Abstract

Membranous nephropathy (MN) and minimal change disease (MCD) are two common causes leading to nephrotic syndrome (NS). They have similar clinical features but different treatment strategies and prognoses. M-type phospholipase A2 receptor (PLA2R) is considered as a specific marker of membranous nephropathy. However, its sensitivity is only about 70%. Therefore, there is a lack of effective and noninvasive tools to distinguish PLA2R-negative MN and MCD patients without renal biopsy. A total 949 patients who were pathologically diagnosed as idiopathic MN or MCD were enrolled in this study, including 805 idiopathic MN and 144 MCD. Based on the basic information and laboratory examination of 200 PLA2R-negative MN and 144 MCD, we used a univariate and multivariate logistic regression to select the relevant variables and develop a discrimination model. A novel model including age, albumin, urea, high density lipoprotein, C3 levels and red blood cell count was established for PLA2R-negative MN and MCD. The discrimination model has great differential capability (with an AUC of 0.904 in training group and an AUC of 0.886 in test group) and calibration capability. When testing in all 949 patients, our model also showed good discrimination ability for all idiopathic MN and MCD.

Highlights

  • Membranous nephropathy (MN) and minimal change disease (MCD) are two common causes leading to nephrotic syndrome (NS)

  • Thrombospondin type-I domain-containing 7A (THSD7A) was identified as the target antigen in about 10% of patients with phospholipase A2 receptor (PLA2R)-negative MN in European and North American populations, but THSD7A-associated membranous nephropathy has a low prevalence in Chinese p­ atients11

  • The results suggested that PLA2R-negative MN patients tended to be older and have higher total protein (TP), ALB levels and greater urine volume

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Summary

Introduction

Membranous nephropathy (MN) and minimal change disease (MCD) are two common causes leading to nephrotic syndrome (NS). They have similar clinical features but different treatment strategies and prognoses. Minimal change disease (MCD) is another primary glomerular disease with high prevalence characterized by rapid onset and development Current studies suggest these two diseases account for about 60% NS patients in ­China. Thrombospondin type-I domain-containing 7A (THSD7A) was identified as the target antigen in about 10% of patients with PLA2R-negative MN in European and North American populations, but THSD7A-associated membranous nephropathy has a low prevalence in Chinese p­ atients. It is urgent to develop a new convenient and noninvasive method to distinguish MN from MCD

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