» Articles » PMID: 29525970

Effects of Discontinuing Oral Bisphosphonate Treatments for Postmenopausal Osteoporosis on Bone Turnover Markers and Bone Density

Overview
Journal Osteoporos Int
Date 2018 Mar 12
PMID 29525970
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Improvement of osteoblast adhesion, viability, and mineralization by restoring the cell cytoskeleton after bisphosphonate discontinuation in vitro.

Patntirapong S, Champakerdsap C, Mathaveechotikul P, Vatanasilp A J Appl Oral Sci. 2024; 32:e20240034.

PMID: 39140581 PMC: 11321799. DOI: 10.1590/1678-7757-2024-0034.


Prolonged bone health benefits for breast cancer patients following adjuvant bisphosphonate therapy: the BoHFAB study.

Brown J, Paggiosi M, Rathbone E, Gregory W, Bertelli G, Din O J Bone Miner Res. 2024; 39(1):8-16.

PMID: 38630878 PMC: 11207765. DOI: 10.1093/jbmr/zjad006.


Comparison of bone mineral density of osteoporotic and osteopenia menopausal women treated with oral bisphosphonates before stopping the treatment and 1 year after drug holiday period.

Rizi M, Salari A, Salesi M, Rasooli L, Karimifar M Clin Rheumatol. 2024; 43(4):1375-1379.

PMID: 38347325 DOI: 10.1007/s10067-024-06906-7.


The Sequential Therapy in Osteoporosis.

Sauhta R, Makkar D, Siwach P Indian J Orthop. 2023; 57(Suppl 1):150-162.

PMID: 38107815 PMC: 10721775. DOI: 10.1007/s43465-023-01067-2.


The why and how of sequential and combination therapy in osteoporosis. A review of the current evidence.

Chandran M Arch Endocrinol Metab. 2022; 66(5):724-738.

PMID: 36382762 PMC: 10118820. DOI: 10.20945/2359-3997000000564.


References
1.
Whitaker M, Guo J, Kehoe T, Benson G . Bisphosphonates for osteoporosis--where do we go from here?. N Engl J Med. 2012; 366(22):2048-51. DOI: 10.1056/NEJMp1202619. View

2.
Eastell R, Hannon R, Wenderoth D, Rodriguez-Moreno J, Sawicki A . Effect of stopping risedronate after long-term treatment on bone turnover. J Clin Endocrinol Metab. 2011; 96(11):3367-73. PMC: 3205892. DOI: 10.1210/jc.2011-0412. View

3.
McClung M, Harris S, Miller P, Bauer D, Davison K, Dian L . Bisphosphonate therapy for osteoporosis: benefits, risks, and drug holiday. Am J Med. 2012; 126(1):13-20. DOI: 10.1016/j.amjmed.2012.06.023. View

4.
Bauer D, Schwartz A, Palermo L, Cauley J, Hochberg M, Santora A . Fracture prediction after discontinuation of 4 to 5 years of alendronate therapy: the FLEX study. JAMA Intern Med. 2014; 174(7):1126-34. PMC: 4409325. DOI: 10.1001/jamainternmed.2014.1232. View

5.
Black D, Delmas P, Eastell R, Reid I, Boonen S, Cauley J . Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis. N Engl J Med. 2007; 356(18):1809-22. DOI: 10.1056/NEJMoa067312. View