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Progression to insulin therapy among patients with type 2 diabetes treated with sitagliptin or sulphonylurea plus metformin dual therapy
Aim To assess time to insulin initiation among patients with type 2 diabetes mellitus (T2DM) treated with sitagliptin versus sulphonylurea as add‐on to metformin. Methods This retrospective cohort study used GE Centricity electronic medical records and included patients aged ≥18 years with continuou...
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Published in: | Diabetes, obesity & metabolism obesity & metabolism, 2015-10, Vol.17 (10), p.956-964 |
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container_title | Diabetes, obesity & metabolism |
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creator | Inzucchi, S. E. Tunceli, K. Qiu, Y. Rajpathak, S. Brodovicz, K. G. Engel, S. S. Mavros, P. Radican, L. Brudi, P. Li, Z. Fan, C. P. S. Hanna, B. Tang, J. Blonde, L. |
description | Aim
To assess time to insulin initiation among patients with type 2 diabetes mellitus (T2DM) treated with sitagliptin versus sulphonylurea as add‐on to metformin.
Methods
This retrospective cohort study used GE Centricity electronic medical records and included patients aged ≥18 years with continuous medical records and an initial prescription of sitagliptin or sulphonylurea (index date) with metformin for ≥90 days during 2006–2013. Sitagliptin and sulphonylurea users were matched 1 : 1 using propensity score matching, and differences in insulin initiation were assessed using Kaplan–Meier curves and Cox regression. We used conditional logistic regression to examine the likelihood of insulin use 1–6 years after the index date for each year.
Results
Propensity score matching produced 3864 matched pairs. Kaplan–Meier analysis showed that sitagliptin users had a lower risk of insulin initiation compared with sulphonylurea users (p = 0.003), with 26.6% of sitagliptin users initiating insulin versus 34.1% of sulphonylurea users over 6 years. This finding remained significant after adjusting for baseline characteristics (hazard ratio 0.76, 95% confidence interval 0.65–0.90). Conditional logistic regression analyses confirmed that sitagliptin users were less likely to initiate insulin compared with sulphonylurea users [odds ratios for years 1–6: 0.77, 0.79, 0.81, 0.57, 0.29 and 0.75, respectively (p |
doi_str_mv | 10.1111/dom.12489 |
format | article |
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To assess time to insulin initiation among patients with type 2 diabetes mellitus (T2DM) treated with sitagliptin versus sulphonylurea as add‐on to metformin.
Methods
This retrospective cohort study used GE Centricity electronic medical records and included patients aged ≥18 years with continuous medical records and an initial prescription of sitagliptin or sulphonylurea (index date) with metformin for ≥90 days during 2006–2013. Sitagliptin and sulphonylurea users were matched 1 : 1 using propensity score matching, and differences in insulin initiation were assessed using Kaplan–Meier curves and Cox regression. We used conditional logistic regression to examine the likelihood of insulin use 1–6 years after the index date for each year.
Results
Propensity score matching produced 3864 matched pairs. Kaplan–Meier analysis showed that sitagliptin users had a lower risk of insulin initiation compared with sulphonylurea users (p = 0.003), with 26.6% of sitagliptin users initiating insulin versus 34.1% of sulphonylurea users over 6 years. This finding remained significant after adjusting for baseline characteristics (hazard ratio 0.76, 95% confidence interval 0.65–0.90). Conditional logistic regression analyses confirmed that sitagliptin users were less likely to initiate insulin compared with sulphonylurea users [odds ratios for years 1–6: 0.77, 0.79, 0.81, 0.57, 0.29 and 0.75, respectively (p < 0.05 for years 4 and 5)].
