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Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study
The risk of osteoporosis in patients with chronic inflammatory neuropathy (CIN) has not been evaluated in detail. We conducted a population-based case-control study nested in a retrospective cohort to analyze osteoporosis risk among patients with CIN using a nationwide database. Patients with CIN ba...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591220/ https://www.ncbi.nlm.nih.gov/pubmed/31235735 http://dx.doi.org/10.1038/s41598-019-45591-4 |
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author | Kim, Seung Woo Kim, Eun Hwa Lee, Jinae Choi, Young-Chul Kim, Seung Min Shin, Ha Young |
author_facet | Kim, Seung Woo Kim, Eun Hwa Lee, Jinae Choi, Young-Chul Kim, Seung Min Shin, Ha Young |
author_sort | Kim, Seung Woo |
collection | PubMed |
description | The risk of osteoporosis in patients with chronic inflammatory neuropathy (CIN) has not been evaluated in detail. We conducted a population-based case-control study nested in a retrospective cohort to analyze osteoporosis risk among patients with CIN using a nationwide database. Patients with CIN based on the Korean Classification of Disease diagnostic code were included and were matched to controls. A Cox proportional hazards regression model was used to evaluate the effect of CIN on osteoporosis. After propensity score matching, 585 CIN patients and 585 controls were selected. Patients with CIN had an increased osteoporosis risk (hazard ratio [HR] = 2.293, 95% confidence interval [CI] 1.460–3.601) compared with controls. The osteoporosis risk was higher among male patients with CIN than among male controls (HR = 5.404, 95% CI 2.252–12.969), while there were no significant differences among women. Among the CIN patients, the average daily dose of corticosteroids was higher in those who developed osteoporosis (19.6 mg [10.8–49.3]) than those who did not (16.2 mg [7.2–29.1], p = 0.001). The osteoporosis risk among CIN patients is higher than among controls. High risk of osteoporosis in male patients may indicate that osteoporosis in CIN patients results from the disease itself or related treatments. |
format | Online Article Text |
id | pubmed-6591220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65912202019-07-02 Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study Kim, Seung Woo Kim, Eun Hwa Lee, Jinae Choi, Young-Chul Kim, Seung Min Shin, Ha Young Sci Rep Article The risk of osteoporosis in patients with chronic inflammatory neuropathy (CIN) has not been evaluated in detail. We conducted a population-based case-control study nested in a retrospective cohort to analyze osteoporosis risk among patients with CIN using a nationwide database. Patients with CIN based on the Korean Classification of Disease diagnostic code were included and were matched to controls. A Cox proportional hazards regression model was used to evaluate the effect of CIN on osteoporosis. After propensity score matching, 585 CIN patients and 585 controls were selected. Patients with CIN had an increased osteoporosis risk (hazard ratio [HR] = 2.293, 95% confidence interval [CI] 1.460–3.601) compared with controls. The osteoporosis risk was higher among male patients with CIN than among male controls (HR = 5.404, 95% CI 2.252–12.969), while there were no significant differences among women. Among the CIN patients, the average daily dose of corticosteroids was higher in those who developed osteoporosis (19.6 mg [10.8–49.3]) than those who did not (16.2 mg [7.2–29.1], p = 0.001). The osteoporosis risk among CIN patients is higher than among controls. High risk of osteoporosis in male patients may indicate that osteoporosis in CIN patients results from the disease itself or related treatments. Nature Publishing Group UK 2019-06-24 /pmc/articles/PMC6591220/ /pubmed/31235735 http://dx.doi.org/10.1038/s41598-019-45591-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Seung Woo Kim, Eun Hwa Lee, Jinae Choi, Young-Chul Kim, Seung Min Shin, Ha Young Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title_full | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title_fullStr | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title_full_unstemmed | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title_short | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
title_sort | risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591220/ https://www.ncbi.nlm.nih.gov/pubmed/31235735 http://dx.doi.org/10.1038/s41598-019-45591-4 |
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