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A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice

Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy, typically affecting males in infancy. The disease causes progressive weakness and atrophy of skeletal muscles, with approximately 20,000 new cases diagnosed yearly. Currently, methods for diagnosing DMD are invasive, la...

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Autores principales: Ralbovsky, Nicole M., Dey, Paromita, Galfano, Andrew, Dey, Bijan K., Lednev, Igor K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407179/
https://www.ncbi.nlm.nih.gov/pubmed/36011258
http://dx.doi.org/10.3390/genes13081342
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author Ralbovsky, Nicole M.
Dey, Paromita
Galfano, Andrew
Dey, Bijan K.
Lednev, Igor K.
author_facet Ralbovsky, Nicole M.
Dey, Paromita
Galfano, Andrew
Dey, Bijan K.
Lednev, Igor K.
author_sort Ralbovsky, Nicole M.
collection PubMed
description Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy, typically affecting males in infancy. The disease causes progressive weakness and atrophy of skeletal muscles, with approximately 20,000 new cases diagnosed yearly. Currently, methods for diagnosing DMD are invasive, laborious, and unable to make accurate early detections. While there is no cure for DMD, there are limited treatments available for managing symptoms. As such, there is a crucial unmet need to develop a simple and non-invasive method for accurately detecting DMD as early as possible. Raman spectroscopy with chemometric analysis is shown to have the potential to fill this diagnostic need.
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spelling pubmed-94071792022-08-26 A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice Ralbovsky, Nicole M. Dey, Paromita Galfano, Andrew Dey, Bijan K. Lednev, Igor K. Genes (Basel) Protocol Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy, typically affecting males in infancy. The disease causes progressive weakness and atrophy of skeletal muscles, with approximately 20,000 new cases diagnosed yearly. Currently, methods for diagnosing DMD are invasive, laborious, and unable to make accurate early detections. While there is no cure for DMD, there are limited treatments available for managing symptoms. As such, there is a crucial unmet need to develop a simple and non-invasive method for accurately detecting DMD as early as possible. Raman spectroscopy with chemometric analysis is shown to have the potential to fill this diagnostic need. MDPI 2022-07-27 /pmc/articles/PMC9407179/ /pubmed/36011258 http://dx.doi.org/10.3390/genes13081342 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Ralbovsky, Nicole M.
Dey, Paromita
Galfano, Andrew
Dey, Bijan K.
Lednev, Igor K.
A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title_full A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title_fullStr A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title_full_unstemmed A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title_short A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice
title_sort novel method for detecting duchenne muscular dystrophy in blood serum of mdx mice
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407179/
https://www.ncbi.nlm.nih.gov/pubmed/36011258
http://dx.doi.org/10.3390/genes13081342
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