4.2 Review

Prevention of glucocorticoid-induced osteoporosis

Journal

EXPERT OPINION ON PHARMACOTHERAPY
Volume 10, Issue 6, Pages 997-1005

Publisher

INFORMA HEALTHCARE
DOI: 10.1517/14656560902868225

Keywords

bone; fracture; glucocorticoids; osteoporosis

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Glucocorticoid-induced osteoporosis is the most common cause of secondary osteoporosis. The role of the Wnt signaling pathway in bone formation and the ratio of receptor activator for NF-kappa B ligand versus osteoprotegerin in bone resorption are exciting new insights. The absolute fracture risk helps both clinicians and patients to interpret the results of bone density measurement, which may have a positive influence on adherence to therapy. The bisphosphonates alendronate and risedronate are the first-line treatment in the prevention of glucocorticoid-induced osteoporosis, because both increase the bone mineral density of the spine and hips and reduce the vertebral fracture rate. Treatment with the anabolic agent parathyroid hormone (1 - 34) strongly stimulates bone turnover, and seems to be superior to treatment with alendronate. it might be attractive for glucocorticoid-treated patients with new vertebral fractures during treatment with bisphosphonates, and/or with severe fracture risk.

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