A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes

A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes Martin St. John Sutton , FRCP 1 , Marc Rendell , MD 2 , Paresh Dandona , MD 3 , Jo F. Dole , PHD 4 , Karen Murphy , MT (ASCP) 4 , Rita Patwardhan , PHD 4 , Jai...

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Veröffentlicht in:Diabetes care 2002-11, Vol.25 (11), p.2058-2064
Hauptverfasser: SUTTON, Martin St, RENDELL, Marc, DANDONA, Paresh, DOLE, Jo F, MURPHY, Karen, PATWARDHAN, Rita, PATEL, Jai, FREED, Martin
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container_end_page 2064
container_issue 11
container_start_page 2058
container_title Diabetes care
container_volume 25
creator SUTTON, Martin St
RENDELL, Marc
DANDONA, Paresh
DOLE, Jo F
MURPHY, Karen
PATWARDHAN, Rita
PATEL, Jai
FREED, Martin
description A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes Martin St. John Sutton , FRCP 1 , Marc Rendell , MD 2 , Paresh Dandona , MD 3 , Jo F. Dole , PHD 4 , Karen Murphy , MT (ASCP) 4 , Rita Patwardhan , PHD 4 , Jai Patel , MD 4 , Martin Freed , MD 4 and For the Rosiglitazone Clinical Trials Study Group 1 University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 2 Creighton University, Omaha, Nebraska 3 State University of New York School of Medicine at Buffalo, Buffalo, New York 4 GlaxoSmithKline, Collegeville, Pennsylvania Abstract OBJECTIVE —This open-label, active-controlled study investigated the cardiac safety and antihyperglycemic effect of rosiglitazone (RSG) in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS —Of the 203 patients randomly assigned to RSG (4 mg b.i.d.) or glyburide (GLB) (titrated to achieve optimal glycemic control for the first 8 weeks only to limit the risk of hypoglycemia; mean 10.5 mg/day), 118 had an echocardiogram performed at week 52. Left ventricular (LV) mass index, ejection fraction, and left ventricular end-diastolic volume were assessed by M-mode echocardiography at baseline and weeks 12, 28, and 52; 24-h ambulatory blood pressure was assessed at baseline and at weeks 28 and 52. Glycemic control was assessed by measuring fasting plasma glucose (FPG) and HbA 1c . RESULTS —Neither treatment produced an increase in LV mass index that exceeded 1 SD. Ejection fraction did not change in either group. Both groups had clinically insignificant increases in LV end-diastolic volume. RSG, but not GLB, caused a statistically significant reduction in ambulatory diastolic blood pressure. Both treatments reduced HbA 1c and FPG. CONCLUSIONS —A total of 52 weeks of therapy with RSG (4 mg b.i.d.) did not adversely affect cardiac structure or function in patients with type 2 diabetes and produced significant and sustained reductions in hyperglycemia. Decreases in ambulatory diastolic blood pressure with RSG were superior to those with GLB. ACEI, ACE inhibitor AE, adverse event BP, blood pressure ECG, electrocardiogram EF, ejection fraction FPG, fasting plasma glucose GLB, glyburide ITT, intent to treat LOCF, last observation carried forward LV, left ventricular LVEDV, LV end-diastolic volume LVM, LV mass LVMI, LV mass index MR, mitral regurgitation RSG, rosiglitazone Footnotes Address correspondence and reprint requests to Martin St.
