, Sara Fortunato, Francesco Ciscato, Patrizia Tiberio, Francesca Sciacco, Monica Moggio, Maurizio Bettica, Paolo Comi, Giacomo P. |
author_sort | Ripolone, Michela |
collection | PubMed |
description | Becker muscular dystrophy (BMD) is a severe X-linked muscle disease. Age of onset, clinical variability, speed of progression and affected tissues display wide variability, making a clinical trial design for drug development very complex. The histopathological changes in skeletal muscle tissue are central to the pathogenesis, but they have not been thoroughly elucidated yet. Here we analysed muscle biopsies from a large cohort of BMD patients, focusing our attention on the histopathological muscle parameters, as fibrosis, fatty replacement, fibre cross sectional area, necrosis, regenerating fibres, splitting fibres, internalized nuclei and dystrophy evaluation. We correlated histological parameters with both demographic features and clinical functional evaluations. The most interesting results of our study are the accurate quantification of fibroadipose tissue replacement and the identification of some histopathological aspects that well correlate with clinical performances. Through correlation analysis, we divided our patients into three clusters with well-defined histological and clinical features. In conclusion, this is the first study that analyses in detail the histological characteristics of muscle biopsies in a large cohort of BMD patients, correlating them to a functional impairment. The collection of these data help to better understand the histopathological progression of the disease and can be useful to validate any pharmacological trial in which the modification of muscle biopsy is utilized as outcome measure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-022-01354-3. |
format | Online Article Text |
id | pubmed-8994373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89943732022-04-10 Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy Ripolone, Michela Velardo, Daniele Mondello, Stefania Zanotti, Simona Magri, Francesca Minuti, Elisa Cazzaniga, Sara Fortunato, Francesco Ciscato, Patrizia Tiberio, Francesca Sciacco, Monica Moggio, Maurizio Bettica, Paolo Comi, Giacomo P. Acta Neuropathol Commun Research Becker muscular dystrophy (BMD) is a severe X-linked muscle disease. Age of onset, clinical variability, speed of progression and affected tissues display wide variability, making a clinical trial design for drug development very complex. The histopathological changes in skeletal muscle tissue are central to the pathogenesis, but they have not been thoroughly elucidated yet. Here we analysed muscle biopsies from a large cohort of BMD patients, focusing our attention on the histopathological muscle parameters, as fibrosis, fatty replacement, fibre cross sectional area, necrosis, regenerating fibres, splitting fibres, internalized nuclei and dystrophy evaluation. We correlated histological parameters with both demographic features and clinical functional evaluations. The most interesting results of our study are the accurate quantification of fibroadipose tissue replacement and the identification of some histopathological aspects that well correlate with clinical performances. Through correlation analysis, we divided our patients into three clusters with well-defined histological and clinical features. In conclusion, this is the first study that analyses in detail the histological characteristics of muscle biopsies in a large cohort of BMD patients, correlating them to a functional impairment. The collection of these data help to better understand the histopathological progression of the disease and can be useful to validate any pharmacological trial in which the modification of muscle biopsy is utilized as outcome measure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-022-01354-3. BioMed Central 2022-04-08 /pmc/articles/PMC8994373/ /pubmed/35395784 http://dx.doi.org/10.1186/s40478-022-01354-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ripolone, Michela Velardo, Daniele Mondello, Stefania Zanotti, Simona Magri, Francesca Minuti, Elisa Cazzaniga, Sara Fortunato, Francesco Ciscato, Patrizia Tiberio, Francesca Sciacco, Monica Moggio, Maurizio Bettica, Paolo Comi, Giacomo P. Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title | Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title_full | Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title_fullStr | Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title_full_unstemmed | Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title_short | Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy |
title_sort | muscle histological changes in a large cohort of patients affected with becker muscular dystrophy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994373/ https://www.ncbi.nlm.nih.gov/pubmed/35395784 http://dx.doi.org/10.1186/s40478-022-01354-3 |
work_keys_str_mv | AT ripolonemichela musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT velardodaniele musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT mondellostefania musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT zanottisimona musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT magrifrancesca musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT minutielisa musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT cazzanigasara musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT fortunatofrancesco musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT ciscatopatrizia musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT tiberiofrancesca musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT sciaccomonica musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT moggiomaurizio musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT betticapaolo musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy AT comigiacomop musclehistologicalchangesinalargecohortofpatientsaffectedwithbeckermusculardystrophy |