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Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis
BACKGROUND: Previous studies have reached mixed conclusions regarding the association between metabolic syndrome (MS) and osteoporosis. We aimed to perform a meta-analysis based on published studies that explored the association between osteoporosis and MS. METHODS: To identify related literature, a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8331299/ https://www.ncbi.nlm.nih.gov/pubmed/34354749 http://dx.doi.org/10.1155/2021/6691487 |
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author | Liu, Weida Wang, Chuangshi Hao, Jun Yin, Lu Wang, Yang Li, Wei |
author_facet | Liu, Weida Wang, Chuangshi Hao, Jun Yin, Lu Wang, Yang Li, Wei |
author_sort | Liu, Weida |
collection | PubMed |
description | BACKGROUND: Previous studies have reached mixed conclusions regarding the association between metabolic syndrome (MS) and osteoporosis. We aimed to perform a meta-analysis based on published studies that explored the association between osteoporosis and MS. METHODS: To identify related literature, a systematic search of PubMed, Cochrane Library, and EMBASE databases from inception to June 2020 was performed. Original studies that reported the risk estimates of osteoporosis morbidity for two or three categories of bone mineral density (BMD) in patients with MS were selected. Two independent investigators screened and selected the articles. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using random-effects models. RESULTS: Of 2632 identified studies, nine cross-sectional studies with 14 datasets were eligible for our meta-analysis. In seven studies (10 datasets), the summarized ORs of osteoporosis for MS were 0.72 (95% CI: 0.52–0.99). Subgroup analyses by gender showed that significant inverse associations were observed only in men (OR = 0.72, 95% CI: 0.55–0.96) but not in women (OR = 0.70, 95% CI: 0.41–1.22). The definition of MS, the source of the study population, and the adjustment of covariates affected the estimates. In two studies (4 datasets), there was no evidence for an association between MS and decreased BMD. CONCLUSIONS: Our findings demonstrated that MS was significantly associated with a lower osteoporosis risk. There might be gender differences in the association between MS and osteoporosis. In addition, the association was likely to relate to the definition of MS, the source of the study population, and the adjustment of covariates. |
format | Online Article Text |
id | pubmed-8331299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-83312992021-08-04 Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis Liu, Weida Wang, Chuangshi Hao, Jun Yin, Lu Wang, Yang Li, Wei Int J Endocrinol Review Article BACKGROUND: Previous studies have reached mixed conclusions regarding the association between metabolic syndrome (MS) and osteoporosis. We aimed to perform a meta-analysis based on published studies that explored the association between osteoporosis and MS. METHODS: To identify related literature, a systematic search of PubMed, Cochrane Library, and EMBASE databases from inception to June 2020 was performed. Original studies that reported the risk estimates of osteoporosis morbidity for two or three categories of bone mineral density (BMD) in patients with MS were selected. Two independent investigators screened and selected the articles. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using random-effects models. RESULTS: Of 2632 identified studies, nine cross-sectional studies with 14 datasets were eligible for our meta-analysis. In seven studies (10 datasets), the summarized ORs of osteoporosis for MS were 0.72 (95% CI: 0.52–0.99). Subgroup analyses by gender showed that significant inverse associations were observed only in men (OR = 0.72, 95% CI: 0.55–0.96) but not in women (OR = 0.70, 95% CI: 0.41–1.22). The definition of MS, the source of the study population, and the adjustment of covariates affected the estimates. In two studies (4 datasets), there was no evidence for an association between MS and decreased BMD. CONCLUSIONS: Our findings demonstrated that MS was significantly associated with a lower osteoporosis risk. There might be gender differences in the association between MS and osteoporosis. In addition, the association was likely to relate to the definition of MS, the source of the study population, and the adjustment of covariates. Hindawi 2021-07-16 /pmc/articles/PMC8331299/ /pubmed/34354749 http://dx.doi.org/10.1155/2021/6691487 Text en Copyright © 2021 Weida Liu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Liu, Weida Wang, Chuangshi Hao, Jun Yin, Lu Wang, Yang Li, Wei Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title | Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title_full | Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title_fullStr | Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title_full_unstemmed | Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title_short | Association between Metabolic Syndrome and Osteoporosis: A Systematic Review and Meta-Analysis |
title_sort | association between metabolic syndrome and osteoporosis: a systematic review and meta-analysis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8331299/ https://www.ncbi.nlm.nih.gov/pubmed/34354749 http://dx.doi.org/10.1155/2021/6691487 |
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