Evidence map›Paper›PMID 38639356›Full record

ArticleJournal of the American Heart Association2024

Imbalance of Iron Availability and Demand in Patients With Acute and Chronic Heart Failure.

Lukas Lanser, Gerhard Poelzl, Moritz Messner, Maria Ungericht, Marc-Michael Zaruba, Jakob Hirsch, Stefan Hechenberger, Stefan Obersteiner, Bernhard Koller, Hanno Ulmer and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Lukas LanserDepartment of Internal Medicine II Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0001-7849-2971
Gerhard PoelzlDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.
Moritz MessnerDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0003-3250-4353
Maria UngerichtDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.ORCID 0009-0008-2098-9772
Marc-Michael ZarubaDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0003-1074-5463
Jakob HirschDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0003-4747-7802
Stefan HechenbergerDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.
Stefan ObersteinerDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.
Bernhard KollerDepartment of Internal Medicine III Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0001-6771-6757
Hanno UlmerInstitute of Medical Statistics and Informatics Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0001-5911-1002
Guenter WeissDepartment of Internal Medicine II Medical University of Innsbruck Innsbruck Austria.ORCID 0000-0003-0709-2158
Innsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIron deficiency (ID) is a frequent comorbidity in patients with acute (AHF) and chronic heart failure (CHF) associated with morbidity and death. We aimed to better characterize iron homeostasis in patients with heart failure applying different biomarkers and to evaluate the accuracy of current ID definition by the European Society of Cardiology/American College of Cardiology/American Heart Association to indicate tissue iron availability and demand. METHODS AND

resultsWe performed a retrospective cohort study investigating 277 patients with AHF and 476 patients with CHF between February 2021 and May 2022. Patients with AHF had more advanced ID than patients with CHF, reflected by increased soluble transferrin receptor and soluble transferrin receptor-ferritin index, and lower ferritin, serum iron, transferrin saturation, hepcidin, and reticulocyte hemoglobin. Decreased iron availability or increased tissue iron demand, reflected by increased soluble transferrin receptor-ferritin index and decreased reticulocyte hemoglobin, was found in 84.1% (AHF) and 28.0% (CHF) with absolute ID and in 50.0% (AHF) and 10.5% (CHF) with combined ID according to the current European Society of Cardiology/American College of Cardiology/American Heart Association-based ID definition. Low hepcidin expression as an indicator of systemic ID was found in 91.1% (AHF) and 80.4% (CHF) of patients with absolute ID and in 32.3% (AHF) and 18.8% (CHF) of patients with combined ID. ID definitions with higher specificity reduce the need for iron supplementation by 25.5% in patients with AHF and by 65.6% in patients with CHF.

conclusionsOur results suggest that the current European Society of Cardiology/American College of Cardiology/American Heart Association-based ID definition might overestimate true ID, particularly in CHF. More stringent thresholds for ID could more accurately identify patients with heart failure with reduced tissue iron availability who benefit from intravenous iron supplementation.

Indexed as

BiomarkersHeart FailureIronAcute DiseaseAgedAged, 80 and overAnemia, Iron-DeficiencyChronic DiseaseFemaleFerritinsHepcidinsHumansIron DeficienciesMaleMiddle AgedReceptors, TransferrinBiomarkersFerritinsHepcidinsIronReceptors, Transferrinacute heart failurechronic heart failurehepcidiniron deficiencyret‐HbsTfR

Identifiers

PMID38639356
PMCPMC11179892
OpenAlexW4394954693

What OpenQuestion holds

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LicenceCC BY-NC
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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.