# Association between serum hepcidin-25 levels and hyporesponsiveness to erythropoiesis-stimulating agents in Japanese patients receiving hemodialysis: a cross-sectional study

**Authors:** Ryo Fujikawa, Nobuo Nagano, Yuko Mitobe, Kyoko Ito

PMC · DOI: 10.1007/s10157-025-02783-9 · Clinical and Experimental Nephrology · 2025-10-31

## TL;DR

This study finds that higher hepcidin-25 levels in hemodialysis patients are linked to better response to erythropoiesis-stimulating agents, along with other iron metabolism markers.

## Contribution

The study provides new evidence on the relationship between hepcidin-25 and ESA hyporesponsiveness in Japanese hemodialysis patients.

## Key findings

- Hepcidin-25 levels were significantly negatively correlated with the ESA resistance index (ERI).
- Hepcidin-25 levels correlated positively with serum iron and ferritin, and negatively with hematocrit and erythropoietin levels.
- Patients receiving oral iron-containing preparations had higher hepcidin-25 levels.

## Abstract

Hepcidin-25 plays an important role in regulating iron metabolism; however, the association between hepcidin-25 levels and hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is controversial. We aimed to clarify the associations between serum hepcidin-25 levels and hyporesponsiveness to ESAs in Japanese patients receiving hemodialysis, and between hepcidin-25 levels and other factors.

This observational cross-sectional study included hemodialysis patients recruited at Heisei-Hidaka Clinic in Japan from August 2023 to June 2024. Serum hepcidin-25 levels were measured by latex immunoassay. Hyporesponsiveness to ESAs was determined by the ESA resistance index (ERI). The correlation between hepcidin-25 levels and ERI was evaluated using Pearson’s correlation coefficient. We also investigated the patient characteristics associated with hepcidin-25 levels using multiple regression analysis.

Hepcidin-25 levels were significantly negatively correlated with ERI (r = − 0.438, p = 0.0005). Hepcidin-25 levels also showed significant positive correlations with serum iron, transferrin saturation (TSAT), serum ferritin, and high sensitive C-reactive protein (hs-CRP), and significant negative correlations with hematocrit, unsaturated iron-binding capacity, total iron-binding capacity, and serum erythropoietin levels. Hepcidin-25 levels were significantly higher in the patients who received oral iron-containing preparations than in those without these preparations. Multiple regression analysis showed significant partial regression coefficients for ERI, hematocrit, TSAT, serum ferritin, hs-CRP, and the administration of oral iron-containing preparations.

Serum hepcidin-25 levels were significantly negatively correlated with the ERI. The results suggest that hepcidin-25 levels might be associated with ERI, hematocrit, TSAT, serum ferritin, hs-CRP, and the administration of oral iron-containing preparations.

## Linked entities

- **Chemicals:** iron (PubChem CID 23925)

## Full-text entities

- **Genes:** TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Chemicals:** iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12886222/full.md

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Source: https://tomesphere.com/paper/PMC12886222