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pubmed-article:17630145pubmed:abstractTextAs the aging population increases, the rising prevalence of osteoporosis-related spine fractures will have a dramatic impact on health care. At present, mainstay treatment relies on systemic medications intended to prevent diminishing bone mineral density (BMD) and bone mass. However, an adjunctive treatment strategy is to target specific areas of the skeletal system that are prone to clinically significant osteoporotic fractures. We term this strategy the "local treatment of osteoporosis" or osteoplasty. Potential use of osteoplasty involves the percutaneous injection of bioresorbable and bioactive bone cements into bones at risk of sustaining osteoporotic fractures. Calcium sulfate (CaSO(4)) is among the candidate bioresorbable bone cements with the material attributes desirable for potential application with osteoplasty, yet previous studies on the osteoconductive properties of CaSO(4) have been limited to animal models exhibiting normal bone biology and architecture. However, osteoporotic bone physiology may potentially interfere with the material properties of common osteoconductive biomaterials, such as that of CaSO(4). To further test this hypothesis, a suitable animal model is needed to evaluate the in vivo behavior of potential biomaterials in osteoporotic bone.lld:pubmed
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pubmed-article:17630145pubmed:articleTitleA rat osteoporotic spine model for the evaluation of bioresorbable bone cements.lld:pubmed
pubmed-article:17630145pubmed:affiliationDepartment of Orthopaedic Surgery, University of California-San Diego, 350 Dickinson Street, Mail Code 8894, San Diego, CA 92103, USA.lld:pubmed
pubmed-article:17630145pubmed:publicationTypeJournal Articlelld:pubmed
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