Liraglutide vs insulin glargine and placebo in combination with metformin and sulfonylurea therapy in type 2 diabetes mellitus (LEAD-5 met+SU): a randomised controlled trial

被引:667
作者
Russell-Jones, D. [1 ]
Vaag, A. [2 ]
Schmitz, O. [3 ]
Sethi, B. K. [4 ]
Lalic, N. [5 ]
Antic, S. [6 ]
Zdravkovic, M. [7 ]
Ravn, G. M. [7 ]
Simo, R. [8 ]
机构
[1] Royal Guildford Hosp, Dept Endocrinol & Diabet, Guildford GU2 7XX, Surrey, England
[2] Steno Diabet Ctr, Dept Endocrinol, DK-2820 Gentofte, Denmark
[3] Univ Aarhus, Univ Hosp, Aarhus, Denmark
[4] Care Hosp, Hyderabad, Andhra Pradesh, India
[5] Sch Med, Belgrade, Serbia
[6] Diabet & Metab Dis Clin, Nish, Serbia
[7] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[8] Univ Vall Hebron, Inst Recerca Hosp, Diabet Res Unit, Barcelona, Spain
关键词
DPP-4; Exenatide; Incretin; Insulin glargine; LEAD-5; GLUCAGON-LIKE PEPTIDE-1; HUMAN GLP-1 ANALOG; GLYCEMIC CONTROL; BASAL INSULIN; NPH INSULIN; EXENATIDE EXENDIN-4; ORAL-AGENTS; NN2211; PHARMACOKINETICS; PHARMACODYNAMICS;
D O I
10.1007/s00125-009-1472-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the study was to compare the efficacy and safety of liraglutide in type 2 diabetes mellitus vs placebo and insulin glargine (A21Gly,B31Arg,B32Arg human insulin), all in combination with metformin and glimepiride. This randomised (using a telephone or web-based randomisation system), parallel-group, controlled 26 week trial of 581 patients with type 2 diabetes mellitus on prior monotherapy (HbA(1c) 7.5-10%) and combination therapy (7.0-10%) was conducted in 107 centres in 17 countries. The primary endpoint was HbA(1c). Patients were randomised (2:1:2) to liraglutide 1.8 mg once daily (n = 232), liraglutide placebo (n = 115) and open-label insulin glargine (n = 234), all in combination with metformin (1 g twice daily) and glimepiride (4 mg once daily). Investigators, participants and study monitors were blinded to the treatment status of the liraglutide and placebo groups at all times. The number of patients analysed as intention to treat were: liraglutide n = 230, placebo n = 114, insulin glargine n = 232. Liraglutide reduced HbA(1c) significantly vs glargine (1.33% vs 1.09%; -0.24% difference, 95% CI 0.08, 0.39; p = 0.0015) and placebo (-1.09% difference, 95% CI 0.90, 1.28; p < 0.0001). There was greater weight loss with liraglutide vs placebo (treatment difference -1.39 kg, 95% CI 2.10, 0.69; p = 0.0001), and vs glargine (treatment difference -3.43 kg, 95% CI 4.00, 2.86; p < 0.0001). Liraglutide reduced systolic BP (-4.0 mmHg) vs glargine (+0.5 mmHg; -4.5 mmHg difference, 95% CI 6.8, -2.2; p = 0.0001) but not vs placebo (p = 0.0791). Rates of hypoglycaemic episodes (major, minor and symptoms only, respectively) were 0.06, 1.2 and 1.0 events/patient/year, respectively, in the liraglutide group (vs 0, 1.3, 1.8 and 0, 1.0, 0.5 with glargine and placebo, respectively). A slightly higher number of adverse events (including nausea at 14%) were reported with liraglutide, but only 9.8% of participants in the group receiving liraglutide developed anti-liraglutide antibodies. Liraglutide added to metformin and sulfonylurea produced significant improvement in glycaemic control and bodyweight compared with placebo and insulin glargine. The difference vs insulin glargine in HbA(1c) was within the predefined non-inferiority margin.
引用
收藏
页码:2046 / 2055
页数:10
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