4.5 Article

Efficacy of weekly teriparatide does not vary by baseline fracture probability calculated using FRAX

期刊

OSTEOPOROSIS INTERNATIONAL
卷 26, 期 9, 页码 2347-2353

出版社

SPRINGER LONDON LTD
DOI: 10.1007/s00198-015-3129-7

关键词

Epidemiology; FRAX; Osteoporosis; Randomised controlled trial; Teriparatide; Vertebral fracture

资金

  1. ActiveSignal
  2. Alliance for Better Bone Health
  3. AMGEN
  4. Bayer
  5. Consilient Healthcare
  6. GE Lunar
  7. Hologic
  8. Internis Pharma
  9. Lilly
  10. MSD
  11. Novartis
  12. Pfizer
  13. Roche
  14. Servier
  15. Tethys
  16. UCB
  17. Univadis
  18. Chugai Pharmaceutical
  19. Teijin Pharma
  20. Asahi Kasei Pharma
  21. Daiichi Sankyo
  22. Chugai
  23. Daiichi-Sankyo-Co.
  24. Eli Lilly Japan
  25. Eli Lilly
  26. lecture fees
  27. MRC [MR/K006312/1, MC_U147585819, G0400491, MC_U147585827] Funding Source: UKRI
  28. Medical Research Council [U1475000001, MC_U147585819, MR/K006312/1, MC_U147585824, G0400491, MC_UU_12011/1, MC_UP_A620_1014, MC_U147585827] Funding Source: researchfish
  29. National Institute for Health Research [NF-SI-0513-10085, NF-SI-0508-10082] Funding Source: researchfish

向作者/读者索取更多资源

The aim of this study was to determine the efficacy of once-weekly teriparatide as a function of baseline fracture risk. Treatment with once-weekly teriparatide was associated with a statistically significant 79 % decrease in vertebral fractures, and in the cohort as a whole, efficacy was not related to baseline fracture risk. Introduction Previous studies have suggested that the efficacy of some interventions may be greater in the segment of the population at highest fracture risk as assessed by the FRAXA(R) algorithms. The aim of the present study was to determine whether the antifracture efficacy of weekly teriparatide was dependent on the magnitude of fracture risk. Methods Baseline fracture probabilities (using FRAX) were computed from the primary data of a phase 3 study (TOWER) of the effects of weekly teriparatide in 542 men and postmenopausal women with osteoporosis. The outcome variable comprised morphometric vertebral fractures. Interactions between fracture probability and efficacy were explored by Poisson regression. Results The 10-year probability of major osteoporotic fractures (without BMD) ranged from 7.2 to 42.2 %. FRAX-based hip fracture probabilities ranged from 0.9 to 29.3 %. Treatment with teriparatide was associated with a 79 % (95 % CI 52-91 %) decrease in vertebral fractures assessed by semiquantitative morphometry. Relative risk reductions for the effect of teriparatide on the fracture outcome did not change significantly across the range of fracture probabilities (p=0.28). In a subgroup analysis of 346 (64 %) participants who had FRAX probabilities calculated with the inclusion of BMD, there was a small but significant interaction (p=0.028) between efficacy and baseline fracture probability such that high fracture probabilities were associated with lower efficacy. Conclusion Weekly teriparatide significantly decreased the risk of morphometric vertebral fractures in men and postmenopausal women with osteoporosis. Overall, the efficacy of teriparatide was not dependent on the level of fracture risk assessed by FRAX in the cohort as a whole.

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