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Study 19 of 21Setmelanotide literatureJAMA · ReviewTop journal2026

Obesity in Children Aged 2 to 12 Years: A Review.

Obesity in children is a significant health issue, and while intensive lifestyle interventions can reduce BMI, pharmacotherapy options like setmelanotide are limited to specific genetic conditions.

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Where it sits

this study against the rest of the setmelanotide corpus
3
Preclinical
12
Observational
0
Open-label
2
Randomised
4
Reviews · this one

Summary and findings

This review addresses obesity in children aged 2 to 12 years, highlighting the prevalence and associated health risks. It discusses the role of body mass index (BMI) in identifying obesity and mentions setmelanotide as a pharmacotherapy approved for specific genetic forms of obesity. The review emphasizes the importance of intensive health behavior and lifestyle treatment in managing obesity.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Intensive health behavior and lifestyle treatment reduces BMI by 0.7 compared with children who do not participate in intensive health behavior and lifestyle treatment.2026

Abstract

The authors’ words, as JAMA supplied them

<h4>Importance</h4>Obesity affects 15% of children aged 2 to 5 years and 22% of children aged 6 to 11 years in the US. Obesity in children is associated with dyslipidemia, hypertension, metabolic dysfunction-associated steatotic liver disease, and obstructive sleep apnea. Compared with normal-weight peers, children with obesity have lower quality of life and are 5 times more likely to have obesity in adulthood.<h4>Observations</h4>Body mass index (BMI; calculated as weight in kilograms divided by height in meters squared) is used to identify children at risk for excess adiposity, and guidelines recommend that clinicians screen for obesity using BMI starting at age 2 years. Among children, obesity is defined using standardized age- and sex-specific growth charts, with obesity defined as BMI in the 95th or higher percentile and severe obesity as BMI of 120% or greater of the 95th percentile. Obesity treatment in children includes intensive health behavior and lifestyle treatment, consisting of at least 26 contact hours of face-to-face group or family-based activities that incorporate nutrition, physical activity, and behavior change education delivered to the child and caregivers over a 3- to 12-month period. Intensive health behavior and lifestyle treatment reduces BMI by 0.7 compared with children who do not participate in intensive health behavior and lifestyle treatment. The only obesity pharmacotherapy currently approved by the US Food and Drug Administration (FDA) for children younger than 12 years is setmelanotide, a melanocortin-4 receptor agonist, which is indicated for 3 forms of rare monogenic obesity (LEPR, POMC, and PCSK1 genetic variants), Bardet-Biedl syndrome, and acquired hypothalamic obesity. Liraglutide is currently only FDA approved for youth aged 12 years or older; however, a randomized clinical trial among children aged 6 to younger than 12 years demonstrated that, compared with placebo, liraglutide reduced BMI by 7.4%. Metabolic and bariatric surgery is rarely used in children younger than age 12 years and evidence supporting its use in children is limited. Early identification and treatment of obesity during childhood may reduce risk of type 2 diabetes, dyslipidemia, hypertension, and mortality in adulthood.<h4>Conclusions and relevance</h4>Obesity in children is associated with chronic disease, such as hypertension, and with poor quality of life. Evidence-based treatment for obesity in children includes intensive health behavior and lifestyle treatment, and pharmacotherapy may provide additional benefit, although short- and long-term safety and efficacy data are limited. Early identification and treatment of obesity during childhood may reduce risk of type 2 diabetes, dyslipidemia, hypertension, and mortality in adulthood.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

Elsewhere in the Setmelanotide corpus

DSetmelanotide for the Treatment of Acquired Hypothalamic Obesity. Reply.The New England journal of medicine · 2026—AImpact of setmelanotide on metabolic syndrome risk in patients with proopiomelanocortin or leptin receptor deficiencies.The Journal of clinical endocrinology and metabolism · 2026 · Overall mean (SD) change in MetS-Z-BMI score after ∼1 year of treatment was -1.05 (0.88).HumanAMeasuring Hunger Severity in Rare MC4R Pathway Diseases: Development and Psychometric Evaluation of the Most Hunger Item.Advances in therapy · 2023 · MWPC thresholds for Most Hunger were estimated as 1.5-2.6, 0.95-1.6, and 2.4-3.7, respectively.HumanBPositioning Incretin-Based and Next-Generation Obesity Management Medications: A Methodological Framework for a Series of Systematic Reviews and Network Meta-Analyses.Diabetes, obesity & metabolism · 2026 · Not reported in abstract.reviewBEffectiveness and Safety of Setmelanotide in a Patient With a Heterozygous PCSK1 Deficiency.Obesity (Silver Spring, Md.) · 2026 · n=1 · 11.8% total weight loss over 3 monthsHumanBGlobal genomics in over 4 million individuals prioritizes therapeutic targets for heart failure and its subtypesbiorxiv-preprint · 2026 · Identified 383 loci associated with heart failure, n=4,468,166.Human