4.6 Article

Inflammatory Bowel Disease and the Risk of Fracture After Controlling for FRAX

期刊

JOURNAL OF BONE AND MINERAL RESEARCH
卷 28, 期 5, 页码 1007-1013

出版社

WILEY-BLACKWELL
DOI: 10.1002/jbmr.1848

关键词

INFLAMMATORY BOWEL DISEASE; OSTEOPOROSIS; BONE MINERAL DENSITY; FRACTURE; FRAX; POPULATION-BASED

资金

  1. Bingham Chair in Gastroenterology
  2. Abbott Canada
  3. Prometheus Laboratories
  4. Aptalis Pharmaceuticals
  5. Novartis
  6. Amgen
  7. AstraZeneca
  8. Pfizer
  9. Bayer
  10. Warner-Chilcott/Procter Gamble
  11. Lilly
  12. Roche
  13. Servier
  14. Hologic
  15. American College of Gastroenterology
  16. Canadian Institutes of Health Research (CIHR)/Osteoporosis Canada New Investigator Grant
  17. University of Manitoba Bingham Chair in Gastroenterology
  18. Manitoba Centre for Health Policy, Manitoba Health

向作者/读者索取更多资源

Subjects with inflammatory bowel disease (IBD) are at increased risk for hip and other major osteoporotic fractures. However, previous analyses have not fully accounted for differences in bone mineral density (BMD) and other clinical factors that affect the risk of fracture. The World Health Organization Fracture Risk Assessment tool (FRAX) can be used to predict the 10-year fracture risk from BMD and clinical risk factors. A population-based database containing clinical information on all IBD subjects in the province of Manitoba, Canada, was linked with the Manitoba Bone Mineral Density Database, which contains results of all dual X-ray absorptiometry (DXA) scans in the province. FRAX probabilities were calculated for all subjects aged 50 years or more undergoing baseline DXA testing. Subjects were followed for occurrence of major osteoporotic fractures (MOF; hip, clinical spine, wrist, humerus). Cox proportional hazards models were used to determine whether IBD was independently predictive of MOF or hip fracture. After controlling for FRAX fracture probability computed with BMD, IBD was not associated with a significantly increased risk for MOF (hazard ratio [HR]=1.12, 95% confidence interval [CI], 0.831.55) but was associated with an increased risk for hip fracture (HR=2.14; 95% CI, 1.263.65). The addition of femoral neck T-score to FRAX probability without knowledge of BMD had a negligible effect on the estimated HRs for IBD, suggesting that IBD mediates any effect on fracture risk independently of femoral neck BMD. After controlling for FRAX probability, subjects with IBD are not at an increased risk for overall MOF, but may be at increased risk of hip fracture. (c) 2013 American Society for Bone and Mineral Research.

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