Literature DB >> 26002394

Arrhythmias in the muscular dystrophies.

Archana Rajdev1, William J Groh2.   

Abstract

In patients with muscular dystrophies, cardiac involvement leading to cardiomyopathy and arrhythmias occurs with variable prevalence, mirroring the phenotypic variability seen among and within the various hereditary myopathies. Knowledge of the incidence of arrhythmias and predictors of sudden death in the various hereditary myopathies can help guide screening and appropriate management of these patients, thereby improving survival. The noncardiac manifestations can lead to delayed recognition of symptoms, affect the decision to implant a prophylactic device, and once a decision is made to proceed with device implant, increase peri-procedural respiratory and anesthesia-related complications. Published by Elsevier Inc.

Entities:  

Keywords:  Arrhythmia; Genetics; Implantable cardioverter-defibrillator; Muscular dystrophy; Pacemaker; Sudden cardiac death

Mesh:

Year:  2015        PMID: 26002394      PMCID: PMC4441951          DOI: 10.1016/j.ccep.2015.03.011

Source DB:  PubMed          Journal:  Card Electrophysiol Clin        ISSN: 1877-9182


  27 in total

1.  Significance of late ventricular potentials in myotonic dystrophy.

Authors:  D Babuty; L Fauchier; D Tena-Carbi; P Poret; J Leche; M Raynaud; J P Fauchier; P Cosnay
Journal:  Am J Cardiol       Date:  1999-11-01       Impact factor: 2.778

2.  Primary prevention of sudden death in patients with lamin A/C gene mutations.

Authors:  Christophe Meune; Jop H Van Berlo; Frédéric Anselme; Gisèle Bonne; Yigal M Pinto; Denis Duboc
Journal:  N Engl J Med       Date:  2006-01-12       Impact factor: 91.245

3.  ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemakers and Antiarrhythmia Devices): developed in collaboration with the American Association for Thoracic Surgery and Society of Thoracic Surgeons.

Authors:  Andrew E Epstein; John P DiMarco; Kenneth A Ellenbogen; N A Mark Estes; Roger A Freedman; Leonard S Gettes; A Marc Gillinov; Gabriel Gregoratos; Stephen C Hammill; David L Hayes; Mark A Hlatky; L Kristin Newby; Richard L Page; Mark H Schoenfeld; Michael J Silka; Lynne Warner Stevenson; Michael O Sweeney; Sidney C Smith; Alice K Jacobs; Cynthia D Adams; Jeffrey L Anderson; Christopher E Buller; Mark A Creager; Steven M Ettinger; David P Faxon; Jonathan L Halperin; Loren F Hiratzka; Sharon A Hunt; Harlan M Krumholz; Frederick G Kushner; Bruce W Lytle; Rick A Nishimura; Joseph P Ornato; Richard L Page; Barbara Riegel; Lynn G Tarkington; Clyde W Yancy
Journal:  Circulation       Date:  2008-05-15       Impact factor: 29.690

4.  The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein.

Authors:  S Manilal; T M Nguyen; C A Sewry; G E Morris
Journal:  Hum Mol Genet       Date:  1996-06       Impact factor: 6.150

5.  QT dispersion in patients with Duchenne-type progressive muscular dystrophy.

Authors:  M Yotsukura; A Yamamoto; T Kajiwara; T Nishimura; K Sakata; T Ishihara; K Ishikawa
Journal:  Am Heart J       Date:  1999-04       Impact factor: 4.749

6.  [Myotonic dystrophy and heart disease: behavior of arrhythmic events and conduction disturbances].

Authors:  Silvana Angelina D'Orio Nishioka; Martino Martinelli Filho; Suely Marie; Mayana Zatz; Roberto Costa
Journal:  Arq Bras Cardiol       Date:  2005-05-02       Impact factor: 2.000

7.  Long-term follow-up of arrhythmias in patients with myotonic dystrophy treated by pacing: a multicenter diagnostic pacemaker study.

