Improved glycaemic control with minimal hypoglycaemia and no weight change with the once-daily human glucagon-like peptide-1 analogue liraglutide as add-on to sulphonylurea in Japanese patients with type 2 diabetes

被引:75
作者
Kaku, K. [1 ]
Rasmussen, M. F. [2 ]
Clauson, P. [2 ]
Seino, Y. [3 ]
机构
[1] Kawasaki Med Sch, Diabet & Endocrine Div, Dept Med, Kurashiki, Okayama 7010192, Japan
[2] Novo Nordisk AS, Bagsvaerd, Denmark
[3] Kansai Elect Power Hosp, Osaka, Japan
关键词
glucagon-like peptide-1; liraglutide; sulphonylurea; type; 2; diabetes; HUMAN GLP-1 ANALOG; BODY-MASS INDEX; EXENATIDE EXENDIN-4; INSULIN SENSITIVITY; GLUCOSE-TOLERANCE; TREATED PATIENTS; METFORMIN; SECRETION; SAFETY; TRIAL;
D O I
10.1111/j.1463-1326.2009.01194.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methods: The efficacy and safety of the once-daily human glucagon-like peptide-1 (GLP-1) analogue liraglutide were compared in 264 Japanese subjects [mean body mass index (BMI) 24.9 kg/m2; mean glycated haemoglobin (HBA1c) 8.4%] randomized and exposed to receive liraglutide 0.6 mg/day (n = 88), 0.9 mg/day (n = 88) or placebo (n = 88) each added to SU monotherapy (glibenclamide, glicazide or glimeprimide) in a 24-week, double-blind, parallel-group trial. Results: The mean change in HBA1c from baseline to week 24 (LOCF) was -1.56 (s.d. 0.84) and -1.46 (s.d. 0.95) with liraglutide 0.9 and 0.6 mg respectively, and -0.40 (s.d. 0.93) with placebo. HBA1c decreased in the placebo group from 8.45 to 8.06%, while liraglutide reduced HBA1c from 8.60 to 7.14%, and from 8.23 to 6.67% at the 0.6 and 0.9 mg doses respectively. Mean HBA1c at week 24 of the two liraglutide groups were significantly lower than the placebo group (p < 0.0001 for both). More subjects reached HBA1c < 7.0% with liraglutide (0.6 mg: 46.5%; 0.9 mg: 71.3%) vs. placebo (14.8%). Fasting plasma glucose (FPG) levels were significantly improved with liraglutide (difference -1.47 mmol/l and -1.80 mmol/l with 0.6 and 0.9 mg vs. placebo; p < 0.0001). Overall safety was similar between treatments: no major hypoglycaemic episodes were reported, while 84/77/38 minor hypoglycaemic episodes occurred in the 0.6 mg/0.9 mg and placebo treatment groups (all in combination with SU), reflecting lower ambient glucose levels. No relevant change in mean body weight occurred in subjects receiving liraglutide (0.6 mg: 0.06 kg; 0.9 mg: -0.37 kg), while mean body weight decreased in subjects receiving placebo (-1.12 kg). Conclusions: The addition of liraglutide to SU treatment for 24 weeks dose-dependently improved glycaemic control vs. SU monotherapy, without causing major hypoglycaemia or weight gain or loss.
引用
收藏
页码:341 / 347
页数:7
相关论文
共 34 条
[1]   Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes [J].
Buse, JB ;
Henry, RR ;
Han, J ;
Kim, DD ;
Fineman, MS ;
Baron, AD .
DIABETES CARE, 2004, 27 (11) :2628-2635
[2]   Liraglutide once a day versus exenatide twice a day for type 2 diabetes: a 26-week randomised, parallel-group, multinational, open-label trial (LEAD-6) [J].
Buse, John B. ;
Rosenstock, Julio ;
Sesti, Giorgio ;
Schmidt, Wolfgang E. ;
Montanya, Eduard ;
Brett, Jason H. ;
Zychma, Marcin ;
Blonde, Lawrence .
LANCET, 2009, 374 (9683) :39-47
[3]   The GLP-1 derivative NN2211 restores β-cell sensitivity to glucose in type 2 diabetic patients after a single dose [J].
Chang, AM ;
Jakobsen, G ;
Sturis, J ;
Smith, MJ ;
Bloem, CJ ;
An, B ;
Galecki, A ;
Halter, JB .
DIABETES, 2003, 52 (07) :1786-1791
[4]   Effects of exenatide (exendin-4) on glycemic control and weight over 30 weeks in metformin-treated patients with type 2 diabetes [J].
DeFronzo, RA ;
Ratner, RE ;
Han, J ;
Kim, DD ;
Fineman, MS ;
Baron, AD .
DIABETES CARE, 2005, 28 (05) :1092-1100
[5]  
Deurenberg P, 2002, Obes Rev, V3, P141, DOI 10.1046/j.1467-789X.2002.00065.x
[6]   PLASMA-INSULIN LEVELS IN JAPANESE AND JAPANESE-AMERICAN MEN WITH TYPE-2 DIABETES MAY BE RELATED TO THE OCCURRENCE OF CARDIOVASCULAR-DISEASE [J].
FUJIMOTO, WY ;
AKANUMA, Y ;
KANAZAWA, Y ;
MASHIKO, S ;
LEONETTI, D ;
WAHL, P .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1989, 6 (02) :121-127
[7]   Insulin secretion capacity in the development from normal glucose tolerance to type 2 diabetes [J].
Fukushima, M ;
Suzuki, H ;
Seino, Y .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2004, 66 :S37-S43
[8]   Insulin secretion and insulin sensitivity at different stages of glucose tolerance: A cross-sectional study of Japanese type 2 diabetes [J].
Fukushima, M ;
Usami, M ;
Ikeda, M ;
Nakai, Y ;
Taniguchi, A ;
Matsuura, T ;
Suzuki, H ;
Kurose, T ;
Yamada, Y ;
Seino, Y .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2004, 53 (07) :831-835
[9]   Liraglutide versus glimepiride monotherapy for type 2 diabetes (LEAD-3 Mono): a randomised, 52-week, phase III, double-blind, parallel-treatment trial [J].
Garber, Alan ;
Henry, Robert ;
Ratner, Robert ;
Garcia-Hernandez, Pedro A. ;
Rodriguez-Pattzi, Hiromi ;
Olvera-Alvarez, Israel ;
Hale, Paula M. ;
Zdravkovic, Milan ;
Bode, Bruce .
LANCET, 2009, 373 (9662) :473-481
[10]   Insulin sensitivity and acute insulin response in African-Americans, non-Hispanic Whites, and Hispanics with NIDDM - The insulin resistance atherosclerosis study [J].
Haffner, SM ;
Howard, G ;
Mayer, E ;
Bergman, RN ;
Savage, PJ ;
Rewers, M ;
Mykkanen, L ;
Karter, AJ ;
Hamman, R ;
Saad, MF .
DIABETES, 1997, 46 (01) :63-69