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Research article2011Peer reviewed

Identification of 2 Loci Associated with Development of Myxomatous Mitral Valve Disease in Cavalier King Charles Spaniels

Madsen Busk, Majbritt; Olsen Hoier, Lisbeth; Häggström, Jens; Höglund, Katja; Bersås Ljungvall, Ingrid; Falk, Torkel; Wess, Gerhard; Stephenson, Hannah; Dukes-McEwan, Joanna; Chetboul, Valérie; Vassiliki, Gouni; Friis Proschowsky, Helle; Cirera, Susanna; Karlskov-Mortensen, Peter; Fredholm, Merete

Abstract

Myxomatous mitral valve disease (MMVD) is the most common heart disease in dogs. It is characterized by chronic progressive degenerative lesions of the mitral valve. The valve leaflets become thickened and prolapse into the left atrium resulting in mitral regurgitation (MR). MMVD is most prevalent in small to medium sized dog breeds, Cavalier King Charles Spaniels (CKCS) in particular. The onset of MMVD is highly age dependent, and at the age of 10 years, nearly all CKCS are affected. The incidence of a similar disease in humans-mitral valve prolapse-is 1-5%. By defining CKCSs with an early onset of MMVD as cases and old dogs with no or mild signs of MMVD as controls, we conducted a genome-wide association study (GWAS) to identify loci associated with development of MMVD. We have identified a 1.58 Mb region on CFA13 (P(genome) = 4.0x 10(-5)) and a 1.68 Mb region on CFA14 (P(genome) = 7.9x 10(-4)) associated with development of MMVD. This confirms the power of using the dog as a model to uncover potential candidate regions involved in the molecular mechanisms behind complex traits.

Keywords

genome-wide association study; myxomatous mitral valve disease; MVP; Cavalier King Charles Spaniel; Dog

Published in

Journal of Heredity
2011, Volume: 102, pages: S62-S67
Publisher: OXFORD UNIV PRESS INC