Zoledronate and Raloxifene combination therapy enhances material and mechanical properties of diseased mouse bone

dc.contributor.authorPowell, Katherine M.
dc.contributor.authorSkaggs, Cayla
dc.contributor.authorPulliam, Alexis
dc.contributor.authorBerman, Alycia
dc.contributor.authorAllen, Matthew R.
dc.contributor.authorWallace, Joseph M.
dc.contributor.departmentBiomedical Engineering, School of Engineering and Technologyen_US
dc.date.accessioned2021-06-10T22:41:40Z
dc.date.available2021-06-10T22:41:40Z
dc.date.issued2019-10-01
dc.description.abstractCurrent interventions to reduce skeletal fragility are insufficient at enhancing both the quantity and quality of bone when attempting to improve overall mechanical integrity. Bisphosphonates, such as Zoledronate (ZOL), are used to treat a variety of bone disorders by increasing bone mass to decrease fracture risk, but long-term use has been shown in some settings to compromise bone quality. Alternatively, Raloxifene (RAL) has recently been demonstrated to improve tissue quality and overall mechanical properties in a cell-independent manner by binding to collagen and increasing tissue hydration. We hypothesized that a combination of RAL and ZOL would improve mechanical and material properties of bone more than either monotherapy alone by enhancing both quantity and quality. In this study, wildtype (WT) and heterozygous (OIM+/−) male mice from the Osteogenesis Imperfecta (OI) murine model were treated with either RAL, ZOL, or both from 8 weeks to 16 weeks of age. Using the OIM model allows for investigation of therapeutic effects on a quality-based bone disease. Combination treatment resulted in higher trabecular architecture, cortical mechanical properties, and cortical fracture toughness in diseased mouse bone. Two fracture toughness properties, which are direct measures of the tissue's ability to resist the initiation and propagation of a crack, were significantly improved with combination treatment in OIM+/− compared to control. There was no significant effect on fracture toughness with either monotherapy alone in either genotype. Following the mass-based effects of ZOL, trabecular bone volume fraction was significantly higher with combination treatment in both genotypes. Combination treatment resulted in higher ultimate stress in both genotypes. RAL and combination treatment in OIM+/− also increased resilience compared to the control. In conclusion, this study demonstrates the beneficial effects of using combination drug treatments to increase bone mass while simultaneously improving tissue quality, especially to enhance the mechanical integrity of diseased bone. Combination therapies could be a potential method to improve bone health and combat skeletal fragility on both the microscopic and macroscopic levels.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationPowell, K. M., Skaggs, C., Pulliam, A., Berman, A., Allen, M. R., & Wallace, J. M. (2019). Zoledronate and Raloxifene combination therapy enhances material and mechanical properties of diseased mouse bone. Bone, 127, 199–206. https://doi.org/10.1016/j.bone.2019.06.018en_US
dc.identifier.issn8756-3282en_US
dc.identifier.urihttps://hdl.handle.net/1805/26126
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.bone.2019.06.018en_US
dc.relation.journalBoneen_US
dc.sourcePMCen_US
dc.subjectOsteogenesis Imperfectaen_US
dc.subjectSERMen_US
dc.subjectBisphosphonateen_US
dc.subjectBone qualityen_US
dc.subjectFracture toughnessen_US
dc.titleZoledronate and Raloxifene combination therapy enhances material and mechanical properties of diseased mouse boneen_US
dc.typeArticleen_US
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