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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9407179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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