Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance - The STOP-NIDDM Ttrial

被引:1189
作者
Chiasson, JL
Josse, RG
Gomis, R
Hanefeld, M
Karasik, A
Laakso, M
机构
[1] Univ Montreal, Ctr Hosp, Hotel Dieu, Res Ctr, Montreal, PQ H2W 1T7, Canada
[2] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[3] Univ Toronto, St Michaels Hosp, Dept Med, Toronto, ON M5B 1W8, Canada
[4] Univ Barcelona, Hosp Clin, Diabet Unit, Barcelona, Spain
[5] Tech Univ Dresden, Ctr Clin Studies GWT, D-8027 Dresden, Germany
[6] Chaim Sheba Med Ctr, Inst Endocrinol, IL-52621 Tel Hashomer, Israel
[7] Univ Kuopio, Dept Med, SF-70210 Kuopio, Finland
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2003年 / 290卷 / 04期
关键词
D O I
10.1001/jama.290.4.486
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The worldwide explosive increase in type 2 diabetes mellitus and its cardiovascular morbidity are becoming major health concerns. Objective To evaluate the effect of decreasing postprandial hyperglycemia with acarbose, an alpha-glucosidase inhibitor, on the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance (IGT). Design, Setting, and Participants International, multicenter double-blind, placebo-controlled, randomized trial, undertaken in hospitals in Canada, Germany, Austria, Norway, Denmark, Sweden, Finland, Israel, and Spain from July 1998 through August 2001. A total of 1429 patients with IGT were randomized with 61 patients (4%) excluded because they did not have IGT or had no postrandomization data, leaving 1368 patients for a modified intent-to-treat analysis. Both men (49%) and women (51%) participated with a mean (SD) age of 54.5 (7.9) years and body mass index of 30.9 (4.2). These patients were followed up for a mean (SD) of 3.3 (1.2) years. Intervention Patients with IGT were randomized to receive either placebo (n=715) or 100 mg of acarbose 3 times a day (n = 714). Main Outcome Measures The development of major cardiovascular events (coronary heart disease, cardiovascular death, congestive heart failure, cerebrovascular event, and peripheral vascular disease) and hypertension (greater than or equal to140/90 mm Hg). Results Three hundred forty-one patients (24%) discontinued their participation prematurely, 211 in the acarbose-treated group and 130 in the placebo group; these patients were also followed up for outcome parameters. Decreasing postprandial hyperglycemia with acarbose was associated with a 49% relative risk reduction in the development of cardiovascular events (hazard ratio [HR], 0.51; 95% confidence interval [CI]; 0.28-0.95; P=.03) and a 2.5% absolute risk reduction. Among cardiovascular events, the major reduction was in the risk of myocardial infarction (HR, 0.09; 95% CI, 0.01-0.72; P=.02). Acarbose was also associated with a 34% relative risk reduction in the incidence of new cases of hypertension (HR, 0.66; 95% CI, 0.49-0.89; P=.006) and a 5.3% absolute risk reduction. Even after adjusting for major risk factors, the reduction in the risk of cardiovascular events (HR, 0.47; 95% CI, 0.24-0.90; P=.02) and hypertension (HR, 0.62; 95% CI, 0.45-0.86; P=.004) associated with acarbose treatment was still statistically significant. Conclusion This study suggests that treating IGT patients with acarbose is associated with a significant reduction in the risk of cardiovascular disease and hypertension.
引用
收藏
页码:486 / 494
页数:9
相关论文
共 50 条
[1]   Cardiovascular disease in older adults with glucose disorders: comparison of American Diabetes Association criteria for diabetes mellitus with WHO criteria [J].
Barzilay, JI ;
Spiekerman, CF ;
Wahl, PW ;
Kuller, LH ;
Cushman, M ;
Furberg, CD ;
Dobs, A ;
Polak, JF ;
Savage, PJ .
LANCET, 1999, 354 (9179) :622-625
[2]   Carotid artery stenosis is related to blood glucose level in an elderly Caucasian population: The Hoorn Study [J].
Beks, PHJ ;
Mackaay, AJC ;
deVries, H ;
deNeeling, JND ;
Bouter, LM ;
Heine, RJ .
DIABETOLOGIA, 1997, 40 (03) :290-298
[3]   Impaired glucose tolerance, Type II diabetes mellitus and carotid atherosclerosis: prospective results from the Bruneck Study [J].
Bonora, E ;
Kiechl, S ;
Oberhollenzer, F ;
Egger, G ;
Bonadonna, RC ;
Muggeo, M ;
Willeit, J .
DIABETOLOGIA, 2000, 43 (02) :156-164
[4]   Glucose tolerance and cardiovascular mortality -: Comparison of fasting and 2-hour diagnostic criteria [J].
Borch-Johnsen, K ;
Neil, A ;
Balkau, B ;
Larsen, S ;
Nissinen, A ;
Pekkanen, J ;
Tuomilehto, J ;
Jousilahti, P ;
Lindstrom, J ;
Pyörälä, M ;
Pyörälä, K ;
Eschwege, E ;
Gallus, G ;
Garancini, MP ;
Bouter, LM ;
Dekker, JM ;
Heine, RJ ;
Nijpels, HG ;
Stehouwer, CDA ;
Feskens, EJM ;
Kromhout, D ;
Peltonen, M ;
Pajak, A ;
Eriksson, J ;
Qiao, Q .
ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (03) :397-405
[5]   Meal-generated oxidative stress in type 2 diabetic patients [J].
Ceriello, A ;
Lizzio, S ;
Bortolotti, N ;
Russo, A ;
Motz, E ;
Tonutti, L ;
Crescentini, A ;
Taboga, C .
DIABETES CARE, 1998, 21 (09) :1529-1533
[6]   Total radical-trapping antioxidant parameter in NIDDM patients [J].
Ceriello, A ;
Bortolotti, N ;
Falleti, E ;
Taboga, C ;
Tonutti, L ;
Crescentini, A ;
Motz, E ;
Lizzio, S ;
Russo, A ;
Bartoli, E .
DIABETES CARE, 1997, 20 (02) :194-197
[7]   Acute hyperglycemia induces nitrotyrosine formation and apoptosis in perfused heart from rat [J].
Ceriello, A ;
Quagliaro, L ;
D'Amico, M ;
Di Filippo, C ;
Marfella, R ;
Nappo, F ;
Berrino, L ;
Rossi, F ;
Giugliano, D .
DIABETES, 2002, 51 (04) :1076-1082
[8]   Post-meal coagulation activation in diabetes mellitus: The effect of acarbose [J].
Ceriello, A ;
Taboga, C ;
Tonutti, L ;
Giacomello, R ;
Stel, L ;
Motz, E ;
Pirisi, M .
DIABETOLOGIA, 1996, 39 (04) :469-473
[9]   The STOP-NIDDM Trial -: An international study on the efficacy of an α-glucosidase inhibitor to prevent type 2 diabetes in a population with impaired glucose tolerance:: rationale, design, and preliminary screening data [J].
Chiasson, JL ;
Gomis, R ;
Hanefeld, M ;
Josse, RG ;
Karasik, A ;
Laakso, M .
DIABETES CARE, 1998, 21 (10) :1720-1725
[10]   The effect of acarbose on insulin sensitivity in subjects with impaired glucose tolerance [J].
Chiasson, JL ;
Josse, RG ;
Leiter, LA ;
Mihic, M ;
Nathan, DM ;
Palmason, C ;
Cohen, RM ;
Wolever, TMS .
DIABETES CARE, 1996, 19 (11) :1190-1193