Abstract
Denosumab is a human monoclonal antibody that neutralizes RANKL, a cytokine able to interact with the RANK receptor on preosteoclasts and osteoclasts, decreasing their recruitment and differentiation, leading to a decreased bone resorption. The aim of this observational real-life study was to analyze adherence to denosumab therapy and assess its efficacy in increasing bone mineral density (BMD) and modulating biochemical skeletal markers following previous treatments with bisphosphonates in a group of post-menopausal women with osteoporosis. Women were recruited in the specialized center from March 2012 to September 2019. Biochemical markers were recorded at baseline and every six months prior to subsequent drug injection. Dual X-ray absorptiometry was requested at baseline and after 18/24 months. Comparing BMD at baseline and after denosumab therapy in naive patients and in those previously treated with bisphosphonates, a positive therapeutic effect was observed in both groups. The results of our real-life study demonstrate, as expected, that BMD values significantly increased upon denosumab treatment. Interestingly, denosumab showed an increased efficacy in patients previously treated with bisphosphonates. Moreover, biochemical markers data indicate that osteoporotic patients, without other concomitant unstable health conditions, could be evaluated once a year, decreasing the number of specialistic center access.
Funder
Ministero dell’Istruzione, dell’Università e della Ricerca
Subject
Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health
Reference44 articles.
1. Population Reference Bureauhttps://www.prb.org/aging-unitedstates-fact-sheet
2. Bone modeling and remodeling: From biology to clinical application;Migliaccio;Aging Clin. Exp. Res.,2004
3. Bone quality
4. The mineralization of bone tissue: a forgotten dimension in osteoporosis research
5. The Contribution of Trabecular Architecture to Cancellous Bone Quality
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献