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Updated: Apr 1, 2026

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours
B Haliloglu1, Z Atay2, T Guran2
1Department of Pediatric Endocrinology, Marmara University Medical School, Istanbul, Turkey. belmahaliloglu26@hotmail.com.
Insights
Hypothalamic obesity in children with hypothalamic tumors has a higher mortality rate. Increased BMI SDS after 6 months of therapy, younger age at diagnosis, and higher BMI SDS are significant risk factors for mortality.
Area of Science:
- Pediatric Endocrinology
- Oncology
- Metabolic Disorders
Background:
- Hypothalamic obesity (HyOb) is a frequent complication in children diagnosed with hypothalamic tumors.
- Patients with HyOb face a potentially elevated mortality risk, often linked to obstructive sleep apnea/hypoventilation.
Purpose of the Study:
- To ascertain predictive factors for mortality in pediatric patients experiencing HyOb.
- To identify key indicators for improved survival outcomes in this vulnerable population.
Main Methods:
- A cohort of twenty children diagnosed with HyOb secondary to hypothalamic tumors was studied.
- Follow-up extended over a minimum of 3 years, with participants under 15 years at diagnosis and receiving short-term glucocorticoid treatment.
Main Results:
- A significant increase in Body Mass Index (BMI) Standard Deviation Score (SDS) was observed within the first 6 months of therapy.
- Mortality risk was notably higher in patients with a BMI SDS increase exceeding 1 after 6 months (RR: 8.4, P<0.05).
- Younger children (age <6 years at diagnosis) and those reaching a maximum BMI SDS ≥3 exhibited substantially higher mortality rates.
Conclusions:
- An escalating BMI SDS after 6 months of therapy emerges as a critical risk factor for HyOb-related mortality.
- Early diagnosis (age <6 years) and achieving a maximum BMI SDS ≥3 are associated with increased mortality, underscoring the need for prompt and intensive obesity management.
Background:
Hypothalamic obesity (HyOb) is a common complication of childhood hypothalamic tumours. Patients with HyOb probably have a higher mortality rate than those with other types of obesity due in many cases to obstructive sleep apnoea/hypoventilation.
Objectives:
To identify predictive factors for mortality caused by HyOb in children.
Methods:
Twenty children with HyOb secondary to hypothalamic tumours that were followed-up for ≥3 years and aged <15 years at diagnosis, and received supraphysiological glucocorticoid treatment for ≤1 month.
Results:
Mean age at diagnosis was 6.36 ± 3.60 years. Mean body mass index (BMI) Standard deviation of the samples (SDS) increased from 0.77 ± 1.26 to 2.66 ± 1.45 during the first 6 months, but slowed from month 6-12 (2.73 ± 1.35). ΔBMI SDS at 0-6 months was significantly higher in patients aged <6 years at diagnosis than in those aged >6 years at diagnosis (3.71 ± 1.96 vs. 0.83 ± 0.73, P < 0.001). Maximum BMI SDS was also significantly higher in the younger group (3.88 ± 1.39 vs. 2.79 ± 0.64, P < 0.05). In all, four patients died and the mortality rate was significantly higher in the patients with a further increase in BMI SDS > 1 SDS after 6 months of therapy (RR: 8.4, P < 0.05). Both overall mortality and obesity-related mortality rates were higher in the patients aged <6 years at diagnosis (4.5-fold, 7.2-fold higher, respectively, P > 0.05). The mortality rate was also 3.7-fold higher in the patients with a maximum BMI SDS ≥ 3 at any time during the first 3 years after therapy(P > 0.05).
Conclusions:
An increase in BMI SDS after 6 months of therapy was observed to be a risk factor for mortality caused by HyOb. In addition, age <6 years at diagnosis and a maximum BMI SDS ≥ 3 were associated with a higher mortality rate, indicating that earlier and more aggressive treatment of obesity is required.
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