Chanoine Jean-Pierre, Hampl Sarah, Jensen Craig, Boldrin Mark, Hauptman Jonathan
Endocrinology and Diabetes Unit, British Columbia Children's Hospital, Vancouver, Canada.
JAMA. 2005 Jun 15;293(23):2873-83. doi: 10.1001/jama.293.23.2873.
The prevalence of overweight and obesity in children and adolescents is increasing rapidly. In this population, behavioral therapy alone has had limited success in providing meaningful, sustained weight reduction, and pharmacological treatment has not been extensively studied.
To determine the efficacy and safety of orlistat in weight management of adolescents.
DESIGN, SETTING, AND PATIENTS: Multicenter, 54-week (August 2000-October 2002), randomized, double-blind study of 539 obese adolescents (aged 12-16 years; body mass index [BMI] >or=2 units above the 95th percentile) at 32 centers in the United States and Canada.
A 120-mg dose of orlistat (n = 357) or placebo (n = 182) 3 times daily for 1 year, plus a mildly hypocaloric diet (30% fat calories), exercise, and behavioral therapy.
Change in BMI; secondary measures included changes in waist and hip circumference, weight loss, lipid measurements, and glucose and insulin responses to oral glucose challenge.
There was a decrease in BMI in both treatment groups up to week 12, thereafter stabilizing with orlistat but increasing beyond baseline with placebo. At the end of the study, BMI had decreased by 0.55 with orlistat but increased by 0.31 with placebo (P = .001). Compared with 15.7% of the placebo group, 26.5% of participants taking orlistat had a 5% or higher decrease in BMI (P = .005); 4.5% and 13.3%, respectively, had a 10% or higher decrease in BMI (P = .002). At study end, weight had increased 0.53 kg with orlistat and 3.14 kg with placebo (P<.001). Dual-energy x-ray absorptiometry showed that this difference was explained by changes in fat mass. Waist circumference decreased in the orlistat group but increased in the placebo group (-1.33 cm vs +0.12 cm; P<.05). Generally mild to moderate gastrointestinal tract adverse events occurred in 9% to 50% of the orlistat group and in 1% to 13% of the placebo group.
In combination with diet, exercise, and behavioral modification, orlistat statistically significantly improved weight management in obese adolescents compared with placebo. The use of orlistat for 1 year in this adolescent population did not raise major safety issues although gastrointestinal adverse events were more common in the orlistat group.
儿童和青少年中超重及肥胖的患病率正在迅速上升。在这一人群中,仅靠行为疗法在实现有意义的、持续的体重减轻方面成效有限,而药物治疗尚未得到广泛研究。
确定奥利司他在青少年体重管理中的疗效和安全性。
设计、地点和患者:在美国和加拿大的32个中心进行的多中心、为期54周(2000年8月至2002年10月)的随机双盲研究,涉及539名肥胖青少年(年龄12 - 16岁;体重指数[BMI]高于第95百分位数至少2个单位)。
120毫克剂量的奥利司他(n = 357)或安慰剂(n = 182),每日3次,持续1年,同时搭配轻度低热量饮食(脂肪热量占30%)、运动和行为疗法。
BMI的变化;次要指标包括腰围和臀围的变化、体重减轻情况、血脂测量结果以及口服葡萄糖耐量试验中的血糖和胰岛素反应。
在第12周前,两个治疗组的BMI均有所下降,此后奥利司他组的BMI保持稳定,而安慰剂组的BMI则超过基线水平上升。研究结束时,奥利司他组的BMI下降了0.55,而安慰剂组上升了0.31(P = 0.001)。与安慰剂组15.7%的参与者相比,服用奥利司他的参与者中有26.5%的BMI下降了5%或更多(P = 0.005);分别有4.5%和13.3%的参与者BMI下降了10%或更多(P = 0.002)。研究结束时,奥利司他组体重增加了0.53千克,安慰剂组增加了3.14千克(P<0.001)。双能X线吸收法显示,这种差异是由体脂变化所致。奥利司他组的腰围减小,而安慰剂组的腰围增加(-1.33厘米对+0.12厘米;P<0.05)。奥利司他组9%至50%的参与者出现一般为轻至中度的胃肠道不良事件,安慰剂组为1%至13%。
与饮食、运动和行为改变相结合,与安慰剂相比,奥利司他在肥胖青少年的体重管理方面有统计学意义上的显著改善。在这一青少年人群中使用奥利司他1年并未引发重大安全问题,尽管胃肠道不良事件在奥利司他组更为常见。