Barkeling B, Elfhag K, Rooth P, Rössner S
Obesity Unit, Institute of Internal Medicine, Huddinge University Hospital, Stockholm, Sweden.
Int J Obes Relat Metab Disord. 2003 Jun;27(6):693-700. doi: 10.1038/sj.ijo.0802298.
To evaluate the short-term effects of sibutramine on appetite and eating behaviour and whether these effects are related to the long-term therapeutic outcome.
Short-term: randomised, double-blind, placebo-controlled, within-subject design. Long-term: prospective open clinical trial.
A total of 36 obese (nine men/27 women) with a body mass index of 39.3+/-4.3 (mean+/-s.d.) (range 30.2 - 45.2) kg/m(2) and age 44.4+/-12.1 y. PROCEDURE AND METHODS:: First phase-short-term effects: At baseline, the subjects were treated for 14 days with 15 mg sibutramine/placebo (period 1) followed by a 2 weeks single-blind placebo washout period, the subjects received the alternative therapy for another 14 days (period 2). At baseline, and at day 14 in each treatment period the subjects arrived fasting to the laboratory for a standardised breakfast and an ad libitum standardised lunch using the VIKTOR set-up (a universal eating monitor) to evaluate the microstructure of the eating behaviour (ie amount of food consumed and eating rate). Visual Analogue Scales were applied before and after the meals as well as every hour between the meals to monitor the appetite. During this first phase, subjects were encouraged to keep their habitual eating habits. Second phase-long-term effects: All subjects received 10 months open treatment with 15 mg sibutramine and dietary advice in monthly group sessions with a dietitian. On the last day of this treatment period, the subjects returned to repeat the measurements of appetite and eating behaviour using the same test procedure as during the first phase of the study.
First phase: Sibutramine influenced appetite and eating behaviour that could be registered after only 14 days of treatment. The amount of food consumed at lunch on VIKTOR was reduced by 16% by sibutramine compared to placebo, 335+/-123 g vs 399+/-126 g (P<0.0001). Second phase: Responders and nonresponders were defined as those who ate less vs more food on VIKTOR when treated with sibutramine compared to the baseline food intake in the first phase of the study. The weight reduction was greater for responders 11.8+/-6.2 (mean+/-s.d.) kg compared to nonresponders 6.8+/-2.7 (mean+/-s.d.) kg (P<0.05).
Short-term effects of sibutramine on appetite and eating behaviour were identified such as a reduction in food intake and in ratings of subjective motivation to eat. Short-term sibutramine effects on eating behaviour are to some extent related to the long-term therapeutic outcome in obese subjects.
评估西布曲明对食欲和进食行为的短期影响,以及这些影响是否与长期治疗结果相关。
短期:随机、双盲、安慰剂对照、受试者自身对照设计。长期:前瞻性开放临床试验。
共36名肥胖者(9名男性/27名女性),体重指数为39.3±4.3(均值±标准差)(范围30.2 - 45.2)kg/m²,年龄44.4±12.1岁。
第一阶段——短期影响:在基线时,受试者接受15毫克西布曲明/安慰剂治疗14天(第1期),随后是2周的单盲安慰剂洗脱期,受试者接受另一种治疗14天(第2期)。在基线时,以及每个治疗期的第14天,受试者空腹到实验室食用标准化早餐和随意食用标准化午餐,使用VIKTOR装置(一种通用饮食监测仪)评估进食行为的微观结构(即食物摄入量和进食速度)。在餐前、餐后以及餐间每小时使用视觉模拟量表监测食欲。在这第一阶段,鼓励受试者保持其习惯的饮食习惯。第二阶段——长期影响:所有受试者接受10个月的开放治疗,服用15毫克西布曲明,并在每月与营养师进行的小组会议中接受饮食建议。在该治疗期的最后一天,受试者返回,使用与研究第一阶段相同的测试程序重复测量食欲和进食行为。
第一阶段:西布曲明影响食欲和进食行为,仅治疗14天后即可显现。与安慰剂相比,西布曲明使VIKTOR上午餐的食物摄入量减少了16%,分别为335±123克和399±126克(P<0.0001)。第二阶段:将与研究第一阶段基线食物摄入量相比,服用西布曲明时在VIKTOR上进食较少和较多的受试者分别定义为反应者和无反应者。反应者的体重减轻幅度更大,为11.8±6.2(均值±标准差)千克,而无反应者为6.8±2.7(均值±标准差)千克(P<0.05)。
确定了西布曲明对食欲和进食行为的短期影响,如食物摄入量减少和主观进食动机评分降低。西布曲明对进食行为的短期影响在一定程度上与肥胖受试者的长期治疗结果相关。