Literature DB >> 34147413

A review of the underlying genetics and emerging therapies for canine cardiomyopathies.

L Shen1, A H Estrada2, K M Meurs3, M Sleeper2, C Vulpe4, C J Martyniuk4, C A Pacak5.   

Abstract

Cardiomyopathies such as dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy are common in large breed dogs and carry an overall poor prognosis. Research shows that these diseases have strong breed predilections, and selective breeding has historically been recommended to reduce the disease prevalence in affected breeds. Treatment of these diseases is typically palliative and aimed at slowing disease progression and managing clinical signs of heart failure as they develop. The discovery of specific genetic mutations underlying cardiomyopathies, such as the striatin mutation in Boxer arrhythmogenic right ventricular cardiomyopathy and the pyruvate dehydrogenase kinase 4 and titin mutations in Doberman Pinschers, has strengthened our ability to screen and selectively breed individuals in an attempt to produce unaffected offspring. The discovery of these disease-linked mutations has also opened avenues for the development of gene therapies, including gene transfer and genome-editing approaches. This review article discusses the known genetics of cardiomyopathies in dogs, reviews existing gene therapy strategies and the status of their development in canines, and discusses ongoing challenges in the clinical translation of these technologies for treating heart disease. While challenges remain in using these emerging technologies, the exponential growth of the gene therapy field holds great promise for future clinical applications.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Arrhythmogenic right ventricular cardiomyopathy; Clustered regularly interspaced short palindromic repeats; Dilated cardiomyopathy; Gene editing; Gene therapy

Mesh:

Year:  2021        PMID: 34147413      PMCID: PMC8606013          DOI: 10.1016/j.jvc.2021.05.003

Source DB:  PubMed          Journal:  J Vet Cardiol        ISSN: 1760-2734            Impact factor:   1.750


  83 in total

Review 1.  Immune responses to gene therapy vectors: influence on vector function and effector mechanisms.

Authors:  N Bessis; F J GarciaCozar; M-C Boissier
Journal:  Gene Ther       Date:  2004-10       Impact factor: 5.250

2.  Canine dilated cardiomyopathy: a retrospective study of prognostic findings in 367 clinical cases.

Authors:  M W S Martin; M J Stafford Johnson; G Strehlau; J N King
Journal:  J Small Anim Pract       Date:  2010-08       Impact factor: 1.522

3.  A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher.

Authors:  Kathryn M Meurs; Sunshine Lahmers; Bruce W Keene; Stephen N White; Mark A Oyama; Evan Mauceli; Kerstin Lindblad-Toh
Journal:  Hum Genet       Date:  2012-03-25       Impact factor: 4.132

4.  Ser67-phosphorylated inhibitor 1 is a potent protein phosphatase 1 inhibitor.

Authors:  K X Huang; H K Paudel
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-23       Impact factor: 11.205

5.  Arrhythmogenic right ventricular cardiomyopathy in boxer dogs: a retrospective study of survival.

Authors:  A Caro-Vadillo; L García-Guasch; E Carretón; J A Montoya-Alonso; J Manubens
Journal:  Vet Rec       Date:  2013-01-12       Impact factor: 2.695

6.  Ventricular arrhythmias in Rhodesian Ridgebacks with a family history of sudden death and results of a pedigree analysis for potential inheritance patterns.

Authors:  Kathryn M Meurs; Jess A Weidman; Steven L Rosenthal; Kevin K Lahmers; Steven G Friedenberg
Journal:  J Am Vet Med Assoc       Date:  2016-05-15       Impact factor: 1.936

7.  Cardiomyopathy prevalence in 780 apparently healthy cats in rehoming centres (the CatScan study).

Authors:  Jessie Rose Payne; David Charles Brodbelt; Virginia Luis Fuentes
Journal:  J Vet Cardiol       Date:  2015-12       Impact factor: 1.701

8.  A substitution mutation in the myosin binding protein C gene in ragdoll hypertrophic cardiomyopathy.

Authors:  Kathryn M Meurs; Michelle M Norgard; Martina M Ederer; Kristina P Hendrix; Mark D Kittleson
Journal:  Genomics       Date:  2007-05-22       Impact factor: 5.736

9.  Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.

Authors:  Leonela Amoasii; John C W Hildyard; Hui Li; Efrain Sanchez-Ortiz; Alex Mireault; Daniel Caballero; Rachel Harron; Thaleia-Rengina Stathopoulou; Claire Massey; John M Shelton; Rhonda Bassel-Duby; Richard J Piercy; Eric N Olson
Journal:  Science       Date:  2018-08-30       Impact factor: 47.728

10.  Development of an intein-mediated split-Cas9 system for gene therapy.

Authors:  Dong-Jiunn Jeffery Truong; Karin Kühner; Ralf Kühn; Stanislas Werfel; Stefan Engelhardt; Wolfgang Wurst; Oskar Ortiz
Journal:  Nucleic Acids Res       Date:  2015-06-16       Impact factor: 16.971

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  1 in total

Review 1.  Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional Model.

Authors:  Karen R Gaar-Humphreys; Talitha C F Spanjersberg; Giorgia Santarelli; Guy C M Grinwis; Viktor Szatmári; Bernard A J Roelen; Aryan Vink; J Peter van Tintelen; Folkert W Asselbergs; Hille Fieten; Magdalena Harakalova; Frank G van Steenbeek
Journal:  Animals (Basel)       Date:  2022-06-29       Impact factor: 3.231

  1 in total

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