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Periostin concentrations in childhood-onset craniopharyngioma patients
K Heinks1, C De Schutter-Nüsse1,2, S Boekhoff1
1Department of Pediatrics and Pediatric Hematology/Oncology, University Children's Hospital, Klinikum Oldenburg AöR, 26133, Oldenburg, Germany.
Insights
Periostin levels in craniopharyngioma (CP) patients did not correlate with non-alcoholic fatty liver disease (NAFLD) risk factors. Therefore, periostin is unlikely to be a useful NAFLD marker in CP patients.
Area of Science:
- Endocrinology
- Hepatology
- Oncology
Background:
- Periostin is elevated in craniopharyngioma (CP)-associated fibroblasts and linked to non-alcoholic fatty liver disease (NAFLD).
- CP patients with hypothalamic syndrome have a high incidence of NAFLD.
- This study investigates periostin as a potential NAFLD marker in CP.
Purpose of the Study:
- To determine if periostin concentrations in biological fluids of CP patients are elevated.
- To assess the association between periostin levels and pathological hepatic parameters in CP.
- To evaluate periostin's potential as an indicator of NAFLD risk in CP.
Main Methods:
- A cross-sectional study involving 35 patients with sellar masses (32 CP) and controls.
- Periostin levels were measured using ELISA in serum, urine, and saliva.
- Associations with hypothalamic involvement, obesity, and hepatic enzymes were analyzed.
Main Results:
- Periostin concentrations in serum, urine, and saliva were similar across CP and control groups.
- No significant association was found between periostin levels and hypothalamic lesions, obesity, or hepatic enzymes.
- A subgroup with decreased insulin-like growth factor (IGF)-1 showed elevated serum periostin.
Conclusions:
- Periostin concentrations in CP patients are not linked to established NAFLD risk factors.
- Periostin does not appear to be a suitable biomarker for NAFLD in the context of craniopharyngioma.
- Further research is needed to clarify the role of periostin in the subgroup with decreased IGF-1.
Purpose:
Periostin is highly expressed in craniopharyngioma (CP)-associated fibroblasts and has been identified as a marker for non-alcoholic fatty liver disease (NAFLD). Half of CP patients with hypothalamic syndrome develop NAFLD. We hypothesized that periostin concentration is elevated in biological fluids of CP and associated with pathological hepatic parameters, indicating increased risk for NAFLD.
Methods:
A cross-sectional study on 35 patients with sellar masses (SMP) recruited in the German Childhood Craniopharyngioma Registry (32 CP, 2 xanthogranuloma, 1 pilocytic astrocytoma), three short-statured patients with isolated growth hormone deficiency, five short-statured patients with normal findings in GH-stimulating tests and decreased insulin-like growth factor (IGF)-1 and seven healthy controls. Periostin was measured by Elisa in serum, urine and saliva.
Results:
Periostin serum, urine and saliva concentrations in CP were similar to concentrations of the other groups. Hypothalamic involvement/hypothalamic lesions, degree of obesity as well as hepatic enzymes were not associated with elevated periostin concentrations. Due to low patient numbers with pathological hepatic parameters, missing imaging data on the degree of steatosis hepatis and the lack of histological proof of NAFLD, no definitive conclusions can be drawn from measured periostin concentrations in serum. Interestingly, the subgroup of patients with decreased IGF-1 levels showed elevated concentrations of serum periostin when compared with other groups.
Conclusions:
In CP, periostin concentrations are not associated with known risk factors for NAFLD such as hepatic and metabolic parameters, obesity and hypothalamic lesions. Accordingly, periostin does not seem to be a suitable marker for NAFLD in CP.
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