Abstract

AimPremixed insulin regimens are commonly used for the treatment of patients with type-2 diabetes mellitus (T2DM). However, limited data are available regarding next-step therapy options in cases where premixed insulin fails to provide adequate glycemic control. This 20-week observational study of everyday clinical practice evaluated the efficacy, safety and treatment satisfaction of insulin glargine plus oral anti-diabetic drugs (OADs) in T2DM patients previously treated with premixed insulin.MethodsIn this open-label, single-arm, 20-week study, 70 subjects with T2DM inadequately controlled with premixed insulin were switched to insulin glargine plus OADs. Changes in glycaemic control, incidence of hypoglycaemia, treatment satisfaction using the Diabetes Treatment Satisfaction Questionnaire (DTSQ), serum superoxide dismutase (SOD), and serum 8-iso-prostaglandin (8-iso-PG) were evaluated at the start and the end of the study.ResultsOver the 20 week treatment period, mean (±SD) HbA1c levels decreased from 8.28 ± 1.24% to 6.83 ± 1.09%, mean (±SD) FBG levels decreased from 7.64 ± 1.36 mmol/L to 5.57 ± 1.21 mmol/L, and 2 h PBG levels decreased from 12.07 ± 1.17 mmol/L to 8.94 ± 1.56 mmol/L, all P < 0.001. A total of 3 symptomatic hypoglycemic episodes were reported. No significant reductions in body weight were observed. The mean daily dose of insulin decreased by 14 U between week 0 (30.20 ± 9.93 U) and week 20 (16.38 ± 5.15 U). The total treatment satisfaction score showed a significant increase from study baseline to end point. Significant increases in SOD(90.00 ± 16.62 to 108.81 ± 27.02 u/ml, P < 0.01) and reductions in 8-iso-PG(2.15 ± 0.61 to 1.64 ± 0.42 pg/ml, P < 0.05) were observed between the start and end of the observation period. There were significant differences in baseline HbA1c, duration of diabetes, and baseline postprandial C-peptide between the A1c ≤ 6.5% group and the A1c > 7.0% group [HbA1c: 7.25% ± 1.02% vs. 9.32% ± 1.23%; duration: 7.84 ± 1.02 vs. 13.96 ± 1.35 years; postprandial C-peptide: 4.83 ± 2.11 vs 2.54 ± 0.87 nmol/L, all P < 0.05].ConclusionsThe observational study shows that, in T2DM patients inadequately controlled with premixed insulin, switching therapy to glargine plus OADs is associated with significant improvements in glycaemic control and treatment satisfaction, and is with low incidence of hypoglycemia. Baseline postprandial C-peptide, HbA1c, and duration of diabetes are the key factors closely related to efficacy of this treatment regimen.

Highlights

  • Type-2 diabetes mellitus (T2DM) is a progressive condition in which the level of glycated hemoglobin rises inexorably over time, and the function of beta cells declines

  • Professional diabetes organizations recommend that basal or premixed insulin could be used as the initial insulin therapy

  • 8 patients treated with premix insulin from diagnosis of DM, 43 patients initiated insulin after failure of one or two oral anti-diabetes drugs (OADs), 19 patients initiated insulin after failure of two or three OADs

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Summary

Introduction

Type-2 diabetes mellitus (T2DM) is a progressive condition in which the level of glycated hemoglobin rises inexorably over time, and the function of beta cells declines. If lifestyle interventions and oral anti-diabetes drugs (OADs) prove inadequate in controlling glycemic levels, insulin therapy becomes necessary. Professional diabetes organizations recommend that basal or premixed insulin could be used as the initial insulin therapy. Premixed insulin alone can be insufficient to achieve and sustain optimal glycemic control, and there are often additional concerns regarding hypoglycemia, weight gain, and lifestyle restrictions [2]. There is limited information available regarding therapeutic options for patients for who premixed insulin provides inadequate glycemic control, who frequently experience episodes of hypoglycemia or those who want to avoid additional injections

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