Literature DB >> 18513510

Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: a comparative study from the Pediatric Cardiomyopathy Registry.

David M Connuck1, Lynn A Sleeper, Steven D Colan, Gerald F Cox, Jeffrey A Towbin, April M Lowe, James D Wilkinson, E John Orav, Leigha Cuniberti, Bonnie A Salbert, Steven E Lipshultz.   

Abstract

OBJECTIVE: The aim of this study was to determine in pediatric Duchenne (DMD) and Becker muscular dystrophy (BMD) or other dilated cardiomyopathies (ODCM) whether outcomes differ by diagnosis.
BACKGROUND: Children with dilated cardiomyopathy are treated as a single undifferentiated group.
METHODS: This cohort study of 128 children with DMD, 15 with BMD, and 312 with ODCM uses outcome measures of left ventricular (LV) size and function, death, heart transplant, and death or transplant.
RESULTS: At cardiomyopathy diagnosis, the DMD and BMD groups had similar mean ages (14.4 and 14.6 years), prevalence of congestive heart failure (CHF) (30% and 33%), and LV fractional shortening (FS) Z-scores (median, -5.2 for DMD and -6.7 for BMD). The BMD group had more severe mitral regurgitation (P = .05) and a higher mean LV end-diastolic dimension Z-score than the DMD group (2.9 +/- 1.5 vs 1.2 +/- 1.9, P = .002). Duchenne muscular dystrophy group survival was lower than in BMD or ODCM groups (P = .06) at 5 years (57%, 100%, and 71%, respectively). In BMD, 25% received cardiac transplants within 0.4 years of cardiomyopathy diagnosis. The combined DMD and BMD group had less LV dilation and a closer-to-normal LV FS at cardiomyopathy diagnosis than the ODCM group. After 2 years, LV dilation increased, and LV FS did not change in the combined DMD and BMD group; for ODCM patients, LV dilation did not progress, and LV FS improved.
CONCLUSIONS: Children with DMD and cardiomyopathy have a higher mortality. Becker muscular dystrophy has a high heart transplantation rate in the 5 years after diagnosis of cardiomyopathy. Serial echocardiography demonstrates a different disease course for DMD and BMD patients compared with ODCM patients.

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Mesh:

Year:  2008        PMID: 18513510      PMCID: PMC2729548          DOI: 10.1016/j.ahj.2008.01.018

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  17 in total

1.  Design and implementation of the North American Pediatric Cardiomyopathy Registry.

Authors:  M A Grenier; S K Osganian; G F Cox; J A Towbin; S D Colan; P R Lurie; L A Sleeper; E J Orav; S E Lipshultz
Journal:  Am Heart J       Date:  2000-02       Impact factor: 4.749

2.  Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy.

Authors: 
Journal:  Pediatrics       Date:  2005-12       Impact factor: 7.124

3.  Incidence, causes, and outcomes of dilated cardiomyopathy in children.

Authors:  Jeffrey A Towbin; April M Lowe; Steven D Colan; Lynn A Sleeper; E John Orav; Sarah Clunie; Jane Messere; Gerald F Cox; Paul R Lurie; Daphne Hsu; Charles Canter; James D Wilkinson; Steven E Lipshultz
Journal:  JAMA       Date:  2006-10-18       Impact factor: 56.272

Review 4.  The heart in human dystrophinopathies.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Cardiology       Date:  2003       Impact factor: 1.869

5.  A family of Becker's progressive muscular dystrophy with severe cardiomyopathy.

Authors:  M Yazawa; S Ikeda; M Owa; S Haruta; N Yanagisawa; E Tanaka; M Watanabe
Journal:  Eur Neurol       Date:  1987       Impact factor: 1.710

6.  Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy.

Authors:  Marly Conceição Silva; Zilda Maria Alves Meira; Juliana Gurgel Giannetti; Marcelo Moreira da Silva; Alysson Félix Oliveira Campos; Márcia de Melo Barbosa; Geraldo Moll Starling Filho; Rogério de Aguiar Ferreira; Mayana Zatz; Carlos Eduardo Rochitte
Journal:  J Am Coll Cardiol       Date:  2007-04-23       Impact factor: 24.094

7.  Improved outcomes of pediatric dilated cardiomyopathy with utilization of heart transplantation.

Authors:  Anna E Tsirka; Kathryn Trinkaus; Su-Chiung Chen; Steven E Lipshultz; Jeffrey A Towbin; Steven D Colan; Vernat Exil; Arnold W Strauss; Charles E Canter
Journal:  J Am Coll Cardiol       Date:  2004-07-21       Impact factor: 24.094

8.  Heart transplantation in patients with muscular dystrophy associated with end-stage cardiomyopathy.

Authors:  W Rees; S Schüler; M Hummel; R Hetzer
Journal:  J Heart Lung Transplant       Date:  1993 Sep-Oct       Impact factor: 10.247

9.  X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Authors:  J A Towbin; J F Hejtmancik; P Brink; B Gelb; X M Zhu; J S Chamberlain; E R McCabe; M Swift
Journal:  Circulation       Date:  1993-06       Impact factor: 29.690

10.  Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.

