Cardiovascular Safety and Effectiveness of Bisphosphonates: From Intervention Trials to Real-Life Data |
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Authors: | Chiara Delli Poggi Maria Fusaro Maria Cristina Mereu Maria Luisa Brandi Luisella Cianferotti |
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Affiliation: | 1.Bone Metabolic Diseases Unit, Department of Experimental, Clinical and Biomedical Sciences, University of Florence, 50139 Florence, Italy;2.National Research Council (CNR), Institute of Clinical Physiology (IFC), 56124 Pisa, Italy;3.Department of Medicine, University of Padova, 35128 Padova, Italy;4.Independent Researcher, 09100 Cagliari, Italy;5.F.I.R.M.O. Italian Foundation for the Research on Bone Diseases, 50141 Florence, Italy; |
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Abstract: | Both osteoporosis with related fragility fractures and cardiovascular diseases are rapidly outspreading worldwide. Since they are often coexistent in elderly patients and may be related to possible common pathogenetic mechanisms, the possible reciprocal effects of drugs employed to treat these diseases have to be considered in clinical practice. Bisphosphonates, the agents most largely employed to decrease bone fragility, have been shown to be overall safe with respect to cardiovascular diseases and even capable of reducing cardiovascular morbidity in some settings, as mainly shown by real life studies. No randomized controlled trials with cardiovascular outcomes as primary endpoints are available. While contradictory results have emerged about a possible BSP-mediated reduction of overall mortality, it is undeniable that these drugs can be employed safely in patients with high fracture risk, since no increased mortality has ever been demonstrated. Although partial reassurance has emerged from meta-analysis assessing the risk of cardiac arrhythmias during bisphosphonates treatment, caution is warranted in administering this class of drugs to patients at risk for atrial fibrillation, possibly preferring other antiresorptives or anabolics, according to osteoporosis guidelines. This paper focuses on the complex relationship between bisphosphonates use and cardiovascular disease and possible co-management issues. |
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Keywords: | osteoporosis fragility fractures zoledronate alendronate risedronate cardiovascular diseases |
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