Van Gaal Luc F, Scheen André J, Rissanen Aila M, Rössner Stephan, Hanotin Corinne, Ziegler Olivier
Department of Diabetology, Metabolism, and Clinical Nutrition, Antwerp University Hospital, Wilrijkstraat 10, B-2650 Edegem-Antwerp, Belgium.
Eur Heart J. 2008 Jul;29(14):1761-71. doi: 10.1093/eurheartj/ehn076. Epub 2008 Apr 15.
Rimonabant, the first selective cannabinoid type 1 receptor blocker, has been shown to produce weight loss and improvements in several cardiometabolic risk factors over 1 year. We report the 2 year efficacy and tolerability data of rimonabant.
Patients with a body mass index > or =30 or >27 kg/m(2) with treated/untreated hypertension, dyslipidaemia, or both, were randomized to double-blind treatment with placebo, rimonabant 5 or 20 mg once daily plus a calorie-restricted diet for 2 years. Weight loss from baseline to 2 years in the intention-to-treat population was significantly greater with rimonabant 20 mg (mean +/- SD: -5.5 +/- 7.7 kg; P < 0.001) and 5 mg (-2.9 +/- 6.5 kg; P = 0.002) than placebo (-1.2 +/- 6.8 kg). Rimonabant 20 mg produced significantly greater improvements than placebo in waist circumference, high-density lipoprotein cholesterol, triglycerides, fasting glucose and insulin levels, insulin resistance, and metabolic syndrome prevalence. Rimonabant 20 mg produced clinically meaningful improvements in all Impact of Weight on Quality of Life-Lite questionnaire domain scores at 2 years. Rimonabant was generally well tolerated and rates of adverse events, including depressed mood disorders and disturbances were similar to placebo during year 2. Proportions of patients with clinically significant depression (Hospital Anxiety and Depression Scale score >11) were similar in all treatment groups.
Rimonabant 20 mg over 2 years promoted clinically relevant and durable weight loss and improvements in cardiometabolic risk factors.
利莫那班是首个选择性1型大麻素受体阻滞剂,已证实其在1年时间内可实现体重减轻,并改善多种心血管代谢风险因素。我们报告了利莫那班的2年疗效和耐受性数据。
体重指数≥30或>27kg/m²,伴有已治疗/未治疗的高血压、血脂异常或两者皆有的患者,被随机分为接受安慰剂、每日一次5mg或20mg利莫那班联合热量限制饮食的双盲治疗组,为期2年。在意向性治疗人群中,与安慰剂组(-1.2±6.8kg)相比,20mg利莫那班组(均值±标准差:-5.5±7.7kg;P<0.001)和5mg利莫那班组(-2.9±6.5kg;P = 0.002)从基线到2年时的体重减轻更为显著。20mg利莫那班组在腰围、高密度脂蛋白胆固醇、甘油三酯、空腹血糖和胰岛素水平、胰岛素抵抗以及代谢综合征患病率方面的改善显著优于安慰剂组。20mg利莫那班组在2年时对生活质量-简易版问卷所有领域得分均产生了具有临床意义的改善。利莫那班总体耐受性良好,在第2年时包括情绪低落障碍和精神障碍在内的不良事件发生率与安慰剂组相似。所有治疗组中具有临床显著抑郁(医院焦虑抑郁量表评分>11)的患者比例相似。
2年内使用20mg利莫那班可促进具有临床相关性且持久的体重减轻以及心血管代谢风险因素的改善。