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西布曲明在肥胖患者中的疗效与耐受性:一项剂量范围研究。

Efficacy and tolerability of sibutramine in obese patients: a dose-ranging study.

作者信息

Hanotin C, Thomas F, Jones S P, Leutenegger E, Drouin P

机构信息

Department of Clinical Research, Laboratoires Knoll France, Levallois-Perret, France.

出版信息

Int J Obes Relat Metab Disord. 1998 Jan;22(1):32-8. doi: 10.1038/sj.ijo.0800540.

Abstract

OBJECTIVES

To assess the weight-reducing effects and tolerability of 5 mg, 10 mg and 15 mg daily doses of sibutramine, a novel serotonin and noradrenaline reuptake inhibitor (SNRI).

DESIGN

Multicentre, double-blind, and placebo-controlled study. After a one week run-in period, patients were randomized to receive placebo or sibutramine over a 12-week period. Advice on diet and behaviour modification was provided. One follow-up was conducted four weeks after cessation of treatment.

SUBJECTS

235 obese outpatients, aged 18-65 y with a body mass index (BMI) within the range 27-40 kg/m2.

MEASUREMENTS

Weight, height, waist and hip circumference, and medical history, assessment of hunger, satiety, appetite and craving for sweet, savoury and carbohydrate foods, and also for carbohydrate snacking, standard laboratory assessments, blood pressure, heart rate and ECG.

RESULTS

The group mean (+/- s.e.m.) weight loss at end-point was 1.4 +/- 0.5 kg for placebo (n = 59), 2.4 +/- 0.5 kg for 5 mg sibutramine (n = 56), 5.1 +/- 0.5 kg for 10 mg sibutramine (n = 59) and 4.9 +/- 0.5 kg (n = 62) for 15 mg sibutramine. The difference observed between the placebo and the 10 mg and 15 mg groups was statistically significant from week 2 onwards (P < 0.01), but there was no significant difference between these sibutramine groups. The percentage of patients losing > 5% of initial bodyweight was significantly greater for 15 mg sibutramine (55%) and 10 mg sibutramine (49%) than for treatment with placebo (19%), (P < 0.001). During the double-blind period, 41 patients (17%) withdrew prematurely and 168 patients (71%) reported 453 adverse events. The incidence and type of adverse event and the rates of withdrawal, were not significantly different in the four groups. No significant differences between the groups were observed, in respect of changes in systolic and diastolic blood pressure, but a significant increase in heart rate (about 4 beats/min) was noted for patients who received 10 mg or 15 mg sibutramine, compared with the placebo (P < 0.001).

CONCLUSION

These data demonstrate dose-related weight loss with sibutramine treatment for up to 12 weeks in obese patients. Doses of 10 mg and 15 mg once daily were shown to be similarly effective, well tolerated and significantly more effective than the placebo.

摘要

目的

评估新型5-羟色胺和去甲肾上腺素再摄取抑制剂(SNRI)西布曲明每日5毫克、10毫克和15毫克剂量的减肥效果及耐受性。

设计

多中心、双盲、安慰剂对照研究。经过1周的导入期后,患者被随机分组,在12周内接受安慰剂或西布曲明治疗。提供了饮食和行为改变方面的建议。治疗停止4周后进行一次随访。

受试者

235名肥胖门诊患者,年龄在18 - 65岁之间,体重指数(BMI)在27 - 40千克/平方米范围内。

测量指标

体重、身高、腰围和臀围、病史、饥饿感、饱腹感、食欲以及对甜、咸和碳水化合物食物的渴望程度,还有碳水化合物零食情况、标准实验室评估、血压、心率和心电图。

结果

终点时,安慰剂组(n = 59)的组平均(±标准误)体重减轻为1.4 ± 0.5千克,5毫克西布曲明组(n = 56)为2.4 ± 0.5千克,10毫克西布曲明组(n = 59)为5.1 ± 0.5千克,15毫克西布曲明组(n = 62)为4.9 ± 0.5千克。从第2周起,安慰剂组与10毫克和15毫克组之间观察到的差异具有统计学意义(P < 0.01),但这些西布曲明组之间无显著差异。体重减轻超过初始体重5%的患者百分比,15毫克西布曲明组(55%)和10毫克西布曲明组(49%)显著高于安慰剂治疗组(19%),(P < 0.001)。在双盲期,41名患者(17%)提前退出,168名患者(71%)报告了453起不良事件。四组中不良事件的发生率和类型以及退出率无显著差异。各组之间在收缩压和舒张压变化方面未观察到显著差异,但与安慰剂相比,接受10毫克或15毫克西布曲明的患者心率显著增加(约4次/分钟),(P < 0.001)。

结论

这些数据表明,在肥胖患者中,西布曲明治疗长达12周可实现与剂量相关的体重减轻。每日10毫克和15毫克的剂量显示出相似的效果、良好的耐受性,且比安慰剂显著更有效。

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