Evidence map›Paper›PMID 42267373›Full record

ArticleERJ open research2026

Comparison of airway mucin 5AC and 5B expression in preterm-born adults and asthma.

Mervi Kreus, Petra Um-Bergström, Heta Merikallio, Elisa Lappi-Blanco, Ilkka Miinalainen, Nicole Y Wagner, Eva Berggren-Broström, Erik Melén, Anders Lindén, Åsa M Wheelock and 2 more

Abstract read
In one paragraph

Article in ERJ open research, 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

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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

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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

12 authors.

Mervi KreusDivision of immunology and Respiratory Medicine, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-1334-7535
Petra Um-BergströmDepartment of Pediatrics, Sachs' Children and Youth Hospital, Södersjukhuset, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-2715-2683
Heta MerikallioResearch Unit of Biomedicine and Internal Medicine, University of Oulu, Oulu, Finland.
Elisa Lappi-BlancoDepartment of Pathology, Oulu University Hospital, Oulu, Finland.
Ilkka MiinalainenBiocenter Oulu, University of Oulu, Oulu, Finland.ORCID https://orcid.org/0000-0002-3922-3442
Nicole Y WagnerDivision of immunology and Respiratory Medicine, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Eva Berggren-BroströmDepartment of Pediatrics, Sachs' Children and Youth Hospital, Södersjukhuset, Stockholm, Sweden.
Erik MelénDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-8248-0663
Anders LindénDepartment of Respiratory Medicine and Allergy and Center for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
Åsa M WheelockDivision of immunology and Respiratory Medicine, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Riitta KaarteenahoResearch Unit of Biomedicine and Internal Medicine, University of Oulu, Oulu, Finland.
C Magnus SköldDivision of immunology and Respiratory Medicine, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: As preterm birth is a risk factor for developing chronic lung disease later in life and has been associated with asthma-like symptoms, we hypothesised that preterm-born adults with and without a history of bronchopulmonary dysplasia (BPD) resemble patients with asthma with respect to altered mucin expression in the airways. Methods: Bronchial biopsies were retrieved from 39 adults born very-to-extremely preterm (of which 22 had a history of BPD), 18 adults with mild allergic asthma and 24 healthy controls. Mucin (MUC) 5AC and MUC5B protein expressions were determined by immunohistochemistry and immunoelectron microscopy. Additionally, the percentage of goblet cells was estimated. Results: MUC5AC expression and the percentage of goblet cells were lower in preterm-born adults than in asthma patients but did not markedly differ from those of healthy controls. In the preterm-born adults, MUC5AC expression correlated negatively with forced expiratory volume in 1 s to forced vital capacity ratio (FEV Conclusions: Unlike patients with asthma, preterm-born adults with or without BPD do not exhibit increased MUC5AC expression compared with healthy controls. However, the associations of MUC5AC and MUC5B expression with lung function, symptoms and quality-of-life indices suggest a potential clinical role for these mucins in this population.

Identifiers

PMID42267373
PMCPMC13244201

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