Acarbose in the prevention of cardiovascular disease in subjects with impaired glucose tolerance and type 2 diabetes mellitus

被引:52
作者
Delorme, S
Chiasson, JL
机构
[1] CHUM, Hotel Dieu, Res Ctr, Montreal, PQ H2W 1T7, Canada
[2] CHUM, Div Metab Endocrinol & Nutr, Montreal, PQ H2W 1T7, Canada
[3] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
关键词
D O I
10.1016/j.coph.2004.11.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The prevalence of glucose intolerance is increasing dramatically worldwide. Both impaired glucose tolerance (IGT) and type 2 diabetes are associated with excess mortality from cardiovascular disease. It is now generally accepted that these cardiovascular complications are related to prevailing hyperglycemia, particularly postprandial hyperglycemia. Acarbose specifically decreases the postprandial glycemic surge in IGT and diabetic subjects. The Study To Prevent Non-insulin-dependent Diabetes Mellitus (STOP-NIDDM) trial has shown that acarbose treatment in IGT subjects decreased the risk of progression to diabetes by 36%. Furthermore, it was associated with a 49% risk reduction of cardiovascular events. In a subgroup of subjects, acarbose treatment was accompanied by a 50% decrease in the progression of intima-media thickness of the carotids. Finally, a meta-analysis of seven major studies on the use of acarbose in the treatment of diabetes indicated that acarbose treatment was associated with a 35% risk reduction of cardiovascular disease. It is proposed that the mechanism by which acarbose can lower the risk of cardiovascular events is through diminution of oxidative stress induced by postprandial glycemic excursion.
引用
收藏
页码:184 / 189
页数:6
相关论文
共 38 条
[1]   Is there glycemic threshold for mortality risk? [J].
Balkau, B ;
Bertrais, S ;
Ducimetiere, P ;
Eschwege, E .
DIABETES CARE, 1999, 22 (05) :696-699
[2]  
Balkau B, 2000, DIABETES METAB, V26, P282
[3]  
Baron AD, 1998, DIABETES RES CLIN PR, V40, pS51
[4]   Isolated postchallenge hyperglycemia and the risk of fatal cardiovascular disease in older women and men - The Rancho Bernardo Study [J].
Barrett-Connor, E ;
Ferrara, A .
DIABETES CARE, 1998, 21 (08) :1236-1239
[5]   Hydroperoxides in plasma are reduced by intensified insulin treatment - A randomized controlled study of IDDM patients with microalbuminuria [J].
Berg, TJ ;
Nourooz-Zadeh, J ;
Wolff, SP ;
Tritschler, HJ ;
Bangstad, HJ ;
Hanssen, KE .
DIABETES CARE, 1998, 21 (08) :1295-1300
[6]  
BISCHOFF H, 1995, CLIN INVEST MED, V18, P303
[7]  
Bonora E, 2002, INT J CLIN PRACT, P5
[8]   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
[9]   Increased circulating intercellular adhesion molecule-1 levels in type II diabetic patients: The possible role of metabolic control and oxidative stress [J].
Ceriello, A ;
Falleti, E ;
Bortolotti, N ;
Motz, E ;
Cavarape, A ;
Russo, A ;
Gonano, F ;
Bartoli, E .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (04) :498-501
[10]   Fibrinogen and diabetes mellitus: Is it time for intervention trials? [J].
Ceriello, A .
DIABETOLOGIA, 1997, 40 (06) :731-734