Evidence map›Paper›PMID 42088641›Full record

ArticleClinical kidney journal2026

Erythroferrone is associated with the hepcidin-to-ferritin ratio and cardiovascular mortality in chronic kidney disease.

Kristin Danielson Pistis, Abdul Rashid Qureshi, Soheir Beshara, Bengt Lindholm, Peter Stenvinkel, Peter Bárány

Abstract read
In one paragraph

Article in Clinical kidney journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kristin Danielson PistisRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Abdul Rashid QureshiRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-0536-5327
Soheir BesharaDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Bengt LindholmRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Peter StenvinkelRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Peter BárányRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0001-6501-8293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The role of erythroferrone, a hormone synthesized in erythroid cells that suppresses hepatic production of hepcidin to increase systemic iron availability during erythropoiesis expansion, has not been sufficiently characterized in chronic kidney disease (CKD). Therefore, we evaluated its determinants and its association with mortality risk in patients with CKD stages 3-5. Methods: In this cross-sectional study with longitudinal follow-up, erythroferrone, hepcidin, ferritin, transferrin saturation (TSAT), C-reactive protein (CRP) and nutritional status were assessed in 377 CKD patients [92 patients with CKD stages 3-4, 210 non-dialysed patients with CKD stage 5 and 75 patients on peritoneal dialysis (PD)]. Regression analyses were performed to investigate the association between erythroferrone and relevant variables. The association between erythroferrone and mortality risk was analysed using Fine-Gray analysis, accounting for kidney transplantation as a competing risk. Results: Erythroferrone, hepcidin and ferritin were higher in PD patients and in CKD 5 patients as compared with CKD 3-4 patients, whereas the hepcidin-to-ferritin ratio did not differ between the cohorts. In linear regression analysis, erythroferrone was positively associated with the reticulocyte count, CRP and CKD severity and negatively associated with TSAT and the hepcidin-to-ferritin ratio (and hepcidin). Further adjustment for erythropoiesis-stimulating agents (ESAs) revealed that erythroferrone no longer showed an association with the severity of CKD or CRP levels. Finally, erythroferrone was linked to both all-cause mortality and cardiovascular mortality. Conclusions: Erythroferrone in CKD patients associated with the reticulocyte count and ESA dose and was inversely correlated with the hepcidin-to-ferritin ratio and TSAT, while its relationship with CKD stage may reflect ESA therapy. Higher circulating erythroferrone levels are associated with an increased mortality risk.

Indexed as

erythroferroneerythropoiesishepcidinironkidney failure

Identifiers

PMID42088641
PMCPMC13136888

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.