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Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients
BACKGROUND: Accelerated atherosclerosis is considered to be the linking factor between low bone mineral density (BMD) and increased cardiovascular events and mortality, while some coronary angiographic studies do not support this point. In this study, we attempt to provide a distinct comprehensive v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112784/ https://www.ncbi.nlm.nih.gov/pubmed/30197509 http://dx.doi.org/10.2147/CIA.S168445 |
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author | Guan, Xue-qiang Xue, Yang-jing Wang, Jie Ma, Jun Li, Yue-chun Zheng, Cheng Wu, Sai-zhu |
author_facet | Guan, Xue-qiang Xue, Yang-jing Wang, Jie Ma, Jun Li, Yue-chun Zheng, Cheng Wu, Sai-zhu |
author_sort | Guan, Xue-qiang |
collection | PubMed |
description | BACKGROUND: Accelerated atherosclerosis is considered to be the linking factor between low bone mineral density (BMD) and increased cardiovascular events and mortality, while some coronary angiographic studies do not support this point. In this study, we attempt to provide a distinct comprehensive view of the relationship between BMD and the angiographically determined coronary atherosclerotic burden. METHODS: A total of 459 consecutive patients with stable chest pain suspected of coronary artery disease (CAD) underwent both dual-energy X-ray absorptiometry scan and selective coronary angiography. The association between BMD and global coronary atherosclerotic plaque burden as represented by the multivessel involvement and the modified Gensini score was analyzed. RESULTS: Multivariable analysis revealed that the low BMD at femoral neck and total hip was an independent correlate of multivessel CAD. The T-scores measured at femoral neck and total hip were both negatively and independently associated to the modified Gensini score. These inversely correlated relationships between BMD and CAD were not observed at lumbar spine 1–4. CONCLUSION: This cross-sectional study elucidated an inverse relationship between hip BMD and the modified Gensini score, and low hip BMD values (T-scores) were significantly and independently associated with increased risk of multivessel coronary disease in patients hospitalized for stable chest pain. |
format | Online Article Text |
id | pubmed-6112784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61127842018-09-07 Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients Guan, Xue-qiang Xue, Yang-jing Wang, Jie Ma, Jun Li, Yue-chun Zheng, Cheng Wu, Sai-zhu Clin Interv Aging Original Research BACKGROUND: Accelerated atherosclerosis is considered to be the linking factor between low bone mineral density (BMD) and increased cardiovascular events and mortality, while some coronary angiographic studies do not support this point. In this study, we attempt to provide a distinct comprehensive view of the relationship between BMD and the angiographically determined coronary atherosclerotic burden. METHODS: A total of 459 consecutive patients with stable chest pain suspected of coronary artery disease (CAD) underwent both dual-energy X-ray absorptiometry scan and selective coronary angiography. The association between BMD and global coronary atherosclerotic plaque burden as represented by the multivessel involvement and the modified Gensini score was analyzed. RESULTS: Multivariable analysis revealed that the low BMD at femoral neck and total hip was an independent correlate of multivessel CAD. The T-scores measured at femoral neck and total hip were both negatively and independently associated to the modified Gensini score. These inversely correlated relationships between BMD and CAD were not observed at lumbar spine 1–4. CONCLUSION: This cross-sectional study elucidated an inverse relationship between hip BMD and the modified Gensini score, and low hip BMD values (T-scores) were significantly and independently associated with increased risk of multivessel coronary disease in patients hospitalized for stable chest pain. Dove Medical Press 2018-08-24 /pmc/articles/PMC6112784/ /pubmed/30197509 http://dx.doi.org/10.2147/CIA.S168445 Text en © 2018 Guan et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Guan, Xue-qiang Xue, Yang-jing Wang, Jie Ma, Jun Li, Yue-chun Zheng, Cheng Wu, Sai-zhu Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title | Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title_full | Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title_fullStr | Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title_full_unstemmed | Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title_short | Low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
title_sort | low bone mineral density is associated with global coronary atherosclerotic plaque burden in stable angina patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112784/ https://www.ncbi.nlm.nih.gov/pubmed/30197509 http://dx.doi.org/10.2147/CIA.S168445 |
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