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Long-term weight gain in children with craniopharyngioma
Sibylle Rovani1, Victoria Butler2, Dinane Samara-Boustani1
1Paediatric Endocrinology, Diabetology, Gynaecology Department, Necker-Enfants Malades University Hospital, AP-HP Centre, Paris 75015, France.
Insights
Children treated for craniopharyngioma experience significant weight gain, even with hypothalamus-sparing approaches. Maintaining hypothalamus integrity is linked to less weight gain, but hypothalamic obesity remains a concern.
Area of Science:
- Pediatric Endocrinology
- Pediatric Oncology
- Neuro-oncology
Background:
- Adamantinomatous craniopharyngioma is a pediatric brain tumor.
- Excessive weight gain is a common long-term complication in survivors.
- Understanding weight changes and associated risk factors is crucial for patient management.
Purpose of the Study:
- To assess long-term weight changes in children treated for craniopharyngioma.
- To identify risk factors contributing to excessive weight gain.
- To investigate the association between hypothalamic damage and weight gain.
Main Methods:
- Retrospective cohort study of 108 children managed between 1990 and 2019.
- Comparison of body mass index (BMI) standard deviation scores (SDS) at baseline and last follow-up.
- Univariate and multivariate analyses to identify variables associated with BMI-SDS variation.
Main Results:
- Mean BMI-SDS increased significantly over 10.4 years of follow-up (2.11 overall).
- Less weight gain was observed in patients without hypothalamic involvement (tumor or treatment).
- Factors associated with BMI-SDS change >2 included female sex, hypothalamic tumor involvement, and higher baseline BMI.
Conclusions:
- Clinically significant weight gain is nearly universal in pediatric craniopharyngioma survivors.
- Hypothalamus integrity is associated with reduced weight gain, but hypothalamic obesity persists.
- Novel treatment strategies are needed to address persistent weight gain despite hypothalamus-sparing approaches.
Objective:
Adamantinomatous craniopharyngioma mainly affects children. Excessive weight gain is a major long-term complication. The primary objective of this study was to assess long-term weight changes in children treated for craniopharyngioma. The secondary objectives were to identify risk factors for excessive weight gain and to look for associations with hypothalamic damage by the tumour or treatment.
Design:
Single-centre retrospective cohort study.
Method:
Children managed for craniopharyngioma at our centre between 1990 and 2019 were included. The body mass index (BMI) standard deviation scores (SDS) at baseline and at last follow-up were compared. Univariate and multivariate analyses were performed in order to identify variables associated with the long-term BMI-SDS variation.
Results:
The 108 patients had a mean follow-up of 10.4 years. The mean BMI-SDS increase over time was 2.11 (P < .001) overall, 1.21 (P < .001) in the group without hypothalamic involvement by the tumour, and 1.95 (P < .001) in the group managed using intended hypothalamus-sparing surgery. The absence of hypothalamic involvement by the tumour or treatment was significantly associated with less weight gain (P = .046 and P < .01, respectively). After adjustment, factors associated with a BMI-SDS change greater than 2 were female sex (P = .023), tumour involving the hypothalamus (P = .04), and higher baseline BMI (P < .001).
Conclusion:
Clinically significant weight gain occurred in nearly all children treated for craniopharyngioma, including those whose hypothalamus was spared by the tumour and intentionally by treatment. However, hypothalamus integrity was associated with less weight gain. Despite hypothalamus-sparing strategies, hypothalamic obesity remains a major concern, indicating a need for novel treatment approaches.
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