尿PLA2R抗体检测在PLA2R相关膜性肾病危险分层中的应用。

Tianyu Zheng, Yuan Qin, Xuanli Tang, Peng Bi, Xuxiang Hui, Zixuan Zhou, Yulin Fu, Huiming Sheng, Xiumei Zhou, Xueqin Zhao, Yuanyuan Du, Qiang He, Biao Huang
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Patients were grouped into remission and nonremission groups according to the outcomes after 12 months of treatment and the data were analyzed.</p><p><strong>Results.—: </strong>The cutoff values of sPLA2R-IgG (sPLA2R-immunoglobulin G), uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 for distinguishing between remission and nonremission groups were 50 relative units (RU)/mL, 3.51 RU/mL, 6835 ng/mL, and 143.4 ng/mL, respectively. The average value in the remission group for sPLA2R-IgG, uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 was 37.39 RU/mL, 1.10 RU/mL, 3498.99 ng/mL, and 33.83 ng/mL, respectively. The average value in the nonremission group for sPLA2R-IgG, uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 was 279.96 RU/mL, 45.36 RU/mL, 25762.47 ng/mL, and 1383.89 ng/mL, respectively. 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引用次数: 0

摘要

上下文。-: m型磷脂酶A2受体(PLA2R)是膜性肾病(MN)的主要自身抗原。作为MN的特异性抗体,血清PLA2R抗体(sPLA2R-Ab)水平与PLA2R相关MN (PMN)危险分层的相关性仍存在争议。-:应用时间分辨荧光免疫分析法(TRFIA)检测尿PLA2R-Ab (uPLA2R-Ab),建立更为灵敏的血清与尿PLA2R-Ab联合检测PMN危害分层的方法。-:采用高灵敏度的TRFIA方法检测PMN患者的初始血清和尿液样本。根据治疗12个月后的结果将患者分为缓解组和非缓解组,并对数据进行分析。-: sPLA2R-IgG (spla2r免疫球蛋白G)、uPLA2R-IgG、sPLA2R-IgG4和uPLA2R-IgG4用于区分缓解组和非缓解组的截止值分别为50相对单位(RU)/mL、3.51 RU/mL、6835 ng/mL和143.4 ng/mL。缓解组sPLA2R-IgG、uPLA2R-IgG、sPLA2R-IgG4和uPLA2R-IgG4的平均值分别为37.39 RU/mL、1.10 RU/mL、3498.99 ng/mL和33.83 ng/mL。非缓解组sPLA2R-IgG、uPLA2R-IgG、sPLA2R-IgG4和uPLA2R-IgG4的平均值分别为279.96 RU/mL、45.36 RU/mL、25762.47 ng/mL和1383.89 ng/mL。以sPLA2R-Ab为主要因素,联合uPLA2R-Ab可将血清和尿液PLA2R-IgG、血清和尿液PLA2R-IgG4联合检测的高危预测值分别从54.55%和75%提高到100%。-:本研究采用高灵敏度的TRFIA方法;血清和尿液PLA2R-Ab联合检测可提高PMN风险分层的效率,并能更好地评估PMN监测情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urine PLA2R Antibody Detection in Hazard Stratification of PLA2R-Associated Membranous Nephropathy.

Context.—: M-type phospholipase A2 receptor (PLA2R) is the major autoantigen of membranous nephropathy (MN). As the specific antibodies of MN, the correlation between serum PLA2R antibody (sPLA2R-Ab) levels and PLA2R-associated MN (PMN) risk stratification is still controversial.

Objective.—: To apply the time-resolved fluorescence immunoassay (TRFIA) method on urine PLA2R-Ab (uPLA2R-Ab), detect, and then establish a more sensitive method of combined serum and urine PLA2R-Ab detection for PMN hazard stratification.

Design.—: A highly sensitive TRFIA method was used to detect the initial serum and urine samples of patients with PMN. Patients were grouped into remission and nonremission groups according to the outcomes after 12 months of treatment and the data were analyzed.

Results.—: The cutoff values of sPLA2R-IgG (sPLA2R-immunoglobulin G), uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 for distinguishing between remission and nonremission groups were 50 relative units (RU)/mL, 3.51 RU/mL, 6835 ng/mL, and 143.4 ng/mL, respectively. The average value in the remission group for sPLA2R-IgG, uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 was 37.39 RU/mL, 1.10 RU/mL, 3498.99 ng/mL, and 33.83 ng/mL, respectively. The average value in the nonremission group for sPLA2R-IgG, uPLA2R-IgG, sPLA2R-IgG4, and uPLA2R-IgG4 was 279.96 RU/mL, 45.36 RU/mL, 25762.47 ng/mL, and 1383.89 ng/mL, respectively. For sPLA2R-Ab as the primary factor, in combination with uPLA2R-Ab, the high-risk predictive value of combined detection of serum and urine PLA2R-IgG and of serum and urine PLA2R-IgG4 was upgraded from 54.55% to 100% and from 75% to 100%, respectively.

Conclusions.—: A highly sensitive TRFIA method was applied in this study; the combined detection of serum and urine PLA2R-Ab improves the efficiency of PMN risk stratification, and can provide a better assessment of PMN monitoring.

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