Literature DB >> 21049175

Comparison of motor strength and function in patients with Duchenne muscular dystrophy with or without steroid therapy.

Samara Lamounier Santana Parreira1, Maria Bernadete Dutra Resende, Edmar Zanoteli, Mary Souza Carvalho, Suely Kazue Marie, Umbertina Conti Reed.   

Abstract

OBJECTIVE: To compare muscle strength (MS) and motor function in patients with Duchenne muscular dystrophy (DMD) receiving steroids for different times against the natural evolution of DMD described by Scott et al.
METHOD: 90 patients with DMD (aged 5- 12 years), receiving steroids for one to seven years, were evaluated by Medical Research Council Scale (MRC) and Hammersmith motor ability score. The relation between MS and motor abilities measurement from our data and Scott's ones were ascertained statistically.
RESULTS: The relation between patient's age and Hammersmith scores revealed decrease of 0.76 point per year for age against decrease of 2.23 points on Scott's study. The relation between MRC scale and patient's age showed decrease of 0.80 point per year of age against decrease of 3.65 points on Scott's study.
CONCLUSION: In patients with DMD aged five to 12 years the progression of the disease is delayed by steroids and the motor function is less reduced than muscular strength.

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Year:  2010        PMID: 21049175     DOI: 10.1590/s0004-282x2010000500002

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


  10 in total

1.  Domains of Daily Physical Activity in Children with Mitochondrial Disease: A 3D Accelerometry Approach.

Authors:  Saskia Koene; Ilse Dirks; Esmee van Mierlo; Pascal R de Vries; Anjo J W M Janssen; Jan A M Smeitink; Arjen Bergsma; Hans Essers; Kenneth Meijer; Imelda J M de Groot
Journal:  JIMD Rep       Date:  2017-01-17

2.  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

3.  International Paediatric Mitochondrial Disease Scale.

Authors:  Saskia Koene; Jan C M Hendriks; Ilse Dirks; Lonneke de Boer; Maaike C de Vries; Mirian C H Janssen; Izelle Smuts; Cheuk-Wing Fung; Virginia C N Wong; I René F M de Coo; Katharina Vill; Claudia Stendel; Thomas Klopstock; Marni J Falk; Elizabeth M McCormick; Robert McFarland; Imelda J M de Groot; Jan A M Smeitink
Journal:  J Inherit Metab Dis       Date:  2016-06-09       Impact factor: 4.982

4.  One in five patients with Duchenne muscular dystrophy dies from other causes than cardiac or respiratory failure.

Authors:  Lisa Wahlgren; Anna-Karin Kroksmark; Mar Tulinius; Kalliopi Sofou
Journal:  Eur J Epidemiol       Date:  2021-11-21       Impact factor: 8.082

5.  Lung function monitoring in patients with duchenne muscular dystrophy on steroid therapy.

Authors:  Darlene L Machado; Elaine C Silva; Maria B D Resende; Celso R F Carvalho; Edmar Zanoteli; Umbertina C Reed
Journal:  BMC Res Notes       Date:  2012-08-13

6.  Improving clinical trial design for Duchenne muscular dystrophy.

Authors:  Luciano Merlini; Patrizia Sabatelli
Journal:  BMC Neurol       Date:  2015-08-26       Impact factor: 2.474

7.  Early myocardial damage assessment in dystrophinopathies using (99)Tc(m)-MIBI gated myocardial perfusion imaging.

Authors:  Li Zhang; Zhe Liu; Ke-You Hu; Qing-Bao Tian; Ling-Ge Wei; Zhe Zhao; Hong-Rui Shen; Jing Hu
Journal:  Ther Clin Risk Manag       Date:  2015-12-10       Impact factor: 2.423

8.  Responsiveness of the domain climbing up and going down stairs of the Functional Evaluation scale for Duchenne Muscular Dystrophy: a one-year follow-up.

Authors:  Priscila S Albuquerque; Mariana C Voos; Mariene S Simões; Joyce Martini; Carlos B M Monteiro; Fatima A Caromano
Journal:  Braz J Phys Ther       Date:  2016-06-16       Impact factor: 3.377

9.  Cost of Illness in Patients with Duchenne Muscular Dystrophy in Portugal: The COIDUCH Study.

Authors:  Pedro Labisa; Valeska Andreozzi; Melina Mota; Susana Monteiro; Rita Alves; João Almeida; Björn Vandewalle; Jorge Felix; Katharina Buesch; Hugo Canhão; Igor Beitia Ortiz de Zarate
Journal:  Pharmacoecon Open       Date:  2021-10-03

Review 10.  Prognostic indicators of disease progression in Duchenne muscular dystrophy: A literature review and evidence synthesis.

Authors:  Nermina Ferizovic; Jessica Summers; Igor Beitia Ortiz de Zárate; Christian Werner; Joel Jiang; Erik Landfeldt; Katharina Buesch
Journal:  PLoS One       Date:  2022-03-25       Impact factor: 3.240

  10 in total

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