Department of Nephrology Dialysis and Transplantation, Gazi University Faculty of Medicine, 06560, Ankara, Turkey.
Department of Pathology, Gazi University Faculty of Medicine, 06560, Ankara, Turkey.
Clin Exp Nephrol. 2021 May;25(5):488-500. doi: 10.1007/s10157-020-02011-6. Epub 2021 Jan 18.
The aim of this study was to define the clinicopathologic features of phospholipase A receptor (PLAR) and/or thrombospondin type-1 domain-containing 7A (THSD7A) associated membranous nephropathy(MN) focusing on their impact to disease relapse and response to treatment.
A total of 201 patients were enrolled for baseline clinical and histopathological features and 102 patients with a clinical follow-up for more than 1 year were evaluated for outcomes. Immunohistochemical staining was performed with PLAR and THSD7A antibodies on kidney biopsies and glomerular staining was evaluated.
PLAR expression was observed in 75% of the patients' biopsies; however, THSD7A expression was present only in 7 patients' biopsies (3.5%). No significant difference was found between histopathological and clinical features of PLAR positive and negative patients, collectively. Glomerular PLAR expression was significantly associated with complete and complete/partial remission with first-line treatment; however, overall complete, and complete/partial remission rates did not differ from PLAR negative patients (p = 0.2 and p = 0.8). Male gender, the presence of IgG4 staining and a necessity of immunosuppressive treatment were significantly associated with glomerular PLAR expression. One patient, who developed end-stage renal disease, had glomerular expression for both PLAR and THSD7A. Three patients with THSD7A-positive MN achieved complete remission.
The probability of achieving complete remission is high in patients with PLAR-positive MN for whom the relapse rate was also higher. The overall renal outcome did not differ from PLAR negative cases. Low incidence of THSD7A-positive MN reduces the possibility of future randomized controlled trials.
本研究旨在定义磷脂酶 A 受体(PLAR)和/或血栓反应蛋白 1 型结构域包含 7A(THSD7A)相关膜性肾病(MN)的临床病理特征,重点关注其对疾病复发和治疗反应的影响。
共纳入 201 例患者进行基线临床和组织病理学特征分析,其中 102 例患者的临床随访时间超过 1 年,以评估结局。对肾活检标本进行 PLAR 和 THSD7A 抗体免疫组织化学染色,并评估肾小球染色。
PLAR 表达在 75%的患者活检标本中可见,但仅在 7 例患者的活检标本中(3.5%)可见 THSD7A 表达。PLAR 阳性和阴性患者的组织病理学和临床特征之间无显著差异。肾小球 PLAR 表达与一线治疗的完全缓解和完全/部分缓解显著相关,但总完全缓解和完全/部分缓解率与 PLAR 阴性患者无差异(p=0.2 和 p=0.8)。男性、IgG4 染色的存在和免疫抑制治疗的必要性与肾小球 PLAR 表达显著相关。1 例发生终末期肾病的患者同时表达 PLAR 和 THSD7A。3 例 THSD7A 阳性 MN 患者达到完全缓解。
PLAR 阳性 MN 患者达到完全缓解的可能性较高,复发率也较高。总体肾脏结局与 PLAR 阴性病例无差异。THSD7A 阳性 MN 的低发生率降低了未来进行随机对照试验的可能性。