The investigation of the efficacy of insulin glargine on glycemic control when combined with either repaglinide or acarbose in obese Type 2 diabetic patients

被引:19
作者
Duran, C. [1 ]
Tuncel, E. [2 ]
Ersoy, C. [2 ]
Ercan, I. [3 ]
Selimoglu, H. [2 ]
Kiyici, S. [2 ]
Guclu, M. [2 ]
Erturk, E. [2 ]
Imamoglu, S. [2 ]
机构
[1] Konya Educ & Res Hosp, Div Endocrinol, Konya, Turkey
[2] Uludag Univ, Fac Med, Div Endocrinol & Metab, Bursa, Turkey
[3] Uludag Univ, Fac Med, Dept Biostat, Bursa, Turkey
关键词
Acarbose; insulin glargine; repaglinide; secondary failure; Type; 2; diabetes; BEDTIME NPH INSULIN; COMBINATION THERAPY; PLACEBO; HYPOGLYCEMIA; MULTICENTER; MONOTHERAPY; SAFETY; TRIAL;
D O I
10.1007/BF03345682
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Combinations of insulin and oral antidiabetic drugs (OAD) are often prescribed instead of insulin alone. In this study, the effects of insulin glargine (IG) in combination with repaglinide or acarbose on glycemic parameters were investigated. Obese Type 2 diabetic patients with fasting blood glucose (FBG) levels >= mmol/l and hemoglobin glycated (A1C) >= 9% under maximal CAD combination therapy were enrolled. Previous therapies were discontinued, and patients were randomized into 2 groups. The combinations of IG and repaglinide were administered to group 1, and of IG and acarbose to group 2 for 13 weeks. Twenty Patients in group 1 and 18 patients in group 2 completed the study. A1C levels were significantly decreased from 10.9 +/- 1.4% to 7.7 +/- 1.1% in group 1 and 11.0 +/- 1.4% to 8.1 +/- 1.4% in group 2. FBG levels were significantly decreased from 11.9 +/- 2.7 to 7.1 +/- 2.3 mmol/l in group 1 and 11.1 +/- 2.5 to 6.8 +/- 1.4 mmol/l in group 2. Post-prandial glucose levels were significantly decreased from 15.3 +/- 3.8 to 10.3 +/- 3.0 mmol/l in group 1 and 14.0 +/- 3.1 to 8.9 +/- 2.2 mmol/l in group 2. Intergroup comparisons indicated no significant differences. More weight gain was detected in group 1, compared to the baseline. Syptomatic hypoglycemia incidence was similar in both groups. Severe hypoglycemic attacks were seen in two patients in group 1. Flatulance incidence was higher in acarbose group. Conclusively, repaglinide and acarbose were equally effective when combined with IG for obese Type 2 diabetic patients controlled inadequately with OAD alone. Furthermore, acarbose seems to have advantages over repaglinide concerning weight gain and severe hypoglycemic attacks.
引用
收藏
页码:69 / 73
页数:5
相关论文
共 30 条
[1]  
[Anonymous], 2005, DIABETES CARE, V28, pS4
[2]   ACARBOSE - AN UPDATE OF ITS PHARMACOLOGY AND THERAPEUTIC USE IN DIABETES-MELLITUS [J].
BALFOUR, JA ;
MCTAVISH, D .
DRUGS, 1993, 46 (06) :1025-1054
[3]  
Borch-Johnsen K, 1999, LANCET, V354, P617
[4]   THE EFFICACY OF ACARBOSE IN THE TREATMENT OF PATIENTS WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS - A MULTICENTER CONTROLLED CLINICAL-TRIAL [J].
CHIASSON, JL ;
JOSSE, RG ;
HUNT, JA ;
PALMASON, C ;
RODGER, NW ;
ROSS, SA ;
RYAN, EA ;
TAN, MH ;
WOLEVER, TMS .
ANNALS OF INTERNAL MEDICINE, 1994, 121 (12) :928-935
[5]   MULTICENTER, PLACEBO-CONTROLLED TRIAL COMPARING ACARBOSE (BAY G-5421) WITH PLACEBO, TOLBUTAMIDE, AND TOLBUTAMIDE-PLUS-ACARBOSE IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
CONIFF, RF ;
SHAPIRO, J ;
SEATON, TB ;
BRAY, GA .
AMERICAN JOURNAL OF MEDICINE, 1995, 98 (05) :443-451
[6]  
De Luis DA, 2002, DIABETES, V51, pA468
[7]   Effect of repaglinide addition to NPH insulin monotherapy on glycemic control in patients with type 2 diabetes [J].
de luis, DA ;
Aller, R ;
Cuellar, L ;
Terroba, C ;
Ovalle, H ;
Izaola, O ;
Romero, E .
DIABETES CARE, 2001, 24 (10) :1844-1845
[8]   Glimepiride combined with morning insulin glargine, bedtime neutral protamine Hagedorn insulin, or bedtime insulin glargine in patients with type 2 diabetes -: A randomized, controlled trial [J].
Fritsche, A ;
Schweitzer, MA ;
Häring, HU .
ANNALS OF INTERNAL MEDICINE, 2003, 138 (12) :952-959
[9]   Comparison of repaglinide vs. gliclazide in combination with bedtime NPH insulin in patients with Type 2 diabetes inadequately controlled with oral hypoglycaemic agents [J].
Furlong, NJ ;
Hulme, SA ;
O'Brien, SV ;
Hardy, KJ .
DIABETIC MEDICINE, 2003, 20 (11) :935-941
[10]   INSULIN USE IN NIDDM [J].
GENUTH, S .
DIABETES CARE, 1990, 13 (12) :1240-1264