The Effectiveness and Safety of Romosozumab and Teriparatide in Postmenopausal Women with Osteoporosis

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Abstract

Purpose: The purpose of this observational study was to investigate the effectiveness and safety of romosozumab (ROMO) and teriparatide (TPTD) in a clinical setting. Methods: A total of 315 postmenopausal women were included based on the reimbursement criteria for ROMO and TPTD at the Department of Endocrinology at Aarhus University Hospital. Criteria for ROMO were bone mineral density (BMD) T-score < -2.5 (femoral neck [FN], total hip [TH], or lumbar spine [LS]) + a fragility fracture (hip, spine, pelvis, distal forearm, or proximal humerus) within 3 years. Criteria for TPTD: within 3 years, ≥ 2 vertebral fractures or 1 vertebral fracture + BMD T-score (FN, TH, or LS) < -3. Data were collected from medical records. The primary end point was percentage change from baseline in BMD (FN, TH, and LS) at month 12. BMD was measured by dual-energy x-ray absorptiometry (DXA). Results: At month 12, ROMO led to significantly (P

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Hartz, M. C., Johannessen, F. B., Harsløf, T., & Langdahl, B. L. (2025). The Effectiveness and Safety of Romosozumab and Teriparatide in Postmenopausal Women with Osteoporosis. Journal of Clinical Endocrinology and Metabolism, 110(5), e1640–e1652. https://doi.org/10.1210/clinem/dgae484

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