» Articles » PMID: 36553559

Genetic Variants at the Nebulette Locus Are Associated with Myxomatous Mitral Valve Disease Severity in Cavalier King Charles Spaniels

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2022 Dec 23
PMID 36553559
Authors
Affiliations
Soon will be listed here.
Abstract

The most common cardiovascular disease in domestic dogs is myxomatous mitral valve disease (MMVD), accounting for 75% of all cardiac disease. An increase in age is generally associated with increased incidence of the disease, but Cavalier King Charles Spaniels (CKCS) exhibit an unusually high prevalence of early-onset MMVD, and thus, potentially greater cardiac morbidity and mortality compared to other breeds. Previous research has suggested that selected candidate risk alleles for MMVD are fixed in CKCSs, including six locations within the () gene on CFA2. The current study analysed genotypes of 180 Australian CKCSs at the identified risk loci. Of these, 178 were phenotyped for severity of disease by echocardiographic measurements of left atrium to aortic root ratio (LA:Ao) and weight normalised left ventricular end diastolic diameter (LVIDdN). Genotyping array markers correctly predicted the genotype at the risk-variant loci in the CKCS population, and the , and variants were observed to be in perfect linkage disequilibrium in this cohort. The CKCS cohort included 6/178 dogs being heterozygous for the protective/wild-type alleles at the NEBL locus. The mean LA:Ao and LVIDdN scores of these dogs heterozygous at variants were significantly smaller, and with significantly lower variance compared to age-matched CKCSs that were homozygous for risk alleles. The lower cardiac measurements in the heterozygous dogs indicate a significantly reduced risk of severe MMVD disease. Our analysis suggests that despite relative fixation of the NEBL risk alleles, healthy reference alleles at exist in low frequency in the CKCS breed and can be used to reduce MMVD severity and mortality.

References
1.
Jung S, Bohan A . Genome-wide sequencing and quantification of circulating microRNAs for dogs with congestive heart failure secondary to myxomatous mitral valve degeneration. Am J Vet Res. 2018; 79(2):163-169. DOI: 10.2460/ajvr.79.2.163. View

2.
Markby G, MacRae V, Corcoran B, Summers K . Comparative transcriptomic profiling of myxomatous mitral valve disease in the cavalier King Charles spaniel. BMC Vet Res. 2020; 16(1):350. PMC: 7509937. DOI: 10.1186/s12917-020-02542-w. View

3.
Bionda A, Cortellari M, Bagardi M, Frattini S, Negro A, Locatelli C . A Genomic Study of Myxomatous Mitral Valve Disease in Cavalier King Charles Spaniels. Animals (Basel). 2020; 10(10). PMC: 7602727. DOI: 10.3390/ani10101895. View

4.
Borgarelli M, Savarino P, Crosara S, Santilli R, Chiavegato D, Poggi M . Survival characteristics and prognostic variables of dogs with mitral regurgitation attributable to myxomatous valve disease. J Vet Intern Med. 2008; 22(1):120-8. DOI: 10.1111/j.1939-1676.2007.0008.x. View

5.
Ancot F, Lemay P, Knowler S, Kennedy K, Griffiths S, Cherubini G . A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels. BMC Genet. 2018; 19(1):16. PMC: 5865342. DOI: 10.1186/s12863-018-0605-z. View