Abstract
This chapter discusses drug therapy used to reduce fracture risk by influencing the material and structural properties of bone. Bone loss is slow before menopause because remodelling is slow. Bone loss accelerates after menopause because remodelling rate increases, reducing bone mineral density (BMD) and bones material rigidity. Anti-resorptive drugs reduce the rate of bone remodelling. Reconstruction the skeleton requires anabolic therapy. Parathyroid hormone (PTH) given intermittently increases bone formation on the endosteal surface increasing both cortical and trabecular thickness. Strontium ranelate reduces vertebral and non-vertebral fractures. The rate of bone remodelling does not appear to be reduced. There may be a reduction the depth of bone resorption while allowing bone formation to continue but remains uncertain.
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Seeman, E. (2007). Material and Structural Basis of Bone Fragility: A Rational Approach to Therapy. In: Qin, L., Genant, H.K., Griffith, J.F., Leung, K.S. (eds) Advanced Bioimaging Technologies in Assessment of the Quality of Bone and Scaffold Materials. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-45456-4_23
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DOI: https://doi.org/10.1007/978-3-540-45456-4_23
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