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单核细胞趋化蛋白-1 作为一种尿生物标志物,用于诊断巴西狼疮肾炎患者的活动期。

Monocyte chemoattractant-1 as a urinary biomarker for the diagnosis of activity of lupus nephritis in Brazilian patients.

机构信息

Department of Rheumatology, and the Department of Immunology, Servidor Publico Estadual Hospital, São Paulo, Brazil.

出版信息

J Rheumatol. 2012 Oct;39(10):1948-54. doi: 10.3899/jrheum.110201. Epub 2012 Sep 1.

DOI:10.3899/jrheum.110201
PMID:22942263
Abstract

OBJECTIVE

Monocyte chemotactic protein (MCP-1), involved in the pathogenesis of lupus nephritis (LN), has recently been indicated as a new biomarker of kidney activity in systemic lupus erythematosus (SLE). Our aim was to assess urinary MCP-1 (uMCP-1) as a biomarker of renal activity in patients with SLE and to compare it to other disease activity markers, using the ELISA.

METHODS

Seventy-five female Brazilian patients with SLE and a control group participated in our study. Patients with SLE were distributed among 3 groups according to kidney involvement and classified according to disease activity based on clinical and laboratory measures such as urinary sediment, proteinuria, kidney function, C3, C4, anti-dsDNA, disease activity index, and renal SLE disease activity index. The serum and uMCP-1 concentrations were measured by sandwich ELISA.

RESULTS

In the A-LN group (active lupus nephritis: SLE with kidney involvement), the concentration of uMCP-1 was significantly higher than in other groups. A cutoff point was established using the results of the control group to apply this test in the detection of LN. A-LN had a higher frequency of positive results for uMCP-1 in comparison to the other groups (p < 0.001). To detect disease activity in patients with LN, a new cutoff was determined based on the results of patients with SLE with kidney involvement. Setting specificity at 90%, the sensitivity of the test was 50%.

CONCLUSION

The high specificity makes uMCP-1 a useful test as a predictor of kidney activity in SLE, especially when associated to other measures used in clinical practice.

摘要

目的

参与狼疮肾炎(LN)发病机制的单核细胞趋化蛋白(MCP-1)最近被认为是系统性红斑狼疮(SLE)中肾脏活动的新生物标志物。我们的目的是评估狼疮患者尿液中 MCP-1(uMCP-1)作为肾脏活动的生物标志物,并使用 ELISA 与其他疾病活动标志物进行比较。

方法

75 名患有 SLE 的巴西女性患者和对照组参与了我们的研究。根据肾脏受累情况,将 SLE 患者分为 3 组,并根据临床和实验室指标(如尿沉渣、蛋白尿、肾功能、C3、C4、抗 dsDNA、疾病活动指数和肾脏 SLE 疾病活动指数)将其分为疾病活动组。通过夹心 ELISA 测量血清和 uMCP-1 浓度。

结果

在 A-LN 组(活动期狼疮肾炎:有肾脏受累的 SLE)中,uMCP-1 的浓度明显高于其他组。使用对照组的结果建立了一个截断点,以将该测试应用于 LN 的检测。与其他组相比,A-LN 中 uMCP-1 的阳性结果频率更高(p <0.001)。为了检测 LN 患者的疾病活动度,根据有肾脏受累的 SLE 患者的结果确定了新的截断值。在设定特异性为 90%的情况下,该测试的灵敏度为 50%。

结论

高特异性使 uMCP-1 成为一种有用的检测方法,可作为预测 SLE 肾脏活动的指标,特别是与临床实践中使用的其他措施结合使用时。

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