Artigo Acesso aberto Revisado por pares

Vildagliptin, a Dipeptidyl Peptidase-IV Inhibitor, Improves Model-Assessed β-Cell Function in Patients with Type 2 Diabetes

2005; Oxford University Press; Volume: 90; Issue: 8 Linguagem: Inglês

10.1210/jc.2004-2460

ISSN

1945-7197

Autores

Andrea Mari, William M. Sallas, Yan‐Ling He, C. E. Watson, Monica Ligueros‐Saylan, Beth E. Dunning, Carolyn F. Deacon, Jens J. Holst, James E. Foley,

Tópico(s)

Neuropeptides and Animal Physiology

Resumo

Aims/Hypothesis: The dipeptidyl peptidase IV inhibitor, vildagliptin, increases levels of intact glucagon-like peptide-1 (GLP-1) and improves glycemic control in patients with type 2 diabetes. Although GLP-1 is known to stimulate insulin secretion, vildagliptin does not affect plasma insulin levels in diabetic patients, suggesting that more sophisticated measures are necessary to ascertain the influence of vildagliptin on β-cell function. Methods: This study examined the effects of 28-d treatment with vildagliptin (100 mg, twice daily; n = 9) vs. placebo (n = 11) on β-cell function in diabetic patients using a mathematical model that describes the insulin secretory rate as a function of glucose levels (β-cell dose response), the change in glucose with time (derivative component), and a potentiation factor, which is a function of time and may reflect the actions of nonglucose secretagogues and other factors. Results: Vildagliptin significantly increased the insulin secretory rate at 7 mmol/liter glucose (secretory tone), calculated from the dose response; the difference in least squares mean (ΔLSM) was 101 ± 51 pmol·min−1·m−2 (P = 0.002). The slope of the β-cell dose response, the derivative component, and the potentiation factor were not affected. Vildagliptin also significantly decreased mean prandial glucose (ΔLSM, −1.2 ± 0.4 mmol/liter; P = 0.01) and glucagon (ΔLSM, −10.7 ± 4.8 ng/liter; P = 0.03) levels and increased plasma levels of intact GLP-1 (ΔLSM, +10.8 ± 1.6 pmol/liter; P < 0.0001) and gastric inhibitory polypeptide (ΔLSM, +43.4 ± 9.4 pmol/liter; P < 0.0001) relative to placebo. Conclusion: Vildagliptin is an incretin degradation inhibitor that improves β-cell function in diabetic patients by increasing the insulin secretory tone.

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