Literature DB >> 24030636

Sibling concordance for clinical features of Duchenne and Becker muscular dystrophies.

Sydney Pettygrove1, Zhenqiang Lu, Jennifer G Andrews, F John Meaney, Daniel W Sheehan, Elinora T Price, Deborah J Fox, Shree Pandya, Lijing Ouyang, Susan D Apkon, Zoe Powis, Christopher Cunniff.   

Abstract

INTRODUCTION: The correlation of markers of disease severity among brothers with Duchenne or Becker muscular dystrophy has implications for clinical guidance and clinical trials.
METHODS: Sibling pairs with Duchenne or Becker muscular dystrophy (n = 60) were compared for ages when they reached clinical milestones of disease progression, including ceased ambulation, scoliosis of ≥ 20°, and development of cardiomyopathy.
RESULTS: The median age at which younger brothers reached each milestone, compared with their older brothers ranged from 25 months younger for development of cardiomyopathy to 2 months older for ceased ambulation. For each additional month of ambulation by the older brother, the hazard of ceased ambulation by the younger brother decreased by 4%.
CONCLUSIONS: The ages when siblings reach clinical milestones of disease vary widely between siblings. However, the time to ceased ambulation for older brothers predicts the time to ceased ambulation for their younger brothers.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  Becker muscular dystrophy; Duchenne muscular dystrophy; ambulation; cardiomyopathy; scoliosis; sibling features

Mesh:

Year:  2014        PMID: 24030636      PMCID: PMC4481732          DOI: 10.1002/mus.24078

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  15 in total

1.  Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation.

Authors:  Michelle Eagle; Simon V Baudouin; Colin Chandler; David R Giddings; Robert Bullock; Kate Bushby
Journal:  Neuromuscul Disord       Date:  2002-12       Impact factor: 4.296

2.  Cardiac and pulmonary function variability in Duchenne/Becker muscular dystrophy: an initial report.

Authors:  David J Birnkrant; Mahi Lakshmi Ashwath; Garey H Noritz; Michelle C Merrill; Tushar A Shah; Carol A Crowe; Robert C Bahler
Journal:  J Child Neurol       Date:  2010-05-25       Impact factor: 1.987

Review 3.  Scoliosis in patients with Duchenne muscular dystrophy.

Authors:  Lori A Karol
Journal:  J Bone Joint Surg Am       Date:  2007-02       Impact factor: 5.284

4.  Predictive factors for the development of scoliosis in Duchenne muscular dystrophy.

Authors:  M Kinali; M Main; J Eliahoo; S Messina; R K Knight; J Lehovsky; G Edge; E Mercuri; A Y Manzur; F Muntoni
Journal:  Eur J Paediatr Neurol       Date:  2007-01-25       Impact factor: 3.140

5.  The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy.

Authors:  G Nigro; L I Comi; L Politano; R J Bain
Journal:  Int J Cardiol       Date:  1990-03       Impact factor: 4.164

Review 6.  Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for management.

Authors:  Richard T Moxley; Shree Pandya; Emma Ciafaloni; Deborah J Fox; Kim Campbell
Journal:  J Child Neurol       Date:  2010-06-25       Impact factor: 1.987

7.  Deflazacort treatment of Duchenne muscular dystrophy.

Authors:  W D Biggar; M Gingras; D L Fehlings; V A Harris; C A Steele
Journal:  J Pediatr       Date:  2001-01       Impact factor: 4.406

Review 8.  Dystrophies and heart disease.

Authors:  G F Cox; L M Kunkel
Journal:  Curr Opin Cardiol       Date:  1997-05       Impact factor: 2.161

Review 9.  Update on the management of Duchenne muscular dystrophy.

Authors:  A Y Manzur; M Kinali; F Muntoni
Journal:  Arch Dis Child       Date:  2008-07-30       Impact factor: 3.791

10.  Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure.

Authors:  Carole Vuillerot; Françoise Girardot; Christine Payan; Jacques Fermanian; Jean Iwaz; Capucine De Lattre; Carole Berard
Journal:  Dev Med Child Neurol       Date:  2009-04-22       Impact factor: 5.449

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  3 in total

1.  Echocardiographic evaluation of left ventricular systolic function by the M-mode lateral mitral annular plane systolic excursion in patients with Duchenne muscular dystrophy age 0-21 years.

Authors:  Melissa K Webb; Poonam P Thankavel; Claudio Ramaciotti
Journal:  Health Sci Rep       Date:  2020-10-05

Review 2.  A Review of MD STAR net's Research Contributions to Pediatric-Onset Dystrophinopathy in the United States; 2002-2017.

Authors:  Kashika M Sahay; Tiffany Smith; Kristin M Conway; Paul A Romitti; Molly M Lamb; Jennifer Andrews; Shree Pandya; Joyce Oleszek; Christopher Cunniff; Rodolfo Valdez
Journal:  J Child Neurol       Date:  2018-10-22       Impact factor: 1.987

3.  Natural History of Histopathologic Changes in Cardiomyopathy of Golden Retriever Muscular Dystrophy.

Authors:  Sarah M Schneider; Garett T Sansom; Lee-Jae Guo; Shinji Furuya; Brad R Weeks; Joe N Kornegay
Journal:  Front Vet Sci       Date:  2022-02-17
  3 in total

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