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Withdrawal of sulfonylureas from patients with type 2 diabetes receiving long-term sulfonylurea and insulin combination therapy results in deterioration of glycemic control: a randomized controlled trial

The benefit of sulfonylureas (SUs) to patients with type 2 diabetes mellitus receiving long-term insulin treatment is unclear. This study evaluated glycemic control and beta-cell function after SU withdrawal in these patients. In this 8-week randomized controlled study, patients with type 2 diabetes...

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Published in:Diabetes, metabolic syndrome and obesity metabolic syndrome and obesity, 2015-01, Vol.8 (default), p.137-145
Main Authors: Srivanichakorn, Weerachai, Sriwijitkamol, Apiradee, Kongchoo, Aroon, Sriussadaporn, Sutin, Plengvidhya, Nattachet, Lertwattanarak, Raweewan, Vannasaeng, Sathit, Thongtang, Nuntakorn
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container_title Diabetes, metabolic syndrome and obesity
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creator Srivanichakorn, Weerachai
Sriwijitkamol, Apiradee
Kongchoo, Aroon
Sriussadaporn, Sutin
Plengvidhya, Nattachet
Lertwattanarak, Raweewan
Vannasaeng, Sathit
Thongtang, Nuntakorn
description The benefit of sulfonylureas (SUs) to patients with type 2 diabetes mellitus receiving long-term insulin treatment is unclear. This study evaluated glycemic control and beta-cell function after SU withdrawal in these patients. In this 8-week randomized controlled study, patients with type 2 diabetes who had been treated with insulin for at least 3 years plus moderate to high doses of SUs were randomly assigned to withdrawal (n=16) or continuation (n=16) of SUs. Clinical characteristics, glycemic control, hypoglycemic events, and insulin secretion, including homeostasis model assessment of beta-cell function (HOMA-B) score, C-peptide concentration, and Matsuda index, were evaluated at baseline and after 2 and 8 weeks. Thirty patients (16 in the SU withdrawal group and 14 in the SU continuation group) completed the study. Median duration of diabetes was 17 (range 5-40) years. Baseline clinical characteristics, glycemic control, and HOMA-B were similar in the two groups, but the mean fasting C-peptide concentration was higher in the SU withdrawal group. After 8 weeks, the SU withdrawal group showed a significant increase in mean glycosylated hemoglobin levels from 7.8%±0.5% (62±5 mmol/mol) to 8.6%±1.2% (71±13 mmol/mol; P=0.002), whereas the SU continuation group showed a slight but not significant increase from 7.7%±0.5% (61±5 mmol/mol) to 7.9%±1.2% (63±13 mmol/mol; P=0.37). Insulin secretion, as measured by C-peptide and HOMA-B, decreased by 18% and 36%, respectively, in the SU withdrawal group. Hypoglycemic events were significantly more frequent in the SU continuation group whereas body weight did not change significantly in either group. Withdrawal of SU from patients with type 2 diabetes receiving long-term combination treatment with SU and insulin resulted in deterioration of glycemic control and insulin secretion.
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This study evaluated glycemic control and beta-cell function after SU withdrawal in these patients. In this 8-week randomized controlled study, patients with type 2 diabetes who had been treated with insulin for at least 3 years plus moderate to high doses of SUs were randomly assigned to withdrawal (n=16) or continuation (n=16) of SUs. Clinical characteristics, glycemic control, hypoglycemic events, and insulin secretion, including homeostasis model assessment of beta-cell function (HOMA-B) score, C-peptide concentration, and Matsuda index, were evaluated at baseline and after 2 and 8 weeks. Thirty patients (16 in the SU withdrawal group and 14 in the SU continuation group) completed the study. Median duration of diabetes was 17 (range 5-40) years. Baseline clinical characteristics, glycemic control, and HOMA-B were similar in the two groups, but the mean fasting C-peptide concentration was higher in the SU withdrawal group. After 8 weeks, the SU withdrawal group showed a significant increase in mean glycosylated hemoglobin levels from 7.8%±0.5% (62±5 mmol/mol) to 8.6%±1.2% (71±13 mmol/mol; P=0.002), whereas the SU continuation group showed a slight but not significant increase from 7.7%±0.5% (61±5 mmol/mol) to 7.9%±1.2% (63±13 mmol/mol; P=0.37). Insulin secretion, as measured by C-peptide and HOMA-B, decreased by 18% and 36%, respectively, in the SU withdrawal group. Hypoglycemic events were significantly more frequent in the SU continuation group whereas body weight did not change significantly in either group. Withdrawal of SU from patients with type 2 diabetes receiving long-term combination treatment with SU and insulin resulted in deterioration of glycemic control and insulin secretion.</description><identifier>ISSN: 1178-7007</identifier><identifier>EISSN: 1178-7007</identifier><identifier>DOI: 10.2147/DMSO.S78008</identifier><identifier>PMID: 25767401</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Analysis ; Care and treatment ; Cholesterol ; Combination therapy ; Diabetes ; Drug dosages ; Endocrinology ; Evidence-based medicine ; Feasibility studies ; Glucose ; Glucose monitoring ; Health aspects ; Hemoglobin ; Homeostasis ; Hypoglycemia ; Insulin ; Insulin resistance ; Laboratories ; Metabolism ; Original Research ; Peptides ; Triglycerides</subject><ispartof>Diabetes, metabolic syndrome and obesity, 2015-01, Vol.8 (default), p.137-145</ispartof><rights>COPYRIGHT 2015 Dove Medical Press Limited</rights><rights>2015. 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After 8 weeks, the SU withdrawal group showed a significant increase in mean glycosylated hemoglobin levels from 7.8%±0.5% (62±5 mmol/mol) to 8.6%±1.2% (71±13 mmol/mol; P=0.002), whereas the SU continuation group showed a slight but not significant increase from 7.7%±0.5% (61±5 mmol/mol) to 7.9%±1.2% (63±13 mmol/mol; P=0.37). Insulin secretion, as measured by C-peptide and HOMA-B, decreased by 18% and 36%, respectively, in the SU withdrawal group. Hypoglycemic events were significantly more frequent in the SU continuation group whereas body weight did not change significantly in either group. Withdrawal of SU from patients with type 2 diabetes receiving long-term combination treatment with SU and insulin resulted in deterioration of glycemic control and insulin secretion.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>25767401</pmid><doi>10.2147/DMSO.S78008</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source Taylor & Francis Open Access; Publicly Available Content Database; PubMed Central
subjects Analysis
Care and treatment
Cholesterol
Combination therapy
Diabetes
Drug dosages
Endocrinology
Evidence-based medicine
Feasibility studies
Glucose
Glucose monitoring
Health aspects
Hemoglobin
Homeostasis
Hypoglycemia
Insulin
Insulin resistance
Laboratories
Metabolism
Original Research
Peptides
Triglycerides
title Withdrawal of sulfonylureas from patients with type 2 diabetes receiving long-term sulfonylurea and insulin combination therapy results in deterioration of glycemic control: a randomized controlled trial
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