Conclusions
In this real‐world matched cohort study, patients with T2DM treated with sitagliptin had a significantly lower risk of insulin initiation compared with patients treated with sulphonylurea, both as add‐on to metformin.</description><identifier>ISSN: 1462-8902</identifier><identifier>EISSN: 1463-1326</identifier><identifier>DOI: 10.1111/dom.12489</identifier><identifier>PMID: 25962401</identifier><identifier>CODEN: DOMEF6</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject><![CDATA[Aged ; Antidiabetics ; Cohort analysis ; Confidence intervals ; database research ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - drug therapy ; DPP-IV inhibitor ; Drug Administration Schedule ; Drug Prescriptions - statistics & numerical data ; Drug Therapy, Combination ; Electronic medical records ; Female ; Health risk assessment ; Humans ; Hypoglycemic Agents - administration & dosage ; Insulin ; Insulin - administration & dosage ; insulin therapy ; Kaplan-Meier Estimate ; Male ; Medical records ; Metformin ; Metformin - administration & dosage ; Middle Aged ; Original ; Propensity Score ; Regression analysis ; Retrospective Studies ; Sitagliptin Phosphate - administration & dosage ; Sulfonylurea Compounds - administration & dosage ; sulphonylureas ; Time Factors ; type 2 diabetes]]></subject><ispartof>Diabetes, obesity & metabolism, 2015-10, Vol.17 (10), p.956-964</ispartof><rights>2015 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.</rights><rights>2015 John Wiley & Sons Ltd</rights><rights>2015. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5799-2862bed2c1984dc6fac856773d2462e6736f0b06dff94c9f853c8c673af29c4d3</citedby><cites>FETCH-LOGICAL-c5799-2862bed2c1984dc6fac856773d2462e6736f0b06dff94c9f853c8c673af29c4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25962401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inzucchi, S. E.</creatorcontrib><creatorcontrib>Tunceli, K.</creatorcontrib><creatorcontrib>Qiu, Y.</creatorcontrib><creatorcontrib>Rajpathak, S.</creatorcontrib><creatorcontrib>Brodovicz, K. G.</creatorcontrib><creatorcontrib>Engel, S. S.</creatorcontrib><creatorcontrib>Mavros, P.</creatorcontrib><creatorcontrib>Radican, L.</creatorcontrib><creatorcontrib>Brudi, P.</creatorcontrib><creatorcontrib>Li, Z.</creatorcontrib><creatorcontrib>Fan, C. P. S.</creatorcontrib><creatorcontrib>Hanna, B.</creatorcontrib><creatorcontrib>Tang, J.</creatorcontrib><creatorcontrib>Blonde, L.</creatorcontrib><title>Progression to insulin therapy among patients with type 2 diabetes treated with sitagliptin or sulphonylurea plus metformin dual therapy</title><title>Diabetes, obesity & metabolism</title><addtitle>Diabetes Obes Metab</addtitle><description>Aim
To assess time to insulin initiation among patients with type 2 diabetes mellitus (T2DM) treated with sitagliptin versus sulphonylurea as add‐on to metformin.
Methods
This retrospective cohort study used GE Centricity electronic medical records and included patients aged ≥18 years with continuous medical records and an initial prescription of sitagliptin or sulphonylurea (index date) with metformin for ≥90 days during 2006–2013. Sitagliptin and sulphonylurea users were matched 1 : 1 using propensity score matching, and differences in insulin initiation were assessed using Kaplan–Meier curves and Cox regression. We used conditional logistic regression to examine the likelihood of insulin use 1–6 years after the index date for each year.
Results
Propensity score matching produced 3864 matched pairs. Kaplan–Meier analysis showed that sitagliptin users had a lower risk of insulin initiation compared with sulphonylurea users (p = 0.003), with 26.6% of sitagliptin users initiating insulin versus 34.1% of sulphonylurea users over 6 years. This finding remained significant after adjusting for baseline characteristics (hazard ratio 0.76, 95% confidence interval 0.65–0.90). Conditional logistic regression analyses confirmed that sitagliptin users were less likely to initiate insulin compared with sulphonylurea users [odds ratios for years 1–6: 0.77, 0.79, 0.81, 0.57, 0.29 and 0.75, respectively (p < 0.05 for years 4 and 5)].
