Astrup Arne, Rössner Stephan, Van Gaal Luc, Rissanen Aila, Niskanen Leo, Al Hakim Mazin, Madsen Jesper, Rasmussen Mads F, Lean Michael E J
Department of Human Nutrition, Faculty of Life Sciences, University of Copenhagen, Frederiksberg, Denmark.
Lancet. 2009 Nov 7;374(9701):1606-16. doi: 10.1016/S0140-6736(09)61375-1. Epub 2009 Oct 23.
The frequency of obesity has risen dramatically in recent years but only few safe and effective drugs are currently available. We assessed the effect of liraglutide on bodyweight and tolerability in obese individuals without type 2 diabetes.
We did a double-blind, placebo-controlled 20-week trial, with open-label orlistat comparator in 19 sites in Europe. 564 individuals (18-65 years of age, body-mass index 30-40 kg/m2) were randomly assigned, with a telephone or web-based system, to one of four liraglutide doses (1.2 mg, 1.8 mg, 2.4 mg, or 3.0 mg, n=90-95) or to placebo (n=98) administered once a day subcutaneously, or orlistat (120 mg, n=95) three times a day orally. All individuals had a 500 kcal per day energy-deficit diet and increased their physical activity throughout the trial, including the 2-week run-in. Weight change analysed by intention to treat was the primary endpoint. An 84-week open-label extension followed. This study is registered with ClinicalTrials.gov, number NCT00422058.
Participants on liraglutide lost significantly more weight than did those on placebo (p=0.003 for liraglutide 1.2 mg and p<0.0001 for liraglutide 1.8-3.0 mg) and orlistat (p=0.003 for liraglutide 2.4 mg and p<0.0001 for liraglutide 3.0 mg). Mean weight loss with liraglutide 1.2-3.0 mg was 4.8 kg, 5.5 kg, 6.3 kg, and 7.2 kg compared with 2.8 kg with placebo and 4.1 kg with orlistat, and was 2.1 kg (95% CI 0.6-3.6) to 4.4 kg (2.9-6.0) greater than that with placebo. More individuals (76%, n=70) lost more than 5% weight with liraglutide 3.0 mg that with placebo (30%, n=29) or orlistat (44%, n=42). Liraglutide reduced blood pressure at all doses, and reduced the prevalence of prediabetes (84-96% reduction) with 1.8-3.0 mg per day. Nausea and vomiting occurred more often in individuals on liraglutide than in those on placebo, but adverse events were mainly transient and rarely led to discontinuation of treatment.
Liraglutide treatment over 20 weeks is well tolerated, induces weight loss, improves certain obesity-related risk factors, and reduces prediabetes.
Novo Nordisk A/S, Bagsvaerd, Denmark.
近年来肥胖发生率急剧上升,但目前仅有少数安全有效的药物。我们评估了利拉鲁肽对无2型糖尿病肥胖个体体重及耐受性的影响。
我们在欧洲19个地点进行了一项双盲、安慰剂对照的20周试验,并设置了开放标签的奥利司他作为对照。564名个体(年龄18 - 65岁,体重指数30 - 40kg/m²)通过电话或基于网络的系统随机分配至四个利拉鲁肽剂量组之一(1.2mg、1.8mg、2.4mg或3.0mg,n = 90 - 95)或安慰剂组(n = 98),每天皮下注射一次,或奥利司他组(120mg,n = 95),每天口服三次。所有个体在整个试验期间,包括2周导入期,采用每日500千卡的能量亏空饮食并增加身体活动。按意向性分析的体重变化是主要终点。随后进行了一项84周的开放标签延长期试验。本研究已在ClinicalTrials.gov注册,编号为NCT00422058。
使用利拉鲁肽的参与者体重减轻显著多于使用安慰剂者(利拉鲁肽1.2mg组p = 0.003,利拉鲁肽1.8 - 3.0mg组p < 0.0001)以及奥利司他组(利拉鲁肽2.4mg组p = 0.003,利拉鲁肽3.0mg组p < 0.0001)。利拉鲁肽1.2 - 3.0mg组的平均体重减轻分别为4.8kg、5.5kg、6.3kg和7.2kg,而安慰剂组为2.8kg,奥利司他组为4.1kg,利拉鲁肽组比安慰剂组多减轻2.1kg(95%CI 0.6 - 3.6)至4.4kg(2.9 - 6.0)。与安慰剂组(30%,n = 29)或奥利司他组(44%,n = 42)相比,更多使用利拉鲁肽3.0mg的个体(76%,n = 70)体重减轻超过5%。利拉鲁肽在所有剂量下均能降低血压,且每天使用1.8 - 3.0mg可降低糖尿病前期的发生率(降低84 - 96%)。使用利拉鲁肽的个体恶心和呕吐发生率高于使用安慰剂者,但不良事件主要是短暂性的,很少导致治疗中断。
20周的利拉鲁肽治疗耐受性良好,可诱导体重减轻,改善某些与肥胖相关的危险因素,并降低糖尿病前期风险。
丹麦 Bagsvaerd 的诺和诺德公司。