Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide

被引:430
|
作者
Astrup, A. [1 ]
Carraro, R. [2 ]
Finer, N. [3 ]
Harper, A. [4 ]
Kunesova, M. [5 ]
Lean, M. E. J. [6 ]
Niskanen, L. [7 ,8 ]
Rasmussen, M. F. [9 ]
Rissanen, A. [10 ]
Rossner, S. [11 ]
Savolainen, M. J. [12 ]
Van Gaal, L. [13 ]
机构
[1] Univ Copenhagen, Fac Life Sci, Dept Human Nutr, DK-1958 Frederiksberg C, Denmark
[2] Univ Hosp La Princesa, Inst Invest Sanitaria Princesa, Dept Endocrinol, Madrid, Spain
[3] UCL, Dept Med, London, England
[4] Novo Nordisk AS, Clin Reporting, Soborg, Denmark
[5] Inst Endocrinol, Obes Management Ctr, Prague, Czech Republic
[6] Univ Glasgow, Glasgow Royal Infirm, Dept Human Nutr, Glasgow G31 2ER, Lanark, Scotland
[7] Cent Hosp Cent Finland, Dept Med, Jyvaskyla, Finland
[8] Univ Eastern Finland, Kuopio, Finland
[9] Novo Nordisk Inc, Med & Sci Dept, Princeton, NJ USA
[10] Univ Helsinki, Cent Hosp, Dept Psychiat, Obes Res Unit, Helsinki, Finland
[11] Karolinska Univ Hosp, Obes Unit, Huddinge, Sweden
[12] Univ Oulu, Inst Clin Med, Oulu, Finland
[13] Univ Antwerp Hosp, Dept Endocrinol Diabetol & Metab, Antwerp, Belgium
关键词
liraglutide; GLP-1; analog; weight loss; OBESITY; REDUCTION; SIBUTRAMINE; OVERWEIGHT; DIET; LIFE;
D O I
10.1038/ijo.2011.158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Having demonstrated short-term weight loss with liraglutide in this group of obese adults, we now evaluate safety/tolerability (primary outcome) and long-term efficacy for sustaining weight loss (secondary outcome) over 2 years. Design: A randomized, double-blind, placebo-controlled 20-week study with 2-year extension (sponsor unblinded at 20 weeks, participants/investigators at 1 year) in 19 European clinical research centers. Subjects: A total of 564 adults (n = 90-98 per group; body mass index 30-40 kg m(-2)) enrolled, 398 entered the extension and 268 completed the 2-year trial. Participants received diet (500 kcal deficit per day) and exercise counseling during 2-week run-in, before being randomly assigned (with a telephone or web-based system) to once-daily subcutaneous liraglutide (1.2, 1.8, 2.4 or 3.0 mg, n = 90-95), placebo (n = 98) or open-label orlistat (120 mg x 3, n = 95). After 1 year, liraglutide/placebo recipients switched to liraglutide 2.4 mg, then 3.0 mg (based on 20-week and 1-year results, respectively). The trial ran from January 2007-April 2009 and is registered with Clinicaltrials.gov, number NCT00480909. Results: From randomization to year 1, liraglutide 3.0 mg recipients lost 5.8 kg (95% confidence interval 3.7-8.0) more weight than those on placebo and 3.8 kg (1.6-6.0) more than those on orlistat (P <= 0.0001; intention-to-treat, last-observation-carried-forward). At year 2, participants on liraglutide 2.4/3.0 mg for the full 2 years (pooled group, n 184) lost 3.0 kg (1.3-4.7) more weight than those on orlistat (n 95; P < 0.001). Completers on liraglutide 2.4/3.0 mg (n 92) maintained a 2-year weight loss of 7.8 kg from screening. With liraglutide 3.0 mg, 20-week body fat decreased by 15.4% and lean tissue by 2.0%. The most frequent drug-related side effects were mild to moderate, transient nausea and vomiting. With liraglutide 2.4/3.0 mg, the 2-year prevalence of prediabetes and metabolic syndrome decreased by 52 and 59%, with improvements in blood pressure and lipids. Conclusion: Liraglutide is well tolerated, sustains weight loss over 2 years and improves cardiovascular risk factors. International Journal of Obesity (2012) 36, 843-854; doi:10.1038/ijo.2011.158; published online 16 August 2011
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收藏
页码:843 / 854
页数:12
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