4.6 Article

Relationship between bone mineral density changes with denosumab treatment and risk reduction for vertebral and nonvertebral fractures

期刊

JOURNAL OF BONE AND MINERAL RESEARCH
卷 27, 期 3, 页码 687-693

出版社

WILEY
DOI: 10.1002/jbmr.1472

关键词

DENOSUMAB; BONE MINERAL DENSITY; FRACTURE; SURROGATE; PERCENT OF TREATMENT EFFECT EXPLAINED

资金

  1. Amgen Inc.
  2. Servier
  3. Novartis
  4. Amgen
  5. Roche
  6. Eli Lilly
  7. Schering Plough
  8. Pfizer
  9. Wyeth-Ayerst
  10. Novo Nordisk
  11. Procter Gamble
  12. Groupe Fournier
  13. Besins EscoVesco
  14. MSD
  15. Chiesi
  16. Boehringer Mannheim
  17. AstraZeneca
  18. California Pacific Medical Center
  19. GlaxoSmithKline
  20. Hologic
  21. Kyphon Inc.
  22. Lilly Industries
  23. Maxygen
  24. Nastech Pharmaceuticals
  25. Nestle Research Center
  26. New Zealand Milk Limited
  27. ONO-Pharma
  28. Organon Laboratories
  29. Osteologix
  30. Procter & Gamble Pharmaceuticals
  31. Diagnostics
  32. Sanofi-Aventis
  33. Shire
  34. Tethys
  35. Trans-Pharma Medical Limited
  36. Unilever
  37. Unipath
  38. Merck
  39. Boehringer
  40. JJ
  41. GSK
  42. Biosante
  43. Lilly
  44. Takeda
  45. Warner-Chilcott
  46. Fund for Scientific Research, Flanders, Belgium (FWO-Vlaanderen)

向作者/读者索取更多资源

Dual-energy X-ray absorptiometric bone mineral density (DXA BMD) is a strong predictor of fracture risk in untreated patients. However, previous patient-level studies suggest that BMD changes explain little of the fracture risk reduction observed with osteoporosis treatment. We investigated the relevance of DXA BMD changes as a predictor for fracture risk reduction using data from the FREEDOM trial, which randomly assigned placebo or denosumab 60?mg every 6 months to 7808 women aged 60 to 90 years with a spine or total hip BMD T-score?100%] and 72% [95% CI: 24% >100%], respectively). Previous patient-level studies may have underestimated the strength of the relationship between BMD change and the effect of treatment on fracture risk or this relationship may be unique to denosumab. (c) 2012 American Society for Bone and Mineral Research

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