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Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study
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 analyz...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916792/ https://www.ncbi.nlm.nih.gov/pubmed/33579002 http://dx.doi.org/10.3390/ijerph18041728 |
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author | Marocco, Chiara Zimatore, Giovanna Mocini, Edoardo Fornari, Rachele Iolascon, Giovanni Gallotta, Maria Chiara Bimonte, Viviana Maria Baldari, Carlo Lenzi, Andrea Migliaccio, Silvia |
author_facet | Marocco, Chiara Zimatore, Giovanna Mocini, Edoardo Fornari, Rachele Iolascon, Giovanni Gallotta, Maria Chiara Bimonte, Viviana Maria Baldari, Carlo Lenzi, Andrea Migliaccio, Silvia |
author_sort | Marocco, Chiara |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7916792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79167922021-03-01 Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study Marocco, Chiara Zimatore, Giovanna Mocini, Edoardo Fornari, Rachele Iolascon, Giovanni Gallotta, Maria Chiara Bimonte, Viviana Maria Baldari, Carlo Lenzi, Andrea Migliaccio, Silvia Int J Environ Res Public Health Article 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. MDPI 2021-02-10 2021-02 /pmc/articles/PMC7916792/ /pubmed/33579002 http://dx.doi.org/10.3390/ijerph18041728 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Marocco, Chiara Zimatore, Giovanna Mocini, Edoardo Fornari, Rachele Iolascon, Giovanni Gallotta, Maria Chiara Bimonte, Viviana Maria Baldari, Carlo Lenzi, Andrea Migliaccio, Silvia Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title | Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title_full | Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title_fullStr | Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title_full_unstemmed | Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title_short | Efficacy of Denosumab Therapy Following Treatment with Bisphosphonates in Women with Osteoporosis: A Cohort Study |
title_sort | efficacy of denosumab therapy following treatment with bisphosphonates in women with osteoporosis: a cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916792/ https://www.ncbi.nlm.nih.gov/pubmed/33579002 http://dx.doi.org/10.3390/ijerph18041728 |
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