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1.
Vet Clin Pathol ; 47(4): 582-588, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30556915

ABSTRACT

BACKGROUND: Markers of lipid and glucose metabolism are used in both clinical practice and research. Detection of abnormal laboratory results often relies on species-specific reference intervals, but interbreed variation can also affect data interpretation. OBJECTIVES: The purpose of the present study was to compare concentrations of selected biochemical variables among different dog breeds. METHODS: We analyzed a database containing information on biochemical variables from 534 dogs belonging to nine different breeds. All dogs were confirmed to be healthy based on history, physical examination, and ancillary tests. Concentrations of glucose, fructosamine, insulin, cholesterol, triglycerides, fatty acids, and C-reactive protein were compared using the nonparametric Kruskal-Wallis and Dunn's tests. RESULTS: All variables tested showed significant interbreed differences, although all breeds remained within the previously established RIs for dogs. Fructosamine, insulin, and cholesterol showed a wide interbreed variation that could affect the interpretation of results. CONCLUSIONS: Breed is an important factor to consider when assessing energy metabolism in dogs, especially for markers like fructosamine, insulin, and cholesterol, which vary considerably among breeds.


Subject(s)
Dogs/blood , Glucose/metabolism , Lipid Metabolism , Animals , Biomarkers/blood , Blood Glucose/analysis , C-Reactive Protein/analysis , Cholesterol/blood , Dogs/metabolism , Fatty Acids, Nonesterified/blood , Female , Fructosamine/blood , Insulin/blood , Male , Reference Values , Species Specificity , Triglycerides/blood
2.
PLoS One ; 10(5): e0123173, 2015.
Article in English | MEDLINE | ID: mdl-25970163

ABSTRACT

Diabetes mellitus is a serious health problem in both dogs and humans. Certain dog breeds show high prevalence of the disease, whereas other breeds are at low risk. Fructosamine and glycated haemoglobin (HbA1c) are two major biomarkers of glycaemia, where serum concentrations reflect glucose turnover over the past few weeks to months. In this study, we searched for genetic factors influencing variation in serum fructosamine concentration in healthy dogs using data from nine dog breeds. Considering all breeds together, we did not find any genome-wide significant associations to fructosamine serum concentration. However, by performing breed-specific analyses we revealed an association on chromosome 3 (pcorrected ≈ 1:68 × 10-6) in Belgian shepherd dogs of the Malinois subtype. The associated region and its close neighbourhood harbours interesting candidate genes such as LETM1 and GAPDH that are important in glucose metabolism and have previously been implicated in the aetiology of diabetes mellitus. To further explore the genetics of this breed specificity, we screened the genome for reduced heterozygosity stretches private to the Belgian shepherd breed. This revealed a region with reduced heterozygosity that shows a statistically significant interaction (p = 0.025) with the association region on chromosome 3. This region also harbours some interesting candidate genes and regulatory regions but the exact mechanisms underlying the interaction are still unknown. Nevertheless, this finding provides a plausible explanation for breed-specific genetic effects for complex traits in dogs. Shepherd breeds are at low risk of developing diabetes mellitus. The findings in Belgian shepherds could be connected to a protective mechanism against the disease. Further insight into the regulation of glucose metabolism could improve diagnostic and therapeutic methods for diabetes mellitus.


Subject(s)
Diabetes Mellitus/veterinary , Dog Diseases/genetics , Fructosamine/genetics , Genetic Loci , Genetic Predisposition to Disease , Animals , Breeding , Chromosomes, Mammalian , Diabetes Mellitus/genetics , Dogs , Female , Genome-Wide Association Study , Glycated Hemoglobin/genetics , Glyceraldehyde-3-Phosphate Dehydrogenase (NADP+)(Phosphorylating)/genetics , Heterozygote , Humans , Leucine Zippers/genetics , Loss of Heterozygosity , Male , Phenotype , Species Specificity
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