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Short‐ and long‐term effect of sitagliptin after near normalization of glycemic control with insulin in poorly controlled Japanese type 2 diabetic patients
Authors:Keiko Fujisawa  Tetsuyuki Yasuda  Hideaki Kaneto  Naoto Katakami  Mayumi Tsuji  Fumiyo Kubo  Shugo Sasaki  Kazuyuki Miyashita  Toyoko Naka  Ryuuichi Kasami  Akio Kuroda  Munehide Matsuhisa  Iichiro Shimomura
Affiliation:1. Department of Metabolic Medicine, Osaka University Graduate School of Medicine, , Osaka, Japan;2. Diabetes Therapeutics and Research Center, Tokushima University, , Tokushima, Japan
Abstract:

Aims/Introduction

The aim of the present study was to examine the short‐ and long‐term effect of sitagliptin on glucose tolerance after near normalization of glycemic control with insulin in poorly controlled type 2 diabetic patients.

Materials and Methods

We consecutively enrolled a total of 30 type 2 diabetic patients whose glycated hemoglobin levels (National Glycohemoglobin Standardization Program) were ≥7.4%, stopped all oral antidiabetic drugs and started insulin therapy. When fasting plasma glucose levels became <140 mg/dL, we carried out the first oral glucose tolerance test (OGTT). After 1‐week sitagliptin treatment (50 mg/day), the second OGTT was carried out. Furthermore, we evaluated the long‐term efficacy of sitagliptin on glucose tolerance after near normalization of glycemic control with insulin.

Results

After 1‐week sitagliptin treatment, the area under the curve of insulin was markedly increased, and the area under the curve of glucagon and glucose was markedly decreased. Duration of diabetes and insulin secretory capacity were correlated with the effect of sitagliptin. Furthermore, interestingly, near normalization of glycemic control with insulin therapy for 1–2 weeks brought out the long‐term effectiveness of sitagliptin on glucose tolerance for 24 weeks, which was not observed with other antidiabetic drugs.

Conclusions

These findings suggest that near normalization of glycemic control with insulin improves the clinical response to sitagliptin in poorly controlled type 2 diabetic patients.
Keywords:Dipeptidyl peptidase‐4 inhibitor  Insulin therapy  Sitagliptin
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