doi_str_mv 10.2337/diacare.25.11.2058
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Dole , PHD 4 , Karen Murphy , MT (ASCP) 4 , Rita Patwardhan , PHD 4 , Jai Patel , MD 4 , Martin Freed , MD 4 and For the Rosiglitazone Clinical Trials Study Group 1 University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 2 Creighton University, Omaha, Nebraska 3 State University of New York School of Medicine at Buffalo, Buffalo, New York 4 GlaxoSmithKline, Collegeville, Pennsylvania Abstract OBJECTIVE —This open-label, active-controlled study investigated the cardiac safety and antihyperglycemic effect of rosiglitazone (RSG) in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS —Of the 203 patients randomly assigned to RSG (4 mg b.i.d.) or glyburide (GLB) (titrated to achieve optimal glycemic control for the first 8 weeks only to limit the risk of hypoglycemia; mean 10.5 mg/day), 118 had an echocardiogram performed at week 52. Left ventricular (LV) mass index, ejection fraction, and left ventricular end-diastolic volume were assessed by M-mode echocardiography at baseline and weeks 12, 28, and 52; 24-h ambulatory blood pressure was assessed at baseline and at weeks 28 and 52. Glycemic control was assessed by measuring fasting plasma glucose (FPG) and HbA 1c . RESULTS —Neither treatment produced an increase in LV mass index that exceeded 1 SD. Ejection fraction did not change in either group. Both groups had clinically insignificant increases in LV end-diastolic volume. RSG, but not GLB, caused a statistically significant reduction in ambulatory diastolic blood pressure. Both treatments reduced HbA 1c and FPG. CONCLUSIONS —A total of 52 weeks of therapy with RSG (4 mg b.i.d.) did not adversely affect cardiac structure or function in patients with type 2 diabetes and produced significant and sustained reductions in hyperglycemia. Decreases in ambulatory diastolic blood pressure with RSG were superior to those with GLB. ACEI, ACE inhibitor AE, adverse event BP, blood pressure ECG, electrocardiogram EF, ejection fraction FPG, fasting plasma glucose GLB, glyburide ITT, intent to treat LOCF, last observation carried forward LV, left ventricular LVEDV, LV end-diastolic volume LVM, LV mass LVMI, LV mass index MR, mitral regurgitation RSG, rosiglitazone Footnotes Address correspondence and reprint requests to Martin St. John Sutton, FRCP, University of Pennsylvania Medical Center, 3400 Spruce St., Philadelphia, PA 19104. E-mail: suttonm{at}mail.med.upenn.edu . Received for publication 15 January 2002 and accepted in revised form 13 August 2002. J.F.D. and R.P. are employed by GlaxoSmithKline, and M.F. is employed by, holds stock in, and has received grant/research support from GlaxoSmithKline. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. DIABETES CARE</description><identifier>ISSN: 0149-5992</identifier><identifier>EISSN: 1935-5548</identifier><identifier>DOI: 10.2337/diacare.25.11.2058</identifier><identifier>PMID: 12401757</identifier><identifier>CODEN: DICAD2</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Blood Glucose - drug effects ; Blood Glucose - metabolism ; Blood Pressure - drug effects ; Body Mass Index ; Cardiovascular Physiological Phenomena ; Cardiovascular System - drug effects ; Comparative analysis ; Continental Population Groups ; Diabetes ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - physiopathology ; Diabetes. Impaired glucose tolerance ; Drug therapy ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Evaluation ; Female ; Glibenclamide ; Glyburide - therapeutic use ; Glycated Hemoglobin A - analysis ; Hemodynamics - drug effects ; Hormones. Endocrine system ; Humans ; Hypoglycemic agents ; Hypoglycemic Agents - therapeutic use ; Male ; Management. Various non-drug treatments. Langerhans islet grafts ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Physiological aspects ; Placebos ; Rosiglitazone ; Rosiglitazone maleate ; Safety ; Side effects ; Thiazoles - therapeutic use ; Thiazolidinediones ; Time Factors ; Type 2 diabetes ; Ventricular Function, Left - drug effects ; Ventricular Function, Left - physiology</subject><ispartof>Diabetes care, 2002-11, Vol.25 (11), p.2058-2064</ispartof><rights>2003 INIST-CNRS</rights><rights>COPYRIGHT 2002 American Diabetes Association</rights><rights>Copyright American Diabetes Association Nov 