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Published on: April 4, 2025
Semaglutide treatment for children with obesity: an observational study
Elizabeth-Jane van Boxel1, Saqib Rahman2, Karen Lai3
1Southampton General Hospital, Southampton, UK elizabeth.vanboxel@uhs.nhs.uk.
Insights
Semaglutide effectively reduced weight and BMI in children with obesity and comorbidities. Mild gastrointestinal side effects were noted, with a few discontinuing treatment.
Area of Science:
- Pediatric Endocrinology
- Obesity Medicine
- Pharmacological Interventions
Background:
- Childhood obesity is a growing global health concern.
- Comorbidities like insulin resistance and type 2 diabetes are common in pediatric obesity.
- Effective weight management strategies are crucial for long-term health outcomes in children.
Purpose of the Study:
- To evaluate the efficacy and tolerability of semaglutide for weight loss in pediatric patients with obesity.
- To assess the impact of semaglutide on body mass index (BMI) standard deviation score (SDS) and overall body weight.
- To identify and report any adverse events associated with semaglutide treatment in this population.
Main Methods:
- A retrospective observational study included 50 children (aged 10-18) with obesity (BMI SDS >2) and comorbidities.
- Patients received once-weekly injectable semaglutide (1 mg) alongside dietary and lifestyle advice.
- Primary outcomes included changes in weight, BMI SDS, and percentage body weight over 6 and 12 months.
Main Results:
- After 6 months, significant reductions were observed in BMI SDS (0.32±0.27) and body weight (7.03±7.50 kg), with a mean weight loss of 6.4±6.3%.
- At 12 months, further significant decreases in BMI SDS (0.54±0.52) and body weight (9.7±10.8 kg) were noted, with 8.9±10.0% total weight loss.
- Mild gastrointestinal side effects were common; five patients discontinued treatment due to adverse events, and one developed gallstones.
Conclusions:
- Semaglutide demonstrates efficacy as a weight loss adjunct in children with obesity and comorbidities.
- The treatment was generally well-tolerated, with manageable side effects in a multidisciplinary setting.
- Semaglutide represents a promising therapeutic option for pediatric weight management programs.
Objective:
To assess efficacy and tolerability of semaglutide as a weight loss treatment for children living with comorbid obesity.
Design:
Retrospective observational study of the first 50 children from a weight management service treated with semaglutide for at least 6 months.
Setting:
A tertiary paediatric multidisciplinary weight management clinic in a UK hospital.
Patients:
Aged 10-18 years old with a body mass index (BMI) SD score (SDS) >2 with a weight-related comorbidity (including insulin resistance (defined as homeostatic model assessment for insulin resistance >4), type 2 diabetes, metabolic-associated fatty liver disease, obstructive sleep apnoea or hypertension).
Interventions:
Once-weekly injectable semaglutide titrated over 8 weeks to a final dose of 1 mg in addition to dietary and lifestyle advice.
Main Outcome Measures:
Primary outcome measures were change in weight, BMI SDS and percentage body weight. Secondary outcomes were side effects and cessation of treatment.
Results:
After 6 months of treatment, statistically significant decreases in BMI SDS (0.32±0.27, p<0.001) and body weight (7.03±7.50 kg, p<0.001) were seen. Mean percentage total weight loss was 6.4±6.3% (p<0.001). For the 14 patients for whom 12-month data were available, statistically significant decreases were seen in mean BMI SDS (0.54±0.52, p<0.001). Mean body weight decreased by 9.7±10.8 kg (p<0.001). Percentage total weight loss at 12 months was 8.9±10.0% (p<0.001). Mild gastrointestinal side effects were common. One patient developed gallstones. Five patients discontinued treatment due to side effects.
Conclusion:
Semaglutide appears to be a safe and effective weight loss adjunct when used in a multidisciplinary weight management clinic.
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