Superiority of denosumab over bisphosphonates in preventing and treating glucocorticoid-induced osteoporosis: a systematic review and meta-analysis with GRADE quality assessment
The increasing prevalence of glucocorticoid-induced osteoporosis (GIOP) due to long-term glucocorticoid therapy underscores the need for effective treatment options. Denosumab and bisphosphonates, both key in managing GIOP, require further comparative evaluation to determine their relative efficacy...
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Published in | Frontiers in endocrinology (Lausanne) Vol. 15; p. 1407692 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
18.12.2024
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Subjects | |
Online Access | Get full text |
ISSN | 1664-2392 1664-2392 |
DOI | 10.3389/fendo.2024.1407692 |
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Summary: | The increasing prevalence of glucocorticoid-induced osteoporosis (GIOP) due to long-term glucocorticoid therapy underscores the need for effective treatment options. Denosumab and bisphosphonates, both key in managing GIOP, require further comparative evaluation to determine their relative efficacy and safety profiles.
We conducted a systematic review and meta-analysis, adhering to PRISMA guidelines. Our analysis included randomized controlled trials (RCTs) comparing denosumab with bisphosphonates in GIOP management. The outcomes were percent changes in bone mineral density (BMD) at various sites, bone turnovers markers (BTMs) and the incidence of adverse events.
Our study comprised five RCTs with 1,043 participants. The results showed a significant mean difference in BMD percentage change from baseline at LS of 2.87% (95% CI: 1.86 to 3.87,
<0.001) and at TH of 1.39% (95% CI: 0.15 to 2.64,
=0.03). Additionally, the safety profile of denosumab was found to be comparable to bisphosphonates, with no significant increase in the incidence of adverse events or serious adverse reactions.
Denosumab proved more effective in enhancing BMD than bisphosphonates in GIOP, maintaining a comparable safety profile. However, the study's limitations, including heterogeneity and the need for longer-term research, were noted. |
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Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Undefined-1 content type line 23 ObjectType-Article-3 These authors have contributed equally to this work Edited by: Jonathan H. Tobias, University of Bristol, United Kingdom Angela Sheu, Garvan Institute of Medical Research, Australia Reviewed by: Dina Keumala Sari, Universitas Sumatera Utara, Indonesia |
ISSN: | 1664-2392 1664-2392 |
DOI: | 10.3389/fendo.2024.1407692 |