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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 |
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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. |
doi_str_mv | 10.2147/DMSO.S78008 |
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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. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Srivanichakorn et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-66743775c8bd4c5925e0f60f099e62b24db062619d9320c7fbf530dc067d082a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2226038453/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2226038453?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25767401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Srivanichakorn, Weerachai</creatorcontrib><creatorcontrib>Sriwijitkamol, Apiradee</creatorcontrib><creatorcontrib>Kongchoo, Aroon</creatorcontrib><creatorcontrib>Sriussadaporn, Sutin</creatorcontrib><creatorcontrib>Plengvidhya, Nattachet</creatorcontrib><creatorcontrib>Lertwattanarak, Raweewan</creatorcontrib><creatorcontrib>Vannasaeng, Sathit</creatorcontrib><creatorcontrib>Thongtang, Nuntakorn</creatorcontrib><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</title><title>Diabetes, metabolic syndrome and obesity</title><addtitle>Diabetes Metab Syndr Obes</addtitle><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.</description><subject>Analysis</subject><subject>Care and treatment</subject><subject>Cholesterol</subject><subject>Combination therapy</subject><subject>Diabetes</subject><subject>Drug dosages</subject><subject>Endocrinology</subject><subject>Evidence-based medicine</subject><subject>Feasibility studies</subject><subject>Glucose</subject><subject>Glucose monitoring</subject><subject>Health aspects</subject><subject>Hemoglobin</subject><subject>Homeostasis</subject><subject>Hypoglycemia</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Laboratories</subject><subject>Metabolism</subject><subject>Original Research</subject><subject>Peptides</subject><subject>Triglycerides</subject><issn>1178-7007</issn><issn>1178-7007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQQCMEolXpiTuyhISQ0C6O49gJB6SqfFUq6qEgjpZjO1lXjr21nVbLX-RPMWHbsotIDrFm3jzH4ymK5yVekpLytx--Xl4sL3mDcfOoOCxL3iw4xvzxzvqgOE7pCs8Px5SQp8UBqTnjFJeHxa8fNq90lLfSodCjNLk--I2bopEJ9TGMaC2zNT4ndAskypu1QQRpKzuTTULRKGNvrB-QC35YZBPHPQmSXiPrIWQ9UmHsrAdf8CivTJTrDQggB3ZIazBGG-IWgL8Z3EaZ0Soo9DkG9w5JFEEYRvvT6Puog2WOVrpnxZNeumSO775HxfdPH7-dflmcX3w-Oz05X6iaV3nB4OgV57VqOk1V3ZLa4J7hHretYaQjVHeYEVa2uq0IVrzv-rrCWmHGNW6IrI6Ks61XB3kl1tGOMm5EkFb8CYQ4CBmzVc6IrmVQXUrDJKZ9K9tK8ZaqjjJZq0514Hq_da2nbjRaQaejdHvS_Yy3KzGEG0GrmlYtA8HrO0EM15NJWYw2KeOc9CZMSZSMUVJimBBAX_6DXoUpemiVIIQwXDW0rv5Sg4QDWN8H2FfNUnFCad3wmlIO1PI_FLx6vrDgTW8hvlfwaqdgZaTLqxTcNN912gffbEEVQ0rR9A_NKLGYZ17MMy-2Mw_0i93-PbD3E179BjmHAKc</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Srivanichakorn, Weerachai</creator><creator>Sriwijitkamol, Apiradee</creator><creator>Kongchoo, Aroon</creator><creator>Sriussadaporn, Sutin</creator><creator>Plengvidhya, Nattachet</creator><creator>Lertwattanarak, Raweewan</creator><creator>Vannasaeng, Sathit</creator><creator>Thongtang, Nuntakorn</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>KB0</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150101</creationdate><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</title><author>Srivanichakorn, Weerachai ; Sriwijitkamol, Apiradee ; Kongchoo, Aroon ; Sriussadaporn, Sutin ; Plengvidhya, Nattachet ; Lertwattanarak, Raweewan ; Vannasaeng, Sathit ; Thongtang, Nuntakorn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-66743775c8bd4c5925e0f60f099e62b24db062619d9320c7fbf530dc067d082a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Care and treatment</topic><topic>Cholesterol</topic><topic>Combination therapy</topic><topic>Diabetes</topic><topic>Drug dosages</topic><topic>Endocrinology</topic><topic>Evidence-based medicine</topic><topic>Feasibility studies</topic><topic>Glucose</topic><topic>Glucose monitoring</topic><topic>Health aspects</topic><topic>Hemoglobin</topic><topic>Homeostasis</topic><topic>Hypoglycemia</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Laboratories</topic><topic>Metabolism</topic><topic>Original Research</topic><topic>Peptides</topic><topic>Triglycerides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srivanichakorn, Weerachai</creatorcontrib><creatorcontrib>Sriwijitkamol, Apiradee</creatorcontrib><creatorcontrib>Kongchoo, Aroon</creatorcontrib><creatorcontrib>Sriussadaporn, Sutin</creatorcontrib><creatorcontrib>Plengvidhya, Nattachet</creatorcontrib><creatorcontrib>Lertwattanarak, Raweewan</creatorcontrib><creatorcontrib>Vannasaeng, Sathit</creatorcontrib><creatorcontrib>Thongtang, Nuntakorn</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Diabetes, metabolic syndrome and obesity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Srivanichakorn, Weerachai</au><au>Sriwijitkamol, Apiradee</au><au>Kongchoo, Aroon</au><au>Sriussadaporn, Sutin</au><au>Plengvidhya, Nattachet</au><au>Lertwattanarak, Raweewan</au><au>Vannasaeng, Sathit</au><au>Thongtang, Nuntakorn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Diabetes, metabolic syndrome and obesity</jtitle><addtitle>Diabetes Metab Syndr Obes</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>8</volume><issue>default</issue><spage>137</spage><epage>145</epage><pages>137-145</pages><issn>1178-7007</issn><eissn>1178-7007</eissn><abstract>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.</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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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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