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.
Abstract

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