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Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis
BACKGROUND: This study's objective was to evaluate the association between proton-pump inhibitor (PPI) use and bone fracture incidence and bone mineral density (BMD) by meta-analyzing the estimates reported by epidemiological and cohort studies. METHODS: Data were acquired from studies identifi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Bone and Mineral Research
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135649/ https://www.ncbi.nlm.nih.gov/pubmed/30237993 http://dx.doi.org/10.11005/jbm.2018.25.3.141 |
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author | Nassar, Yousef Richter, Seth |
author_facet | Nassar, Yousef Richter, Seth |
author_sort | Nassar, Yousef |
collection | PubMed |
description | BACKGROUND: This study's objective was to evaluate the association between proton-pump inhibitor (PPI) use and bone fracture incidence and bone mineral density (BMD) by meta-analyzing the estimates reported by epidemiological and cohort studies. METHODS: Data were acquired from studies identified after a literature search in electronic databases. Odds ratios (ORs), hazard ratios (HRs), and risk ratios (RRs) between PPI use and bone fracture incidence were pooled under the random effects model, and meta-analysis of standardized mean differences between PPI users and controls in cross-sectional values and BMD changes was conducted. RESULTS: Thirty-three studies fulfilled the eligibility criteria. These studies provided data from 2,714,502 individuals with a mean age of 66.91 years (95% confidence interval [CI], 63.37–70.46); 33.21% (95% CI, 30.44–35.99) were males and 64.61% (95% CI, 60.73–68.49) were females. Overall, fracture incidence was 22.04% (95% CI, 16.10–27.97) in PPI users and 15.57% (95% CI, 12.28–18.86) in controls. The overall effect size of the point estimate was 1.28 (95% CI, 1.22–1.35) between PPI use and bone fracture incidence. There was a trend towards increased fracture incidence from short duration use: OR 1.29 (95% CI, 1.19–1.40), medium duration use: OR 1.33 (95% CI, 1.12–1.55) and long duration use: OR 1.62 (95% CI, 1.33–1.90). There was no significant difference in the standardized mean differences between PPI users and controls, either in cross-sectional BMD values or in the BMD change observed in longitudinal studies. CONCLUSIONS: Pooling of ORs, HRs, and RRs suggested that PPI use might increase fracture risk. However, there was no effect of PPI use on BMD. |
format | Online Article Text |
id | pubmed-6135649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society for Bone and Mineral Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-61356492018-09-20 Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis Nassar, Yousef Richter, Seth J Bone Metab Original Article BACKGROUND: This study's objective was to evaluate the association between proton-pump inhibitor (PPI) use and bone fracture incidence and bone mineral density (BMD) by meta-analyzing the estimates reported by epidemiological and cohort studies. METHODS: Data were acquired from studies identified after a literature search in electronic databases. Odds ratios (ORs), hazard ratios (HRs), and risk ratios (RRs) between PPI use and bone fracture incidence were pooled under the random effects model, and meta-analysis of standardized mean differences between PPI users and controls in cross-sectional values and BMD changes was conducted. RESULTS: Thirty-three studies fulfilled the eligibility criteria. These studies provided data from 2,714,502 individuals with a mean age of 66.91 years (95% confidence interval [CI], 63.37–70.46); 33.21% (95% CI, 30.44–35.99) were males and 64.61% (95% CI, 60.73–68.49) were females. Overall, fracture incidence was 22.04% (95% CI, 16.10–27.97) in PPI users and 15.57% (95% CI, 12.28–18.86) in controls. The overall effect size of the point estimate was 1.28 (95% CI, 1.22–1.35) between PPI use and bone fracture incidence. There was a trend towards increased fracture incidence from short duration use: OR 1.29 (95% CI, 1.19–1.40), medium duration use: OR 1.33 (95% CI, 1.12–1.55) and long duration use: OR 1.62 (95% CI, 1.33–1.90). There was no significant difference in the standardized mean differences between PPI users and controls, either in cross-sectional BMD values or in the BMD change observed in longitudinal studies. CONCLUSIONS: Pooling of ORs, HRs, and RRs suggested that PPI use might increase fracture risk. However, there was no effect of PPI use on BMD. The Korean Society for Bone and Mineral Research 2018-08 2018-08-31 /pmc/articles/PMC6135649/ /pubmed/30237993 http://dx.doi.org/10.11005/jbm.2018.25.3.141 Text en Copyright © 2018 The Korean Society for Bone and Mineral Research http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nassar, Yousef Richter, Seth Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title | Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title_full | Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title_fullStr | Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title_full_unstemmed | Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title_short | Proton-pump Inhibitor Use and Fracture Risk: An Updated Systematic Review and Meta-analysis |
title_sort | proton-pump inhibitor use and fracture risk: an updated systematic review and meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135649/ https://www.ncbi.nlm.nih.gov/pubmed/30237993 http://dx.doi.org/10.11005/jbm.2018.25.3.141 |
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