Authors:  Arnaud Lazarus; Jean Varin; Dominique Babuty; Frédéric Anselme; Joel Coste; Denis Duboc
Journal:  J Am Coll Cardiol       Date:  2002-11-06       Impact factor: 24.094

8.  Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

Authors:  Jop H van Berlo; Willem G de Voogt; Anneke J van der Kooi; J Peter van Tintelen; Gisèle Bonne; Rabah Ben Yaou; Denis Duboc; Tom Rossenbacker; Hein Heidbüchel; Marianne de Visser; Harry J G M Crijns; Yigal M Pinto
Journal:  J Mol Med (Berl)       Date:  2004-11-13       Impact factor: 4.599

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

Authors:  David M Connuck; 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
Journal:  Am Heart J       Date:  2008-03-19       Impact factor: 4.749

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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  10 in total

Review 1.  Cardiomyopathy in becker muscular dystrophy: Overview.

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

2.  Cardiac manifestations in Emery-Dreifuss muscular dystrophy.

Authors:  Whitney Faiella; Ricardo Bessoudo
Journal:  CMAJ       Date:  2018-12-03       Impact factor: 8.262

3.  Functional correction of dystrophin actin binding domain mutations by genome editing.

Authors:  Viktoriia Kyrychenko; Sergii Kyrychenko; Malte Tiburcy; John M Shelton; Chengzu Long; Jay W Schneider; Wolfram-Hubertus Zimmermann; Rhonda Bassel-Duby; Eric N Olson
Journal:  JCI Insight       Date:  2017-09-21

Review 4.  Dilated cardiomyopathy as the initial presentation of Becker muscular dystrophy: a systematic review of published cases.

Authors:  Gaspar Del Rio-Pertuz; Cristina Morataya; Kanak Parmar; Sarah Dubay; Erwin Argueta-Sosa
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

5.  Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients.

Authors:  Binyamin Eisen; Ronen Ben Jehuda; Ashley J Cuttitta; Lucy N Mekies; Yuval Shemer; Polina Baskin; Irina Reiter; Lubna Willi; Dov Freimark; Mihaela Gherghiceanu; Lorenzo Monserrat; Michaela Scherr; Denise Hilfiker-Kleiner; Michael Arad; Daniel E Michele; Ofer Binah
Journal:  J Cell Mol Med       Date:  2019-01-08       Impact factor: 5.310

Review 6.  The Added Value of Cardiac Magnetic Resonance in Muscular Dystrophies.

Authors:  Mariana M Lamacie; Jodi Warman-Chardon; Andrew M Crean; Anca Florian; Karim Wahbi
Journal:  J Neuromuscul Dis       Date:  2019

7.  Bioenergetic and Metabolic Impairments in Induced Pluripotent Stem Cell-Derived Cardiomyocytes Generated from Duchenne Muscular Dystrophy Patients.

Authors:  Lubna Willi; Ifat Abramovich; Jonatan Fernandez-Garcia; Bella Agranovich; Margarita Shulman; Helena Milman; Polina Baskin; Binyamin Eisen; Daniel E Michele; Michael Arad; Ofer Binah; Eyal Gottlieb
Journal:  Int J Mol Sci       Date:  2022-08-29       Impact factor: 6.208

8.  Antagonism of the Thromboxane-Prostanoid Receptor as a Potential Therapy for Cardiomyopathy of Muscular Dystrophy.

Authors:  James D West; Cristi L Galindo; Kyungsoo Kim; John Jonghyun Shin; James B Atkinson; Ines Macias-Perez; Leo Pavliv; Bjorn C Knollmann; Jonathan H Soslow; Larry W Markham; Erica J Carrier
Journal:  J Am Heart Assoc       Date:  2019-10-30       Impact factor: 5.501

9.  Depressed β-adrenergic inotropic responsiveness and intracellular calcium handling abnormalities in Duchenne Muscular Dystrophy patients' induced pluripotent stem cell-derived cardiomyocytes.

Authors:  Lucy N Mekies; Danielle Regev; Binyamin Eisen; Jonatan Fernandez-Gracia; Polina Baskin; Ronen Ben Jehuda; Rita Shulman; Irina Reiter; Raz Palty; Michael Arad; Eyal Gottlieb; Ofer Binah
Journal:  J Cell Mol Med       Date:  2021-02-22       Impact factor: 5.310

Review 10.  Role of CMR Imaging in Diagnostics and Evaluation of Cardiac Involvement in Muscle Dystrophies.

Authors:  Edyta Blaszczyk; Jan Gröschel; Jeanette Schulz-Menger
Journal:  Curr Heart Fail Rep       Date:  2021-07-28
  10 in total

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