Evidence map›Paper›PMID 40443456›Full record

ArticleJCEM case reports2025

Weight Management in a Patient With Smith-Magenis Syndrome: The Role of GLP-1 Receptor Agonists.

Jorge César Correia, Timothy Frayling, Zoltan Pataky

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jorge César CorreiaUnit of Therapeutic Patient Education, WHO Collaborating Centre, Department of Primary Care Medicine, University Hospitals of Geneva, 1206 Geneva, Switzerland.ORCID https://orcid.org/0000-0002-7020-0695
Timothy FraylingFaculty Diabetes Centre, University of Geneva, 1206 Geneva, Switzerland.ORCID https://orcid.org/0000-0001-8362-2603
Zoltan PatakyUnit of Therapeutic Patient Education, WHO Collaborating Centre, Department of Primary Care Medicine, University Hospitals of Geneva, 1206 Geneva, Switzerland.ORCID https://orcid.org/0000-0002-8720-3833

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smith-Magenis syndrome (SMS) is a rare genetic disorder characterized by intellectual disability, behavioral challenges, sleep disturbances, and obesity. Managing obesity in SMS is complex due to the behavioral dysregulation. This case involves a patient with SMS who experienced significant weight gain from early in childhood, developing complications such as type 2 diabetes, dyslipidemia, and steatotic liver disease. Initial management with lifestyle changes was insufficient, leading to progressive weight gain. At age 18 years, subcutaneous semaglutide was introduced, resulting in marked improvements in impulsivity, food cravings, and weight control. However, because of a global shortage of this medication, at age 21 years, she was switched to the oral formulation of semaglutide, which led to a relapse in violent behavior, increased food intake, and weight regain. When subcutaneous semaglutide became available again, it was reinstated, stabilizing her weight and behavior. This case underscores the potential of glucagon-like peptide 1 receptor agonists (GLP-1 RAs) in managing both obesity and behavioral symptoms in SMS. While injectable GLP-1 RAs show promise, further research is needed to determine why they may be more effective than oral formulations. Further studies are needed to confirm the effectiveness of GLP-1 RAs and the dosage and explore alternative treatments for long-term obesity management in genetic syndromes.

Indexed as

behavioral impulsivityGLP-1 receptor agonistsobesity managementSmith-Magenis syndrome

Identifiers

PMID40443456
PMCPMC12119458

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.