Key result
Canine diabetes is linked to ~74% lower serum betatrophin levels, unresolved by insulin therapy.
Why the study?
Visfatin and betatrophin are adipokines involved in insulin resistance and altered lipid metabolism, and the authors hypothesized their serum concentrations are altered in diabetic dogs irrespective of body condition.
Cross-Sectional (n=81)
DM-associated visfatin and betatrophin alterations persist despite insulin; hypothesis-generating for adipokine roles in canine DM, prospective studies needed.
Canine diabetes mellitus (DM) is associated with hyperglycemia and hyperlipidemia. Visfatin and betatrophin are adipokines involved in the pathophysiology of insulin resistance and deranged lipid metabolism, and are also altered in obesity. We hypothesized that visfatin and betatrophin serum concentrations are altered in diabetic dogs, irrespective of their body condition. The study included 23 newly-diagnosed DM (NDDM) dogs, 34 insulin-treated DM (ITDM) dogs and 24 healthy dogs. Body condition score was determined and fasted serum samples were collected for measurement of betatrophin, visfatin and insulin serum concentrations. Visfatin concentrations (mean, 95% CI) were lower in overweight NDDM (4.5 ng/mL, 2.5-8.1, P=0.05) and ITDM (2.8 ng/mL 1.8-4.3, P=0.006) than healthy (7.7 ng/mL, 5.0-11.7) dogs, but were not different among lean dogs, and were negatively correlated to betahydroxybutyric acid in ITDM dogs (r=-0.59, P=0.05). Betatrophin concentrations were lower in NDDM (69 pg/mL, 43-112, P<0.001) and ITDM (53 pg/mL, 34-84, P<0.001) than healthy (267 pg/mL, 167-426) dogs. Among NDDM dogs, betatrophin concentrations were higher in those with concurrent liver disease (203 pg/mL, 49-844) than those with no evidence of liver disease (19 pg/mL, 4-90, P=0.007), and were negatively correlated with glucose concentrations (r=-0.44, P=0.04) and creatinine (r=-0.60, P=0.003). Insulin concentrations were not different among NDDM and healthy dogs. Among NDDM dogs, insulin concentrations were negatively correlated to concentrations of betahydroxybutyric acid (r=-0.65, P=0.002) and were lower in dogs with concurrent kidney disease (5.6 mU/L, 2.1-15.3) compared to those with no evidence of kidney disease (20.6 mU/L, 8.0-53.2, P=0.018). In conclusion, DM in dogs is associated with alteration in visfatin and betatrophin concentrations that are not resolved by insulin treatment.
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Slon et al. (2025) conducted a cross-sectional in Canine diabetes mellitus (n=81). Diabetes mellitus vs. Healthy dogs was evaluated on Serum concentrations of visfatin and betatrophin (p=<0.001). Diabetic dogs had lower serum betatrophin (69 pg/mL in newly-diagnosed, 53 pg/mL in insulin-treated vs 267 pg/mL in healthy; P<0.001) and visfatin concentrations, unresolved by insulin.
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