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The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea

Systemic lupus erythematosus (SLE) is known to be one of the leading causes of end-stage renal disease (ESRD). The aim of this study was to estimate the incidence rate of ESRD and the risk for progression to ESRD in SLE patients compared to the general population. A total of 21,253 SLE patients were...

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Autores principales: Choi, Hong Sang, Han, Kyung-Do, Jung, Jin-Hyung, Kim, Chang Seong, Bae, Eun Hui, Ma, Seong Kwon, Kim, Soo Wan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641670/
https://www.ncbi.nlm.nih.gov/pubmed/31305460
http://dx.doi.org/10.1097/MD.0000000000016420
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author Choi, Hong Sang
Han, Kyung-Do
Jung, Jin-Hyung
Kim, Chang Seong
Bae, Eun Hui
Ma, Seong Kwon
Kim, Soo Wan
author_facet Choi, Hong Sang
Han, Kyung-Do
Jung, Jin-Hyung
Kim, Chang Seong
Bae, Eun Hui
Ma, Seong Kwon
Kim, Soo Wan
author_sort Choi, Hong Sang
collection PubMed
description Systemic lupus erythematosus (SLE) is known to be one of the leading causes of end-stage renal disease (ESRD). The aim of this study was to estimate the incidence rate of ESRD and the risk for progression to ESRD in SLE patients compared to the general population. A total of 21,253 SLE patients were extracted from the Korean National Health Insurance Service database between 2008 and 2013. Age-and sex-matched controls (n = 106,265) were randomly sampled in a 5:1 ratio from non-SLE individuals. Both cohorts were followed up for development of ESRD until 2015. During the median 7.53 years of follow-up, 533 (2.51%) cases of ESRD were newly developed in SLE patients and 145 (0.14%) cases in matched controls (incidence rate: 4.075 and 0.219 per 1000 person-year, respectively). SLE patients were at higher risk for ESRD development compared to matched controls (hazard ratio [HR], 9.84; 95% confidence interval [CI] 8.10–11.96) after multivariate adjustment. In subgroup analysis, the risk for ESRD was higher in male (HR, 7.76; 95% CI 5.07–11.90) and female patients with SLE (HR, 10.48; 95% CI 8.41–13.07) than in matched controls. When analyzed by age group, the younger the age, the higher the risk of ESRD versus non-SLE matched controls; this result was also significant after adjustment. In subgroup analysis according to comorbidities, the SLE group had a significantly higher risk of ESRD than the non-SLE group in almost all subgroups. SLE was associated with an increased incidence of ESRD.
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spelling pubmed-66416702019-08-15 The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea Choi, Hong Sang Han, Kyung-Do Jung, Jin-Hyung Kim, Chang Seong Bae, Eun Hui Ma, Seong Kwon Kim, Soo Wan Medicine (Baltimore) Research Article Systemic lupus erythematosus (SLE) is known to be one of the leading causes of end-stage renal disease (ESRD). The aim of this study was to estimate the incidence rate of ESRD and the risk for progression to ESRD in SLE patients compared to the general population. A total of 21,253 SLE patients were extracted from the Korean National Health Insurance Service database between 2008 and 2013. Age-and sex-matched controls (n = 106,265) were randomly sampled in a 5:1 ratio from non-SLE individuals. Both cohorts were followed up for development of ESRD until 2015. During the median 7.53 years of follow-up, 533 (2.51%) cases of ESRD were newly developed in SLE patients and 145 (0.14%) cases in matched controls (incidence rate: 4.075 and 0.219 per 1000 person-year, respectively). SLE patients were at higher risk for ESRD development compared to matched controls (hazard ratio [HR], 9.84; 95% confidence interval [CI] 8.10–11.96) after multivariate adjustment. In subgroup analysis, the risk for ESRD was higher in male (HR, 7.76; 95% CI 5.07–11.90) and female patients with SLE (HR, 10.48; 95% CI 8.41–13.07) than in matched controls. When analyzed by age group, the younger the age, the higher the risk of ESRD versus non-SLE matched controls; this result was also significant after adjustment. In subgroup analysis according to comorbidities, the SLE group had a significantly higher risk of ESRD than the non-SLE group in almost all subgroups. SLE was associated with an increased incidence of ESRD. Wolters Kluwer Health 2019-07-12 /pmc/articles/PMC6641670/ /pubmed/31305460 http://dx.doi.org/10.1097/MD.0000000000016420 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Choi, Hong Sang
Han, Kyung-Do
Jung, Jin-Hyung
Kim, Chang Seong
Bae, Eun Hui
Ma, Seong Kwon
Kim, Soo Wan
The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title_full The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title_fullStr The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title_full_unstemmed The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title_short The risk of end-stage renal disease in systemic lupus erythematosus: A nationwide population-based study in Korea
title_sort risk of end-stage renal disease in systemic lupus erythematosus: a nationwide population-based study in korea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641670/
https://www.ncbi.nlm.nih.gov/pubmed/31305460
http://dx.doi.org/10.1097/MD.0000000000016420
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