Reducing BMI below the obesity threshold in adolescents treated with once‐weekly subcutaneous semaglutide 2.4 mg

Author:

Kelly Aaron S.1ORCID,Arslanian Silva2,Hesse Dan3,Iversen Aske Thorn3,Körner Antje45,Schmidt Signe3,Sørrig Rasmus3,Weghuber Daniel6,Jastreboff Ania M.7ORCID

Affiliation:

1. Department of Pediatrics and Center for Pediatric Obesity Medicine University of Minnesota Medical School Minneapolis Minnesota USA

2. Division of Pediatric Endocrinology, Diabetes and Metabolism, Center for Pediatric Research in Obesity and Metabolism University of Pittsburgh School of Medicine, UPMC Children's Hospital of Pittsburgh Pittsburgh Pennsylvania USA

3. Novo Nordisk A/S Søborg Denmark

4. Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI‐MAG) of the Helmholtz Zentrum München at the University of Leipzig and University Hospital Leipzig Leipzig Germany

5. Center for Pediatric Research (CPL) Leipzig University, Medical Faculty, Hospital for Children and Adolescents Leipzig Germany

6. Department of Pediatrics Paracelsus Medical University Salzburg Austria

7. Department of Medicine (Endocrinology and Metabolism) and Department of Pediatrics (Pediatric Endocrinology) Yale University School of Medicine New Haven Connecticut USA

Abstract

AbstractObjectiveThe aim of this study was to examine how improvement in BMI with the glucagon‐like peptide‐1 receptor agonist semaglutide translated to changes in BMI category in a post hoc analysis of the double‐blind, phase 3a randomized controlled Semaglutide Treatment Effect in People with obesity (STEP) TEENS trial.MethodsAdolescents with obesity received once‐weekly subcutaneous semaglutide 2.4 mg or placebo plus lifestyle intervention, which comprised counseling in healthy nutrition and a goal of 60 minutes of moderate‐ to high‐intensity physical activity per day. Achievement of an improvement in BMI category and attainment of normal‐weight or overweight BMI by week 68 were analyzed using logistic regression models.ResultsIn the overall population, 44.9% of participants receiving semaglutide achieved weight reduction resulting in reclassification to a normal‐weight or overweight BMI category versus 12.1% receiving placebo at week 68 (odds ratio: 22.7; 95% CI: 7.6–67.9). The proportion of semaglutide‐treated participants in obesity class III decreased from 37.3% to 13.6% but increased with placebo. The odds ratio for achieving an improvement of at least one BMI category was significantly greater with semaglutide versus placebo (23.5; 95% CI: 9.9–55.5); an improvement of at least one BMI category was seen in 73.7% of participants receiving semaglutide compared with 19.0% of participants receiving placebo.ConclusionsSemaglutide was highly effective in reducing BMI category. While on treatment, most trial participants' BMI improved by at least one category, and >40% reached a category below the obesity threshold.

Publisher

Wiley

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)

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