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-592717ca2fcf5b939e908e9319a4a87c7f22d34051a42d8a19d388b0d2b9c3603</citedby><cites>FETCH-LOGICAL-c511t-592717ca2fcf5b939e908e9319a4a87c7f22d34051a42d8a19d388b0d2b9c3603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14361584$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12401757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUTTON, Martin St</creatorcontrib><creatorcontrib>RENDELL, Marc</creatorcontrib><creatorcontrib>DANDONA, Paresh</creatorcontrib><creatorcontrib>DOLE, Jo F</creatorcontrib><creatorcontrib>MURPHY, Karen</creatorcontrib><creatorcontrib>PATWARDHAN, Rita</creatorcontrib><creatorcontrib>PATEL, Jai</creatorcontrib><creatorcontrib>FREED, Martin</creatorcontrib><creatorcontrib>For the Rosiglitazone Clinical Trials Study Group</creatorcontrib><title>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes</title><title>Diabetes care</title><addtitle>Diabetes Care</addtitle><description>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes Martin St. John Sutton , FRCP 1 , Marc Rendell , MD 2 , Paresh Dandona , MD 3 , Jo F. Dole , PHD 4 , Karen Murphy , MT (ASCP) 4 , Rita Patwardhan , PHD 4 , Jai Patel , MD 4 , Martin Freed , MD 4 and For the Rosiglitazone Clinical Trials Study Group 1 University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 2 Creighton University, Omaha, Nebraska 3 State University of New York School of Medicine at Buffalo, Buffalo, New York 4 GlaxoSmithKline, Collegeville, Pennsylvania Abstract OBJECTIVE —This open-label, active-controlled study investigated the cardiac safety and antihyperglycemic effect of rosiglitazone (RSG) in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS —Of the 203 patients randomly assigned to RSG (4 mg b.i.d.) or glyburide (GLB) (titrated to achieve optimal glycemic control for the first 8 weeks only to limit the risk of hypoglycemia; mean 10.5 mg/day), 118 had an echocardiogram performed at week 52. Left ventricular (LV) mass index, ejection fraction, and left ventricular end-diastolic volume were assessed by M-mode echocardiography at baseline and weeks 12, 28, and 52; 24-h ambulatory blood pressure was assessed at baseline and at weeks 28 and 52. Glycemic control was assessed by measuring fasting plasma glucose (FPG) and HbA 1c . RESULTS —Neither treatment produced an increase in LV mass index that exceeded 1 SD. Ejection fraction did not change in either group. Both groups had clinically insignificant increases in LV end-diastolic volume. RSG, but not GLB, caused a statistically significant reduction in ambulatory diastolic blood pressure. Both treatments reduced HbA 1c and FPG. CONCLUSIONS —A total of 52 weeks of therapy with RSG (4 mg b.i.d.) did not adversely affect cardiac structure or function in patients with type 2 diabetes and produced significant and sustained reductions in hyperglycemia. Decreases in ambulatory diastolic blood pressure with RSG were superior to those with GLB. ACEI, ACE inhibitor AE, adverse event BP, blood pressure ECG, electrocardiogram EF, ejection fraction FPG, fasting plasma glucose GLB, glyburide ITT, intent to treat LOCF, last observation carried forward LV, left ventricular LVEDV, LV end-diastolic volume LVM, LV mass LVMI, LV mass index MR, mitral regurgitation RSG, rosiglitazone Footnotes Address correspondence and reprint requests to Martin St. John Sutton, FRCP, University of Pennsylvania Medical Center, 3400 Spruce St., Philadelphia, PA 19104. E-mail: suttonm{at}mail.med.upenn.edu . Received for publication 15 January 2002 and accepted in revised form 13 August 2002. J.F.D. and R.P. are employed by GlaxoSmithKline, and M.F. is employed by, holds stock in, and has received grant/research support from GlaxoSmithKline. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. DIABETES CARE</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - drug effects</subject><subject>Blood Glucose - metabolism</subject><subject>Blood Pressure - drug effects</subject><subject>Body Mass Index</subject><subject>Cardiovascular Physiological Phenomena</subject><subject>Cardiovascular System - drug effects</subject><subject>Comparative analysis</subject><subject>Continental Population Groups</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Drug therapy</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Evaluation</subject><subject>Female</subject><subject>Glibenclamide</subject><subject>Glyburide - therapeutic use</subject><subject>Glycated Hemoglobin A - analysis</subject><subject>Hemodynamics - drug effects</subject><subject>Hormones. Endocrine system</subject><subject>Humans</subject><subject>Hypoglycemic agents</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Male</subject><subject>Management. Various