Abstract

BackgroundBezafibrate is mainly used to treat hypertriglyceridemia. Studies have reported that bezafibrate also improves type 2 diabetes mellitus, but the mechanism has not been fully elucidated. We performed euglycemic hyperinsulinemic clamps (glucose clamp) and meal tolerance tests (MTT) to examine the effects of bezafibrate on insulin resistance in patients with type 2 diabetes mellitus.MethodsTwelve Japanese patients with type 2 diabetes mellitus and dyslipidemia (mean age: 59.5 years; fasting plasma glucose: 7.95 mmol/L; hemoglobin A1c [HbA1c]: 7.3%; body mass index: 26.5 kg/m2) underwent a glucose clamp and MTT before and after 12 weeks of treatment with 400 mg/day bezafibrate. The glucose infusion rate was measured during the glucose clamp. The patients took a test meal (460 kcal) in the MTT. Plasma glucose and immunoreactive insulin levels were measured at 0 (fasting), 30, 60, 120, and 180 min. Serum C-peptide immunoreactivity, serum lipids, and liver function markers were also measured during the MTT.ResultsBezafibrate significantly increased the mean glucose infusion rate from 5.78 ± 1.94 to 6.78 ± 2.52 mg/kg/min (p < 0.05). HbA1c improved from 7.30 ± 0.55% to 7.02 ± 0.52% (p < 0.05). In the MTT, fasting plasma glucose decreased from 7.95 ± 1.15 to 6.98 ± 1.07 mmol/L (p < 0.05). The area under the plasma glucose curve from 0 to 180 min decreased significantly from 29.48 ± 5.07 to 27.12 ± 3.98 mmol/h/L (p < 0.05), whereas immunoreactive insulin was unchanged. Furthermore, bezafibrate also significantly improved serum lipids, with decreases in triglyceride levels from 1.84 ± 0.88 to 1.14 ± 0.41 mmol/L (p < 0.05), low-density lipoprotein cholesterol levels from 3.56 ± 0.83 to 2.92 ± 0.55 mmol/L (p < 0.05), and remnant-like particle cholesterol levels decreased from 0.25 ± 0.16 to 0.14 ± 0.06 mmol/L (p < 0.05), and increases in high-density lipoprotein cholesterol levels from 1.50 ± 0.24 to 1.66 ± 0.29 mmol/L (p < 0.05).ConclusionsBezafibrate improved glucose intolerance and peripheral insulin resistance in these Japanese patients with type 2 diabetes mellitus and dyslipidemia. Therefore, bezafibrate could be used to treat insulin resistance in patients with type 2 diabetes mellitus and dyslipidemia.Trial registrationUniversity Hospital Medical Information Network (UMIN) Clinical Trials Registry, UMIN000012462.

Highlights

  • Bezafibrate is mainly used to treat hypertriglyceridemia

  • In the Japan bezafibrate clinical effectiveness and tolerability (JBENEFIT) study, a large-scale study of 3316 patients with type 2 diabetes mellitus and dyslipidemia, administration of 200–400 mg/day of bezafibrate for 24 weeks decreased hemoglobin A1c (HbA1c) from 7.69% to 7.22% and fasting blood glucose levels from 9.00 to 7.81 mmol/L [6]. These results indicate that bezafibrate is effective for the treatment of type 2 diabetes mellitus

  • The glucose infusion rate (GIR) significantly increased from 5.78 mg/kg/min before bezafibrate

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Summary

Introduction

Bezafibrate is mainly used to treat hypertriglyceridemia. Studies have reported that bezafibrate improves type 2 diabetes mellitus, but the mechanism has not been fully elucidated. In the Japan bezafibrate clinical effectiveness and tolerability (JBENEFIT) study, a large-scale study of 3316 patients with type 2 diabetes mellitus and dyslipidemia, administration of 200–400 mg/day of bezafibrate for 24 weeks decreased hemoglobin A1c (HbA1c) from 7.69% to 7.22% and fasting blood glucose levels from 9.00 to 7.81 mmol/L [6]. These results indicate that bezafibrate is effective for the treatment of type 2 diabetes mellitus

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