Urine Nephrin and Podocalyxin Reflecting Podocyte Damage and Severity of Kidney Disease in Various Glomerular Diseases—A Cross-Sectional Study

Author:

Giannou Panagiota1ORCID,Gakiopoulou Harikleia2,Stambolliu Emelina1ORCID,Petras Dimitrios1,Chalkia Aglaia1,Kapota Athanasia1,Palamaris Kostas2ORCID,Hadziyannis Emilia3,Thomas Konstantinos4ORCID,Alexakou Zoe1,Bora Margarita1,Mintzias Theodoros5,Vassilopoulos Dimitrios3ORCID,Patsouris Eustratios2,Deutsch Melanie6

Affiliation:

1. Nephrology Department, Hippokration General Hospital, 11527 Athens, Greece

2. 1st Department of Pathology, School of Medicine, National and Kapodistrian University of Athens, 10679 Athens, Greece

3. 2nd Department of Medicine and Laboratory, Clinical Immunology—Rheumatology Unit, School of Medicine, National and Kapodistrian University of Athens, 10679 Athens, Greece

4. 4th Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens, 10679 Athens, Greece

5. Athens School of Medicine, Hellenic Society of Occupational and Environmental Medicine, 10445 Athens, Greece

6. 2nd Academic Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, Hippokration General Hospital of Athens, 11527 Athens, Greece

Abstract

Background/Objectives: Glomerulopathy is a term used to describe a broad spectrum of renal diseases, characterized by dysfunction of glomerular filtration barrier, especially of podocytes. Several podocyte-associated proteins have been found and proved their usefulness as urine markers of podocyte dysfunction. Two of them are nephrin (NEP) and prodocalyxin (PDC). This study aims to evaluate the association of podocyte damage, as it is demonstrated via the concentrations of urinary proteins, with clinical and histological data from patients with several types of glomerulonephritis. Methods: We measured urine levels of two podocyte-specific markers, NEP and PDC (corrected for urine creatinine levels), in patients with a wide range of glomerulopathies. Serum and urine parameters as well as histological parameters from renal biopsy were recorded. Results: In total, data from 37 patients with glomerulonephritis and 5 healthy controls were analyzed. PDC and NEP concentrations correlated between them and with serum creatinine levels (p = 0.001 and p = 0.013 respectively), and with histological lesions associated with chronicity index of renal cortex, such as severe interstitial fibrosis, severe tubular atrophy and hyalinosis (for PDC/NEP, all p < 0.05). In addition, the PDC and NEP demonstrated statistically significant correlations with interstitial inflammation (p = 0.018/p = 0.028). Regarding electron microscopy evaluation, PDC levels were correlated with distinct characteristics, such as fibrils and global podocyte foot process fusion, whereas the NEP/CR ratio was uniquely significantly associated with podocyte fusion only in non-immune-complex-mediated glomerulonephritis (p = 0.02). Among the other clinical and histological parameters included in our study, a strong correlation between proteinuria >3 g/24 h and diffuse fusion of podocyte foot processes (p = 0.016) was identified. Conclusions: Podocalyxin and nephrin concentrations in urine are markers of podocyte dysfunction, and in our study, they were associated both with serum creatinine and histological chronicity indices.

Publisher

MDPI AG

Reference23 articles.

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