non-drug treatments. Langerhans islet grafts</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Physiological aspects</subject><subject>Placebos</subject><subject>Rosiglitazone</subject><subject>Rosiglitazone maleate</subject><subject>Safety</subject><subject>Side effects</subject><subject>Thiazoles - therapeutic use</subject><subject>Thiazolidinediones</subject><subject>Time Factors</subject><subject>Type 2 diabetes</subject><subject>Ventricular Function, Left - drug effects</subject><subject>Ventricular Function, Left - physiology</subject><issn>0149-5992</issn><issn>1935-5548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkt-KUzEQxg-iuOvqC3ghQdAbbc3fnuSy1N1VWFBkxcswJ8lps5wm3SRHqa_gS5vaAwtSchEy_Ga-yXzTNC8JnlPG2g_Wg4Hk5lTMCZlTLOSj5pwoJmZCcPm4OceEq5lQip41z3K-wxhzLuXT5oxQjkkr2vPmzxKt4nYHyecYUOxR2Th02ffOlHx4fovZrwdf4HcMDkGw6HrYd2Py1qGasIJkffwJ2YwDJHQ1BlN8jU-gcVtvqkAoKQ7IB_QVinehlv7hywbd7ncOUfTRQ-eKy8-bJz0M2b2Y7ovm-9Xl7erT7ObL9efV8mZmBCGlfoi2pDVAe9OLTjHlFJZOMaKAg2xN21NqGceCAKdWAlGWSdlhSztl2AKzi-btse4uxfvR5aK3Phs3DBBcHLNu6YIq0YoKvv4PvItjCrU3TSkmTDBJK_T-CK1hcNqHPpYEZu2CSzDUofW-hpeKE07pP_HZCbwee5jVKZ4eeZNizsn1epf8FtJeE6wPa6CnNdBUaEL0YQ1q0qup8bHbOvuQMvlegTcTUK2DoU8QjM8PHGcLIiSv3Lsjt_HrzS9fVexk1inZv9dDyrE</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>SUTTON, Martin St</creator><creator>RENDELL, Marc</creator><creator>DANDONA, Paresh</creator><creator>DOLE, Jo F</creator><creator>MURPHY, Karen</creator><creator>PATWARDHAN, Rita</creator><creator>PATEL, Jai</creator><creator>FREED, Martin</creator><general>American Diabetes Association</general><scope>IQODW</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>3V.</scope><scope>7RV</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0K</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20021101</creationdate><title>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes</title><author>SUTTON, Martin St ; RENDELL, Marc ; DANDONA, Paresh ; DOLE, Jo F ; MURPHY, Karen ; PATWARDHAN, Rita ; PATEL, Jai ; FREED, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-592717ca2fcf5b939e908e9319a4a87c7f22d34051a42d8a19d388b0d2b9c3603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - drug effects</topic><topic>Blood Glucose - metabolism</topic><topic>Blood Pressure - drug effects</topic><topic>Body Mass Index</topic><topic>Cardiovascular Physiological Phenomena</topic><topic>Cardiovascular System - drug effects</topic><topic>Comparative analysis</topic><topic>Continental Population Groups</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Drug therapy</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Evaluation</topic><topic>Female</topic><topic>Glibenclamide</topic><topic>Glyburide - therapeutic use</topic><topic>Glycated Hemoglobin A - analysis</topic><topic>Hemodynamics - drug effects</topic><topic>Hormones. Endocrine system</topic><topic>Humans</topic><topic>Hypoglycemic agents</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Male</topic><topic>Management. Various non-drug treatments. Langerhans islet grafts</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Physiological aspects</topic><topic>Placebos</topic><topic>Rosiglitazone</topic><topic>Rosiglitazone maleate</topic><topic>Safety</topic><topic>Side effects</topic><topic>Thiazoles - therapeutic use</topic><topic>Thiazolidinediones</topic><topic>Time Factors</topic><topic>Type 2 diabetes</topic><topic>Ventricular Function, Left - drug effects</topic><topic>Ventricular Function, Left - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SUTTON, Martin St</creatorcontrib><creatorcontrib>RENDELL, Marc</creatorcontrib><creatorcontrib>DANDONA, Paresh</creatorcontrib><creatorcontrib>DOLE, Jo F</creatorcontrib><creatorcontrib>MURPHY, Karen</creatorcontrib><creatorcontrib>PATWARDHAN, Rita</creatorcontrib><creatorcontrib>PATEL, Jai</creatorcontrib><creatorcontrib>FREED, Martin</creatorcontrib><creatorcontrib>For the Rosiglitazone Clinical Trials Study Group</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Allied Health Premium</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>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUTTON, Martin St</au><au>RENDELL, Marc</au><au>DANDONA, Paresh</au><au>DOLE, Jo F</au><au>MURPHY, Karen</au><au>PATWARDHAN, Rita</au><au>PATEL, Jai</au><au>FREED, Martin</au><aucorp>For the Rosiglitazone Clinical Trials Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes</atitle><jtitle>Diabetes care</jtitle><addtitle>Diabetes