Abstract

Childhood obesity is now considered to be an epidemic. Drug therapy in this age group remains a topic of research. The objective of this study was to examine the effect of treatment with sibutramine (10 mg) on body composition and energy expenditure in obese adolescents. The study was conducted as a randomized, double-blind, placebo-controlled trial. The study was set in an obesity research center. The patients were 24 obese adolescents (age 12-17 yr, 11 boys); four patients withdrew. Intervention was sibutramine (Meridia) or placebo in combination with an energy-restricted diet and exercise plan for 12 wk, followed by an identical, but medication-free, treatment period (follow-up). Change in body mass index (BMI) sd score (BMI-SDS) was the principal measure of efficacy. Body composition and total energy expenditure were measured by stable isotopes and further calculated according to the four-component model, using underwater weighing and dual x-ray absorptiometry. Basal metabolic rate (BMR) was measured by ventilated hood and adjusted for sex and body composition (BMRadj). After intervention, the decrease in BMI-SDS was comparable in both groups. During follow-up, BMI further decreased in the placebo group but stabilized in the sibutramine group. Changes in the percentage of fat mass were not different between both groups. BMRadj decreased in the placebo group and remained constant in the sibutramine group. During follow-up, BMRadj decreased in the sibutramine group and increased in the placebo group. Changes in total energy expenditure were not significantly different. The effect of sibutramine on BMI-SDS was not significant. Sibutramine may diminish the decrease in BMRadj associated with energy restriction in obese adolescents.

Highlights

  • MethodsObese adolescents from the regional public health department and pediatric outpatient clinic of the University Hospital Maastricht participated in the study

  • Context: Childhood obesity is considered to be an epidemic

  • BMRadj decreased in the placebo group and remained constant in the sibutramine group

Read more

Summary

Methods

Obese adolescents from the regional public health department and pediatric outpatient clinic of the University Hospital Maastricht participated in the study. Participants were between 12–18 yr of age, initially selected for BMI greater than or equal to the 97th percentile, and further selected for triceps skinfold thickness greater than or equal to the 97th percentile for age and sex [9] with persisting obesity despite previous. Van Mil et al Sibutramine in Obese Adolescents professionally supervised weight loss attempts (97.5th percentile is equivalent to 2 sd). Patients with endocrine causes or other secondary causes of obesity were excluded as well as patients with any significant physical or medical illness, that could influence the results of the study. Before the start of the study, the adolescents gave oral approval, confirmed by written informed consent by the caregivers. The study was approved by the Medical Ethical Committee of Maastricht University

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call