Conclusions
In this real‐world matched cohort study, patients with T2DM treated with sitagliptin had a significantly lower risk of insulin initiation compared with patients treated with sulphonylurea, both as add‐on to metformin.</description><subject>Aged</subject><subject>Antidiabetics</subject><subject>Cohort analysis</subject><subject>Confidence intervals</subject><subject>database research</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>DPP-IV inhibitor</subject><subject>Drug Administration Schedule</subject><subject>Drug Prescriptions - statistics & numerical data</subject><subject>Drug Therapy, Combination</subject><subject>Electronic medical records</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Hypoglycemic Agents - administration & dosage</subject><subject>Insulin</subject><subject>Insulin - administration & dosage</subject><subject>insulin therapy</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical records</subject><subject>Metformin</subject><subject>Metformin - administration & dosage</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Propensity Score</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Sitagliptin Phosphate - administration & dosage</subject><subject>Sulfonylurea Compounds - administration & dosage</subject><subject>sulphonylureas</subject><subject>Time Factors</subject><subject>type 2 diabetes</subject><issn>1462-8902</issn><issn>1463-1326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp9kk9vFCEUwCdGY2v14BcwJF70MC3_BoaLSVPtqqmtB43GC2GB2aUywwiMdb-BH1va6W7URLnwwvvxgwevqh4jeIjKODKhP0SYtuJOtY8oIzUimN29iXHdCoj3qgcpXUIIKWn5_WoPN4JhCtF-9fN9DKtoU3JhADkAN6TJuxKubVTjBqg-DCswquzskBO4cnkN8ma0AAPj1NJmm0COVmVr5mRyWa28G3ORhAiKbVyHYeOnAoHRTwn0Nnch9iVvJuW3Jz2s7nXKJ_vodj6oPp6--nDyuj67WLw5OT6rdcOFqHHL8NIarJFoqdGsU7ptGOfE4FKsZZywDi4hM10nqBZd2xDd6rKsOiw0NeSgejF7x2nZW6NLWVF5OUbXq7iRQTn5Z2Zwa7kK32UDCYGYF8GzW0EM3yabsuxd0tZ7NdgwJYk4YoLQFrGCPv0LvQxTHEp5ksBGUIwxxP-jiotTggm8dj2fKR1DStF2uysjKK-7QJYukDddUNgnv9e4I7ffXoCjGbhy3m7-bZIvL95tlfW8w6Vsf-x2qPhVlsfljfx0vpCLzw3hp2-_yHPyC0vLzjE</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Inzucchi, S. E.</creator><creator>Tunceli, K.</creator><creator>Qiu, Y.</creator><creator>Rajpathak, S.</creator><creator>Brodovicz, K. G.</creator><creator>Engel, S. S.</creator><creator>Mavros, P.</creator><creator>Radican, L.</creator><creator>Brudi, P.</creator><creator>Li, Z.</creator><creator>Fan, C. P. S.</creator><creator>Hanna, B.</creator><creator>Tang, J.</creator><creator>Blonde, L.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201510</creationdate><title>Progression to insulin therapy among patients with type 2 diabetes treated with sitagliptin or sulphonylurea plus metformin dual therapy</title><author>Inzucchi, S. E. ; Tunceli, K. ; Qiu, Y. ; Rajpathak, S. ; Brodovicz, K. G. ; Engel, S. S. ; Mavros, P. ; Radican, L. ; Brudi, P. ; Li, Z. ; Fan, C. P. S. ; Hanna, B. ; Tang, J. ; Blonde, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5799-2862bed2c1984dc6fac856773d2462e6736f0b06dff94c9f853c8c673af29c4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Antidiabetics</topic><topic>Cohort analysis</topic><topic>Confidence intervals</topic><topic>database research</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>DPP-IV inhibitor</topic><topic>Drug Administration Schedule</topic><topic>Drug Prescriptions - statistics & numerical data</topic><topic>Drug Therapy, Combination</topic><topic>Electronic medical records</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Hypoglycemic Agents - administration & dosage</topic><topic>Insulin</topic><topic>Insulin - administration & dosage</topic><topic>insulin therapy</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Medical records</topic><topic>Metformin</topic><topic>Metformin - administration & dosage</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Propensity Score</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Sitagliptin Phosphate - administration & dosage</topic><topic>Sulfonylurea Compounds - administration & dosage</topic><topic>sulphonylureas</topic><topic>Time Factors</topic><topic>type 2 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inzucchi, S. E.</creatorcontrib><creatorcontrib>Tunceli, K.