Clinicopathological characteristics of patients with low titer anti-phospholipase A2 receptor antibodies verified by indirect immunofluorescence assay.

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2025-02-01 Epub Date: 2024-12-02 DOI:10.1016/j.cca.2024.120070
Hao-Yuan Cui, Chao Li, Yu-Bing Wen, Wei Ye, Wen-Ling Ye, Hang Li, Li-Meng Chen
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Abstract

Objective: Laboratory extensively applied enzyme-linked immunosorbent assay (ELISA) to measure anti-phospholipase A2 receptor antibodies (PLA2R-abs) since its diagnostic significance on PLA2R related primary membranous nephropathy (PLA2R-related pMN) was discovered. However, PLA2R-abs determined by ELISA (PLA2R-ELISA) could infrequently yield inconclusive results, specifically a grey-zone defined as PLA2R-abs ranging from 2 to 20 RU/mL. Recently, researchers suggested that double-check grey-zone PLA2R-abs by indirect immunofluorescence (IIF) could improve diagnostic accuracy. We evaluated the diagnostic performance of PLA2R-IIF in assessing PLA2R-related pMN and summarized clinicopathological characteristics of grey-zone population to provide more evidence for clinical practice.

Methods: Data on demographics, serology and pathology of patients with PLA2R-ELISA grey-zone results and a native kidney biopsy at Peking Union Medical College Hospital from September 2020 to April 2023 were reviewed. Grey-zone samples were analyzed using PLA2R-IIF. Negative results were defined as no fluorescence and positive results were graded according to fluorescence intensity.

Results: This study included a total of 52 grey-zone patients divided into pMN group (n = 36, 69 %) and non-pMN group (n = 16, 31 %) according to renal pathology reports. The pMN patients had higher PLA2R-abs and lower serum creatinine compared to the non-pMN patients (P = 0.003, P < 0.001). No statistically significant differences were observed in 24-hour urine protein and albumin between the two groups. Multiple pathological types were identified in the non-pMN group. The sensitivity and specificity of PLA2R-IIF in PLA2R-ELISA grey-zone population were 72 % and 88 %, respectively, with a total consistent rate of 77 % and a positive predictive value of 93 %.

Conclusion: Both pMN and non-pMN patients presented grey-zone PLA2R-ELISA results. It was necessary to perform PLA2R-IIF to assist in the diagnosis of patients with PLA2R-ELISA grey-zone results.

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间接免疫荧光法验证低效价抗磷脂酶A2受体抗体患者的临床病理特征。
目的:发现抗磷脂酶A2受体抗体(PLA2R-abs)在PLA2R相关原发性膜性肾病(PLA2R相关pMN)中的诊断意义后,实验室广泛应用酶联免疫吸附试验(ELISA)检测抗磷脂酶A2受体抗体(PLA2R-abs)。然而,通过ELISA (PLA2R-ELISA)检测PLA2R-abs通常会产生不确定的结果,特别是定义为PLA2R-abs的灰色区域范围为2至20 RU/mL。最近,研究人员提出通过间接免疫荧光(IIF)双重检查灰色区PLA2R-abs可以提高诊断准确性。我们评价PLA2R-IIF在评估pla2r相关pMN中的诊断效能,总结灰色地带人群的临床病理特征,为临床实践提供更多依据。方法:回顾2020年9月至2023年4月北京协和医院PLA2R-ELISA灰区结果患者的人口学、血清学和病理学数据以及本地肾活检数据。灰色区样品采用PLA2R-IIF分析。阴性结果定义为无荧光,阳性结果根据荧光强度分级。结果:本研究共纳入52例灰色区患者,根据肾脏病理报告分为pMN组(n = 36,69 %)和非pMN组(n = 16,31 %)。pMN患者PLA2R-abs高于非pMN患者,血清肌酐低于非pMN患者(P = 0.003,P )结论:pMN与非pMN患者PLA2R-ELISA结果均呈现灰色区。有必要进行PLA2R-IIF以协助诊断PLA2R-ELISA灰色区结果的患者。
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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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