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一项生活方式改变和 taranabant 联合用于维持低热量饮食减肥效果的随机试验。

A randomized trial of lifestyle modification and taranabant for maintaining weight loss achieved with a low-calorie diet.

机构信息

University of Pennsylvania School of Medicine, Department of Psychiatry, Center for Weight and Eating Disorders, Philadelphia, Pennsylvania, USA.

出版信息

Obesity (Silver Spring). 2010 Dec;18(12):2301-10. doi: 10.1038/oby.2010.67. Epub 2010 Apr 8.

Abstract

Improving the maintenance of weight loss remains a critical challenge for obesity researchers. The present 1-year, randomized, placebo-controlled trial evaluated the safety and efficacy of weight maintenance counseling combined with either placebo or the cannabinoid-1 receptor inverse agonist, taranabant, for sustaining prior weight loss achieved on a low-calorie diet (LCD). Seven hundred eighty-four individuals who had lost ≥ 6% of body weight during six initial weeks of treatment with an 800 kcal/day liquid LCD were randomly assigned to placebo or once-daily taranabant in doses of 0.5, 1, or 2 mg. All participants were provided monthly, on-site behavioral weight maintenance counseling, as well as monthly phone calls. The primary end point was change in body weight from randomization to week 52. The randomized participants lost an average of 9.6 kg (9.5% of initial weight) during the 6-week LCD. The model-adjusted mean change in body weight during the subsequent 1 year was +1.7 kg for placebo, compared with -0.1, -0.6, and -1.2 kg for the taranabant 0.5, 1, and 2 mg doses, respectively (all P values ≤ 0.007 vs. placebo). The incidences of psychiatric-related adverse events, including irritability, were higher for taranabant 1 and 2 mg vs. placebo (P ≤ 0.038). In addition to reporting data on the safety and efficacy of taranabant, this study provides a method for studying the combination of lifestyle modification and pharmacotherapy for weight maintenance after diet-induced weight loss.

摘要

维持体重减轻仍然是肥胖研究人员面临的一项关键挑战。本为期 1 年、随机、安慰剂对照试验评估了体重维持咨询与安慰剂或大麻素 1 型受体反向激动剂 taranabant联合用于维持低热量饮食 (LCD) 初始体重减轻的安全性和有效性。784 名参与者在接受为期 6 周的 800kcal/天液体 LCD 治疗期间体重减轻了≥6%,他们被随机分配至安慰剂组或每天接受 taranabant 0.5、1 或 2mg 治疗。所有参与者每月接受一次现场行为体重维持咨询,并每月接受一次电话咨询。主要终点是从随机分组到第 52 周时体重的变化。随机参与者在 6 周的 LCD 期间平均减轻了 9.6kg(初始体重的 9.5%)。随后 1 年期间体重的模型调整平均变化为安慰剂组增加 1.7kg,而 taranabant 0.5、1 和 2mg 剂量组分别减少 0.1、-0.6 和-1.2kg(所有 P 值均≤0.007 与安慰剂相比)。与安慰剂相比,taranaabant 1mg 和 2mg 组的精神相关不良事件(包括易怒)发生率更高(P≤0.038)。除了报告 taranabant 的安全性和有效性数据外,本研究还提供了一种研究生活方式改变和药物治疗联合用于饮食诱导的体重减轻后的体重维持的方法。

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