Effect of intermittent cyclical etidronate therapy on corticosteroid induced osteoporosis in Japanese patients with connective tissue disease: 3 year followup
- PMID: 14719212
Effect of intermittent cyclical etidronate therapy on corticosteroid induced osteoporosis in Japanese patients with connective tissue disease: 3 year followup
Abstract
Objective: A 3 year prospective randomized study was conducted to clarify the efficacy of intermittent cyclical etidronate therapy on corticosteroid induced osteoporosis.
Methods: A group of 102 Japanese patients were enrolled, each taking > 7.5 mg of prednisolone daily for at least 90 days. Patients were randomly divided into 2 treatment groups: Group E (etidronate) took 200 mg etidronate disodium per day for 2 weeks with 3.0 g calcium lactate and 0.75 microg alphacalcidol daily; Group C (control) took 3.0 g calcium lactate and 0.75 microg alphacalcidol daily. Outcome measurements included changes from baseline in bone mineral density (BMD) of the lumbar spine and the rate of new vertebral fractures at 48 and 144 weeks.
Results: The mean (+/- SD) lumbar spine BMD increased 3.7 +/- 5.6% (p < 0.01) and 1.5 +/- 4.1% (NS) from baseline at 48 weeks and 4.8 +/- 6.9% (p < 0.005) and 0.4 +/- 5.0% (NS) from baseline at 144 weeks in Group E and Group C, respectively. The improvement of BMD in Group E was significantly greater than in Group C at 144 weeks (p < 0.01). In 3 subgroups, men and premenopausal and postmenopausal women, the postmenopausal women showed the greatest improvement. Mean percentage change in this subgroup was 10.1 +/- 8.0% and 1.35 +/- 6.4% in Group E and Group C, respectively. We noted that 2 patients in Group C had new vertebral fractures, whereas no fractures were observed in Group E.
Conclusion: These results indicate that intermittent cyclical etidronate therapy is effective for the prevention and treatment of corticosteroid induced osteoporosis in patients with connective tissue diseases.
Similar articles
-
A comparison of the effect of risedronate and etidronate on lumbar bone mineral density in Japanese patients with osteoporosis: a randomized controlled trial.Osteoporos Int. 2002 Dec;13(12):971-9. doi: 10.1007/s001980200135. Osteoporos Int. 2002. PMID: 12459940 Clinical Trial.
-
Intermittent etidronate therapy to prevent corticosteroid-induced osteoporosis.N Engl J Med. 1997 Aug 7;337(6):382-7. doi: 10.1056/NEJM199708073370603. N Engl J Med. 1997. PMID: 9241127 Clinical Trial.
-
A pooled data analysis on the use of intermittent cyclical etidronate therapy for the prevention and treatment of corticosteroid induced bone loss.J Rheumatol. 2000 Oct;27(10):2424-31. J Rheumatol. 2000. PMID: 11036840
-
[Evidence and utility of etidronate for the treatment of osteoporosis].Clin Calcium. 2008 Oct;18(10):1427-33. Clin Calcium. 2008. PMID: 18830039 Review. Japanese.
-
[Etidronate].Nihon Rinsho. 2003 Feb;61(2):226-30. Nihon Rinsho. 2003. PMID: 12638212 Review. Japanese.
Cited by
-
Bisphosphonates for the prevention and treatment of osteoporosis in patients with rheumatic diseases: a systematic review and meta-analysis.PLoS One. 2013 Dec 6;8(12):e80890. doi: 10.1371/journal.pone.0080890. eCollection 2013. PLoS One. 2013. PMID: 24324644 Free PMC article.
-
Dilemmas in the Management of Osteoporosis in Younger Adults.JBMR Plus. 2022 Jan 19;6(1):e10594. doi: 10.1002/jbm4.10594. eCollection 2022 Jan. JBMR Plus. 2022. PMID: 35079682 Free PMC article. Review.
-
Efficacy of oral etidronate for skeletal diseases in Japan.Yonsei Med J. 2005 Jun 30;46(3):313-20. doi: 10.3349/ymj.2005.46.3.313. Yonsei Med J. 2005. Retraction in: Yonsei Med J. 2023 May;64(5):349. doi: 10.3349/ymj.2003.0386.re. PMID: 15988801 Free PMC article. Retracted. Review.
-
A framework for the development of guidelines for the management of glucocorticoid-induced osteoporosis.Osteoporos Int. 2012 Sep;23(9):2257-76. doi: 10.1007/s00198-012-1958-1. Epub 2012 Mar 21. Osteoporos Int. 2012. PMID: 22434203
-
Bisphosphonates for steroid-induced osteoporosis.Cochrane Database Syst Rev. 2016 Oct 5;10(10):CD001347. doi: 10.1002/14651858.CD001347.pub2. Cochrane Database Syst Rev. 2016. PMID: 27706804 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous