Osteoporosis in pediatric patients suffering from chronic inflammatory bowel disease with and without steroid

Frank Walther1, Christoph Fusch, Michael Radke

  • 1University Children's Hospital, Faculty of Medicine, University of Rostock, Rembrandtstrasse 16/17, D-18057 Rostock. frank.walther@med.uni-rostock.de

Insights

Pediatric inflammatory bowel disease (IBD) patients have similar osteoporosis rates whether or not they use steroids. Osteoporosis is present before steroid treatment, highlighting the need for accurate bone density measurements in these children.

Area of Science:

  • Pediatric Endocrinology
  • Gastroenterology
  • Bone Metabolism

Background:

  • Children with inflammatory bowel disease (IBD) face increased osteoporosis risk due to corticosteroids, inflammation, and malnutrition.
  • Assessing osteoporosis in pediatric IBD is crucial due to potential long-term bone health consequences.

Purpose of the Study:

  • To compare osteoporosis rates in steroid-naive versus steroid-treated pediatric IBD patients.
  • To investigate the impact of inflammation and malnutrition on bone health in pediatric IBD.

Main Methods:

  • Dual-energy X-ray absorptiometry (DXA) assessed lumbar spine bone mineral density (BMD) in 90 IBD patients and 52 controls.
  • Areal BMD was converted to bone mineral apparent density (BMAD) and expressed as standard deviation scores (SDS) relative to controls.

Main Results:

  • Osteoporosis (BMAD-SDS < -2) affected 8% of girls and 20% of boys.
  • Osteoporosis prevalence was similar in steroid-naive (12%) and steroid-treated (11%) IBD patients.
  • Body height SDS correlated with BMD-SDS, not BMAD-SDS, indicating bone size influences BMD measurements.

Conclusions:

  • Osteoporosis is prevalent in pediatric IBD patients, mirroring adult rates, and exists before steroid therapy.
  • Volumetric bone parameters (BMAD) are essential for accurate assessment, compensating for short stature in IBD patients.
  • Accurate assessment using BMAD prevents misdiagnosis of osteopenia in growth-stunted pediatric IBD patients.
Abstract

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