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A well‐tolerated core needle muscle biopsy process suitable for children and adults
Serial muscle biopsies within clinical trials for Duchenne muscular dystrophy (DMD) are critical to document therapeutic responses. Less invasive means of sampling muscle are needed. We analyzed a retrospective consecutive case‐series cohort of vacuum‐assisted core needle muscle biopsy procedures pe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756388/ https://www.ncbi.nlm.nih.gov/pubmed/32820569 http://dx.doi.org/10.1002/mus.27041 |
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author | Barthelemy, Florian Woods, Jeremy D. Nieves‐Rodriguez, Shirley Douine, Emilie D. Wang, Richard Wanagat, Jonathan Miceli, M. Carrie Nelson, Stanley F. |
author_facet | Barthelemy, Florian Woods, Jeremy D. Nieves‐Rodriguez, Shirley Douine, Emilie D. Wang, Richard Wanagat, Jonathan Miceli, M. Carrie Nelson, Stanley F. |
author_sort | Barthelemy, Florian |
collection | PubMed |
description | Serial muscle biopsies within clinical trials for Duchenne muscular dystrophy (DMD) are critical to document therapeutic responses. Less invasive means of sampling muscle are needed. We analyzed a retrospective consecutive case‐series cohort of vacuum‐assisted core needle muscle biopsy procedures performed on healthy and dystrophic individuals at a single institution assessing for safety and reliability of obtaining sufficient high‐quality biopsy tissue for histologic assessment in adult and pediatric subjects. Of 471 muscle cores from 128 biopsy procedures, 377‐550 mg of total muscle tissue was obtained per procedure with mean core weight of 129 mg (SD, 25.1 mg). All biopsies were adequate for histological assessment. There were no significant adverse events. This core needle biopsy approach, when combined with improved sample processing, provides a safe means to consistently obtain muscle samples for diagnostic and clinical trial applications. |
format | Online Article Text |
id | pubmed-7756388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77563882020-12-28 A well‐tolerated core needle muscle biopsy process suitable for children and adults Barthelemy, Florian Woods, Jeremy D. Nieves‐Rodriguez, Shirley Douine, Emilie D. Wang, Richard Wanagat, Jonathan Miceli, M. Carrie Nelson, Stanley F. Muscle Nerve Clinical Research Articles Serial muscle biopsies within clinical trials for Duchenne muscular dystrophy (DMD) are critical to document therapeutic responses. Less invasive means of sampling muscle are needed. We analyzed a retrospective consecutive case‐series cohort of vacuum‐assisted core needle muscle biopsy procedures performed on healthy and dystrophic individuals at a single institution assessing for safety and reliability of obtaining sufficient high‐quality biopsy tissue for histologic assessment in adult and pediatric subjects. Of 471 muscle cores from 128 biopsy procedures, 377‐550 mg of total muscle tissue was obtained per procedure with mean core weight of 129 mg (SD, 25.1 mg). All biopsies were adequate for histological assessment. There were no significant adverse events. This core needle biopsy approach, when combined with improved sample processing, provides a safe means to consistently obtain muscle samples for diagnostic and clinical trial applications. John Wiley & Sons, Inc. 2020-09-20 2020-12 /pmc/articles/PMC7756388/ /pubmed/32820569 http://dx.doi.org/10.1002/mus.27041 Text en © 2020 The Authors. Muscle & Nerve published by Wiley Periodicals LLC. This is an open access article under the terms of the http://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 Barthelemy, Florian Woods, Jeremy D. Nieves‐Rodriguez, Shirley Douine, Emilie D. Wang, Richard Wanagat, Jonathan Miceli, M. Carrie Nelson, Stanley F. A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title | A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title_full | A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title_fullStr | A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title_full_unstemmed | A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title_short | A well‐tolerated core needle muscle biopsy process suitable for children and adults |
title_sort | well‐tolerated core needle muscle biopsy process suitable for children and adults |
topic | Clinical Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756388/ https://www.ncbi.nlm.nih.gov/pubmed/32820569 http://dx.doi.org/10.1002/mus.27041 |
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