A candidate gene analysis of canine hypoadrenocorticism in 3 dog breeds

• Published in: The Journal of heredity Vol. 104; no. 6; pp. 807 - 820
• Main Authors: Short, Andrea D, Boag, Alisdair, Catchpole, Brian, Kennedy, Lorna J, Massey, Jonathan, Rothwell, Simon, Husebye, Eystein, Ollier, Bill
• Format: Journal Article
• Language: English
• Published: United States Oxford Publishing Limited (England) 01.11.2013
• Subjects: Adrenal Insufficiency - veterinary; Alleles; Animal diseases; Animals; Base Sequence; Breeding; Breeding of animals; Chromosome Mapping; Dog Diseases - genetics; Dog Diseases - immunology; Dogs; Gene Frequency; Genes; Genetic Association Studies; Genetics; Genomes; Genotype; Haplotypes; Molecular Sequence Annotation; Polymorphism, Single Nucleotide; hypoadrenocorticism; genetics; Addison’s disease; candidate genes; dog
• ISSN: 0022-1503; 1465-7333
• DOI: 10.1093/jhered/est051

Canine hypoadrenocorticism is believed to be an immune-related condition. It is rare in the overall dog population but shows a breed-related predisposition with Standard poodles and Portuguese water dogs having a greater prevalence of the condition. It shares many similarities with human primary adrenal insufficiency and is believed to be a naturally occurring, spontaneous model for the human condition. Short haplotype blocks and low levels of linkage disequilibrium in the human genome mean that the identification of genetic contributors to the condition requires large sample numbers. Pedigree dogs have high linkage disequilibrium and long haplotypes within a breed, increasing the potential of identifying novel genes that contribute to canine genetic disease. We investigated 222 SNPs from 42 genes that have been associated or may be implicated in human Addison's disease. We conducted case-control analyses in 3 pedigree dog breeds (Labrador retriever: affected n = 30, unaffected = 76; Cocker Spaniel: affected n = 19, unaffected = 53; Springer spaniel: affected n = 26, unaffected = 46) and identified 8 associated alleles in genes COL4A4, OSBPL9, CTLA4, PTPN22, and STXBP5 in 3 pedigree breeds. Association with immune response genes PTPN22 and CTLA4 in certain breeds suggests an underlying immunopathogenesis of the disease. These results suggest that canine hypoadrenocorticism could be a useful model for studying comparative genetics relevant to human Addison's disease.