On the human side, this is exciting for those suffering from Lou Gehrig's Disease (ALS), as the mutation that causes canine DM is the same as that which causes human ALS.
Oreo many thanks for that. When I have some more free time I'll have to look closely into that. Regarding some Hereditary Diseases and DNA Research I think that dogs can help humans, and humans can help dogs. The LUPA Project certainly thinks so and I think that so do many other DNA Research Centres around the world.
Some time ago I thought of things, even things like this where Cavaliers may suggest an excellent comparative and spontaneously occurring disease model of human Type 1 Diabetes, and the following from this address. Abstract as below and document in PDF format from this address.
http://jhered.oxfordjournals.org/cgi/reprint/98/5/518.pdf
Abstract
Canine diabetes is a complex genetic disease of unknown aetiology. It affects 0.005–1.5% of the canine population and shows a clear breed predisposition with the Samoyed being at high risk and the Boxer being at low risk of developing the disease. Canine diabetes is considered to be a disease homologue for human type 1 diabetes (T1D). It results in insulin deficiency as a consequence of autoimmune destruction of islet b-cells in the pancreas and is believed to be mediated by Th1 cytokines (IFNc, TNFa, and IL-2). A number of genes have been associated with type 1 diabetes in humans, including the human leukocyte antigen region, the insulin variable number tandem repeat, PTPN22, CTLA4, IL-4, and IL-13. As yet, these genes have not been evaluated in canine diabetes. In this study, 483 cases of canine diabetes and 869 controls of known breed were analyzed for association with IFNc, IGF2, IL-10, IL-12b, IL-6, insulin, PTPN22, RANTES, IL-4, IL-1a and TNFa. Minor allele frequencies were determined for these genes in each breed. These data were used for comparative analyses in a case control study, and clear associations with diabetes were identified in some breeds with certain alleles of candidate genes. Some associations were with increased susceptibility to the disease (IFNc, IL-10, IL-12b, IL-6, insulin, PTPN22, IL-4, and TNFa), whereas others were protective (IL-4, PTPN22, IL-6, insulin, IGF2, TNFa). This study demonstrates that a number of the candidate genes previously associated with human T1D also appear to be associated with canine diabetes and identifies an IL-10 haplotype which is associated with diabetes in the Cavalier King Charles Spaniel. This suggests that canine diabetes is an excellent comparative and spontaneously occurring disease model of human T1D.
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