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Hip BMD is associated with visceral fat change: a registry study of osteoporosis and sarcopenia
BACKGROUND: Osteoporosis increases the risk of fractures. Visceral fat is associated with cardiovascular disease (CVD). There is inadequate knowledge on the relationship between osteoporosis and visceral fat. The study aimed to evaluate the relationship between bone mineral density (BMD) and viscera...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677287/ https://www.ncbi.nlm.nih.gov/pubmed/36420044 http://dx.doi.org/10.1177/20406223221134051 |
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author | Chen, Ying-Chou Wang, Yu-Wei Ko, Chi-Hua Chen, Jia-Feng Hsu, Chung-Yuan Yu, Shan-Fu Cheng, Tien-Tsai |
author_facet | Chen, Ying-Chou Wang, Yu-Wei Ko, Chi-Hua Chen, Jia-Feng Hsu, Chung-Yuan Yu, Shan-Fu Cheng, Tien-Tsai |
author_sort | Chen, Ying-Chou |
collection | PubMed |
description | BACKGROUND: Osteoporosis increases the risk of fractures. Visceral fat is associated with cardiovascular disease (CVD). There is inadequate knowledge on the relationship between osteoporosis and visceral fat. The study aimed to evaluate the relationship between bone mineral density (BMD) and visceral fat mass in the elderly. METHODS: This was a prospective cohort study. Subjects were enrolled from the Rheumatology Clinic. All subjects underwent baseline bone mineral density and body composition measurements using dual-energy X-ray absorptiometry. RESULTS: A total of 321 patients including 288 females and 33 males were enrolled in this study. We followed up DEXA for 1 year for fat and muscle mass change and found that 162 (50.5%) had a decrease in fat mass, 129 (40.2%) had decreased visceral fat, and 138 (43%) had decreased muscle mass. Furthermore, we found that the baseline hip T score was correlated with visceral fat decrease. Using visceral fat decrease as the outcome, we found that hip T score could predict visceral fat loss: the higher the T score, the more visceral fat loss was found [p < 0.001, OR: 1.6, CI: (1.3–2.1)]. CONCLUSION: A high hip T score was associated with a future decrease in visceral fat, which may decrease the risk of atherosclerosis and CV risk. Therefore, evaluation of visceral fat may be useful for assessing CVD risk in patients with osteoporosis. Effective management of the risk of atherosclerosis and CVD is important in improving the life expectancy of these patients. |
format | Online Article Text |
id | pubmed-9677287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-96772872022-11-22 Hip BMD is associated with visceral fat change: a registry study of osteoporosis and sarcopenia Chen, Ying-Chou Wang, Yu-Wei Ko, Chi-Hua Chen, Jia-Feng Hsu, Chung-Yuan Yu, Shan-Fu Cheng, Tien-Tsai Ther Adv Chronic Dis Original Research BACKGROUND: Osteoporosis increases the risk of fractures. Visceral fat is associated with cardiovascular disease (CVD). There is inadequate knowledge on the relationship between osteoporosis and visceral fat. The study aimed to evaluate the relationship between bone mineral density (BMD) and visceral fat mass in the elderly. METHODS: This was a prospective cohort study. Subjects were enrolled from the Rheumatology Clinic. All subjects underwent baseline bone mineral density and body composition measurements using dual-energy X-ray absorptiometry. RESULTS: A total of 321 patients including 288 females and 33 males were enrolled in this study. We followed up DEXA for 1 year for fat and muscle mass change and found that 162 (50.5%) had a decrease in fat mass, 129 (40.2%) had decreased visceral fat, and 138 (43%) had decreased muscle mass. Furthermore, we found that the baseline hip T score was correlated with visceral fat decrease. Using visceral fat decrease as the outcome, we found that hip T score could predict visceral fat loss: the higher the T score, the more visceral fat loss was found [p < 0.001, OR: 1.6, CI: (1.3–2.1)]. CONCLUSION: A high hip T score was associated with a future decrease in visceral fat, which may decrease the risk of atherosclerosis and CV risk. Therefore, evaluation of visceral fat may be useful for assessing CVD risk in patients with osteoporosis. Effective management of the risk of atherosclerosis and CVD is important in improving the life expectancy of these patients. SAGE Publications 2022-11-17 /pmc/articles/PMC9677287/ /pubmed/36420044 http://dx.doi.org/10.1177/20406223221134051 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 | Original Research Chen, Ying-Chou Wang, Yu-Wei Ko, Chi-Hua Chen, Jia-Feng Hsu, Chung-Yuan Yu, Shan-Fu Cheng, Tien-Tsai Hip BMD is associated with visceral fat change: a registry study of osteoporosis and sarcopenia |
title | Hip BMD is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
title_full | Hip BMD is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
title_fullStr | Hip BMD is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
title_full_unstemmed | Hip BMD is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
title_short | Hip BMD is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
title_sort | hip bmd is associated with visceral fat change: a registry study of
osteoporosis and sarcopenia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677287/ https://www.ncbi.nlm.nih.gov/pubmed/36420044 http://dx.doi.org/10.1177/20406223221134051 |
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