Literature DB >> 33892842

Therapeutic Approaches for Duchenne Muscular Dystrophy: Old and New.

Samuel J Mackenzie1, Stefan Nicolau2, Anne M Connolly3, Jerry R Mendell3.   

Abstract

Duchenne muscular dystrophy (DMD) is marked by pathogenic variants in the DMD gene, leading to reduced or absent dystrophin translation, muscle fiber destruction, loss of ambulation, cardiomyopathy, respiratory failure, and eventually death. Disease progression is slowed with use of prednisone or other corticosteroid agents. Gene replacement therapy, which is one of the focus points of this review, has emerged as the most promising potential treatment for DMD, though alternative RNA-based strategies have been employed for patients with specific pathogenic variants. While challenges remain, many of these novel therapeutic approaches hold promise for treating this devastating disease.
Copyright © 2021 Elsevier Inc. All rights reserved.

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Year:  2021        PMID: 33892842     DOI: 10.1016/j.spen.2021.100877

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  5 in total

Review 1.  Control of satellite cell function in muscle regeneration and its disruption in ageing.

Authors:  Pedro Sousa-Victor; Laura García-Prat; Pura Muñoz-Cánoves
Journal:  Nat Rev Mol Cell Biol       Date:  2021-10-18       Impact factor: 94.444

Review 2.  Histopathology of Duchenne muscular dystrophy in correlation with changes in proteomic biomarkers.

Authors:  Margit Zweyer; Hemmen Sabir; Paul Dowling; Stephen Gargan; Sandra Murphy; Dieter Swandulla; Kay Ohlendieck
Journal:  Histol Histopathol       Date:  2021-12-07       Impact factor: 2.303

3.  Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular Dystrophy.

Authors:  Nathalie Bourg; Ai Vu Hong; William Lostal; Abbass Jaber; Nicolas Guerchet; Guillaume Tanniou; Fanny Bordier; Emilie Bertil-Froidevaux; Christophe Georger; Nathalie Daniele; Isabelle Richard; David Israeli
Journal:  Int J Mol Sci       Date:  2022-02-11       Impact factor: 5.923

Review 4.  Molecular and cellular basis of genetically inherited skeletal muscle disorders.

Authors:  James J Dowling; Conrad C Weihl; Melissa J Spencer
Journal:  Nat Rev Mol Cell Biol       Date:  2021-07-13       Impact factor: 94.444

Review 5.  In vivo Gene Therapy to the Liver and Nervous System: Promises and Challenges.

Authors:  Alessio Cantore; Alessandro Fraldi; Vasco Meneghini; Angela Gritti
Journal:  Front Med (Lausanne)       Date:  2022-01-18
  5 in total

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