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.

Nephron
|November 21, 2021
PubMed
Abstract

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.

Related Concept Videos

Nephrotic Syndrome I : Introduction01:24

Nephrotic Syndrome I : Introduction

Nephrotic Syndrome is a chronic kidney disorder defined by clinical findings such as severe proteinuria, hypoalbuminemia, hyperlipidemia, and edema. These symptoms result from damage to the glomeruli, the kidney’s filtering units, increasing their permeability to proteins.Definition and Meaning:Proteinuria, defined as the loss of more than 3.5 grams of protein per day in adults, is a crucial feature of nephrotic syndrome. This condition is often accompanied by edema, the accumulation of...
93
Nephrotic Syndrome II : Assessment and Medical Management01:26

Nephrotic Syndrome II : Assessment and Medical Management

IntroductionNephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.AssessmentPatient History: Document...
35
Renal Corpuscle01:20

Renal Corpuscle

The glomerulus and Bowman's capsule are two essential components of the nephron, which is the functional unit of the kidney. These microscopic structures play a critical role in the process of blood filtration to produce urine.
Glomerulus: Structure and Function
The glomerulus is a tiny, intricate network of capillaries located at the beginning of the nephron. It's enveloped by the Bowman's capsule and receives its blood supply from an afferent arteriole, which divides into numerous...
3.7K