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Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population
Childhood-onset systemic lupus erythematosus (SLE) is associated with greater disease activity, more aggressive course, and high rates of organ damage. The prolonged use of corticosteroids in childhood SLE contributes to increased morbidity, including avascular necrosis (AVN). We conducted this retr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512010/ https://www.ncbi.nlm.nih.gov/pubmed/32968109 http://dx.doi.org/10.1038/s41598-020-71923-w |
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author | Tsai, Hsin-Lin Chang, Jei-Wen Lu, Jen-Her Liu, Chin-Su |
author_facet | Tsai, Hsin-Lin Chang, Jei-Wen Lu, Jen-Her Liu, Chin-Su |
author_sort | Tsai, Hsin-Lin |
collection | PubMed |
description | Childhood-onset systemic lupus erythematosus (SLE) is associated with greater disease activity, more aggressive course, and high rates of organ damage. The prolonged use of corticosteroids in childhood SLE contributes to increased morbidity, including avascular necrosis (AVN). We conducted this retrospective study using claims data from the Taiwan National Health Insurance Research Database, enrolling 1,472 children with newly-diagnosed SLE between 2005 and 2013. The mean age at the diagnosis of SLE was 15.5 ± 3.3 years, and the female to male ratio was 6.2:1. Thirty-nine patients (2.6%) developed symptomatic AVN during a mean follow-up of 4.6 ± 2.5 years. In multivariate analysis, the risk of AVN was higher in the patients with a daily prednisolone dose between 7.5 mg and 30 mg (HR 7.435, 95% CI 2.882–19.178, p < 0.001) and over 30 mg (HR 9.366, 95% CI 2.225–39.418, p = 0.002) than in those with a dose ≤ 7.5 mg/day. In addition, AVN was inversely correlated with the use of hydroxychloroquine > 627 days (HR 0.335, 95% CI 0.162–0.694, p = 0.003). In conclusion, high daily doses of prednisolone were associated with a significant risk of AVN, whereas the use of hydroxychloroquine > 627 days conferred an advantage. We suggest that the judicious use of corticosteroids combined with hydroxychloroquine might be a promising preventive strategy for AVN. |
format | Online Article Text |
id | pubmed-7512010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75120102020-09-29 Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population Tsai, Hsin-Lin Chang, Jei-Wen Lu, Jen-Her Liu, Chin-Su Sci Rep Article Childhood-onset systemic lupus erythematosus (SLE) is associated with greater disease activity, more aggressive course, and high rates of organ damage. The prolonged use of corticosteroids in childhood SLE contributes to increased morbidity, including avascular necrosis (AVN). We conducted this retrospective study using claims data from the Taiwan National Health Insurance Research Database, enrolling 1,472 children with newly-diagnosed SLE between 2005 and 2013. The mean age at the diagnosis of SLE was 15.5 ± 3.3 years, and the female to male ratio was 6.2:1. Thirty-nine patients (2.6%) developed symptomatic AVN during a mean follow-up of 4.6 ± 2.5 years. In multivariate analysis, the risk of AVN was higher in the patients with a daily prednisolone dose between 7.5 mg and 30 mg (HR 7.435, 95% CI 2.882–19.178, p < 0.001) and over 30 mg (HR 9.366, 95% CI 2.225–39.418, p = 0.002) than in those with a dose ≤ 7.5 mg/day. In addition, AVN was inversely correlated with the use of hydroxychloroquine > 627 days (HR 0.335, 95% CI 0.162–0.694, p = 0.003). In conclusion, high daily doses of prednisolone were associated with a significant risk of AVN, whereas the use of hydroxychloroquine > 627 days conferred an advantage. We suggest that the judicious use of corticosteroids combined with hydroxychloroquine might be a promising preventive strategy for AVN. Nature Publishing Group UK 2020-09-23 /pmc/articles/PMC7512010/ /pubmed/32968109 http://dx.doi.org/10.1038/s41598-020-71923-w Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tsai, Hsin-Lin Chang, Jei-Wen Lu, Jen-Her Liu, Chin-Su Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title | Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title_full | Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title_fullStr | Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title_full_unstemmed | Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title_short | Epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a Taiwanese population |
title_sort | epidemiology and risk factors for avascular necrosis in childhood systemic lupus erythematosus in a taiwanese population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512010/ https://www.ncbi.nlm.nih.gov/pubmed/32968109 http://dx.doi.org/10.1038/s41598-020-71923-w |
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