Evidence map›Paper›PMID 40638437›Full record

ArticleSao Paulo medical journal = Revista paulista de medicina2025

HFE mutations in patients with iron overload in Santa Catarina: a cross-sectional study.

Cristiane Manfé Pagliosa, Vivian Karla Brognoli Franco, Thiago Sousa Matias, Bruno Vieira Dias, Andrea Thives de Carvalho Hoepers

Abstract read
In one paragraph

Article in Sao Paulo medical journal = Revista paulista de medicina, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Cristiane Manfé PagliosaDepartamento de Nutrição, Universidade do Oeste de Santa Catarina (Unoesc), Joaçaba (SC), Brazil; Clinical Nutritionist and Consultant, Department of Nutrition and Food Sciences at Nectalimentos, Joaçaba (SC), Brazil.ORCID 0000-0002-0553-4621
Vivian Karla Brognoli FrancoCentro de Hemoterapia, Hospital Universitário Professor Polydoro Ernani de São Thiago, Universidade Federal de Santa Catarina (UFSC), Florianópolis (SC), Brazil.ORCID 0000-0002-0297-1455
Thiago Sousa MatiasDepartamento de Educação Física, Escola de Esportes, Universidade Federal de Santa Catarina (UFSC), Florianópolis (SC), Brazil.ORCID 0000-0003-0241-3776
Bruno Vieira DiasCentro de Hematologia e Hemoterapia de Santa Catarina, Florianópolis (SC), Brazil.ORCID 0000-0003-4717-1950
Andrea Thives de Carvalho HoepersCentro de Hemoterapia, Hospital Universitário Professor Polydoro Ernani de São Thiago, Universidade Federal de Santa Catarina (UFSC), Florianópolis (SC), Brazil.ORCID 0000-0002-1615-486X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInvestigating the frequency and characteristics of iron overload cases with HFE gene mutation is crucial, given the population-level risks associated with excessive iron.

objectiveTo determine the frequency of HFE mutations in patients with iron overload in Santa Catarina, Brazil. DESIGN AND

settingA cross-sectional study of patients with iron overload at the Ambulatory Department of the Centro de Hematologia e Hemoterapia de Santa Catarina (Hemorrede-HEMOSC) in Santa Catarina.

methodsHFE genotype frequencies were determined, and a division were made between carriers of HFE -C282Y/C282Y mutations and carriers of other HFE-non-C282Y/C282Y mutations, according to each region of Santa Catarina. Binary logistic regression was used for association between sex and age with genetic mutation trait.

resultsAmong the 1,022 patients, 10.4% had secondary hemochromatosis, and 89.6% were evaluated for iron overload due to hereditary hemochromatosis (HH). Of these, 367 underwent genetic testing, which revealed HFE mutations in 77.3%. Most patients with HFE mutations had non-C282Y/C282Y-hemochromatosis, especially H63D/WT (> 39%), regardless of the Santa Catarina region. The frequency of C282Y/C282Y was higher in the West (20.9%) and North (28.3%) regions. Adjusted association analysis showed that men have an increased chance of hemochromatosis when involving 'non-C282Y/C282Y' mutations (OR: 2.77; 95% CI: 1.60-6.608).

conclusionsThe data show the magnitude and characteristics of iron overload cases with HFE mutations in Santa Catarina. As most patients referred for treatment have H63D mutation, we suggest further studies to assess whether other factors, including dietary habits and mandatory iron fortification policies, contribute to iron overload or HH manifestation.

Indexed as

HemochromatosisHemochromatosis ProteinIron OverloadMutationAdolescentAdultAgedBrazilCross-Sectional StudiesFemaleGene FrequencyGenotypeHumansMaleMiddle AgedYoung AdultHemochromatosis ProteinHFE protein, human

Identifiers

PMID40638437
PMCPMC12233034

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