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Bone mineral density in patients with chronic heart failure: a meta-analysis
OBJECTIVE: This study aimed to verify the existing relationship between bone mineral density (BMD) and chronic heart failure (CHF) by meta-analysis. METHODS: Databases, including PubMed, Web of Science, and Chinese National Knowledge Infrastructure, published in English or Chinese up to February 28,...
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/PMC5833795/ https://www.ncbi.nlm.nih.gov/pubmed/29520133 http://dx.doi.org/10.2147/CIA.S154356 |
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author | Xing, Wenmin Lv, Xiaoling Gao, Wenyan Wang, Jirong Yang, Zhouxin Wang, Sanying Zhang, Jing Yan, Jing |
author_facet | Xing, Wenmin Lv, Xiaoling Gao, Wenyan Wang, Jirong Yang, Zhouxin Wang, Sanying Zhang, Jing Yan, Jing |
author_sort | Xing, Wenmin |
collection | PubMed |
description | OBJECTIVE: This study aimed to verify the existing relationship between bone mineral density (BMD) and chronic heart failure (CHF) by meta-analysis. METHODS: Databases, including PubMed, Web of Science, and Chinese National Knowledge Infrastructure, published in English or Chinese up to February 28, 2017, were searched for studies on the association between CHF and BMD. Two independent reviewers collected the relevant articles. The standard mean deviation (SMD) and 95% confidence interval were calculated for BMD with fixed- and random-effect models. Subgroup and sensitivity analyses were also conducted. RESULTS: A total of six studies (552 CHF and 243 non-CHF patients) were included. The results indicated that the patients with CHF had a lower total BMD compared with the non-CHF patients. Similar effects were also observed for femoral neck, arm, leg, and trunk BMD. However, no difference was observed in the lumbar spine BMD. The SMD of total BMD in New York Heart Association classes I or II (NYHA I or II) patients was −0.62, while that in NYHA III or IV patients was −0.87, and the SMD of femoral bone mineral density in NYHA I or II patients was −0.47, while that in NYHA III or IV patients was −1.07. Moreover, vitamin D and parathyroid hormone (PTH) were also found to be associated with CHF. CONCLUSION: Patients with CHF had a lower total BMD and femoral neck, arm, leg, or trochanter BMD than patients with non-CHF. Vitamin D reduced, whereas PTH increased, with the severity of CHF. The clinical significance of the present findings remains uncertain and should be confirmed by future studies. |
format | Online Article Text |
id | pubmed-5833795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58337952018-03-08 Bone mineral density in patients with chronic heart failure: a meta-analysis Xing, Wenmin Lv, Xiaoling Gao, Wenyan Wang, Jirong Yang, Zhouxin Wang, Sanying Zhang, Jing Yan, Jing Clin Interv Aging Original Research OBJECTIVE: This study aimed to verify the existing relationship between bone mineral density (BMD) and chronic heart failure (CHF) by meta-analysis. METHODS: Databases, including PubMed, Web of Science, and Chinese National Knowledge Infrastructure, published in English or Chinese up to February 28, 2017, were searched for studies on the association between CHF and BMD. Two independent reviewers collected the relevant articles. The standard mean deviation (SMD) and 95% confidence interval were calculated for BMD with fixed- and random-effect models. Subgroup and sensitivity analyses were also conducted. RESULTS: A total of six studies (552 CHF and 243 non-CHF patients) were included. The results indicated that the patients with CHF had a lower total BMD compared with the non-CHF patients. Similar effects were also observed for femoral neck, arm, leg, and trunk BMD. However, no difference was observed in the lumbar spine BMD. The SMD of total BMD in New York Heart Association classes I or II (NYHA I or II) patients was −0.62, while that in NYHA III or IV patients was −0.87, and the SMD of femoral bone mineral density in NYHA I or II patients was −0.47, while that in NYHA III or IV patients was −1.07. Moreover, vitamin D and parathyroid hormone (PTH) were also found to be associated with CHF. CONCLUSION: Patients with CHF had a lower total BMD and femoral neck, arm, leg, or trochanter BMD than patients with non-CHF. Vitamin D reduced, whereas PTH increased, with the severity of CHF. The clinical significance of the present findings remains uncertain and should be confirmed by future studies. Dove Medical Press 2018-02-27 /pmc/articles/PMC5833795/ /pubmed/29520133 http://dx.doi.org/10.2147/CIA.S154356 Text en © 2018 Xing 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 Xing, Wenmin Lv, Xiaoling Gao, Wenyan Wang, Jirong Yang, Zhouxin Wang, Sanying Zhang, Jing Yan, Jing Bone mineral density in patients with chronic heart failure: a meta-analysis |
title | Bone mineral density in patients with chronic heart failure: a meta-analysis |
title_full | Bone mineral density in patients with chronic heart failure: a meta-analysis |
title_fullStr | Bone mineral density in patients with chronic heart failure: a meta-analysis |
title_full_unstemmed | Bone mineral density in patients with chronic heart failure: a meta-analysis |
title_short | Bone mineral density in patients with chronic heart failure: a meta-analysis |
title_sort | bone mineral density in patients with chronic heart failure: a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833795/ https://www.ncbi.nlm.nih.gov/pubmed/29520133 http://dx.doi.org/10.2147/CIA.S154356 |
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