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The Prevalence of Mesangial Electron-Dense Deposits in PLA2R-Positive Membranous Nephropathy
Gabriel Giannini1, Lois J Arend1
1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Introduction:
Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults and can be primary or secondary. The antigenic target of antibodies in 70% of primary cases is phospholipase A2 receptor (PLA2R). The presence or absence of mesangial electron-dense deposits has been used to distinguish between primary and secondary MN. Mesangial deposits suggest MN due to lupus, infection, or other causes, though they are reported to occur in approximately 10% of primary MN. Staining for PLA2R is now frequently used for confirming a diagnosis of primary MN. If mesangial deposits predict a secondary cause, they should be more frequent in PLA2R-negative biopsies.
Methods:
A review of institutional kidney biopsies between March 2017 and June 2020 identified all cases of MN. Cases with a diagnosis of lupus or near "full-house" staining by immunofluorescence microscopy (IF) were excluded. Light microscopy, IF, and electron microscopy (EM) were performed. PLA2R staining was performed by IF. EM for all cases was reviewed and electron-dense deposit location, distribution, and size were determined.
Results:
Ninety-three cases of MN were identified, of which 86 had both PLA2R staining and EM performed. Of these, 51 cases (59%) were positive for PLA2R and 35 (41%) were negative. Mesangial electron-dense deposits were present in 22 (25.6%) of the 86 cases, including 27.5% (14/51) of PLA2R-positive cases and 22.8% (8/35) of PLA2R-negative cases. No difference was seen in size or distribution of deposits, or other features considered suggestive of secondary MN.
Conclusion:
PLA2R-negative cases were not more likely to have mesangial deposits than PLA2R-positive cases. Mesangial deposits should not be used as an indicator of secondary MN.
Insights
Mesangial deposits do not reliably distinguish primary from secondary membranous nephropathy (MN). Phospholipase A2 receptor (PLA2R) staining is key for diagnosing primary MN, regardless of deposit location.
Area of Science:
- Nephrology
- Immunopathology
- Diagnostic Pathology
Background:
- Membranous nephropathy (MN) is a leading cause of nephrotic syndrome in adults.
- Primary MN is often associated with antibodies against phospholipase A2 receptor (PLA2R).
- Mesangial electron-dense deposits have been traditionally used to differentiate primary MN from secondary causes, though their reliability is debated.
Purpose of the Study:
- To investigate the association between mesangial electron-dense deposits and PLA2R staining in adult MN cases.
- To determine if the presence of mesangial deposits can predict secondary causes of MN.
Main Methods:
- Retrospective review of 93 adult kidney biopsies diagnosed with MN.
- Exclusion of cases with lupus or "full-house" immunofluorescence (IF).
- Analysis of light microscopy, IF, electron microscopy (EM), and PLA2R staining, focusing on deposit location and characteristics.
Main Results:
- Of 86 evaluable cases, 51 (59%) were PLA2R-positive and 35 (41%) were PLA2R-negative.
- Mesangial deposits were present in 25.6% of cases.
- There was no significant difference in the prevalence (27.5% vs. 22.8%) or characteristics of mesangial deposits between PLA2R-positive and PLA2R-negative biopsies.
Conclusions:
- Mesangial electron-dense deposits are not more frequent in PLA2R-negative MN biopsies.
- The presence of mesangial deposits should not be relied upon to indicate a secondary cause of membranous nephropathy.
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