Evidence map›Paper›PMID 41856675›Full record

ArticleOpen heart2026

Biomarkers of iron deficiency and prognosis in patients hospitalised with new-onset heart failure and a reduced left ventricular ejection fraction.

Jonathan S M Johansson, Josefin Henrysson, Carmen Basic, John G F Cleland, Michael Fu, Charlotta Ljungman

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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jonathan S M JohanssonDepartment of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden jonathan.johansson@vgregion.se.ORCID 0000-0002-4767-7524
Josefin HenryssonDepartment of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Carmen BasicDepartment of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
John G F ClelandUniversity of Glasgow School of Cardiovascular & Metabolic Health, Glasgow, UK.ORCID 0000-0002-1471-7016
Michael FuDepartment of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Charlotta LjungmanDepartment of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIron deficiency (ID) is common in patients with heart failure (HF). Current guidelines define ID based on serum ferritin and transferrin saturation (TSAT) rather than soluble transferrin receptor (STFR) or ratios such as iron/STFR or TSAT/STFR. We investigated the associations between these biomarkers and prognosis in patients with new-onset HF with reduced ejection fraction (HFrEF).

methodsAll patients hospitalised in 2016-2020 at Sahlgrenska University Hospital with new-onset HFrEF who had iron biomarkers measured within 6 months of discharge were included, with follow-up from the date of the iron biomarker test until 31 December 2021. The primary composite event of interest was first re-hospitalisation for HF (HHF) or all-cause mortality. The associations between ID biomarkers and endpoints were analysed using Cox regression adjusted for age, sex, previous HF, left ventricular ejection fraction, HF medications and comorbidity. Bonferroni-Holm correction was applied for multiple testing.

resultsOf 325 patients included (median age 68 (57-76) years, 70.2% men), 168 (52%) had ID using current guideline criteria and STFR was available for 224 (69%) patients. Median follow-up was 2.2 years. In the prespecified analysis plan, biomarkers of ID were not statistically significantly associated with the primary composite endpoint, although each SD increase in TSAT was associated with 56% lower risk of HHF (0.44 [0.27-0.71]) as were increased ratios of iron/STFR (0.58 [0.40-0.86]) and TSAT/STFR (0.55 [0.37-0.83]). However, in a post hoc sensitivity analysis in which patients with extreme values were excluded, each increase in SD of TSAT was associated with 47% lower risk of the primary composite endpoint (0.53 [0.35-0.79]).

conclusionsLower TSAT is associated with a greater risk of clinical events in patients with new-onset HF, as were the ratios of iron/STFR and TSAT/STFR. However, neither ratio appeared to offer a substantial advantage compared with TSAT alone.

Indexed as

FerritinsHeart FailureHospitalizationIronIron DeficienciesStroke VolumeVentricular Function, LeftAgedBiomarkersFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkersFerritinsIronTransferrinBiomarkersEPIDEMIOLOGYHeart Failure, Systolic

Identifiers

PMID41856675
PMCPMC13007192

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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.