Literature DB >> 23632738

Cardiac asynchrony in Duchenne muscular dystrophy.

Abdallah Fayssoil1, Olivier Nardi, David Orlikowski, Djillali Annane.   

Abstract

Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. Heart failure is a classical complication in this disease. Little data are available about systolic dyssynchrony in DMD. We sought to assess the prevalence of left ventricular dysfunction and systolic asynchrony in DMD patients using echocardiographic parameters. We performed electrocardiography and echocardiography for adult's patients with DMD. For systolic dyssynchrony assessment, echocardiography-Doppler was performed and completed by tissular Doppler imaging. 48 DMD were included in our study. Age ranged from 20 to 37 years. QRS duration >120 ms was present in 10 patients/48 and 1 patient disclosed a QRS duration >150 ms. Left ventricular (LV) ejection fraction (EF) ranged from 10 to 62 % with a median of 43 %. Inter-ventricular asynchrony was found in 11.9 % of patients with EF < 35 % and in 2.6 % of patients with EF > 35 %. Intra-ventricular asynchrony was present in 6 % of patients with EF < 35 %. We found a high prevalence of LV dysfunction in DMD. Systolic ventricular asynchrony seems frequent particularly in patients with EF < 35 %.

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Year:  2013        PMID: 23632738     DOI: 10.1007/s10877-013-9472-3

Source DB:  PubMed          Journal:  J Clin Monit Comput        ISSN: 1387-1307            Impact factor:   2.502


  3 in total

1.  2010 Focused Update of ESC Guidelines on device therapy in heart failure: an update of the 2008 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure and the 2007 ESC Guidelines for cardiac and resynchronization therapy. Developed with the special contribution of the Heart Failure Association and the European Heart Rhythm Association.

Authors:  Kenneth Dickstein; Panos E Vardas; Angelo Auricchio; Jean-Claude Daubert; Cecilia Linde; John McMurray; Piotr Ponikowski; Silvia Giuliana Priori; Richard Sutton; Dirk J van Veldhuisen
Journal:  Europace       Date:  2010-11       Impact factor: 5.214

Review 2.  The heart in human dystrophinopathies.

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

3.  Presence of mechanical dyssynchrony in Duchenne muscular dystrophy.

Authors:  Kan N Hor; Janaka P Wansapura; Hussein R Al-Khalidi; William M Gottliebson; Michael D Taylor; Richard J Czosek; Sherif F Nagueh; Nandakishore Akula; Eugene S Chung; Woodrow D Benson; Wojciech Mazur
Journal:  J Cardiovasc Magn Reson       Date:  2011-02-02       Impact factor: 5.364

  3 in total
  5 in total

1.  Cardiac pathologies in female carriers of Duchenne muscular dystrophy assessed by cardiovascular magnetic resonance imaging.

Authors:  Juliane Schelhorn; Anne Schoenecker; Ulrich Neudorf; Haemi Schemuth; Felix Nensa; Kai Nassenstein; Michael Forsting; Ulrike Schara; Thomas Schlosser
Journal:  Eur Radiol       Date:  2015-03-20       Impact factor: 5.315

Review 2.  Cardiac involvement in Duchenne and Becker muscular dystrophy.

Authors:  Sophie Mavrogeni; George Markousis-Mavrogenis; Antigoni Papavasiliou; Genovefa Kolovou
Journal:  World J Cardiol       Date:  2015-07-26

Review 3.  Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms.

Authors:  Alberto Palladino; Paola D'Ambrosio; Andrea Antonio Papa; Roberta Petillo; Chiara Orsini; Marianna Scutifero; Gerardo Nigro; Luisa Politano
Journal:  Acta Myol       Date:  2016-12

Review 4.  Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results.

Authors:  Alberto Palladino; Andrea A Papa; Salvatore Morra; Vincenzo Russo; Manuela Ergoli; Anna Rago; Chiara Orsini; Gerardo Nigro; Luisa Politano
Journal:  Acta Myol       Date:  2019-03-01

5.  A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy.

Authors:  Tatianna Wai Ying Wong; Abdalla Ahmed; Grace Yang; Eleonora Maino; Sydney Steiman; Elzbieta Hyatt; Parry Chan; Kyle Lindsay; Nicole Wong; Diane Golebiowski; Joel Schneider; Paul Delgado-Olguín; Evgueni A Ivakine; Ronald D Cohn
Journal:  Dis Model Mech       Date:  2020-09-21       Impact factor: 5.758

  5 in total

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