Authors:  P Melacini; M Fanin; G A Danieli; C Villanova; F Martinello; M Miorin; M P Freda; M Miorelli; M L Mostacciuolo; G Fasoli; C Angelini; S Dalla Volta
Journal:  Circulation       Date:  1996-12-15       Impact factor: 29.690

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  69 in total

Review 1.  The pediatric cardiomyopathy registry and heart failure: key results from the first 15 years.

Authors:  James D Wilkinson; David C Landy; Steven D Colan; Jeffrey A Towbin; Lynn A Sleeper; E John Orav; Gerald F Cox; Charles E Canter; Daphne T Hsu; Steven A Webber; Steven E Lipshultz
Journal:  Heart Fail Clin       Date:  2010-10       Impact factor: 3.179

2.  Central Arterial Function Measured by Non-invasive Pulse Wave Analysis is Abnormal in Patients with Duchenne Muscular Dystrophy.

Authors:  Thomas D Ryan; John J Parent; Zhiqian Gao; Philip R Khoury; Elizabeth Dupont; Jennifer N Smith; Brenda Wong; Elaine M Urbina; John L Jefferies
Journal:  Pediatr Cardiol       Date:  2017-06-21       Impact factor: 1.655

3.  DOT1L regulates dystrophin expression and is critical for cardiac function.

Authors:  Anh T Nguyen; Bin Xiao; Ronald L Neppl; Eric M Kallin; Juan Li; Taiping Chen; Da-Zhi Wang; Xiao Xiao; Yi Zhang
Journal:  Genes Dev       Date:  2011-02-01       Impact factor: 11.361

Review 4.  Cardiomyopathy in becker muscular dystrophy: Overview.

Authors:  Rady Ho; My-Le Nguyen; Paul Mather
Journal:  World J Cardiol       Date:  2016-06-26

5.  Factors affecting the health-related quality of life of caregivers of patients with muscular dystrophy.

Authors:  Yi-Jing Lue; Shun-Sheng Chen; Yen-Mou Lu
Journal:  J Neurol       Date:  2018-04-26       Impact factor: 4.849

6.  Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.

Authors:  Elizabeth M McNally; Jonathan R Kaltman; D Woodrow Benson; Charles E Canter; Linda H Cripe; Dongsheng Duan; Jonathan D Finder; William J Groh; Eric P Hoffman; Daniel P Judge; Naomi Kertesz; Kathi Kinnett; Roxanne Kirsch; Joseph M Metzger; Gail D Pearson; Jill A Rafael-Fortney; Subha V Raman; Christopher F Spurney; Shari L Targum; Kathryn R Wagner; Larry W Markham
Journal:  Circulation       Date:  2015-05-05       Impact factor: 29.690

7.  Acute Myocardial Injury in a Child with Duchenne Muscular Dystrophy: Pulse Steroid Therapy?

Authors:  Eliza Cinteza; Claudiu Stoicescu; Niculina Butoianu; Mihaela Balgradean; Alin Nicolescu; Matthias Angrés
Journal:  Maedica (Bucur)       Date:  2017-09

8.  Early right ventricular fibrosis and reduction in biventricular cardiac reserve in the dystrophin-deficient mdx heart.

Authors:  Tatyana A Meyers; DeWayne Townsend
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-12-05       Impact factor: 4.733

9.  Variations in native T1 values in patients with Duchenne muscular dystrophy with and without late gadolinium enhancement.

Authors:  Sean M Lang; Tarek Alsaied; Philip R Khoury; Thomas D Ryan; Michael D Taylor
Journal:  Int J Cardiovasc Imaging       Date:  2020-09-20       Impact factor: 2.357

10.  Proteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins.

Authors:  Caroline Lewis; Harald Jockusch; Kay Ohlendieck
Journal:  J Biomed Biotechnol       Date:  2010-05-23
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