Effect of Ramipril and of Rosiglitazone on Carotid Intima-Media Thickness in People With Impaired Glucose Tolerance or Impaired Fasting Glucose STARR (STudy of Atherosclerosis with Ramipril and Rosiglitazone)

被引:52
作者
Lonn, Eva M. [1 ,2 ]
Gerstein, Hertzel C. [1 ,2 ]
Sheridan, Patrick [2 ]
Smith, Sandra [2 ]
Diaz, Rafael [3 ]
Mohan, Viswanathan [4 ]
Bosch, Jackie [2 ]
Yusuf, Salim [1 ,2 ]
Dagenais, Gilles R. [5 ]
机构
[1] McMaster Univ, Dept Med, Hamilton, ON, Canada
[2] McMaster Univ, Populat Hlth Res Inst, Hamilton, ON, Canada
[3] Estudios Cardiol Latino Amer, Rosario, Santa Fe, Argentina
[4] Madras Diabet Res Fdn, Madras, Tamil Nadu, India
[5] Univ Laval, Laval Hosp, Quebec Heart Inst, Quebec City, PQ, Canada
关键词
ACE inhibitors; atherosclerosis; carotid intima-media thickness; pre-diabetes; thiazolidinediones; RANDOMIZED CONTROLLED-TRIAL; CONVERTING-ENZYME-INHIBITORS; TYPE-2; DIABETES-MELLITUS; ARTERIAL-WALL THICKNESS; CARDIOVASCULAR EVENTS; CLINICAL-TRIALS; HEART-FAILURE; PIOGLITAZONE; METAANALYSIS; PROGRESSION;
D O I
10.1016/j.jacc.2008.12.072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The aim of this study was to evaluate effects of the angiotensin-converting enzyme (ACE) inhibitor ramipril and the thiazolidinedione (TZD) rosiglitazone on carotid intima-media thickness (CIMT) in people with impaired glucose tolerance (IGT) and/or impaired fasting glucose (IFG). Background People with IGT and/or IFG are at increased long-term risk for cardiovascular disease. Effects of ACE inhibitors and of TZDs on vascular disease in this population are unknown. Methods One thousand four hundred twenty-five people with IGT and/or IFG but without cardiovascular disease or diabetes were randomized to ramipril 15 mg/day or its placebo and to rosiglitazone 8 mg/day or its placebo with a 2 x 2 factorial design. The primary study outcome was the annualized change of the aggregate maximum CIMT, computed as the average of the maximum CIMTs across 12 carotid arterial segments. The secondary study outcome was the annualized change of the mean far wall left and right common CIMT. Median follow-up was 3 years and carotid ultrasound examinations were obtained at baseline and yearly thereafter. Results There were no differences in the primary and secondary outcomes between the ramipril and placebo groups. Compared with placebo, rosiglitazone reduced the primary CIMT outcome, but the difference was not statistically significant (difference = 0.0027 +/- 0.0015 mm/year; p = 0.08) and significantly reduced the secondary CIMT outcome (difference = 0.0043 +/- 0.0017 mm/year; p = 0.01). Conclusions In people with IGT and/or IFG without cardiovascular disease and diabetes, treatment with ramipril had a neutral effect on CIMT, whereas rosiglitazone modestly reduced CIMT progression. (The Study of Atherosclerosis With Ramipril and Rosiglitazone; NCT00140647). (J Am Coll Cardiol 2009; 53: 2028-35) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:2028 / 2035
页数:8
相关论文
共 29 条
[1]   Angiotensin-converting enzyme inhibitors or angiotensin receptor blockers for prevention of type 2 diabetes - A meta-analysis of randomized clinical trials [J].
Abuissa, H ;
Jones, PG ;
Marso, SP ;
O'Keefe, JH .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 46 (05) :821-826
[2]  
Bosch J, 2006, NEW ENGL J MED, V355, P1551
[3]   Carotid intima-media thickness measurements in intervention studies - Design options, progression rates, and sample size considerations: A point of view [J].
