A genome-wide association study to investigate genetic loci associated with primary glaucoma in American Cocker Spaniels

• Published in: American journal of veterinary research Vol. 83; no. 11; pp. 1 - 8
• Main Authors: Gomes, Filipe Espinheira, Casanova, Maria Isabel, Mouttham, Lara, Bannasch, Danika L, Park, Sangwan, Kim, Soohyun, Young, Laura J, Daley, Nicole L, Thomasy, Sara M, Castelhano, Marta G, Ledbetter, Eric C, Holmberg, Bradford, Boyd, Ryan, Van Der Woerdt, Alexandra, McDonald, Jessica, Hayward, Jessica J
• Format: Journal Article
• Language: English
• Published: United States 01.11.2022
• Subjects: Animals; Case-Control Studies; Dog Diseases - genetics; Dogs; Extracellular Matrix Proteins - genetics; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study - veterinary; Genotype; Glaucoma - genetics; Glaucoma - veterinary; Glaucoma, Open-Angle - genetics; Glaucoma, Open-Angle - veterinary; Polymorphism, Single Nucleotide
• ISSN: 0002-9645; 1943-5681
• DOI: 10.2460/ajvr.22.07.0106

To identify genetic associations with primary glaucoma (PG) in American Cocker Spaniels using a genome-wide association study (GWAS). A nationwide ambidirectional case-control cohort study was performed in American Cocker Spaniels that had an ophthalmic examination performed by a veterinarian. Ninety-four dogs with PG (cases) and 111 dogs without glaucoma (controls) met phenotypic criteria and had a blood sample collected after receiving informed owner consent. Genomic DNA was extracted from whole blood samples and genotyped (CanineHD BeadChip, Illumina Inc). A case-control GWAS using a linear mixed model was performed, and 3 significance thresholds were calculated (1) using a Bonferroni correction on all single nucleotide polymorphisms (SNPs) included in the GWAS, (2) using a Bonferroni correction on only the unlinked SNPs from a pruned data set, and (3) using 10,000 random phenotype permutations. Following genotype data quality control, 89 cases and 93 controls were included in the GWAS. We identified an association on canine chromosome (CFA10); however, it did not reach statistical significance. Potential candidate genes within the surrounding linkage disequilibrium interval include coiled-coil domain containing 85A (CCDC85A) and extracellular growth factor containing fibulin extracellular matrix protein 1 (EFEMP1). Primary glaucoma in the American Cocker Spaniel is a complex heterogeneous disease that may be influenced by a locus on CFA10. The candidate genes CCDC85A and EFEMP1 within the identified linkage disequilibrium interval have been shown to be involved in human open-angle glaucoma.