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Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study
BACKGROUND: Long-term glucocorticoid use increases fracture risk by reducing bone mass. This study evaluated the relationship between hip and vertebral fractures and the total amount of systematic glucocorticoid use. METHODS: We randomly selected 1,896,159 people aged 20 to 100 years who participate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Endocrine Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520587/ https://www.ncbi.nlm.nih.gov/pubmed/32981298 http://dx.doi.org/10.3803/EnM.2020.659 |
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author | Koh, Ji Weon Kim, Junkang Cho, Hyemin Ha, Yong-Chan Kim, Tae-Young Lee, Young-Kyun Kim, Ha Young Jang, Sunmee |
author_facet | Koh, Ji Weon Kim, Junkang Cho, Hyemin Ha, Yong-Chan Kim, Tae-Young Lee, Young-Kyun Kim, Ha Young Jang, Sunmee |
author_sort | Koh, Ji Weon |
collection | PubMed |
description | BACKGROUND: Long-term glucocorticoid use increases fracture risk by reducing bone mass. This study evaluated the relationship between hip and vertebral fractures and the total amount of systematic glucocorticoid use. METHODS: We randomly selected 1,896,159 people aged 20 to 100 years who participated in the National Health Checkup program in 2006. The amount of glucocorticoids prescribed was calculated based on the defined daily dose (DDD). The total DDD was obtained by adding oral and parenteral glucocorticoids for 6 months from the index date. Subjects were categorized into four groups according to total glucocorticoid DDDs: non-users (DDDs=0), low users (0< DDDs ≤45), intermediate users (45< DDDs ≤90), and high users (90< DDDs). We followed them for 2 years. A multivariate Cox proportional hazard model was used to evaluate the effects of the total amount of glucocorticoid use on hip and vertebral fractures. RESULTS: Higher glucocorticoid use was associated with a higher risk of vertebral fracture. Relative to non-users, the vertebral fracture risk was 1.39 times higher in the low-user group, 1.94 times higher in the intermediate-user group, and 2.43 times higher in the high-user group. The risk of hip fracture was 1.72 times higher in intermediate users and 3.28 times higher in high users than in non-users. CONCLUSION: As the amount of glucocorticoid use for 6 months increased, the risk of hip and vertebral fractures became higher. In order to prevent fractures, it is necessary for doctors to evaluate the total amount of glucocorticoid prescribed to the patient and to provide appropriate treatment. |
format | Online Article Text |
id | pubmed-7520587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75205872020-10-05 Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study Koh, Ji Weon Kim, Junkang Cho, Hyemin Ha, Yong-Chan Kim, Tae-Young Lee, Young-Kyun Kim, Ha Young Jang, Sunmee Endocrinol Metab (Seoul) Original Article BACKGROUND: Long-term glucocorticoid use increases fracture risk by reducing bone mass. This study evaluated the relationship between hip and vertebral fractures and the total amount of systematic glucocorticoid use. METHODS: We randomly selected 1,896,159 people aged 20 to 100 years who participated in the National Health Checkup program in 2006. The amount of glucocorticoids prescribed was calculated based on the defined daily dose (DDD). The total DDD was obtained by adding oral and parenteral glucocorticoids for 6 months from the index date. Subjects were categorized into four groups according to total glucocorticoid DDDs: non-users (DDDs=0), low users (0< DDDs ≤45), intermediate users (45< DDDs ≤90), and high users (90< DDDs). We followed them for 2 years. A multivariate Cox proportional hazard model was used to evaluate the effects of the total amount of glucocorticoid use on hip and vertebral fractures. RESULTS: Higher glucocorticoid use was associated with a higher risk of vertebral fracture. Relative to non-users, the vertebral fracture risk was 1.39 times higher in the low-user group, 1.94 times higher in the intermediate-user group, and 2.43 times higher in the high-user group. The risk of hip fracture was 1.72 times higher in intermediate users and 3.28 times higher in high users than in non-users. CONCLUSION: As the amount of glucocorticoid use for 6 months increased, the risk of hip and vertebral fractures became higher. In order to prevent fractures, it is necessary for doctors to evaluate the total amount of glucocorticoid prescribed to the patient and to provide appropriate treatment. Korean Endocrine Society 2020-09 2020-09-22 /pmc/articles/PMC7520587/ /pubmed/32981298 http://dx.doi.org/10.3803/EnM.2020.659 Text en Copyright © 2020 Korean Endocrine Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Koh, Ji Weon Kim, Junkang Cho, Hyemin Ha, Yong-Chan Kim, Tae-Young Lee, Young-Kyun Kim, Ha Young Jang, Sunmee Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title | Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title_full | Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title_fullStr | Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title_full_unstemmed | Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title_short | Effects of Systemic Glucocorticoid Use on Fracture Risk: A Population-Based Study |
title_sort | effects of systemic glucocorticoid use on fracture risk: a population-based study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520587/ https://www.ncbi.nlm.nih.gov/pubmed/32981298 http://dx.doi.org/10.3803/EnM.2020.659 |
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