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Development and validation of a discrimination model between primary PLA2R-negative membranous nephropathy and
Feng Wu1, Yiding Zhang1, Wen Cui1
1Department of Nephrology, The First Affiliated Hospital, Zhengzhou University, No. 1, East Jianshe Road, Zhengzhou, 450052, Henan, People's Republic of China.
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.
Insights
A new model using age, albumin, urea, HDL, C3, and RBC count can help differentiate between membranous nephropathy (MN) and minimal change disease (MCD) in patients without a biopsy. This noninvasive tool aids in diagnosis when M-type phospholipase A2 receptor (PLA2R) testing is inconclusive.
Area of Science:
- Nephrology
- Immunology
Background:
- Membranous nephropathy (MN) and minimal change disease (MCD) are leading causes of nephrotic syndrome (NS) with overlapping clinical presentations.
- Distinguishing between MN and MCD is crucial as they require different therapeutic approaches and have varied prognoses.
- While M-type phospholipase A2 receptor (PLA2R) is a marker for MN, its sensitivity is limited (approx. 70%), necessitating alternative diagnostic methods for PLA2R-negative cases.
Purpose of the Study:
- To develop and validate a noninvasive diagnostic model to differentiate between PLA2R-negative idiopathic MN and MCD.
- To identify key clinical and laboratory parameters that can effectively distinguish these two conditions without the need for renal biopsy.
Main Methods:
- A cohort of 949 patients with pathologically confirmed idiopathic MN (805) or MCD (144) was analyzed.
- A logistic regression model was developed using data from 200 PLA2R-negative MN and 144 MCD patients, incorporating basic information and laboratory results.
- The model's performance was evaluated using area under the curve (AUC) in training and testing groups, and further validated on the entire patient cohort.
Main Results:
- A novel discrimination model incorporating age, albumin, urea, high-density lipoprotein (HDL) levels, C3 levels, and red blood cell (RBC) count was established.
- The model demonstrated strong discriminatory power, with an AUC of 0.904 in the training group and 0.886 in the test group.
- The model also showed good discrimination when applied to the entire cohort of 949 patients, highlighting its robustness.
Conclusions:
- The developed model offers a promising noninvasive tool for differentiating PLA2R-negative MN from MCD.
- This approach can aid clinicians in making timely and accurate diagnoses, potentially avoiding invasive procedures like kidney biopsies.
- The model's inclusion of readily available clinical and laboratory parameters makes it a practical diagnostic aid in nephrotic syndrome management.
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