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DOI 10.1093/jhered/esr041

Медицинская библиотека · The Journal of heredity · 2011

Identification of 2 loci associated with development of myxomatous mitral valve disease in Cavalier King Charles Spaniels.

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

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Аннотация

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) = 4.0 × 10(-5)) and a 1.68 Mb region on CFA14 (P(genome) = 7.9 × 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.

Для цитирования: Madsen Majbritt Busk, Olsen Lisbeth Høier, Häggström Jens, Höglund Katja, Ljungvall Ingrid, Falk Torkel, Wess Gerhard, Stephenson Hannah, Dukes-McEwan Joanna, Chetboul Valérie, Gouni Vassiliki, Proschowsky Helle Friis, Cirera Susanna, Karlskov-Mortensen Peter, Fredholm Merete. Identification of 2 loci associated with development of myxomatous mitral valve disease in Cavalier King Charles Spaniels.. The Journal of heredity. 2011. DOI: 10.1093/jhered/esr041.

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