4.5 Article

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

Journal

MEDICINE
Volume 98, Issue 28, Pages -

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MD.0000000000016420

Keywords

end-stage renal disease; risk; systemic lupus erythematosus

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2016R1D1A1B03931229]
  2. Chonnam National University Hospital Biomedical Research Institute [BCRI18024]
  3. Bio & Medical Technology Development Program of the National Research Foundation of Korea (NRF) - Korean government, MSIT [2017M3A9E8023001, 2017M3A9E8023016]
  4. National Research Foundation of Korea [2017M3A9E8023016] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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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