Effects of sibutramine treatment in obese adolescents - A randomized trial

被引:147
作者
Berkowitz, Robert I.
Fujioka, Ken
Daniels, Stephen R.
Hoppin, Alison G.
Owen, Stanford
Perry, Arlette C.
Sothern, Melinda S.
Renz, Cheryl L.
Pirner, Mark A.
Walch, Julia K.
Jasinsky, Olga
Hewkin, Ann C.
Blakesley, Vicky A.
机构
[1] Childrens Hosp Philadelphia, Behav Hlth Unit, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] Penn Scripps Clin, San Diego, CA USA
[4] Univ Cincinnati, Coll Med, Cincinnati, OH 45221 USA
[5] Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
[6] Massachusetts Gen Hosp, Boston, MA 02114 USA
[7] Ctr Hlth Management, Gulfport, MS USA
[8] Univ Miami, Sch Educ, Coral Gables, FL 33124 USA
[9] Louisiana State Univ, Hlth Sci Ctr, New Orleans, LA 70112 USA
[10] Pennington Biomed Res Ctr, New Orleans, LA USA
[11] Abbott Labs, Abbott Pk, IL 60064 USA
关键词
D O I
10.7326/0003-4819-145-2-200607180-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Increased prevalence of adolescent obesity requires effective treatment options beyond behavior therapy. Objective: To see whether sibutramine reduced weight more than placebo in obese adolescents who were receiving a behavior therapy program. Design: 12-month, 3:1 randomized, double-blind trial conducted from July 2000 to February 2002. Setting: 33 U.S. outpatient clinics. Participants: 498 participants 12 to 16 years of age with a body mass index (BMI) that was at least 2 units more than the U.S. weighted mean of the 95th percentile based on age and sex, to the upper limit of 44 kg/m(2). Interventions: Site-specific behavior therapy plus 10 mg of sibutramine or placebo. Blinded study medication dose was uptitrated to 15 mg or placebo at month 6 if initial BMI was not reduced by 10%. Measurements: Body mass index, waist circumference, body weight, fasting lipid and glycemic variables, safety, and tolerability. Results: Seventy-six percent of patients in the sibutramine group and 62% of patients in the placebo group completed the study. The estimated mean treatment group difference at month 12 (linear mixed-effects model) favored sibutramine for change from baseline in BMI (-2.9 kg/m(2) [95% Cl, -3.5 to -2.2 kg/m(2)]) and body weight (-8.4 kg [Cl, -9.7 to -7.2 kg]) (P < 0.001 for both). The sibutramine group had greater improvements in triglyceride levels, high-density lipoprotein cholesterol levels, insulin levels, and insulin sensitivity (P <= 0.001 for all). The rate of tachycardia was greater with sibutramine vs. placebo (12.5% vs. 6.2%; difference, 6.3 percentage points [Cl, 1.0 to 11.7 percentage points]) but did not lead to increased withdrawal (2.4% vs. 1.5%; difference, 0.9 percentage point [Cl, -1.7 to 3.5 percentage points]). Limitations: The 1-year study duration precluded assessment of long-term weight maintenance and putative health benefits and harms, and 24% and 38% of the sibutramine and placebo groups, respectively, did not complete follow-up. Conclusions: Sibutramine added to a behavior therapy program reduced BMI and body weight more than placebo and improved the profile of several metabolic risk factors in obese adolescents.
引用
收藏
页码:81 / 90
页数:10
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