4.5 Article

Updated trabecular bone score accounting for the soft tissue thickness (TBSTT) demonstrated significantly improved bone microstructure with denosumab in the FREEDOM TBS post hoc analysis

期刊

OSTEOPOROSIS INTERNATIONAL
卷 33, 期 12, 页码 2517-2525

出版社

SPRINGER LONDON LTD
DOI: 10.1007/s00198-022-06549-x

关键词

Trabecular bone score (TBS); Soft tissue thickness; Bone mineral density (BMD); Denosumab; Postmenopausal women; Osteoporosis

资金

  1. University of Lausanne
  2. Amgen Inc., Thousand Oaks, CA, USA

向作者/读者索取更多资源

The study evaluated the effect of denosumab on bone microarchitecture and found that it significantly improved bone microstructure in postmenopausal women with osteoporosis, independent of body mass index.
TBS algorithm has been updated to account for regional soft tissue noise. In postmenopausal women with osteoporosis, denosumab improved tissue thickness-adjusted TBS vs placebo independently of bone mineral density over 3 years, with the magnitude of changes from baseline or placebo numerically greater than body mass index-adjusted TBS. Introduction To evaluate the effect of denosumab on bone microarchitecture assessed by trabecular bone score (TBS) in the FREEDOM study using the updated algorithm that accounts for regional soft tissue thickness -(TBSTT) in dual-energy X-ray absorptiometry (DXA) images and to compare percent changes from baseline and placebo with classical body mass index (BMI)-adjusted TBS -(TBSBMI). Methods Postmenopausal women with lumbar spine or total hip bone mineral density (BMD) T score < - 2.5 and = - 4.0 received placebo or denosumab 60 mg subcutaneously every 6 months. -TBSBMI and -TBSTT were assessed on lumbar spine DXA scans at baseline and months 1, 12, 24, and 36 in a subset of 279 women (129 placebo, 150 denosumab) who completed the 3-year FREEDOM DXA substudy and rolled over to open-label extension study. Results Baseline characteristics were similar between groups. -TBSTT in the denosumab group showed numerically greater changes from both baseline and placebo than -TBSBMI at months 12, 24, and 36. Denosumab led to progressive increases in BMD (1.2, 5.6, 8.1, and 10.5%) and -TBSTT (0.4, 2.3, 2.6, and 3.3%) from baseline to months 1, 12, 24, and 36, respectively. Both TBS changes were significant vs baseline and placebo from months 12 to 36 (p < 0.0001). As expected, BMD and -TBSTT were poorly correlated both at baseline and for changes during treatment. Conclusion In postmenopausal women with osteoporosis, denosumab significantly improved bone microstructure assessed by -TBSTT over 3 years. -TBSTT seemed more responsive to denosumab treatment than -TBSBMI and was independent of BMD.

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