Peer-reviewed veterinary case report
Genetic study of itchy skin allergy in West Highland White Terriers
By Salzmann, Cary A et al.·Published in BMC genetics·2011·College of Veterinary Medicine, United States·View original on PubMed →
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Original publication title: Genome-wide linkage study of atopic dermatitis in West Highland White Terriers.
- Species:
- dog
Plain-English summary
A group of West Highland White Terriers (WHWTs) with atopic dermatitis (a chronic allergic skin condition causing itching and skin lesions) was studied to find genetic links to the disorder. Researchers collected blood samples and health information from 108 dogs but did not find any significant genetic markers associated with the condition. They noted that factors like environmental influences or the nature of the mutation might have affected their results. Future studies with more dogs and advanced techniques may help identify genetic causes of atopic dermatitis in these pets.
People also search for: West Highland White Terrier skin problems · dog itching treatment · atopic dermatitis in dogs · WHWT allergy symptoms · dog skin infection treatment
Abstract
BACKGROUND: Canine atopic dermatitis (AD) is a common, heritable, chronic allergic skin condition prevalent in the West Highland White Terrier (WHWT). In canine AD, environmental allergens trigger an inflammatory response causing visible skin lesions and chronic pruritus that can lead to secondary bacterial and yeast infections. The disorder shares many of the clinical and histopathological characteristics of human AD and represents an animal model of this disorder that could be used to further elucidate genetic causes of human AD. Microsatellite markers genotyped in families of WHWTs affected with AD were used to perform a genome-wide linkage study in order to isolate chromosomal regions associated with the disorder. RESULTS: Blood samples and health questionnaires were collected from 108 WHWTs spanning three families. A linkage simulation using these 108 dogs showed high power to detect a highly penetrant mutation. Ninety WHWTs were genotyped using markers from the Minimal Screening Set 2 (MSS-2). Two hundred and fifty six markers were informative and were used for linkage analysis. Using a LOD score of 2.7 as a significance threshold, no chromosomal regions were identified with significant linkage to AD. LOD scores greater than 1.0 were located in a 56 cM region of chromosome 7. CONCLUSIONS: The study was unable to detect any chromosomal regions significantly linked to canine AD. This could be a result of factors such as environmental modification of phenotype, incorrect assignment of phenotype, a mutation of low penetrance, or incomplete genome coverage. A genome-wide SNP association study in a larger cohort of WHWTs may prove more successful by providing higher density coverage and higher statistical power.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/21510878/