Evidence map›Paper›PMID 42315257›Full record

ArticleBMJ open respiratory research2026

Role of oral bacteria composition and functional gene profiles in respiratory diseases.

Christine Cramer, Ian Philip George Marshall, Michael J Abramson, Nils Oskar Jõgi, Maryia Khomich, Shyamal D Peddada, Bente Sved Skottvoll, Vivi Schlünssen, Randi Jacobsen Bertelsen

Abstract readMulticenter Study
In one paragraph

Article in BMJ open respiratory 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.

0numbers the graph read from it
0cells of the map it votes in
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

9 authors.

Christine CramerDepartment of Public Health, Research Unit for Environment, Danish Ramazzini Centre, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-7873-435X
Ian Philip George MarshallDepartment of Biology, Section for Microbiology, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-9264-4687
Michael J AbramsonSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-9954-0538
Nils Oskar JõgiDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Maryia KhomichDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0002-6840-5739
Shyamal D PeddadaBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, Durham, North Carolina, USA.
Bente Sved SkottvollDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0002-1969-7165
Vivi SchlünssenDepartment of Public Health, Research Unit for Environment, Danish Ramazzini Centre, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0003-4915-1734
Randi Jacobsen BertelsenDepartment of Clinical Science, University of Bergen, Bergen, Norway randi.j.bertelsen@uib.no.ORCID http://orcid.org/0000-0001-5319-525X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe oral microbiome has been shown to be associated with respiratory health, primarily in adult case studies or among children. This relationship has been scarcely investigated in adult population-based cohorts.

objectivesTo investigate the association between oral microbiome and respiratory health, more specifically asthma, chronic rhinosinusitis (CRS), lung function and fractional exhaled nitric oxide (FeNO) in a population-based cross-continental multicentre study among adults.

methodsSubgingival samples from 355 adult European Community Respiratory Health Survey participants from Norway, Australia and Estonia underwent metagenomic sequencing. Respiratory disease was defined from questionnaires and sensitisation from specific immunoglobulin E (IgE)/skin prick tests. Spirometry and FeNO were measured. The associations between alpha diversity and disease status were evaluated in cross-sectional analyses using logistic regression adjusting for sex, smoking and study centre. Differential abundance analyses were performed using analysis of compositions of microbiomes with bias correction.

resultsAlpha diversity differed by study centre and sensitisation status and was associated with non-allergic CRS (richness: 1.12, 95% CI 1.03 to 1.22). A similar though not statistically significant pattern was seen for forced vital capacity (FVC) below the lower limit of normal (LLN).

conclusionIncreased alpha diversity was associated with non-allergic CRS and a similar trend was seen for FVC below LLN. Bacterial composition and functional profiles of the oral microbiome differed by respiratory health status. This study is novel in exploring functional gene profiling in relation to asthma and FeNO.

Indexed as

AsthmaBacteriaMicrobiotaMouthRhinosinusitisAdultAustraliaChronic DiseaseCross-Sectional StudiesEstoniaFemaleFractional Exhaled Nitric Oxide TestingHumansMaleMiddle AgedNitric OxideNitric OxideAllergic lung diseaseAsthmaAsthma EpidemiologyMicrobiotaRespiratory Function Test

Identifiers

PMID42315257
PMCPMC13289405

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Registered trials

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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.