Liraglutide, a once-daily human GLP-1 analogue, added to a sulphonylurea over 26 weeks produces greater improvements in glycaemic and weight control compared with adding rosiglitazone or placebo in subjects with Type 2 diabetes (LEAD-1 SU)

被引:662
作者
Marre, M. [1 ]
Shaw, J. [2 ]
Braendle, M. [3 ]
Bebakar, W. M. W. [4 ]
Kamaruddin, N. A. [5 ]
Strand, J. [6 ]
Zdravkovic, M. [7 ]
Le Thi, T. D. [7 ]
Colagiuri, S. [8 ]
机构
[1] Grp Hosp Bichat Claude Bernard, Serv Endocrinol Diabetol Nutr, F-75722 Paris 18, France
[2] Int Diabet Inst, Melbourne, Vic, Australia
[3] Kantonsspital St Gallen, Div Endocrinol Diabet & Osteol, St Gallen, Switzerland
[4] Hosp Univ Sains, Dept Med, Kelantan, Malaysia
[5] Univ Kebangsaan Malaysia, Dept Med, Kuala Lumpur, Malaysia
[6] Oulun Diakonissalaitos, Oulu, Finland
[7] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[8] Univ Sydney, Inst Obes Nutr & Exercise, Sydney, NSW 2006, Australia
关键词
dipeptidyl peptidase-4; glucagon-like peptide-1 receptor agonist; incretin; insulinotropic; thiazolidinedione; GLUCAGON-LIKE PEPTIDE-1; BETA-CELL FUNCTION; METFORMIN; SAFETY; HYPERGLYCEMIA; GLIMEPIRIDE; REDUCTION; EXENDIN-4; MELLITUS; EFFICACY;
D O I
10.1111/j.1464-5491.2009.02666.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To compare the effects of combining liraglutide (0.6, 1.2 or 1.8 mg/day) or rosiglitazone 4 mg/day (all n >= 228) or placebo (n = 114) with glimepiride (2-4 mg/day) on glycaemic control, body weight and safety in Type 2 diabetes. In total, 1041 adults (mean +/- sd), age 56 +/- 10 years, weight 82 +/- 17 kg and glycated haemoglobin (HbA(1c)) 8.4 +/- 1.0% at 116 sites in 21 countries were stratified based on previous oral glucose-lowering mono : combination therapies (30 : 70%) to participate in a five-arm, 26-week, double-dummy, randomized study. Liraglutide (1.2 or 1.8 mg) produced greater reductions in HbA(1c) from baseline, (-1.1%, baseline 8.5%) compared with placebo (+0.2%, P < 0.0001, baseline 8.4%) or rosiglitazone (-0.4%, P < 0.0001, baseline 8.4%) when added to glimepiride. Liraglutide 0.6 mg was less effective (-0.6%, baseline 8.4%). Fasting plasma glucose decreased by week 2, with a 1.6 mmol/l decrease from baseline at week 26 with liraglutide 1.2 mg (baseline 9.8 mmol/l) or 1.8 mg (baseline 9.7 mmol/l) compared with a 0.9 mmol/l increase (placebo, P < 0.0001, baseline 9.5 mmol/l) or 1.0 mmol/l decrease (rosiglitazone, P < 0.006, baseline 9.9 mmol/l). Decreases in postprandial plasma glucose from baseline were greater with liraglutide 1.2 or 1.8 mg [-2.5 to -2.7 mmol/l (baseline 12.9 mmol/l for both)] compared with placebo (-0.4 mmol/l, P < 0.0001, baseline 12.7 mmol/l) or rosiglitazone (-1.8 mmol/l, P < 0.05, baseline 13.0 mmol/l). Changes in body weight with liraglutide 1.8 mg (-0.2 kg, baseline 83.0 kg), 1.2 mg (+0.3 kg, baseline 80.0 kg) or placebo (-0.1 kg, baseline 81.9 kg) were less than with rosiglitazone (+2.1 kg, P < 0.0001, baseline 80.6 kg). Main adverse events for all treatments were minor hypoglycaemia (< 10%), nausea (< 11%), vomiting (< 5%) and diarrhoea (< 8%). Liraglutide added to glimepiride was well tolerated and provided improved glycaemic control and favourable weight profile. Diabet. Med. 26, 268-278 (2009).
引用
收藏
页码:268 / 278
页数:11
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