Effects of discontinuing oral bisphosphonate treatments for postmenopausal osteoporosis on bone turnover markers and bone density
- PMID: 29525970
- DOI: 10.1007/s00198-018-4460-6
Effects of discontinuing oral bisphosphonate treatments for postmenopausal osteoporosis on bone turnover markers and bone density
Abstract
The antiresorptive potency varies between different bisphosphonates. We investigated the effect of stopping oral bisphosphonate treatment for postmenopausal osteoporosis (ibandronate, alendronate, risedronate) on BTMs and BMD. After stopping treatment, all three groups showed an increase in BTMs and a decrease in hip BMD; however, none returned to pre-treatment baseline values.
Introduction: Bisphosphonates (BPs) continue to suppress bone turnover markers (BTMs) after treatment has stopped, leading to the suggestion that a pause in treatment could be considered for low-risk patients. Indirect comparisons suggest that after cessation of treatment, the effects on bone may differ between drugs. We investigated the effects of stopping oral BP treatments for postmenopausal osteoporosis on BTMs and bone mineral density (BMD).
Methods: We studied postmenopausal osteoporotic women who had previously taken part in a 2-year randomised study of three oral BPs (ibandronate, alendronate, or risedronate). At the end of the study, women with hip BMD T-score > - 2.5 and considered clinically appropriate to discontinue treatment were invited to participate in a further 2-year observational study. Biochemical response was assessed using BTMs, and BMD was measured by dual-energy X-ray absorptiometry.
Results: All BTMs increased after treatment withdrawal but remained below the pre-treatment baseline with less suppression of BTMs for the risedronate group compared to alendronate and ibandronate up to 48 weeks. There was no difference between the BP groups 96 weeks after stopping treatment. The change in BMD during the 96 weeks after stopping treatment was - 1.6% (95% CI - 1.9 to - 1.2, P < 0.001) for the total hip and - 0.6% (95% CI - 1.1 to - 0.2, P = 0.17) at the lumbar spine with no difference between the three BP groups (P = 0.85 and P = 0.48, respectively).
Conclusion: For all treatment groups, there was an increase in BTMs and a decrease in hip BMD after stopping BPs for 2 years; however, none returned to pre-treatment baseline values.
Keywords: Alendronate; Bone density; Bone markers; Ibandronate; Risedronate.
Similar articles
-
Response of bone turnover markers to three oral bisphosphonate therapies in postmenopausal osteoporosis: the TRIO study.Osteoporos Int. 2016 Jan;27(1):21-31. doi: 10.1007/s00198-015-3145-7. Epub 2015 May 20. Osteoporos Int. 2016. PMID: 25990354 Clinical Trial.
-
Comparison of the effects of three oral bisphosphonate therapies on the peripheral skeleton in postmenopausal osteoporosis: the TRIO study.Osteoporos Int. 2014 Dec;25(12):2729-41. doi: 10.1007/s00198-014-2817-z. Epub 2014 Jul 30. Osteoporos Int. 2014. PMID: 25074351 Clinical Trial.
-
Denosumab significantly increases bone mineral density and reduces bone turnover compared with monthly oral ibandronate and risedronate in postmenopausal women who remained at higher risk for fracture despite previous suboptimal treatment with an oral bisphosphonate.Osteoporos Int. 2014 Jul;25(7):1953-61. doi: 10.1007/s00198-014-2692-7. Epub 2014 Mar 28. Osteoporos Int. 2014. PMID: 24676847
-
Significance of a decline in bone mineral density while receiving oral bisphosphonate treatment.Clin Ther. 2008 Mar;30(3):443-52. doi: 10.1016/j.clinthera.2008.03.008. Clin Ther. 2008. PMID: 18405784 Review.
-
The challenge of long-term adherence: The role of bone turnover markers in monitoring bisphosphonate treatment of osteoporosis.Bone. 2020 Jul;136:115336. doi: 10.1016/j.bone.2020.115336. Epub 2020 Mar 28. Bone. 2020. PMID: 32234415 Review.
Cited by
-
Duration of Bisphosphonate Drug Holidays in Osteoporosis Patients: A Narrative Review of the Evidence and Considerations for Decision-Making.J Clin Med. 2021 Mar 9;10(5):1140. doi: 10.3390/jcm10051140. J Clin Med. 2021. PMID: 33803095 Free PMC article. Review.
-
Fracture risk following intermission of osteoporosis therapy.Osteoporos Int. 2019 Sep;30(9):1733-1743. doi: 10.1007/s00198-019-05002-w. Epub 2019 Jun 7. Osteoporos Int. 2019. PMID: 31175404
-
Sustained anti-osteoporotic action of risedronate compared to anti-RANKL antibody following discontinuation in ovariectomized mice.Bone Rep. 2020 Jun 5;13:100289. doi: 10.1016/j.bonr.2020.100289. eCollection 2020 Dec. Bone Rep. 2020. PMID: 32577437 Free PMC article.
-
[Long-term treatment concepts for osteoporosis].Internist (Berl). 2021 May;62(5):474-485. doi: 10.1007/s00108-021-00993-3. Epub 2021 Mar 12. Internist (Berl). 2021. PMID: 33710362 Free PMC article. Review. German.
-
A Vitronectin-Derived Peptide Restores Ovariectomy-Induced Bone Loss by Dual Regulation of Bone Remodeling.Tissue Eng Regen Med. 2022 Dec;19(6):1359-1376. doi: 10.1007/s13770-022-00486-w. Epub 2022 Oct 7. Tissue Eng Regen Med. 2022. PMID: 36207661 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical