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可溶性尿激酶型纤溶酶原激活物受体(suPAR)在局灶节段性肾小球硬化症中的诊断和预后价值及其检测方法的影响。

Diagnostic and Prognostic Value of Soluble Urokinase-type Plasminogen Activator Receptor (suPAR) in Focal Segmental Glomerulosclerosis and Impact of Detection Method.

机构信息

Department of Medicine III, Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.

Department of Emergency Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Sci Rep. 2019 Sep 24;9(1):13783. doi: 10.1038/s41598-019-50405-8.

DOI:10.1038/s41598-019-50405-8
PMID:31551522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6760112/
Abstract

The plasma soluble urokinase-type plasminogen activator receptor (suPAR) is a biomarker for focal segmental glomerulosclerosis (FSGS), but its value is under discussion because of ambiguous results arising from different ELISA methods in previous studies. The aim of this study was to compare diagnostic performance of two leading suPAR ELISA kits and examine four objectives in 146 subjects: (1) plasma suPAR levels according to glomerular disease (primary, secondary and recurrent FSGS after kidney transplantation, other glomerulonephritis) and in healthy controls; (2) suPAR levels based on glomerular filtration rate; (3) sensitivity and specificity of suPAR for FSGS diagnosis and determination of optimal cut-offs; (4) suPAR as prognostic tool. Patients with FSGS showed significant higher suPAR values than patients with other glomerulonephritis and healthy individuals. This applied to subjects with and without chronic kidney disease. Although both suPARnostic™ assay and Quantikine Human uPAR ELISA Kit exerted high sensitivity and specificity for FSGS diagnosis, their cut-off values of 4.644 ng/mL and 2.789 ng/mL were significantly different. Higher suPAR was furthermore predictive for progression to end-stage renal disease. In summary, suPAR values must be interpreted in the context of population and test methods used. Knowing test specific cut-offs makes suPAR a valuable biomarker for FSGS.

摘要

血浆可溶性尿激酶型纤溶酶原激活物受体 (suPAR) 是局灶节段性肾小球硬化症 (FSGS) 的生物标志物,但由于之前的研究中不同 ELISA 方法得出的结果存在歧义,其价值仍存在争议。本研究旨在比较两种领先的 suPAR ELISA 试剂盒的诊断性能,并在 146 名受试者中检验四个目标:(1) 根据肾小球疾病(原发性、继发性和肾移植后复发性 FSGS、其他肾小球肾炎)和健康对照者的血浆 suPAR 水平;(2) 基于肾小球滤过率的 suPAR 水平;(3) suPAR 对 FSGS 诊断的敏感性和特异性以及确定最佳截止值;(4) suPAR 作为预后工具。FSGS 患者的 suPAR 值明显高于其他肾小球肾炎患者和健康个体。这适用于有和没有慢性肾脏病的受试者。尽管 suPARnostic™测定法和 Quantikine Human uPAR ELISA 试剂盒对 FSGS 诊断均具有较高的敏感性和特异性,但它们的 4.644ng/mL 和 2.789ng/mL 截止值存在显著差异。较高的 suPAR 水平进一步预示着向终末期肾病进展。总之,suPAR 值必须结合使用的人群和测试方法进行解释。了解特定的测试截止值可使 suPAR 成为 FSGS 的有价值的生物标志物。

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