# Urinary Podocyte Loss is Associated With Treatment Response in Patients With Primary Nephrotic Syndrome

**Authors:** Bartholomeus T. van den Berge, Jitske Jansen, Quinty Leusink, Sanne Kleuskens, Sharon Bootsman, Anne-Els van de Logt, Jack F.M. Wetzels, Bart Smeets, Rutger J. Maas

PMC · DOI: 10.1016/j.ekir.2025.11.017 · Kidney International Reports · 2025-11-17

## TL;DR

Measuring urinary podocyte loss could help predict treatment outcomes in patients with primary nephrotic syndrome.

## Contribution

This study shows that baseline podocyturia can predict treatment response in primary nephrotic syndrome patients.

## Key findings

- Podocyturia levels differentiate early and late treatment responders in MCD/FSGS patients.
- Podocyturia correlates with proteinuria and normalizes with remission.
- Low podocyturia in MN patients is linked to spontaneous remission.

## Abstract

The disease course of primary nephrotic syndrome (PNS) is highly variable, and is difficult to predict at onset. PNS is characterized by podocyte injury and loss. We hypothesized that measurement of urinary podocyte loss is associated with treatment response in patients with PNS.

We included 21 controls, and 59 patients with PNS (minimal change disease [MCD], n =8; focal segmental glomerulosclerosis [FSGS], n = 9; membranous nephropathy [MN]. n = 42). MCD and FSGS were considered manifestations of the same disease entity, and analyzed as one group. Patients’ baseline clinical and follow-up data were recorded. Urinary sediments were collected and stained for podocyte-specific markers, and analyzed using fluorescence-activated cell sorting (FACS).

In patients with MCD/FSGS, the respective partial and complete remission rates were 24% and 59% during a median follow-up of 12.9 months, and all patients received immunosuppressive treatment. In patients with MN, the respective partial and complete remission rates were 64% and 19% during a median follow-up of 15.5 month, and the majority of patients received immunosuppressive treatment. Patients with PNS had elevated levels of podocyturia when compared with controls, and repeat measurements revealed that podocyturia follows proteinuria course over time, normalizing following complete proteinuria remission. In treatment-responsive immunosuppresive-treated patients with MCD/FSGS, podocyturia at baseline significantly differentiated between early and late treatment responders at 4 weeks, contrary to proteinuria and serum albumin. In symptomatically treated patients with MN, low levels of podocyturia at baseline were associated with spontaneous remission.

Patients with PNS have increased podocyturia compared with healthy individuals. Quantitative detection of podocyturia may have prognostic relevance in patients with PNS.

## Linked entities

- **Diseases:** minimal change disease (MONDO:0006835), focal segmental glomerulosclerosis (MONDO:0100313), membranous nephropathy (MONDO:0005376)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** PNS (MESH:D009404), focal segmental glomerulosclerosis (MESH:D005923), MCD (MESH:D012514), minimal change disease (MESH:D009402), proteinuria (MESH:D011507), membranous nephropathy (MESH:D015433)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12800585/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12800585/full.md

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Source: https://tomesphere.com/paper/PMC12800585