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Determining the association between hypertension and bone metabolism markers in osteoporotic patients
The aim of the case study is to examine the association between hypertension and the level of bone metabolism markers in newly diagnosed osteoporotic patients. A cross-sectional study of 518 subjects was done to see the association between hypertension and the level of osteocalcin (OC), bone-specifi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213284/ https://www.ncbi.nlm.nih.gov/pubmed/34128860 http://dx.doi.org/10.1097/MD.0000000000026276 |
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author | Hu, Zhuoqing Yang, Kevin Hu, Zhihui Li, Miaosheng Wei, Hao Tang, Zheng Chen, Baitong Su, Chengbiao Cai, De Xu, Jinrong |
author_facet | Hu, Zhuoqing Yang, Kevin Hu, Zhihui Li, Miaosheng Wei, Hao Tang, Zheng Chen, Baitong Su, Chengbiao Cai, De Xu, Jinrong |
author_sort | Hu, Zhuoqing |
collection | PubMed |
description | The aim of the case study is to examine the association between hypertension and the level of bone metabolism markers in newly diagnosed osteoporotic patients. A cross-sectional study of 518 subjects was done to see the association between hypertension and the level of osteocalcin (OC), bone-specific alkaline phosphatase (B-ALP), Tartrate-resistant acid phosphatase (TRAP.5B), and 25-hydroxy vitamin D (25-OHD). There were 243 (46.9%) osteoporosis patients with hypertension. Both univariate and multivariate analysis have suggested that lower OC and 25-OHD levels were associated with hypertension. The potential confounders-adjusted OC level was significantly lower in hypertensive female group than that in the female without hypertension group [β = -0.20, 95% confidence interval (95% CI) = -0.37 to -0.03, P = .02 in final adjust model]. The potential confounders-adjusted 25-OHD level was significantly lower in hypertensive male group than that in male without hypertension group (β = -0.34, 95% CI = -0.58 to -0.10, P = .01 in final adjust model). The B-ALP and TRACP.5B levels were positively associated with hypertension in all patients or subgroup analysis. However, all the correlations had no statistical significance for the B-ALP and TRACP.5B. In conclusion, the hypertension was associated with low level of OC and 25-OHD. Hypertension probably led to low bone turnover, which may be one of the mechanisms of hypertension-related osteoporosis. |
format | Online Article Text |
id | pubmed-8213284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-82132842021-06-21 Determining the association between hypertension and bone metabolism markers in osteoporotic patients Hu, Zhuoqing Yang, Kevin Hu, Zhihui Li, Miaosheng Wei, Hao Tang, Zheng Chen, Baitong Su, Chengbiao Cai, De Xu, Jinrong Medicine (Baltimore) 4300 The aim of the case study is to examine the association between hypertension and the level of bone metabolism markers in newly diagnosed osteoporotic patients. A cross-sectional study of 518 subjects was done to see the association between hypertension and the level of osteocalcin (OC), bone-specific alkaline phosphatase (B-ALP), Tartrate-resistant acid phosphatase (TRAP.5B), and 25-hydroxy vitamin D (25-OHD). There were 243 (46.9%) osteoporosis patients with hypertension. Both univariate and multivariate analysis have suggested that lower OC and 25-OHD levels were associated with hypertension. The potential confounders-adjusted OC level was significantly lower in hypertensive female group than that in the female without hypertension group [β = -0.20, 95% confidence interval (95% CI) = -0.37 to -0.03, P = .02 in final adjust model]. The potential confounders-adjusted 25-OHD level was significantly lower in hypertensive male group than that in male without hypertension group (β = -0.34, 95% CI = -0.58 to -0.10, P = .01 in final adjust model). The B-ALP and TRACP.5B levels were positively associated with hypertension in all patients or subgroup analysis. However, all the correlations had no statistical significance for the B-ALP and TRACP.5B. In conclusion, the hypertension was associated with low level of OC and 25-OHD. Hypertension probably led to low bone turnover, which may be one of the mechanisms of hypertension-related osteoporosis. Lippincott Williams & Wilkins 2021-06-18 /pmc/articles/PMC8213284/ /pubmed/34128860 http://dx.doi.org/10.1097/MD.0000000000026276 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 4300 Hu, Zhuoqing Yang, Kevin Hu, Zhihui Li, Miaosheng Wei, Hao Tang, Zheng Chen, Baitong Su, Chengbiao Cai, De Xu, Jinrong Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title | Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title_full | Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title_fullStr | Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title_full_unstemmed | Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title_short | Determining the association between hypertension and bone metabolism markers in osteoporotic patients |
title_sort | determining the association between hypertension and bone metabolism markers in osteoporotic patients |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213284/ https://www.ncbi.nlm.nih.gov/pubmed/34128860 http://dx.doi.org/10.1097/MD.0000000000026276 |
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