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Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis

BACKGROUND: The studies about the correlation between bone mineral density (BMD) and coronary arterial calcification (CAC) were still controversial. The aim of this study was to conduct a meta-analysis to evaluate the association between BMD and CAC. METHODS: We systematically searched PubMed, Embas...

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Autores principales: Zhang, Peiyu, Yang, Liu, Xu, Qingwen, Zeng, Yidi, Yu, Yipin, Peng, Qinghua, Liang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972925/
https://www.ncbi.nlm.nih.gov/pubmed/35371431
http://dx.doi.org/10.1177/20406223221086998
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author Zhang, Peiyu
Yang, Liu
Xu, Qingwen
Zeng, Yidi
Yu, Yipin
Peng, Qinghua
Liang, Hao
author_facet Zhang, Peiyu
Yang, Liu
Xu, Qingwen
Zeng, Yidi
Yu, Yipin
Peng, Qinghua
Liang, Hao
author_sort Zhang, Peiyu
collection PubMed
description BACKGROUND: The studies about the correlation between bone mineral density (BMD) and coronary arterial calcification (CAC) were still controversial. The aim of this study was to conduct a meta-analysis to evaluate the association between BMD and CAC. METHODS: We systematically searched PubMed, Embase, Google scholar and Cochrane library for observational studies. We pooled odds ratio (OR) or correlation coefficient, and 95% confidence interval (CI) of the studies. Continuous data were pooled by mean difference (MD). Sub-group analysis was applied to investigate sources of heterogeneity. Funnel plots for publication bias was also performed. RESULTS: Seventeen studies met the inclusion criteria. Pooled ORs for the prevalence of CAC in patients with low BMD versus patients with normal BMD was 2.11 (95% CI: 1.11 - 4.02, P = 0.02). The data pooled for comparing CAC score of low BMD and normal BMD patients is 33.77 (95% CI: 23.77 - 43.77, p = 0.000). The pooled ORs of multivariate logistic regression to predict the association were 1.00 (95% CI: 0.92 - 1.10, p = 0.95, age-adjusted), and 0.95 (95% CI: 0.86 - 1.05, p = 0.33, multivariable-adjusted). Cohort category and BMD assessment method were the main sources of heterogeneity. CONCLUSIONS: Low BMD is associated with higher prevalence and severity of CAC, especially in postmenopausal women. But the relation is not significant after adjusting age and other confounding variables. Low BMD and CAC may be two independent processes with aging. More large-scale studies with high-quality design are still needed to increase the understanding of them.
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spelling pubmed-89729252022-04-02 Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis Zhang, Peiyu Yang, Liu Xu, Qingwen Zeng, Yidi Yu, Yipin Peng, Qinghua Liang, Hao Ther Adv Chronic Dis Meta-Analysis BACKGROUND: The studies about the correlation between bone mineral density (BMD) and coronary arterial calcification (CAC) were still controversial. The aim of this study was to conduct a meta-analysis to evaluate the association between BMD and CAC. METHODS: We systematically searched PubMed, Embase, Google scholar and Cochrane library for observational studies. We pooled odds ratio (OR) or correlation coefficient, and 95% confidence interval (CI) of the studies. Continuous data were pooled by mean difference (MD). Sub-group analysis was applied to investigate sources of heterogeneity. Funnel plots for publication bias was also performed. RESULTS: Seventeen studies met the inclusion criteria. Pooled ORs for the prevalence of CAC in patients with low BMD versus patients with normal BMD was 2.11 (95% CI: 1.11 - 4.02, P = 0.02). The data pooled for comparing CAC score of low BMD and normal BMD patients is 33.77 (95% CI: 23.77 - 43.77, p = 0.000). The pooled ORs of multivariate logistic regression to predict the association were 1.00 (95% CI: 0.92 - 1.10, p = 0.95, age-adjusted), and 0.95 (95% CI: 0.86 - 1.05, p = 0.33, multivariable-adjusted). Cohort category and BMD assessment method were the main sources of heterogeneity. CONCLUSIONS: Low BMD is associated with higher prevalence and severity of CAC, especially in postmenopausal women. But the relation is not significant after adjusting age and other confounding variables. Low BMD and CAC may be two independent processes with aging. More large-scale studies with high-quality design are still needed to increase the understanding of them. SAGE Publications 2022-03-29 /pmc/articles/PMC8972925/ /pubmed/35371431 http://dx.doi.org/10.1177/20406223221086998 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Meta-Analysis
Zhang, Peiyu
Yang, Liu
Xu, Qingwen
Zeng, Yidi
Yu, Yipin
Peng, Qinghua
Liang, Hao
Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title_full Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title_fullStr Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title_full_unstemmed Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title_short Associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
title_sort associations between bone mineral density and coronary artery calcification: a systematic review and meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972925/
https://www.ncbi.nlm.nih.gov/pubmed/35371431
http://dx.doi.org/10.1177/20406223221086998
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