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...
Gespeichert in:
Veröffentlicht in: | Diabetes care 2002-11, Vol.25 (11), p.2058-2064 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_gale_infotracgeneralonefile_A94142260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A94142260</galeid><sourcerecordid>A94142260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c511t-592717ca2fcf5b939e908e9319a4a87c7f22d34051a42d8a19d388b0d2b9c3603</originalsourceid><addsrcrecordid>eNptkt-KUzEQxg-iuOvqC3ghQdAbbc3fnuSy1N1VWFBkxcswJ8lps5wm3SRHqa_gS5vaAwtSchEy_Ga-yXzTNC8JnlPG2g_Wg4Hk5lTMCZlTLOSj5pwoJmZCcPm4OceEq5lQip41z3K-wxhzLuXT5oxQjkkr2vPmzxKt4nYHyecYUOxR2Th02ffOlHx4fovZrwdf4HcMDkGw6HrYd2Py1qGasIJkffwJ2YwDJHQ1BlN8jU-gcVtvqkAoKQ7IB_QVinehlv7hywbd7ncOUfTRQ-eKy8-bJz0M2b2Y7ovm-9Xl7erT7ObL9efV8mZmBCGlfoi2pDVAe9OLTjHlFJZOMaKAg2xN21NqGceCAKdWAlGWSdlhSztl2AKzi-btse4uxfvR5aK3Phs3DBBcHLNu6YIq0YoKvv4PvItjCrU3TSkmTDBJK_T-CK1hcNqHPpYEZu2CSzDUofW-hpeKE07pP_HZCbwee5jVKZ4eeZNizsn1epf8FtJeE6wPa6CnNdBUaEL0YQ1q0qup8bHbOvuQMvlegTcTUK2DoU8QjM8PHGcLIiSv3Lsjt_HrzS9fVexk1inZv9dDyrE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>220135382</pqid></control><display><type>article</type><title>A Comparison of the Effects of Rosiglitazone and Glyburide on Cardiovascular Function and Glycemic Control in Patients With Type 2 Diabetes</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>SUTTON, Martin St ; RENDELL, Marc ; DANDONA, Paresh ; DOLE, Jo F ; MURPHY, Karen ; PATWARDHAN, Rita ; PATEL, Jai ; FREED, Martin</creator><creatorcontrib>SUTTON, Martin St ; RENDELL, Marc ; DANDONA, Paresh ; DOLE, Jo F ; MURPHY, Karen ; PATWARDHAN, Rita ; PATEL, Jai ; FREED, Martin ; For the Rosiglitazone Clinical Trials Study Group</creatorcontrib><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><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&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 & Allied Health Database</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & 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> |
fulltext | fulltext |
identifier | ISSN: 0149-5992 |
ispartof | Diabetes care, 2002-11, Vol.25 (11), p.2058-2064 |
issn | 0149-5992 1935-5548 |
language | eng |
recordid | cdi_gale_infotracgeneralonefile_A94142260 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T17%3A33%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Comparison%20of%20the%20Effects%20of%20Rosiglitazone%20and%20Glyburide%20on%20Cardiovascular%20Function%20and%20Glycemic%20Control%20in%20Patients%20With%20Type%202%20Diabetes&rft.jtitle=Diabetes%20care&rft.au=SUTTON,%20Martin%20St&rft.aucorp=For%20the%20Rosiglitazone%20Clinical%20Trials%20Study%20Group&rft.date=2002-11-01&rft.volume=25&rft.issue=11&rft.spage=2058&rft.epage=2064&rft.pages=2058-2064&rft.issn=0149-5992&rft.eissn=1935-5548&rft.coden=DICAD2&rft_id=info:doi/10.2337/diacare.25.11.2058&rft_dat=%3Cgale_proqu%3EA94142260%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=220135382&rft_id=info:pmid/12401757&rft_galeid=A94142260&rfr_iscdi=true |