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Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis
OBJECTIVE: Glucocorticoid-induced osteoporosis (GIOP) is the most common form of secondary osteoporosis. In May 2018, denosumab was approved for the treatment of GIOP in men and women at high risk of fracture. We undertook a systematic review and meta-analysis to summarize the efficacy and safety of...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698580/ https://www.ncbi.nlm.nih.gov/pubmed/31616133 http://dx.doi.org/10.2147/DDDT.S148654 |
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author | Yanbeiy, Zeina A Hansen, Karen E |
author_facet | Yanbeiy, Zeina A Hansen, Karen E |
author_sort | Yanbeiy, Zeina A |
collection | PubMed |
description | OBJECTIVE: Glucocorticoid-induced osteoporosis (GIOP) is the most common form of secondary osteoporosis. In May 2018, denosumab was approved for the treatment of GIOP in men and women at high risk of fracture. We undertook a systematic review and meta-analysis to summarize the efficacy and safety of denosumab in the prevention and treatment of GIOP. METHODS: We searched PubMed, CINAHL, American College of Rheumatology and American Society for Bone and Mineral Research meeting abstracts for relevant studies. We included studies in which subjects were taking systemic glucocorticoid therapy and were assigned to take denosumab or control therapy, and assessed the effect of treatment on areal bone mineral density (BMD), fractures and/or safety. RESULTS: Three eligible studies were included in the primary meta-analysis. Denosumab significantly increased lumbar spine BMD (2.32%, 95% CI 1.73%, 2.91%, P<0.0001) and hip BMD (1.52%, 95% CI 1.1%,1.94%, P<0.0001) compared to bisphosphonates. Adverse events, serious adverse events and fractures were similar between denosumab and bisphosphonate arms. CONCLUSION: Results suggest that denosumab is superior to bisphosphonates in its effects on lumbar spine and total hip BMD in patients with GIOP. There was no difference in the incidence of infections, adverse events or serious adverse events. Studies were underpowered to detect differences in the risk of fracture. Denosumab is a reasonable option for treatment of GIOP. However, further studies are needed to guide transitions off denosumab. |
format | Online Article Text |
id | pubmed-6698580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66985802019-10-15 Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis Yanbeiy, Zeina A Hansen, Karen E Drug Des Devel Ther Review OBJECTIVE: Glucocorticoid-induced osteoporosis (GIOP) is the most common form of secondary osteoporosis. In May 2018, denosumab was approved for the treatment of GIOP in men and women at high risk of fracture. We undertook a systematic review and meta-analysis to summarize the efficacy and safety of denosumab in the prevention and treatment of GIOP. METHODS: We searched PubMed, CINAHL, American College of Rheumatology and American Society for Bone and Mineral Research meeting abstracts for relevant studies. We included studies in which subjects were taking systemic glucocorticoid therapy and were assigned to take denosumab or control therapy, and assessed the effect of treatment on areal bone mineral density (BMD), fractures and/or safety. RESULTS: Three eligible studies were included in the primary meta-analysis. Denosumab significantly increased lumbar spine BMD (2.32%, 95% CI 1.73%, 2.91%, P<0.0001) and hip BMD (1.52%, 95% CI 1.1%,1.94%, P<0.0001) compared to bisphosphonates. Adverse events, serious adverse events and fractures were similar between denosumab and bisphosphonate arms. CONCLUSION: Results suggest that denosumab is superior to bisphosphonates in its effects on lumbar spine and total hip BMD in patients with GIOP. There was no difference in the incidence of infections, adverse events or serious adverse events. Studies were underpowered to detect differences in the risk of fracture. Denosumab is a reasonable option for treatment of GIOP. However, further studies are needed to guide transitions off denosumab. Dove 2019-08-14 /pmc/articles/PMC6698580/ /pubmed/31616133 http://dx.doi.org/10.2147/DDDT.S148654 Text en © 2019 Yanbeiy and Hansen. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Yanbeiy, Zeina A Hansen, Karen E Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title | Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title_full | Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title_fullStr | Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title_full_unstemmed | Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title_short | Denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
title_sort | denosumab in the treatment of glucocorticoid-induced osteoporosis: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698580/ https://www.ncbi.nlm.nih.gov/pubmed/31616133 http://dx.doi.org/10.2147/DDDT.S148654 |
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