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狼疮继发终末期肾病的非裔美国患者死亡风险增加。

Increased risk of death in African American patients with end-stage renal disease secondary to lupus.

作者信息

Sule Sangeeta, Fivush Barbara, Neu Alicia, Furth Susan

机构信息

Johns Hopkins University , Baltimore, MD , USA.

Children's Hospital of Philadelphia , Philadelphia, PA , USA.

出版信息

Clin Kidney J. 2014 Feb;7(1):40-4. doi: 10.1093/ckj/sft157. Epub 2014 Jan 2.

Abstract

BACKGROUND

Systemic lupus erythematosus (SLE) is a devastating systemic disease that can lead to end-stage renal disease (ESRD). Our goal was to assess the relative mortality risk associated with race in pediatric and adult populations with ESRD secondary to SLE maintained on hemodialysis (HD).

METHODS

We identified an inception cohort of patients who were started on HD in January 1990 from data collected by the United States Renal Data System (USRDS). Kaplan-Meier survival analyses were performed in these patients using the time at risk from 1 January 1990 through 31 December 2010, the last date of the USRDS data collection period in this dataset. Cox proportional hazard models were used to assess mortality, adjusted for age at dialysis initiation. Subjects were censored at transplantation or end of follow-up.

RESULTS

There were 1580 patients with ESRD secondary to SLE, 252 pediatric patients (62% African American) and 1328 adults (56% African American). African American pediatric patients with ESRD secondary to SLE had a 2-fold increased risk of death compared with African American children with other causes of ESRD [hazard ratio (HR): 2.1, 95% confidence interval (CI): 1.4-2.9, P < 0.01]. Increased risk of death was also seen in African American adults with ESRD secondary to SLE compared with both Caucasians with ESRD secondary to SLE (HR: 2.3, 95% CI: 1.2-4.2, P < 0.01) and African American adults with ESRD secondary to other diseases (HR: 1.2, 95% CI: 1.1-1.4, P < 0.01).

CONCLUSION

Our study suggests that there is a significant increased risk for mortality in African American children and adults with ESRD secondary to SLE. This suggests that African Americans with ESRD secondary to SLE need aggressive monitoring.

摘要

背景

系统性红斑狼疮(SLE)是一种严重的全身性疾病,可导致终末期肾病(ESRD)。我们的目标是评估因SLE继发ESRD并维持血液透析(HD)的儿童和成人人群中与种族相关的相对死亡风险。

方法

我们从美国肾脏数据系统(USRDS)收集的数据中确定了一个起始队列,该队列中的患者于1990年1月开始进行HD治疗。使用从1990年1月1日至2010年12月31日(该数据集中USRDS数据收集期的最后日期)的风险时间,对这些患者进行Kaplan-Meier生存分析。使用Cox比例风险模型评估死亡率,并根据透析开始时的年龄进行调整。在移植或随访结束时对受试者进行截尾。

结果

共有1580例因SLE继发ESRD的患者,其中252例为儿童患者(62%为非裔美国人),1328例为成人患者(56%为非裔美国人)。与因其他原因导致ESRD的非裔美国儿童相比,因SLE继发ESRD的非裔美国儿童死亡风险增加了2倍[风险比(HR):2.1,95%置信区间(CI):1.4 - 2.9,P < 0.01]。与因SLE继发ESRD的白人相比(HR:2.3,95%CI:1.2 - 4.2,P < 0.01)以及与因其他疾病继发ESRD的非裔美国成人相比(HR:1.2,95%CI:1.1 - 1.4,P < 0.01),因SLE继发ESRD的非裔美国成人死亡风险也增加。

结论

我们的研究表明,因SLE继发ESRD的非裔美国儿童和成人的死亡风险显著增加。这表明因SLE继发ESRD的非裔美国人需要积极监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc8e/4389169/ec0f46af3688/sft15701.jpg

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