Care</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>25</volume><issue>11</issue><spage>2058</spage><epage>2064</epage><pages>2058-2064</pages><issn>0149-5992</issn><eissn>1935-5548</eissn><coden>DICAD2</coden><abstract>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes Martin St. John Sutton , FRCP 1 , Marc Rendell , MD 2 , Paresh Dandona , MD 3 , Jo F. Dole , PHD 4 , Karen Murphy , MT (ASCP) 4 , Rita Patwardhan , PHD 4 , Jai Patel , MD 4 , Martin Freed , MD 4 and For the Rosiglitazone Clinical Trials Study Group 1 University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 2 Creighton University, Omaha, Nebraska 3 State University of New York School of Medicine at Buffalo, Buffalo, New York 4 GlaxoSmithKline, Collegeville, Pennsylvania Abstract OBJECTIVE —This open-label, active-controlled study investigated the cardiac safety and antihyperglycemic effect of rosiglitazone (RSG) in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS —Of the 203 patients randomly assigned to RSG (4 mg b.i.d.) or glyburide (GLB) (titrated to achieve optimal glycemic control for the first 8 weeks only to limit the risk of hypoglycemia; mean 10.5 mg/day), 118 had an echocardiogram performed at week 52. Left ventricular (LV) mass index, ejection fraction, and left ventricular end-diastolic volume were assessed by M-mode echocardiography at baseline and weeks 12, 28, and 52; 24-h ambulatory blood pressure was assessed at baseline and at weeks 28 and 52. Glycemic control was assessed by measuring fasting plasma glucose (FPG) and HbA 1c . RESULTS —Neither treatment produced an increase in LV mass index that exceeded 1 SD. Ejection fraction did not change in either group. Both groups had clinically insignificant increases in LV end-diastolic volume. RSG, but not GLB, caused a statistically significant reduction in ambulatory diastolic blood pressure. Both treatments reduced HbA 1c and FPG. CONCLUSIONS —A total of 52 weeks of therapy with RSG (4 mg b.i.d.) did not adversely affect cardiac structure or function in patients with type 2 diabetes and produced significant and sustained reductions in hyperglycemia. Decreases in ambulatory diastolic blood pressure with RSG were superior to those with GLB. ACEI, ACE inhibitor AE, adverse event BP, blood pressure ECG, electrocardiogram EF, ejection fraction FPG, fasting plasma glucose GLB, glyburide ITT, intent to treat LOCF, last observation carried forward LV, left ventricular LVEDV, LV end-diastolic volume LVM, LV mass LVMI, LV mass index MR, mitral regurgitation RSG, rosiglitazone Footnotes Address correspondence and reprint requests to Martin St. John Sutton, FRCP, University of Pennsylvania Medical Center, 3400 Spruce St., Philadelphia, PA 19104. E-mail: suttonm{at}mail.med.upenn.edu . Received for publication 15 January 2002 and accepted in revised form 13 August 2002. J.F.D. and R.P. are employed by GlaxoSmithKline, and M.F. is employed by, holds stock in, and has received grant/research support from GlaxoSmithKline. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. DIABETES CARE</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>12401757</pmid><doi>10.2337/diacare.25.11.2058</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0149-5992
ispartof Diabetes care, 2002-11, Vol.25 (11), p.2058-2064
issn 0149-5992
1935-5548
language eng
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Aged
Biological and medical sciences
Blood Glucose - drug effects
Blood Glucose - metabolism
Blood Pressure - drug effects
Body Mass Index
Cardiovascular Physiological Phenomena
Cardiovascular System - drug effects
Comparative analysis
Continental Population Groups
Diabetes
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - drug therapy
Diabetes Mellitus, Type 2 - physiopathology
Diabetes. Impaired glucose tolerance
Drug therapy
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Evaluation
Female
Glibenclamide
Glyburide - therapeutic use
Glycated Hemoglobin A - analysis
Hemodynamics - drug effects
Hormones. Endocrine system
Humans
Hypoglycemic agents
Hypoglycemic Agents - therapeutic use
Male
Management. Various non-drug treatments. Langerhans islet grafts
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Physiological aspects
Placebos
Rosiglitazone
Rosiglitazone maleate
Safety
Side effects
Thiazoles - therapeutic use
Thiazolidinediones
Time Factors
Type 2 diabetes
Ventricular Function, Left - drug effects
Ventricular Function, Left - physiology
title A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes
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