Rodas Lida M, Matas-García Ana, Barros Xoana, Blasco Miquel, Viñas Odette, Llobell Arturo, Martin Nadia, Quintana Luis F
Servicio de Nefrología y Trasplante Renal, Hospital Clínic, Departamento de Medicina, Universidad de Barcelona, Institut d' Invesigacions biomèdiques Agust Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Servicio de Nefrología, Hospital Josep Trueta, Girona, Spain.
Clin Kidney J. 2019 Feb;12(1):36-41. doi: 10.1093/ckj/sfy005. Epub 2018 Mar 9.
M-type phospholipase A2 receptor (APLA2R) is considered the major antigen involved in the pathogenesis of adult primary membranous nephropathy (MN), which is the leading cause of non-diabetic nephrotic syndrome. Antibodies to this antigen have been proved to be an excellent biomarker of disease activity in primary MN. In fact, preliminary data suggest that the higher the antibody level the more proteinuria, and that a decrease in antibody level precedes the remission of proteinuria, but more solid evidence is needed.
The present work aims to characterize the predictive value of the level of antibodies against PLA2R as a biomarker of disease course and treatment response in a well-defined cohort of 62 patients from University Hospitals Clinic of Barcelona and Josep Trueta in Girona. The primary outcome was the appearance of a spontaneous complete remission (CR), defined as induction of a CR without the use of immunosuppressive agents.
In common with other reports, this work confirms that spontaneous CR is more frequent in patients with low titre of APLA2R at diagnosis, but strikingly, in this cohort we found that spontaneous CR was achieved in patients with APLA2R levels <40 UI/mL. Furthermore, spontaneous CR were less frequently observed in patients with proteinuria >8 g/day.
In conclusion, these findings point out the important role of APLA2R as a tool to predict the disease course and establish personalized therapeutic options at the moment of diagnosis of primary MN. Specifically, patients with low titre of APLA2R (<40 UI/mL) and proteinuria <4/day could obtain benefit of a longer period of follow-up with conservative treatment after diagnosis.
M型磷脂酶A2受体(APLA2R)被认为是成人原发性膜性肾病(MN)发病机制中的主要抗原,MN是非糖尿病肾病综合征的主要病因。针对该抗原的抗体已被证明是原发性MN疾病活动的优良生物标志物。事实上,初步数据表明抗体水平越高蛋白尿越严重,且蛋白尿缓解前抗体水平会下降,但仍需要更确凿的证据。
本研究旨在明确来自巴塞罗那大学医院诊所和赫罗纳的何塞普·特鲁埃塔医院的62例患者队列中,抗PLA2R抗体水平作为疾病进程和治疗反应生物标志物的预测价值。主要结局是出现自发完全缓解(CR),定义为在未使用免疫抑制剂的情况下诱导出CR。
与其他报告一致,本研究证实诊断时APLA2R滴度低的患者自发CR更常见,但引人注目的是,在该队列中我们发现APLA2R水平<40 UI/mL的患者实现了自发CR。此外,蛋白尿>8 g/天的患者自发CR较少见。
总之,这些发现指出APLA2R作为预测原发性MN疾病进程和在诊断时制定个性化治疗方案的工具具有重要作用。具体而言,APLA2R滴度低(<40 UI/mL)且蛋白尿<4/天的患者在诊断后采用保守治疗进行较长时间随访可能有益。