Bots, ML ;
Evans, GW ;
Riley, WA ;
Grobbee, DE .
STROKE, 2003, 34 (12) :2985-2994
[4]   Peroxisome proliferator-activated receptors as transcriptional nodal points and therapeutic targets [J].
Brown, Jonathan D. ;
Plutzky, Jorge .
CIRCULATION, 2007, 115 (04) :518-533
[5]   The relationship between glucose and incident cardiovascular events [J].
Coutinho, M ;
Gerstein, HC ;
Wang, Y ;
Yusuf, S .
DIABETES CARE, 1999, 22 (02) :233-240
[6]   Effects of ramipril and rosiglitazone on cardiovascular and renal outcomes in people with impaired glucose tolerance or impaired fasting glucose - Results of the Diabetes Reduction Assessment with ramipril and rosiglitazone Medication (DREAM) trial [J].
Dagenais, G. R. ;
Gerstein, H. C. ;
Holman, R. ;
Budaj, A. ;
Escalante, A. ;
Hedner, T. ;
Keltai, M. ;
Lonn, E. ;
McFarlane, S. ;
McQueen, M. ;
Teo, K. ;
Sheridan, P. ;
Bosch, J. ;
Pogue, J. ;
Yusuf, S. .
DIABETES CARE, 2008, 31 (05) :1007-1014
[7]   Angiotensin-converting-enzyme inhibitors in stable vascular disease without left ventricular systolic dysfunction or heart failure: a combined analysis of three trials [J].
Dagenais, Gilles R. ;
Pogue, Janice ;
Fox, Kim ;
Simoons, Marteen L. ;
Yusuf, Salim .
LANCET, 2006, 368 (9535) :581-588
[8]   Measurement of carotid intima-media thickness to assess progression and regression of atherosclerosis [J].
de Groot, Eric ;
van Leuven, Sander I. ;
Duivenvoorden, Raphael ;
Meuwese, Marijn C. ;
Akdim, Fatima ;
Bots, Michiel L. ;
Kastelein, John Jp .
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE, 2008, 5 (05) :280-288
[9]   Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events):: a randomised controlled trial [J].
Dormandy, JA ;
Charbonnel, B ;
Eckland, DJA ;
Erdmann, E ;
Massi-Benedetti, M ;
Kmoules, IK ;
Skene, AM ;
Tan, MH ;
Lefébvre, PJ ;
Murray, GD ;
Standl, E ;
Wilcox, RG ;
Wlhelmsen, L ;
Betteridge, J ;
Birkeland, K ;
Golay, A ;
Heine, RJ ;
Korányi, L ;
Laakso, M ;
Mokán, M ;
Norkus, A ;
Pirags, V ;
Podar, T ;
Scheen, A ;
Scherbaum, W ;
Schernthaner, G ;
Schmitz, O ;
Skrha, J ;
Smith, U ;
Taton, J .
LANCET, 2005, 366 (9493) :1279-1289
[10]   Pathophysiologic and therapeutic importance of tissue ACE:: A consensus report [J].
Dzau, VJ ;
Bernstein, K ;
Celermajer, D ;
Cohen, J ;
Dahlöf, B ;
Deanfield, J ;
Diez, J ;
Drexler, H ;
Ferrari, R ;
van Gilst, W ;
Hansson, L ;
Hornig, B ;
Husain, A ;
Johnston, C ;
Lazar, H ;
Lonn, E ;
Lüscher, T ;
Mancini, J ;
Mimran, A ;
Pepine, C ;
Rabelink, T ;
Remme, W ;
Ruilope, L ;
Ruzicka, M ;
Schunkert, H ;
Swedberg, K ;
Unger, T ;
Vaughan, D ;
Weber, M .
CARDIOVASCULAR DRUGS AND THERAPY, 2002, 16 (02) :149-160