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Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis
Aims: To review the effects of bisphosphonates on bone density, fractures, and bone markers in osteopenic older women. Methods: Relevant articles published before February 2022 were searched in PubMed, EMBASE, and the Cochrane Library. All randomized controlled trials that reported incident fracture...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160388/ https://www.ncbi.nlm.nih.gov/pubmed/35662708 http://dx.doi.org/10.3389/fphar.2022.892091 |
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author | Li, Jiangbi Sun, Yang Chen, Zhuo Xie, Xiaoping Gu, Feng Bi, Songqi Yu, Tiecheng |
author_facet | Li, Jiangbi Sun, Yang Chen, Zhuo Xie, Xiaoping Gu, Feng Bi, Songqi Yu, Tiecheng |
author_sort | Li, Jiangbi |
collection | PubMed |
description | Aims: To review the effects of bisphosphonates on bone density, fractures, and bone markers in osteopenic older women. Methods: Relevant articles published before February 2022 were searched in PubMed, EMBASE, and the Cochrane Library. All randomized controlled trials that reported incident fractures, bone mineral density (BMD), bone markers, or adverse events with bisphosphonates in osteopenic older women were included. The quality of included studies was assessed using the Cochrane Risk of Bias tool. The risk ratios (RRs) for fractures, net percent change in bone mineral density and differences in bone markers were calculated using a meta-analysis. Results: A total of 11 studies were included in our meta-analysis. Bisphosphonates significantly increased the percent changes in the lumbar spine BMD (WMD, 5.60; 95% CI, 4.16–7.03; I (2) = 93.6%), hip BMD (WMD, 4.80; 95% CI, 2.93 to 6.66; I (2) = 97.1%), total body BMD (WMD, 3.24; 95% CI, 2.12–4.35; I (2) = 90.9%), femoral neck BMD (WMD, 4.02; 95% CI, 1.70–6.35; I (2) = 91.8%) and trochanter BMD (WMD, 5.22; 95% CI, 3.51–6.93; I (2) = 83.6%) when compared to placebo. Zoledronate was associated with a great treatment effect on fragility fracture (RR, 0.63; 95% CI, 0.50–0.79), clinical vertebral fracture (RR, 0.41; 95% CI, 0.22–0.76), and radiographic vertebral fracture (RR, 0.60; 95% CI, 0.27–1.35) compared to placebo. Meanwhile, alendronate was also associated with beneficial effects on fragility fracture (RR, 0.40; 95% CI, 0.15–1.07), clinical vertebral fracture (RR, 0.46; 95% CI, 0.17–1.24), and radiographic vertebral fracture (RR, 0.64; 95% CI, 0.38–1.09). In addition, the use of bisphosphonates reduced the concentration of procollagen type I N-terminal propeptide (PINP) and C-terminal telopeptide of type I collagen (CTX) over placebo by 15.79 (95% CI, −18.92 to −12.66; I (2) = 28.4%), −0.23 (95% CI, −0.35 to −0.10; I (2) = 91.3%), respectively. Although there was insufficient evidence to determine their safety, these bisphosphonates may have an effect on cancer, cardiac events, and mortality in osteopenic older women. Conclusion: All bisphosphonates examined were associated with beneficial effects on fractures, BMD, and bone markers in women with osteopenia. Further randomized controlled trials are necessary to clarify the safety of bisphosphonates in women with osteopenia. |
format | Online Article Text |
id | pubmed-9160388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91603882022-06-03 Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis Li, Jiangbi Sun, Yang Chen, Zhuo Xie, Xiaoping Gu, Feng Bi, Songqi Yu, Tiecheng Front Pharmacol Pharmacology Aims: To review the effects of bisphosphonates on bone density, fractures, and bone markers in osteopenic older women. Methods: Relevant articles published before February 2022 were searched in PubMed, EMBASE, and the Cochrane Library. All randomized controlled trials that reported incident fractures, bone mineral density (BMD), bone markers, or adverse events with bisphosphonates in osteopenic older women were included. The quality of included studies was assessed using the Cochrane Risk of Bias tool. The risk ratios (RRs) for fractures, net percent change in bone mineral density and differences in bone markers were calculated using a meta-analysis. Results: A total of 11 studies were included in our meta-analysis. Bisphosphonates significantly increased the percent changes in the lumbar spine BMD (WMD, 5.60; 95% CI, 4.16–7.03; I (2) = 93.6%), hip BMD (WMD, 4.80; 95% CI, 2.93 to 6.66; I (2) = 97.1%), total body BMD (WMD, 3.24; 95% CI, 2.12–4.35; I (2) = 90.9%), femoral neck BMD (WMD, 4.02; 95% CI, 1.70–6.35; I (2) = 91.8%) and trochanter BMD (WMD, 5.22; 95% CI, 3.51–6.93; I (2) = 83.6%) when compared to placebo. Zoledronate was associated with a great treatment effect on fragility fracture (RR, 0.63; 95% CI, 0.50–0.79), clinical vertebral fracture (RR, 0.41; 95% CI, 0.22–0.76), and radiographic vertebral fracture (RR, 0.60; 95% CI, 0.27–1.35) compared to placebo. Meanwhile, alendronate was also associated with beneficial effects on fragility fracture (RR, 0.40; 95% CI, 0.15–1.07), clinical vertebral fracture (RR, 0.46; 95% CI, 0.17–1.24), and radiographic vertebral fracture (RR, 0.64; 95% CI, 0.38–1.09). In addition, the use of bisphosphonates reduced the concentration of procollagen type I N-terminal propeptide (PINP) and C-terminal telopeptide of type I collagen (CTX) over placebo by 15.79 (95% CI, −18.92 to −12.66; I (2) = 28.4%), −0.23 (95% CI, −0.35 to −0.10; I (2) = 91.3%), respectively. Although there was insufficient evidence to determine their safety, these bisphosphonates may have an effect on cancer, cardiac events, and mortality in osteopenic older women. Conclusion: All bisphosphonates examined were associated with beneficial effects on fractures, BMD, and bone markers in women with osteopenia. Further randomized controlled trials are necessary to clarify the safety of bisphosphonates in women with osteopenia. Frontiers Media S.A. 2022-05-19 /pmc/articles/PMC9160388/ /pubmed/35662708 http://dx.doi.org/10.3389/fphar.2022.892091 Text en Copyright © 2022 Li, Sun, Chen, Xie, Gu, Bi and Yu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Jiangbi Sun, Yang Chen, Zhuo Xie, Xiaoping Gu, Feng Bi, Songqi Yu, Tiecheng Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title | Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title_full | Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title_fullStr | Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title_full_unstemmed | Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title_short | Effects of Bisphosphonates Treatments in Osteopenic Older Women: A Systematic Review and Meta-Analysis |
title_sort | effects of bisphosphonates treatments in osteopenic older women: a systematic review and meta-analysis |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160388/ https://www.ncbi.nlm.nih.gov/pubmed/35662708 http://dx.doi.org/10.3389/fphar.2022.892091 |
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