Evidence map›Paper›PMID 42524924›Full record

ArticleEinstein (Sao Paulo, Brazil)2026

Serum hepcidin measurement is related to clinical parameters and interferon-gamma in anemia of inflammation.

Raysa Oliveira Maciel, Priscila da Silva Mendonça, Anacélia Gomes de Matos Mota, Deysi Viviana Tenazoa Wong, Roberto César Pereira Lima Júnior, Ronald Feitosa Pinheiro, Silvia Maria Meira Magalhães

Abstract read
In one paragraph

Article in Einstein (Sao Paulo, Brazil), 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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0citing papers in PubMed
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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

7 authors.

Raysa Oliveira MacielCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-7245-5894
Priscila da Silva MendonçaCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0001-6474-9019
Anacélia Gomes de Matos MotaCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-5477-7929
Deysi Viviana Tenazoa WongCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-9741-7560
Roberto César Pereira Lima JúniorCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-7033-655X
Ronald Feitosa PinheiroCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0003-3546-0974
Silvia Maria Meira MagalhãesCancer Cytogenomic Laboratory, Universidade Federal do Ceará, Fortaleza, CE, Brazil.ORCID http://orcid.org/0009-0001-2285-3026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to assess the relationship between hepcidin, IFN-γ, iron biomarkers, and clinical variables in patients with anemia of inflammation.

methodsA cross-sectional study was conducted. Ninety patients with inflammatory anemia and 70 healthy controls were evaluated. Laboratory parameters, serum hepcidin, and IFN-γ were determined using ELISA.

resultsThe mean age of patients with anemia of inflammation was 74.1±7.8 years, and most were female. Most patients reported ≥3 comorbidities (70%). Patients with ≥3 comorbidities had significantly higher levels of hepcidin (p<0.001). Hemoglobin, transferrin saturation index, and serum iron levels were significantly lower in patients with anemia of inflammation than in the control group (p<0.001). The erythrocyte sedimentation rate and ferritin and hepcidin levels increased in the anemia group (p<0.05). A significant positive correlation was observed between hepcidin and ferritin (r=0.372; p=0.001) and IFN-γ (r=0.228; p=0.004). Conversely, a significant negative correlation was found between hepcidin and hemoglobin (r=-0.355; p<0.001).

conclusionUnderstanding how inflammatory parameters and upregulated hepcidin levels act as biomarkers to assess iron homeostasis in anemia of inflammation may be effective for differential diagnosis and therapeutic approaches, such as iron supplementation.

Indexed as

AnemiaHepcidinsInflammationInterferon-gammaAgedAged, 80 and overBiomarkersBlood SedimentationCase-Control StudiesCross-Sectional StudiesEnzyme-Linked Immunosorbent AssayFemaleFerritinsHemoglobinsHumansIronBiomarkersFerritinsHemoglobinsHepcidinsInterferon-gammaIron

Identifiers

PMID42524924
PMCPMC13399299

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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.