Literature DB >> 22392111

Motor function measure scale, steroid therapy and patients with Duchenne muscular dystrophy.

Elaine C da Silva1, Darlene L Machado, Maria B D Resende, Renata F Silva, Edmar Zanoteli, Umbertina C Reed.   

Abstract

OBJECTIVE: To assess the evolution of motor function in patients with Duchenne muscular dystrophy (DMD) treated with steroids (prednisolone or deflazacort) through the Motor Function Measure (MFM), which evaluates three dimensions of motor performance (D1, D2, D3).
METHODS: Thirty-three patients with DMD (22 ambulant, 6 non-ambulant and 5 who lost the capacity to walk during the period of the study) were assessed using the MFM scale six times over a period of 18 months.
RESULTS: All the motor functions remained stable for 14 months in all patients, except D1 for those who lost their walking ability. In ambulant patients, D2 (axial and proximal motor capacities) motor functions improved during six months; an improvement in D3 (distal motor capacity) was noted during the total follow-up. D1 (standing posture and transfers) and total score were useful to predict the loss of the ability to walk.
CONCLUSIONS: The use of the MFM in DMD patients confirms the benefits of the steroid treatment for slowing the progression of the disease.

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Year:  2012        PMID: 22392111     DOI: 10.1590/s0004-282x2012000300007

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  4 in total

1.  Relationship between the climbing up and climbing down stairs domain scores on the FES-DMD, the score on the Vignos Scale, age and timed performance of functional activities in boys with Duchenne muscular dystrophy.

Authors:  Lilian A Y Fernandes; Fátima A Caromano; Silvana M B Assis; Michele E Hukuda; Mariana C Voos; Eduardo V Carvalho
Journal:  Braz J Phys Ther       Date:  2014 Nov-Dec       Impact factor: 3.377

2.  Resveratrol improves motor function in patients with muscular dystrophies: an open-label, single-arm, phase IIa study.

Authors:  Kentaro Kawamura; Shinobu Fukumura; Koki Nikaido; Nobutada Tachi; Naoki Kozuka; Tsugumi Seino; Kingya Hatakeyama; Mitsuru Mori; Yoichi M Ito; Akiyoshi Takami; Shiro Hinotsu; Atsushi Kuno; Yukihiko Kawasaki; Yoshiyuki Horio; Hiroyuki Tsutsumi
Journal:  Sci Rep       Date:  2020-11-25       Impact factor: 4.379

3.  Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy.

Authors:  Charlotte Lilien; Harmen Reyngoudt; Andreea Mihaela Seferian; Teresa Gidaro; Mélanie Annoussamy; Virginie Chê; Valérie Decostre; Isabelle Ledoux; Julien Le Louër; Eric Guemas; Francesco Muntoni; Jean-Yves Hogrel; Pierre Georges Carlier; Laurent Servais
Journal:  Ann Clin Transl Neurol       Date:  2021-08-28       Impact factor: 4.511

4.  Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study.

Authors:  Patricia Hafner; Ulrike Bonati; Beat Erne; Maurice Schmid; Daniela Rubino; Urs Pohlman; Thomas Peters; Erich Rutz; Stephan Frank; Cornelia Neuhaus; Stefanie Deuster; Monika Gloor; Oliver Bieri; Arne Fischmann; Michael Sinnreich; Nuri Gueven; Dirk Fischer
Journal:  PLoS One       Date:  2016-01-22       Impact factor: 3.240

  4 in total

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