Pediatric-onset inflammatory bowel disease poses risk for low bone mineral density at early adulthood

Anat Guz-Mark1, Firas Rinawi2, Oxana Egotubov3

  • 1Institute of Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center, Petah-Tikva, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Insights

Pediatric-onset inflammatory bowel disease (IBD) is linked to reduced bone mineral density (BMD) in adulthood. Low weight at diagnosis is associated with osteopenia and osteoporosis in these patients.

Area of Science:

  • Pediatric Gastroenterology
  • Bone Metabolism
  • Inflammatory Bowel Disease Research

Background:

  • Inflammatory bowel disease (IBD) is a known risk factor for diminished bone mineral density (BMD) in both pediatric and adult populations.
  • Early-onset IBD may have long-term consequences on skeletal health that persist into adulthood.

Purpose of the Study:

  • To investigate the long-term effects of pediatric-onset IBD on adult bone mineral density (BMD).
  • To identify potential correlations between disease characteristics and bone health outcomes in adulthood.

Main Methods:

  • Retrospective review of medical records for pediatric IBD patients.
  • Dual-energy X-ray absorptiometry (DXA) scans in adulthood were analyzed for bone mineral density (BMD) z-scores.
  • Statistical analysis to correlate BMD with various clinical factors.

Main Results:

  • A significant proportion of adult patients (44.3%) with pediatric-onset IBD exhibited osteopenia, and 8.2% had osteoporosis.
  • Lower bone mineral density (BMD) z-scores were observed compared to the normal population (median z-score -1.2, p<0.001).
  • Low weight z-score at diagnosis positively correlated with abnormal bone status in adulthood (r=0.306).

Conclusions:

  • Adults with a history of pediatric-onset IBD frequently experience osteopenia and osteoporosis.
  • Low weight at the time of pediatric IBD diagnosis is a significant predictor of poor bone health in adulthood.
Abstract

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