Long-term renal outcomes of systemic lupus erythematosus in a Taiwanese population: a single-center retrospective study.

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Chao-Han Liu, Chew-Teng Kor, Kai-Hung Hsiao, Ya-Chih Tien
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引用次数: 0

Abstract

Objective: To investigate the long-term outcome of patients with systemic lupus erythematosus (SLE) who presented with renal involvement in a Taiwanese population.

Methods: Data of patients diagnosed with SLE at Changhua Christian Hospital Clinical Research Database from January 2010 until December 2021 were retrospectively reviewed. Participants were categorized according to the presence of renal involvement, defined as a high protein-to-creatinine ratio or positive histopathology of kidney biopsy. Incidence rates and risk factors of chronic kidney disease (CKD) and end-stage renal disease (ESRD) were analyzed.

Results: A total of 2184 eligible patients with SLE were enrolled, of which 293 had renal involvement. The risk of CKD/ESRD development was higher among participants with renal involvement compared with those without renal involvement. The median times to development of CKD and ESRD were 2.03 years (IQR: 0.13-6.33) and 7.34 years (IQR: 3.13-10.41), respectively, among renal involvement participants. The cumulative incidence rates of CKD were 46.6%, 54.5%, and 63% at 1, 2, and 5 years after renal involvement, respectively, and those of ESRD were 4%, 7%, and 11%, respectively. In the subgroups of two definitions (PCR- or biopsy-defined renal involvement) for renal involvement, the incidence rate of developing CKD/ESRD was not significantly different between the groups. Multivariate analysis revealed that factors associated with CKD development were renal involvement, age, hypertension, and serositis.

Conclusion: Among the Taiwanese population, compared with patients without renal involvement, patients with renal involvement were at a higher risk of developing CKD, and the 5-year incidence rate of ESRD is 11% in this study. Key Points • Among the patients with systemic lupus erythematosus in the Taiwanese population, patients with renal involvement were at a higher risk of developing CKD and ESRD. • The median times-to-development of CKD and ESRD were 2.03 (IQR: 0.13-6.33) years and 7.34 (IQR: 3.13-10.41) years, respectively, among renal involvement participants, whilst the cumulative incidence rates of CKD and ESRD at 5 years after renal involvement were 63% and 11%, respectively. • Subgroup analyses to investigate patients with PCR- and biopsy-defined renal involvement were additionally performed in this study, revealing similar incidence rates of CKD and ESRD in both subgroups.

台湾人群系统性红斑狼疮的长期肾脏预后:一项单中心回顾性研究。
目的:探讨台湾系统性红斑狼疮(SLE)患者肾脏受累的长期预后。方法:回顾性分析2010年1月至2021年12月在彰化基督教医院临床研究数据库中诊断为SLE的患者资料。参与者根据肾脏受累的存在进行分类,定义为高蛋白与肌酐比率或肾活检组织病理学阳性。分析慢性肾脏疾病(CKD)和终末期肾脏疾病(ESRD)的发病率和危险因素。结果:共有2184例符合条件的SLE患者入组,其中293例有肾脏受累。有肾脏受累的受试者发生CKD/ESRD的风险高于无肾脏受累的受试者。在肾脏受累的参与者中,CKD和ESRD发展的中位时间分别为2.03年(IQR: 0.13-6.33)和7.34年(IQR: 3.13-10.41)。肾脏受累后1年、2年和5年,CKD的累积发病率分别为46.6%、54.5%和63%,ESRD的累积发病率分别为4%、7%和11%。在肾受累的两种定义(PCR或活检定义的肾受累)的亚组中,两组之间发生CKD/ESRD的发生率无显著差异。多因素分析显示与CKD发展相关的因素有肾脏受累、年龄、高血压和浆膜炎。结论:在台湾人群中,与无肾受累患者相比,肾受累患者发生CKD的风险更高,本研究中ESRD的5年发病率为11%。•台湾人群系统性红斑狼疮患者中,肾脏受累的患者发生CKD和ESRD的风险较高。•肾脏受累参与者的CKD和ESRD发展的中位时间分别为2.03 (IQR: 0.13-6.33)年和7.34 (IQR: 3.13-10.41)年,而肾脏受累后5年CKD和ESRD的累积发病率分别为63%和11%。•本研究还进行了亚组分析,以调查PCR和活检定义的肾脏受累患者,结果显示两个亚组中CKD和ESRD的发病率相似。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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