Early changes in bone turnover and bone mineral density after discontinuation of long-term oral bisphosphonates: a post hoc analysis
Autor: | Annpey Pong, Bente L. Langdahl, T. J. de Villiers, Felicia Cosman, Andrew Denker, Arthur C. Santora, Kenneth G. Saag, Boyd B. Scott |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Endocrinology Diabetes and Metabolism medicine.medical_treatment Osteoporosis Urology 030209 endocrinology & metabolism Discontinuation Placebo Bone remodeling 03 medical and health sciences 0302 clinical medicine Long-term Post-hoc analysis Bone mineral density medicine Femoral neck Bone mineral Alendronate Oral bisphosphonates business.industry Bisphosphonate medicine.disease medicine.anatomical_structure Post hoc 030101 anatomy & morphology business |
Zdroj: | Saag, K, Cosman, F, De Villiers, T, Langdahl, B, Scott, B B, Denker, A E, Pong, A & Santora, A C 2021, ' Early changes in bone turnover and bone mineral density after discontinuation of long-term oral bisphosphonates : a post hoc analysis ', Osteoporosis International, vol. 32, no. 9, pp. 1879-1888 . https://doi.org/10.1007/s00198-020-05785-3 |
ISSN: | 1433-2965 0937-941X |
DOI: | 10.1007/s00198-020-05785-3 |
Popis: | Summary: This post hoc analysis of a randomized, double-blind study of postmenopausal women with osteoporosis found that there were early increases in bone turnover markers and decreases in bone mineral density after discontinuation of long-term alendronate. These findings might help guide treatment decisions, including monitoring after alendronate withdrawal. Introduction: The short-term effects of discontinuing long-term bisphosphonates are poorly characterized. This post hoc analysis investigated 1–12-month changes in bone mineral density (BMD) and bone turnover markers (BTM) after alendronate (ALN) discontinuation. Methods: Data were from a randomized, double-blind trial of MK-5442 (calcium-sensing receptor antagonist) following oral bisphosphonates, with placebo and continued ALN controls (ClinicalTrials.gov NCT00996801). Postmenopausal women with osteoporosis had received oral bisphosphonate (≥ 3–4 preceding years; ALN for the 12 months pre-screening), continuing on ALN 70 mg/week (n = 87) or placebo (n = 88). Results: At 12 months, least-squares mean percent changes from baseline BMD (placebo vs. ALN) were lumbar spine (LS): – 0.36 vs. 1.29, total hip: – 1.44 vs. 0.46, and femoral neck (FN): – 1.26 vs. – 0.08 (all P < 0.05). BTM levels increased by 1–3 months, to 12 months, with placebo vs. ALN (P < 0.001). FN BMD decline was greater in the placebo subgroup with higher urinary N-terminal cross-linked telopeptides of type I collagen/creatinine [uNTx/Cr] (P < 0.01), and higher serum N-terminal pro-peptide of type 1 collagen [P1NP] levels (P < 0.05), at baseline. There was a trend toward greater FN BMD loss with higher BTM levels at 3 and/or 6 months. Younger age and higher LS BMD at baseline were associated with greater LS BMD loss at 12 months (P = 0.04 and < 0.01, respectively); higher baseline FN BMD predicted greater FN BMD loss (P = 0.04). Conclusion: Early changes in BTM levels and BMD were observed after discontinuation of long-term ALN. Further characterization of factors associated with patients’ risk of bone loss upon bisphosphonate discontinuation is warranted. |
Databáze: | OpenAIRE |
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