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系统性红斑狼疮患者终末期肾病的患病率和结局:一项基于人群的研究。

Prevalence and outcomes of end-stage kidney disease in patients with systemic lupus erythematous: a population-based study.

机构信息

Medical Research Centre, The University of Waikato, Private Bag 3105, Hamilton, 3240, New Zealand.

Rheumatology Department, Waikato Hospital, Hamilton, New Zealand.

出版信息

Rheumatol Int. 2024 Mar;44(3):469-475. doi: 10.1007/s00296-023-05409-z. Epub 2023 Aug 14.

Abstract

This study aims to examine the prevalence and outcomes of end-stage kidney disease (ESKD) among systemic lupus erythematosus (SLE) patients. SLE patients identified from the national administrative datasets were linked to the Australia and New Zealand Dialysis and Transplant Registry (ANZDATA) to identify the ESKD cases. Period prevalence of ESKD among SLE patients was calculated. The risk of developing ESKD by ethnicity was explored with Cox Proportional Hazards model. The adjusted hazard ratio (HR) of all-cause mortality for Māori, Pacific, Asian compared to European/others was estimated. Of the 2837 SLE patients, 210 (7.4%) developed ESKD. The average period prevalence of ESKD among SLE patients was 5.7%. Men had twice the prevalence rate of ESKD than women (10.0% vs 5.2%). Māori and Pacific had higher prevalence rate than Asian and European/others (9.4%, 9.8% vs 4.4% and 3.8%). The adjusted HR of developing ESKD for men compared to women was 3.37 (95% CI 1.62-7.02). The adjusted HR of developing ESKD for Māori and Pacific compared to European/others was 4.63 (95% CI 1.61-13.29) and 4.66 (95% CI 1.67-13.00), respectively. Compared to European/others, Māori had an HR of 2.17 (95% CI 1.18-4.00) for all-cause mortality. SLE patients had a high prevalence rate of ESKD. Men, Māori, and Pacific patients with SLE were more likely to develop ESKD. Māori patients with ESKD had poorer survival than other patients. Interventions are needed to reduce the risk of ESKD and to improve the survival of ESKD patients for the disadvantaged groups.

摘要

本研究旨在探讨系统性红斑狼疮(SLE)患者终末期肾病(ESKD)的患病率和结局。从国家行政数据库中确定的 SLE 患者与澳大利亚和新西兰透析和移植登记处(ANZDATA)相关联,以确定 ESKD 病例。计算了 SLE 患者中 ESKD 的时期患病率。采用 Cox 比例风险模型探讨了不同种族发生 ESKD 的风险。估计了毛利人、太平洋岛民、亚洲人与欧洲/其他人相比的全因死亡率的调整后危险比(HR)。在 2837 名 SLE 患者中,有 210 名(7.4%)发展为 ESKD。SLE 患者中 ESKD 的平均时期患病率为 5.7%。男性的 ESKD 患病率是女性的两倍(10.0%比 5.2%)。毛利人和太平洋岛民的患病率高于亚洲人和欧洲/其他人(9.4%、9.8%比 4.4%和 3.8%)。与女性相比,男性发生 ESKD 的调整后 HR 为 3.37(95%CI 1.62-7.02)。与欧洲/其他人相比,毛利人和太平洋岛民发生 ESKD 的调整后 HR 分别为 4.63(95%CI 1.61-13.29)和 4.66(95%CI 1.67-13.00)。与欧洲/其他人相比,毛利人因各种原因导致死亡率的 HR 为 2.17(95%CI 1.18-4.00)。SLE 患者的 ESKD 患病率较高。男性、毛利人和太平洋岛民 SLE 患者更易发生 ESKD。患有 ESKD 的毛利人患者的生存率低于其他患者。需要采取干预措施,以降低 ESKD 的风险,并改善弱势群体 ESKD 患者的生存率。

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