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)

被引:1154
|
作者
Buse, John B. [1 ]
Rosenstock, Julio [2 ]
Sesti, Giorgio [3 ]
Schmidt, Wolfgang E. [4 ]
Montanya, Eduard [5 ]
Brett, Jason H. [6 ]
Zychma, Marcin [7 ]
Blonde, Lawrence [8 ]
机构
[1] Univ N Carolina, Sch Med, Div Endocrinol, Chapel Hill, NC 27515 USA
[2] Dallas Diabet & Endocrine Ctr Med City, Dallas, TX USA
[3] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, Catanzaro, Italy
[4] Ruhr Univ Bochum, Fac Med, St Josef Hosp, Dept Med, Bochum, Germany
[5] Univ Barcelona, CIBERDEM, Hosp Univ Bellivtge IDIBELL, Barcelona, Spain
[6] Novo Nordisk AS, Princeton, NJ USA
[7] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[8] Ochsner Med Ctr, Ochsner Diabet Clin Res Unit, Dept Endocrinol, New Orleans, LA USA
来源
LANCET | 2009年 / 374卷 / 9683期
关键词
GLUCAGON-LIKE PEPTIDE-1; HUMAN GLP-1 ANALOG; BETA-CELL MASS; GLYCEMIC CONTROL; ACUTE-PANCREATITIS; TREATED PATIENTS; METFORMIN; SULFONYLUREA; EXENDIN-4; WEIGHT;
D O I
10.1016/S0140-6736(09)60659-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Unlike most antihyperglycaemic drugs, glucagon-like peptide-1 (GLP-1) receptor agonists have a glucose-dependent action and promote weight loss. We compared the efficacy and safety of liraglutide, a human GLP-1 analogue, with exenatide, an exendin-based GLP-1 receptor agonist. Methods Adults with inadequately controlled type 2 diabetes on maximally tolerated doses of metformin, sulphon urea, or both, were stratified by previous oral antidiabetic therapy and randomly assigned to receive additional liraglutide 1.8 mg once a day (n=233) or exenatide 10 mu g twice a day (n=231) in a 26-week open-label, parallel-group, multinational (15 countries) study. The primary outcome was change in glycosylated haemoglobin (HbA(1c)). Efficacy analyses were by intention to treat. The trial is registered with ClinicalTrials.gov, number NCT00518882. Findings Mean baseline HbA(1c) for the study population was 8.2%. Liraglutide reduced mean HbA(1c) significantly more than did exenatide (-1.12% [SE 0.08] vs -0.79% [0.08]; estimated treatment difference -0.33; 95% CI -0.47 to -0.18; p<0.0001) and more patients achieved a HbA(1c) value of less than 7% (54% vs 43%, respectively; odds ratio 2.02; 95% CI 1.31 to 3.11; p=0.0015). Liraglutide reduced mean fasting plasma glucose more than did exenatide (-1.61 mmol/L [S E 0.20] vs -0.60 mmol/L [0.20]; estimated treatment difference -1.01 mmol/L; 95% CI -1.37 to -0.65; p<0.0001) but postprandial glucose control was less effective after breakfast and dinner. Both drugs promoted similar weight losses (liraglutide -3.24 kg vs exenatide -2.87 kg). Both drugs were well tolerated, but nausea was less persistent (estimated treatment rate ratio 0.448, p<0.0001) and minor hypoglycaemia less frequent with liraglutide than with exenatide (1.93 vs 2.60 events per patient per year; rate ratio 0.55; 95% CI 0.34 to 0.88; p=0.0131; 25.5% vs 33.6% had minor hypoglycaemia). Two patients taking both exenatide and a sulphonylurea had a major hypoglycaemic episode. Interpretation Liraglutide once a day provided significantly greater improvements in glycaemic control than did exenatide twice a day, and was generally better tolerated. The results suggest that liraglutide might be a treatment option for type 2 diabetes, especially when weight loss and risk of hypoglycaemia are major considerations.
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收藏
页码:39 / 47
页数:9
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