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Autoantibodies against nephrin and podocin are associated with disease severity and steroid dependence in adult-onset nephrotic syndrome
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  • Published: 16 March 2026

Autoantibodies against nephrin and podocin are associated with disease severity and steroid dependence in adult-onset nephrotic syndrome

  • Norifumi Hayashi1 na1,
  • Ryoko Akai2 na1,
  • Yu Kagaya1,
  • Keiji Fujimoto1,
  • Takao Iwawaki2,
  • Hitoshi Yokoyama1 &
  • …
  • Kengo Furuichi1 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Diseases
  • Nephrology

Abstract

Nephrotic syndrome is a glomerular disorder characterized by heavy proteinuria and hypoalbuminemia. Autoantibodies against slit diaphragm proteins such as nephrin and podocin have been identified in subsets of patients, but their prevalence and clinical significance in adult-onset disease are not fully understood. We retrospectively studied 114 adults with biopsy-proven nephrotic syndrome, including minimal change nephrotic syndrome, focal segmental glomerulosclerosis, and phospholipase A2 receptor- and neural epidermal growth factor-like 1-associated membranous nephropathy. Serum anti-nephrin and anti-podocin autoantibodies were quantified using enzyme-linked immunosorbent assays.

Anti-nephrin autoantibodies were detected predominantly in minimal change nephrotic syndrome (38.2%) and less frequently in focal segmental glomerulosclerosis (14.3%), but were rare in membranous nephropathy. In contrast, anti-podocin autoantibodies were observed across disease types and were most frequent in neural epidermal growth factor-like 1-associated membranous nephropathy (30.8%). Autoantibody-positive patients presented with more severe nephrotic syndrome, and antibody positivity was associated with a higher incidence of steroid-dependent nephrotic syndrome in exploratory multivariable analyses. In patients with paired samples, autoantibody titers decreased or disappeared in remission.

Notably, anti-nephrin antibodies were preferentially associated with MCNS, whereas anti-podocin antibodies were detected across disease entities and may reflect the extent of podocyte injury rather than disease specificity. Moreover, combined assessment of anti-nephrin and anti-podocin antibody status provided improved stratification of baseline disease severity and relapse-prone disease compared with anti-nephrin antibody status alone.

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Data availability

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.

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Funding

This work was supported by Ministry of Education, Culture, Sports, Science, and Technology Grants-in-Aid for Scientific Research (KAKENHI 24K19138) (to Y.K.).

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Author notes
  1. These authors contributed equally to this work: Norifumi Hayashi and Ryoko Akai.

Authors and Affiliations

  1. Department of Nephrology, School of Medicine, Kanazawa Medical University, Uchinada, Ishikawa, Japan

    Norifumi Hayashi, Yu Kagaya, Keiji Fujimoto, Hitoshi Yokoyama & Kengo Furuichi

  2. Division of Cell Medicine, Department of Life Science, Medical Research Institute, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Ishikawa, 920-0293, Japan

    Ryoko Akai & Takao Iwawaki

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Contributions

N. Hayashi and R. Akai designed the study; N. Hayashi, R. Akai, and T. Iwawaki carried out the experiments; N. Hayashi, Y. Kagaya and K. Fujimoto collected human blood samples. N. Hayashi, H. Yokoyama and K. Furuichi drafted and revised the manuscript. All authors have read and approved the manuscript.

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Correspondence to Norifumi Hayashi.

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Cite this article

Hayashi, N., Akai, R., Kagaya, Y. et al. Autoantibodies against nephrin and podocin are associated with disease severity and steroid dependence in adult-onset nephrotic syndrome. Sci Rep (2026). https://doi.org/10.1038/s41598-026-43612-7

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  • Received: 11 December 2025

  • Accepted: 05 March 2026

  • Published: 16 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-43612-7

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