Literature DB >> 20423733

Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks.

Ellen Otten1, Angeliki Asimaki, Alexander Maass, Irene M van Langen, Allard van der Wal, Nicolaas de Jonge, Maarten P van den Berg, Jeffrey E Saffitz, Arthur A M Wilde, Jan D H Jongbloed, J Peter van Tintelen.   

Abstract

BACKGROUND: Mutations in the gene encoding desmin (DES), an intermediate filament protein, underlie a heterogeneous phenotype, which is referred to as desmin-related myopathy (DRM). Right ventricular involvement including an arrhythmogenic right ventricular cardiomyopathy (ARVC)(-like) phenotype has occasionally been described in DES mutation-carrying patients.
OBJECTIVE: To determine the effects of a DES missense mutation on the structure of different intercalated disk proteins, to evaluate right ventricular involvement in DES mutation carriers, and to establish the role of DES mutations in ARVC(-like) phenotypes.
METHODS: We evaluated the clinical phenotype in two families carrying two different DES mutations. One family was diagnosed with DRM, with an ARVC(-like) phenotype in one patient, while the other family presented with a severe biventricular cardiomyopathy. Additional immunohistochemistry of desmosomal proteins was performed in myocardial tissue from two patients of the last family. The DES gene was screened for mutations in 50 ARVC(-like) patients.
RESULTS: Except for two different DES mutations (p.N342D and p.R454W) in two families with DRM and severe biventricular cardiomyopathy, respectively, we did not find additional DES mutations in ARVC(-like) patients. In addition to desmin aggregates, immunohistochemistry demonstrated a decreased amount of desmoplakin and plakophilin-2 at the intercalated disk in p.R454W mutation carriers.
CONCLUSIONS: We confirmed that either an ARVC-like phenotype or a severe cardiomyopathy with right ventricular involvement are possible, yet infrequent, cardiac phenotypes in DRM. Moreover, we demonstrated that the DES mutation p.R454W affects the localization of desmoplakin and plakophilin-2 at the intercalated disk, suggesting a link between desmosomal cardiomyopathies (mainly affecting the right ventricle) and cardiomyopathies caused by DES mutations. Copyright 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20423733     DOI: 10.1016/j.hrthm.2010.04.023

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  38 in total

1.  Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants.

Authors:  Andreas Brodehl; Per Niklas Hedde; Mareike Dieding; Azra Fatima; Volker Walhorn; Susan Gayda; Tomo Šarić; Bärbel Klauke; Jan Gummert; Dario Anselmetti; Mike Heilemann; Gerd Ulrich Nienhaus; Hendrik Milting
Journal:  J Biol Chem       Date:  2012-03-08       Impact factor: 5.157

2.  Right ventricular protein expression profile in end-stage heart failure.

Authors:  Yan Ru Su; Manuel Chiusa; Evan Brittain; Anna R Hemnes; Tarek S Absi; Chee Chew Lim; Thomas G Di Salvo
Journal:  Pulm Circ       Date:  2015-09       Impact factor: 3.017

3.  Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes.

Authors:  Matthew Taylor; Sharon Graw; Gianfranco Sinagra; Carl Barnes; Dobromir Slavov; Francesca Brun; Bruno Pinamonti; Ernesto E Salcedo; William Sauer; Stylianos Pyxaras; Brian Anderson; Bernd Simon; Julius Bogomolovas; Siegfried Labeit; Henk Granzier; Luisa Mestroni
Journal:  Circulation       Date:  2011-08-01       Impact factor: 29.690

4.  An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis.

Authors:  Diptendu Chatterjee; Meena Fatah; Deniz Akdis; Danna A Spears; Tamara T Koopmann; Kirti Mittal; Muhammad A Rafiq; Bruce M Cattanach; Qili Zhao; Jeff S Healey; Michael J Ackerman; Johan Martijn Bos; Yu Sun; Jason T Maynes; Corinna Brunckhorst; Argelia Medeiros-Domingo; Firat Duru; Ardan M Saguner; Robert M Hamilton
Journal:  Eur Heart J       Date:  2018-11-21       Impact factor: 29.983

5.  Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutation.

Authors:  Carola Hedberg; Atle Melberg; Angelika Kuhl; Dieter Jenne; Anders Oldfors
Journal:  Eur J Hum Genet       Date:  2012-03-07       Impact factor: 4.246

6.  The role of endomyocardial biopsy in ARVC: looking beyond histology in search of new diagnostic markers.

Authors:  Angeliki Asimaki; Jeffrey E Saffitz
Journal:  J Cardiovasc Electrophysiol       Date:  2010-11-18

Review 7.  The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.

Authors:  Jaeger P Ackerman; Daniel C Bartos; Jamie D Kapplinger; David J Tester; Brian P Delisle; Michael J Ackerman
Journal:  Mayo Clin Proc       Date:  2016-10-08       Impact factor: 7.616

Review 8.  Intermediate filaments in cardiomyopathy.

Authors:  Mary Tsikitis; Zoi Galata; Manolis Mavroidis; Stelios Psarras; Yassemi Capetanaki
Journal:  Biophys Rev       Date:  2018-07-19

9.  Autophagic vacuolar pathology in desminopathies.

Authors:  Conrad C Weihl; Stanley Iyadurai; Robert H Baloh; Sara K Pittman; Robert E Schmidt; Glenn Lopate; Alan Pestronk; Matthew B Harms
Journal:  Neuromuscul Disord       Date:  2014-12-12       Impact factor: 4.296

Review 10.  Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy.

Authors:  Angeliki Asimaki; Jeffrey E Saffitz
Journal:  Cell Commun Adhes       Date:  2014-02
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