Evidence map›Paper›PMID 41610123›Full record

ArticlePloS one2026

MUC5B rs35705950 and its association with survival in Brazilian patients with idiopathic pulmonary fibrosis: A longitudinal cohort study.

Rogerio Rufino, Luana Faria, Marcelo Ribeiro-Alves, Lucas Resende Martinez Araujo, Leonardo Palermo, Elizabeth Bessa, Bruno Rangel, Mariana Carneiro Lopes, Mariana Costa Rufino, Cláudia Henrique da Costa and 3 more

Abstract read
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Article in PloS one, 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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1 · What the graph read from it

What it found

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2 · The registry

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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

13 authors.

Rogerio RufinoRio de Janeiro State University, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-5071-6045
Luana FariaRio de Janeiro State University, Rio de Janeiro, Brazil.
Marcelo Ribeiro-AlvesFundacao Oswaldo Cruz, Rio de Janeiro, Brazil.
Lucas Resende Martinez AraujoIdomed, Rio de Janeiro, Brazil.
Leonardo PalermoRio de Janeiro State University, Rio de Janeiro, Brazil.
Elizabeth BessaRio de Janeiro State University, Rio de Janeiro, Brazil.
Bruno RangelRio de Janeiro State University, Rio de Janeiro, Brazil.
Mariana Carneiro LopesRio de Janeiro State University, Rio de Janeiro, Brazil.
Mariana Costa RufinoSão Paulo University, Bauru, Brazil.
Cláudia Henrique da CostaRio de Janeiro State University, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-6785-0753
Jeane de Souza NogueiraTIXUS - Technologic Core for Tissue Repair and Histocompatibility, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Cíntia Barros Santos-RebouçasHuman Genetics Laboratory (SERVGEN), Department of Genetics, Institute of Biology Roberto Alcantara Gomes, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Luís Cristóvão PortoTIXUS - Technologic Core for Tissue Repair and Histocompatibility, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0003-1499-1821

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with heterogeneous clinical outcomes. The MUC5B promoter polymorphism (rs35705950) is the most consistent genetic factor associated with IPF susceptibility, but data from Latin American populations remain limited.

methodsWe conducted a longitudinal cohort study including 50 patients with IPF and 45 healthy controls, recruited between August 1, 2018, and April 30, 2025, at a tertiary referral center in Brazil. Genotyping of rs35705950 was performed by real-time PCR. Demographic, clinical, and functional data were collected at baseline. Survival was analyzed using Kaplan-Meier curves and Cox regression models, with follow-up defined from symptom onset to death or censoring.

resultsThe T-allele frequency was higher in IPF patients compared with controls (47.1% vs 8.3%, p < 0.001). Carriers of the T allele (G/T or T/T) comprised 82.4% of cases versus 16.7% of controls. Among patients with IPF, T-carriers tended to have worse lung function and shorter survival, although survival differences were not statistically significant. In multivariable models, the presence of the T allele was not an independent predictor of mortality. By contrast, higher New York Heart Association (NYHA) functional class was consistently associated with increased mortality risk.

conclusionsIn this Brazilian cohort, the MUC5B promoter variant was strongly associated with susceptibility to IPF but not with independent survival differences. Functional impairment, particularly NYHA class, remained the key prognostic factor. These findings highlight the importance of integrating genetic and clinical information in diverse populations and provide novel data from an underrepresented Latin American setting.

Indexed as

Idiopathic Pulmonary FibrosisMucin-5BPolymorphism, Single NucleotideAgedAllelesBrazilCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseHumansKaplan-Meier EstimateLongitudinal StudiesMaleMiddle AgedPromoter Regions, GeneticMUC5B protein, humanMucin-5B

Identifiers

PMID41610123
PMCPMC12854480

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