Use of C-peptide and homeostasis model assessment of insulin resistance to assess insulin resistance in dogs.
Torsahakul C, Rodprasert W, Simphaisarn K, Kanthathong N, Kaonarsanga S, Sannamwong N, Jeamsripong S, Sawangmake C · Journal of Veterinary Internal Medicine · 4 May 2026
HOMA-IR by C-peptide and HOMA-IRCP2 are reliable, non-invasive tools for detecting insulin resistance in diabetic dogs.
This cross-sectional prospective study evaluated the diagnostic utility of C-peptide and homeostasis model assessment (HOMA) indices for detecting insulin resistance (IR) in dogs. Seventy-six dogs from a referral center were classified into four groups: healthy (n=17), pre-diabetes mellitus (PreDM, n=11), insulin-dependent diabetes mellitus (IDDM, n=20), and diabetes mellitus with insulin resistance (DMIR, n=28). Fasting blood samples were analyzed for glucose, C-peptide, and metabolic markers, with HOMA-IR by C-peptide, HOMA-IRCP2, and HOMA2-IR calculated and compared across groups. The DMIR group demonstrated significantly elevated C-peptide and all HOMA indices compared to other groups. ROC curve analysis confirmed diagnostic accuracy for IR detection: HOMA-IR by C-peptide achieved the highest AUC (0.897), followed by HOMA-IRCP2 (0.893), C-peptide alone (0.843), and HOMA2-IR (0.789), all statistically significant (P<0.001). Optimal cutoff values identified were C-peptide ≥0.7 ng/mL and HOMA-IR by C-peptide ≥120 for highest sensitivity (92.9%), while HOMA-IRCP2 ≥1.65 provided the highest specificity (97.9%). These non-invasive biomarkers offer clinically practical alternatives to more complex diagnostic methods such as euglycemic-hyperinsulinemic clamps. Early identification of IR through these indices may enable timely therapeutic intervention, potentially improving glycemic management and overall clinical outcomes in diabetic dogs. The findings support integration of C-peptide-based HOMA indices into routine diabetic monitoring protocols in small animal practice.
This summary was distilled by AI and may occasionally misinterpret data. Confirm critical details with the primary literature before clinical application.