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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...

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Detalles Bibliográficos
Autores principales: Barthelemy, Florian, Woods, Jeremy D., Nieves‐Rodriguez, Shirley, Douine, Emilie D., Wang, Richard, Wanagat, Jonathan, Miceli, M. Carrie, Nelson, Stanley F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
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
Descripción
Sumario: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.