4.3 Article

Efficacy of romosozumab in patients with osteoporosis on maintenance hemodialysis in Japan; an observational study

Journal

JOURNAL OF BONE AND MINERAL METABOLISM
Volume 39, Issue 6, Pages 1082-1090

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s00774-021-01253-y

Keywords

Romosozumab; Osteoporosis; Hemodialysis; Bone mineral density; TRACP-5b

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Romosozumab significantly increased BMD at the lumbar spine and femoral neck in HD patients after 1 year of treatment. Despite occurrences of hypocalcemia during treatment, there were no intolerable events reported. The rate of new CVD events did not show a significant increase during the 1-year study, suggesting romosozumab as a promising agent for severe osteoporosis in HD patients.
Introduction Romosozumab reportedly increases bone mineral density (BMD) potently but might adversely affect cardiovascular disease (CVD). We evaluated the efficacy of romosozumab in osteoporotic HD patients with a high risk of fracture. Materials and methods This was a single-center 1-year study in Japanese HD patients. Among 96 HD romosozumab-treated HD patients with high risk of fracture, 76 HD patients completed 1 year of subcutaneous administration of romosozumab (210 mg/4 weeks) for 1 year. Romosozumab-untreated HD patients (n = 55) were also included. Changes in BMD and serum markers, together with fracture occurrence, and CVD events, were monitored. Results During romosozumab treatment of 76 HD patients, BMD time-dependently increased significantly by 15.3% +/- 12.9% at the lumbar spine (L1-4), and 7.2% +/- 8.3% at the femoral neck at 1 year. Serum BAP and total P1NP increased significantly and serum TRACP-5b decreased at 4 weeks. Fragility fractures occurred in three (3.8%) patients. Hypocalcemia occurred at 4-48 weeks despite the increased dosing of active vitamin-D derivatives, but without any symptom. New CVD events occurred in 5.2% of romosozumab-treated HD patients and10.9% in romosozumab-untreated HD patients. Conclusions BMD was increased significantly during romosozumab treatment at the lumbar spine, and the femoral neck, respectively, at 1 year in HD patients. Hypocalcemia occurred but without any intolerable event. There was no apparent increase in CVD events during 1 year of study, suggesting romosozumab as a promising agent for HD patients with severe osteoporosis.

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