New canine models of copper toxicosis: diagnosis, treatment, and genetics

Files

Access status: Embargo until 2050-01-01 , Hille_14_NYAS_ (2).pdf (283.43 KB)

Publication date

2014-05

Authors

Fieten, HilleISNI 0000000419428066
Penning, LouisISNI 000000039077188X
Leegwater, Peter A JISNI 0000000388261936
Rothuizen, JanISNI 0000000117341627

Editors

Advisors

Supervisors

Document Type

Article
Open Access logo

License

Abstract

The One Health principle recognizes that human health, animal health, and environmental health are inextricably linked. An excellent example is the study of naturally occurring copper toxicosis in dogs to help understand human disorders of copper metabolism. Besides the Bedlington terrier, where copper toxicosis is caused by a mutation in the COMMD1 gene, more complex hereditary forms of copper-associated hepatitis were recognized recently in other dog breeds. The Labrador retriever is one such breed, where an interplay between genetic susceptibility and exposure to copper lead to clinical copper toxicosis. Purebred dog populations are ideal for gene mapping studies, and because genes involved in copper metabolism are highly conserved across species, newly identified gene mutations in the dog may help unravel the genetic complexity of different human forms of copper toxicosis. Furthermore, increasing knowledge with respect to diagnosis and treatment strategies will benefit both species.

Keywords

copper, dog, liver, genetics, One Health, SDG 3 - Good Health and Well-being

Citation

Fieten, H, Penning, L C, Leegwater, P A J & Rothuizen, J 2014, 'New canine models of copper toxicosis: diagnosis, treatment, and genetics', Annals of the New York Academy of Sciences, vol. 1314, pp. 42-48. https://doi.org/10.1111/nyas.12442