</creatorcontrib><creatorcontrib>Qiu, Y.</creatorcontrib><creatorcontrib>Rajpathak, S.</creatorcontrib><creatorcontrib>Brodovicz, K. G.</creatorcontrib><creatorcontrib>Engel, S. S.</creatorcontrib><creatorcontrib>Mavros, P.</creatorcontrib><creatorcontrib>Radican, L.</creatorcontrib><creatorcontrib>Brudi, P.</creatorcontrib><creatorcontrib>Li, Z.</creatorcontrib><creatorcontrib>Fan, C. P. S.</creatorcontrib><creatorcontrib>Hanna, B.</creatorcontrib><creatorcontrib>Tang, J.</creatorcontrib><creatorcontrib>Blonde, L.</creatorcontrib><collection>Istex</collection><collection>Wiley_OA刊</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes, obesity & metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inzucchi, S. E.</au><au>Tunceli, K.</au><au>Qiu, Y.</au><au>Rajpathak, S.</au><au>Brodovicz, K. G.</au><au>Engel, S. S.</au><au>Mavros, P.</au><au>Radican, L.</au><au>Brudi, P.</au><au>Li, Z.</au><au>Fan, C. P. S.</au><au>Hanna, B.</au><au>Tang, J.</au><au>Blonde, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progression to insulin therapy among patients with type 2 diabetes treated with sitagliptin or sulphonylurea plus metformin dual therapy</atitle><jtitle>Diabetes, obesity & metabolism</jtitle><addtitle>Diabetes Obes Metab</addtitle><date>2015-10</date><risdate>2015</risdate><volume>17</volume><issue>10</issue><spage>956</spage><epage>964</epage><pages>956-964</pages><issn>1462-8902</issn><eissn>1463-1326</eissn><coden>DOMEF6</coden><abstract>Aim
To assess time to insulin initiation among patients with type 2 diabetes mellitus (T2DM) treated with sitagliptin versus sulphonylurea as add‐on to metformin.
Methods
This retrospective cohort study used GE Centricity electronic medical records and included patients aged ≥18 years with continuous medical records and an initial prescription of sitagliptin or sulphonylurea (index date) with metformin for ≥90 days during 2006–2013. Sitagliptin and sulphonylurea users were matched 1 : 1 using propensity score matching, and differences in insulin initiation were assessed using Kaplan–Meier curves and Cox regression. We used conditional logistic regression to examine the likelihood of insulin use 1–6 years after the index date for each year.
Results
Propensity score matching produced 3864 matched pairs. Kaplan–Meier analysis showed that sitagliptin users had a lower risk of insulin initiation compared with sulphonylurea users (p = 0.003), with 26.6% of sitagliptin users initiating insulin versus 34.1% of sulphonylurea users over 6 years. This finding remained significant after adjusting for baseline characteristics (hazard ratio 0.76, 95% confidence interval 0.65–0.90). Conditional logistic regression analyses confirmed that sitagliptin users were less likely to initiate insulin compared with sulphonylurea users [odds ratios for years 1–6: 0.77, 0.79, 0.81, 0.57, 0.29 and 0.75, respectively (p < 0.05 for years 4 and 5)].
Conclusions
In this real‐world matched cohort study, patients with T2DM treated with sitagliptin had a significantly lower risk of insulin initiation compared with patients treated with sulphonylurea, both as add‐on to metformin.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>25962401</pmid><doi>10.1111/dom.12489</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antidiabetics Cohort analysis Confidence intervals database research Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - drug therapy DPP-IV inhibitor Drug Administration Schedule Drug Prescriptions - statistics & numerical data Drug Therapy, Combination Electronic medical records Female Health risk assessment Humans Hypoglycemic Agents - administration & dosage Insulin Insulin - administration & dosage insulin therapy Kaplan-Meier Estimate Male Medical records Metformin Metformin - administration & dosage Middle Aged Original Propensity Score Regression analysis Retrospective Studies Sitagliptin Phosphate - administration & dosage Sulfonylurea Compounds - administration & dosage sulphonylureas Time Factors type 2 diabetes |
title | Progression to insulin therapy among patients with type 2 diabetes treated with sitagliptin or sulphonylurea plus metformin dual therapy |
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