Literature DB >> 8289083

Corticosteroid therapy in Duchenne muscular dystrophy.

M A Khan1.   

Abstract

In recent years, various clinical trials have documented the benefit of glucocorticoid therapy in the palliation of Duchenne muscular dystrophy (DMD). Prednisone therapy, daily or on alternate days, has been confirmed to be of value in enhancing muscle strength and function in DMD for up to two years. However, there is evidence that corticosteroid treatment results in muscle weakness and degeneration. This review, therefore, examines the available studies and addresses various possible mechanisms involved in the efficacy of prednisone therapy and amelioration of DMD. The progression of DMD is known to be associated with profound changes in structure, biochemistry and physiology of the affected muscles. It is hypothesized, therefore, that these very changes offer a fortunate set of circumstances, and it is owing to these alterations, as well as the well known anti-inflammatory/immunosuppressive action of steroid, that muscles in DMD are rendered responsive resulting in significant improvement of muscle bulk and function.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8289083     DOI: 10.1016/0022-510x(93)90017-s

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  10 in total

1.  Prednisolone treatment does not interfere with 2'-O-methyl phosphorothioate antisense-mediated exon skipping in Duchenne muscular dystrophy.

Authors:  Ingrid E C Verhaart; Hans Heemskerk; Tatyana G Karnaoukh; Ingrid G M Kolfschoten; Anne Vroon; Gert-Jan B van Ommen; Judith C T van Deutekom; Annemieke Aartsma-Rus
Journal:  Hum Gene Ther       Date:  2012-01-26       Impact factor: 5.695

2.  Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress.

Authors:  W J Leijendekker; A C Passaquin; L Metzinger; U T Rüegg
Journal:  Br J Pharmacol       Date:  1996-06       Impact factor: 8.739

3.  Prednisone can protect against exercise-induced muscle damage.

Authors:  S C Jacobs; A L Bootsma; P W Willems; P R Bär; J H Wokke
Journal:  J Neurol       Date:  1996-05       Impact factor: 4.849

4.  Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein.

Authors:  A O Gramolini; L M Angus; L Schaeffer; E A Burton; J M Tinsley; K E Davies; J P Changeux; B J Jasmin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

5.  Glucocorticoid-induced leucine zipper (GILZ) and long GILZ inhibit myogenic differentiation and mediate anti-myogenic effects of glucocorticoids.

Authors:  Stefano Bruscoli; Valerio Donato; Enrico Velardi; Moises Di Sante; Graziella Migliorati; Rosario Donato; Carlo Riccardi
Journal:  J Biol Chem       Date:  2010-02-02       Impact factor: 5.157

6.  Bone mineral density and bone metabolism in Duchenne muscular dystrophy.

Authors:  M L Bianchi; A Mazzanti; E Galbiati; S Saraifoger; A Dubini; F Cornelio; L Morandi
Journal:  Osteoporos Int       Date:  2003-07-29       Impact factor: 4.507

7.  Modulation by prednisolone of calcium handling in skeletal muscle cells.

Authors:  L Metzinger; A C Passaquin; W J Leijendekker; P Poindron; U T Rüegg
Journal:  Br J Pharmacol       Date:  1995-12       Impact factor: 8.739

8.  The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy.

Authors:  D M Bonifati; S F Witchel; M Ermani; E P Hoffman; C Angelini; E Pegoraro
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-10       Impact factor: 10.154

Review 9.  Influence of immune responses in gene/stem cell therapies for muscular dystrophies.

Authors:  Andrea Farini; Clementina Sitzia; Silvia Erratico; Mirella Meregalli; Yvan Torrente
Journal:  Biomed Res Int       Date:  2014-05-19       Impact factor: 3.411

Review 10.  Teaching an Old Molecule New Tricks: Drug Repositioning for Duchenne Muscular Dystrophy.

Authors:  Libero Vitiello; Lucia Tibaudo; Elena Pegoraro; Luca Bello; Marcella Canton
Journal:  Int J Mol Sci       Date:  2019-11-30       Impact factor: 5.923

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.