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M-type phospholipase A2 receptor autoantibodies and renal function in patients with primary membranous nephropathy
Elion Hoxha1, Sigrid Harendza1, Hans Pinnschmidt2
1III. Department of Internal Medicine and.
Background And Objectives:
Loss of renal function in patients with primary membranous nephropathy cannot be reliably predicted by laboratory or clinical markers at the time of diagnosis. M-type phospholipase A2 receptor autoantibodies have been shown to be associated with changes in proteinuria. Their eventual effect on renal function, however, is unclear.
Design, Setting, Participants, & Measurements:
In this prospective, open, multicenter study, the potential role of M-type phospholipase A2 receptor autoantibodies levels on the increase of serum creatinine in 118 consecutive patients with membranous nephropathy and positivity for serum M-type phospholipase A2 receptor autoantibodies was analyzed. Patients were included in the study between April of 2010 and December of 2012 and observed until December of 2013. The clinical end point was defined as an increase of serum creatinine by ≥ 25% and serum creatinine reaching ≥ 1.3 mg/dl.
Results:
Patients were divided into tertiles according to their M-type phospholipase A2 receptor autoantibody levels at the time of inclusion in the study: tertile 1 levels=20-86 units/ml (low), tertile 2 levels=87-201 units/ml (medium), and tertile 3 levels ≥ 202 units/ml (high). The median follow-up time of all patients in the study was 27 months (interquartile range=18-33 months). The clinical end point was reached in 69% of patients with high M-type phospholipase A2 receptor autoantibodies levels (tertile 3) but only 25% of patients with low M-type phospholipase A2 receptor autoantibodies levels. The average time to reach the study end point was 17.7 months in patients with high M-type phospholipase A2 receptor autoantibodies levels and 30.9 months in patients with low M-type phospholipase A2 receptor autoantibodies levels. A multivariate Cox regression analysis showed that high M-type phospholipase A2 receptor autoantibodies levels-in addition to men and older age-are an independent predictor for progressive loss of renal function.
Conclusions:
High M-type phospholipase A2 receptor autoantibodies levels were associated with more rapid loss of renal function in this cohort of patients with primary membranous nephropathy and therefore, could be helpful for treatment decisions.
Insights
High levels of M-type phospholipase A2 receptor autoantibodies predict faster kidney function decline in primary membranous nephropathy patients. This finding may aid in treatment decisions for kidney disease progression.
Area of Science:
- Nephrology
- Immunology
Background:
- Primary membranous nephropathy (MN) progression is difficult to predict using standard markers.
- M-type phospholipase A2 receptor (MPR) autoantibodies are linked to proteinuria but their impact on renal function is unclear.
Purpose of the Study:
- To investigate the association between MPR autoantibody levels and the rate of renal function decline in patients with MN.
- To determine if MPR autoantibody levels can predict an increase in serum creatinine.
Main Methods:
- Prospective, open, multicenter study of 118 MN patients with positive MPR autoantibodies.
- Patients were stratified into tertiles based on MPR autoantibody levels (low, medium, high).
- Clinical endpoint: serum creatinine increase ≥ 25% and reaching ≥ 1.3 mg/dl over a median follow-up of 27 months.
Main Results:
- High MPR autoantibody levels (tertile 3) were associated with reaching the endpoint in 69% of patients, versus 25% in the low level group (tertile 1).
- The average time to reach the endpoint was significantly shorter in the high MPR autoantibody group (17.7 months) compared to the low group (30.9 months).
- Multivariate analysis identified high MPR autoantibody levels, male sex, and older age as independent predictors of progressive renal function loss.
Conclusions:
- Elevated MPR autoantibody levels are linked to a more rapid decline in kidney function in primary MN.
- MPR autoantibody levels may serve as a valuable biomarker for predicting disease progression and guiding treatment strategies in MN.
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