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Peer-reviewed veterinary case report

Gene variant in Doberman dogs linked to heart disease and sudden death

By Meurs, Kathryn M et al.·Published in Human genetics·2019·Department of Veterinary Clinical Sciences, United States·View original on PubMed

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Original publication title: A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.

Species:
dog

Plain-English summary

A family of Doberman Pinschers was found to have a genetic variant linked to dilated cardiomyopathy, a serious heart condition that can lead to sudden cardiac death. This condition can cause symptoms like weakness, coughing, or difficulty breathing in affected dogs. Researchers discovered a specific change in the titin gene that was strongly associated with the disease in these dogs. Understanding this genetic link can help veterinarians better diagnose and manage heart problems in Doberman Pinschers.

People also search for: Doberman Pinscher heart problems · dilated cardiomyopathy in dogs · sudden cardiac death in dogs · titin gene and dog health

Abstract

The dog provides a large animal model of familial dilated cardiomyopathy for the study of important aspects of this common familial cardiovascular disease. We have previously demonstrated a form of canine dilated cardiomyopathy in the Doberman pinscher breed that is inherited as an autosomal dominant trait and is associated with a splice site variant in the pyruvate dehydrogenase kinase 4 (PDK4) gene, however, genetic heterogeneity exists in this species as well and not all affected dogs have the PDK4 variant. Whole genome sequencing of a family of Doberman pinchers with dilated cardiomyopathy and sudden cardiac death without the PDK4 variant was performed. A pathologic missense variant in the titin gene located in an immunoglobulin-like domain in the I-band spanning region of the molecule was identified and was highly associated with the disease (p&#x2009;<&#x2009;0.0001). We demonstrate here the identification of a variant in the titin gene highly associated with the disease in this spontaneous canine model of dilated cardiomyopathy. This large animal model of familial dilated cardiomyopathy shares many similarities with the human disease including mode of inheritance, clinical presentation, genetic heterogeneity and a pathologic variant in the titin gene. The dog is an excellent model to improve our understanding of the genotypic phenotypic relationships, penetrance, expression and the pathophysiology of variants in the titin gene.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30715562/