24-hour glycemic profile in type 2 diabetic patients treated with gliclazide modified release once daily

被引:1
作者
Guillausseau, PJ
Greb, W
机构
[1] Hop Lariboisiere, Serv Med B, F-75010 Paris, France
[2] Univ Paris 07, Fac Med Lariboisiere St Louis, Paris, France
[3] Focus Clin Drug Dev, D-41460 Neuss, Germany
关键词
type 2 diabetes mellitus; treatment; sulfonylurea; glicrazide modified release; compliance; glycemic profile; HbA(1C);
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: In type 2 diabetes, the primary and secondary prevention of long-term micro- and macrovascular complications requires a control of blood glucose levels 24 hours a day. The present study was undertaken to assess the effect of a new formulation of gliclazide administered once daily, gliclazide modified release((1)), on plasma glucose levels over 24 hours. Material and Methods: in 21 type 2 diabetic patients previously treated by diet alone or oral antidiabetic agents, glycemic profile (8 am, 10 am, 12 am, 2 pm, 5 pm, 8 pm, 10 pm, 3 am and 8 am), overall glycemic control, acceptability,, and compliance with treatment were assessed before and after a 10-week treatment with gliclazide modified release, (30-60 mg), given once daily at breakfast. Results: The results indicate a significant decrease in plasma glucose levels at all points of the cycle. Mean plasma glucose levels over 24 hours and mean plasma glucose levels during the fasting and the postprandial periods were significantly improved after treatment. In previous drug-naive patients, decrease in HbA(1c) was observed 11.0 +/- 1.1%, P = 0.022). The acceptability was good, with no hypoglycemic events, and a high compliance with treatment was also observed. Conclusion: We can therefore conclude that gliclazide modified release, given once daily at breakfast, is effective over 24 hours in reducing plasma glucose levels in type 2 diabetes. This once-daily administration should lead to an optimal patient compliance with treatment.
引用
收藏
页码:133 / 137
页数:5
相关论文
共 21 条
[1]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[2]  
2-S
[3]   ATP-sensitive K+ channels and insulin secretion:: their role in health and disease [J].
Ashcroft, FM ;
Gribble, FM .
DIABETOLOGIA, 1999, 42 (08) :903-919
[4]   Nonfasting plasma glucose is a better marker of diabetic control than fasting plasma glucose in type 2 diabetes [J].
Avignon, A ;
Radauceanu, A ;
Monnier, L .
DIABETES CARE, 1997, 20 (12) :1822-1826
[5]   Therapy focused on lowering postprandial glucose, not fasting glucose, may be superior for lowering HbA1c [J].
Bastyr, EJ ;
Stuart, CA ;
Brodows, RG ;
Schwartz, S ;
Graf, CJ ;
Zagar, A ;
Robertson, KE .
DIABETES CARE, 2000, 23 (09) :1236-1241
[6]   HOW OFTEN IS MEDICATION TAKEN AS PRESCRIBED - A NOVEL ASSESSMENT TECHNIQUE [J].
CRAMER, JA ;
MATTSON, RH ;
PREVEY, ML ;
SCHEYER, RD ;
OUELLETTE, VL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 261 (22) :3273-3277
[7]   Diamicron®MR once daily is effective and well tolerated in type 2 diabetes -: A double-blind, randomized, multinational study [J].
Drouin, P .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2000, 14 (04) :185-191
[8]  
EILSEN SA, 1990, ARCH INTERN MED, V150, P1881
[9]  
Gavin JR, 1997, DIABETES CARE, V20, P1183
[10]   Intensified multifactorial intervention in patients with type 2 diabetes mellitus and microalbuminuria:: the Steno type 2 randomised study [J].
Gæde, P ;
Vedel, P ;
Parving, HH ;
Pedersen, O .
LANCET, 1999, 353 (9153) :617-622