Evidence map›Paper›PMID 39694676›Full record

Observational studyBMJ open respiratory research2024

Bile acids in the lower airways is associated with airway microbiota changes in chronic obstructive pulmonary disease: an observational study.

Jose A Caparros-Martin, Montserrat Saladié, S Patricia Agudelo-Romero, Kristy S Nichol, F Jerry Reen, Yuben P Moodley, Siobhain Mulrennan, Stephen Stick, Peter A B Wark, Fergal O'Gara

Abstract readObservational Study
In one paragraph

Observational study in BMJ open respiratory research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

10 authors.

Jose A Caparros-Martin *Wal-yan Respiratory Research Centre, The Kids Research Institute Australia, Nedlands, Western Australia, Australia.ORCID 0000-0003-1214-4952
Montserrat Saladié *Curtin Health Innovation Research Institute (CHIRI), Curtin University, Bentley, Western Australia, Australia.
S Patricia Agudelo-RomeroWal-yan Respiratory Research Centre, The Kids Research Institute Australia, Nedlands, Western Australia, Australia.
Kristy S NicholImmune Health Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, Australia.
F Jerry ReenSchool of Microbiology, University College Cork, Cork, Ireland.
Yuben P MoodleyCentre for Respiratory Health, School of Biomedical Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Siobhain MulrennanInstitute of Respiratory Health and Medical School, The University of Western Australia, Nedlands, Western Australia, Australia.ORCID 0000-0002-1766-2612
Stephen StickThe University of Western Australia, Perth, Western Australia, Australia.
Peter A B WarkFaculty of Medicine Nursing and Health Sciences, Monash University, Prahran, Victoria, Australia.ORCID 0000-0001-5676-6126
Fergal O'GaraWal-yan Respiratory Research Centre, The Kids Research Institute Australia, Nedlands, Western Australia, Australia f.ogara@ucc.ie.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic obstructive pulmonary disease (COPD) is a complex disorder with a high degree of interindividual variability. Gastrointestinal dysfunction is common in patients with COPD and has been proposed to influence the clinical progression of the disease. Using the presence of bile acid(s) (BA) in bronchoalveolar lavage (BAL) fluid as a marker of gastric aspiration, we evaluated the relationships between BAs, clinical outcomes and bacterial lung colonisation.

methodsWe used BAL specimens from a cohort of patients with COPD and healthy controls. BAs were profiled and quantified in BAL supernatants using mass spectrometry. Microbial DNA was extracted from BAL pellets and quantified using quantitative PCR. We profiled the BAL microbiota using an amplicon sequencing approach targeting the V3-V4 region of the 16S rRNA gene.

resultsDetection of BAs in BAL was more likely at the earliest clinical stages of COPD and was independent of the degree of airway obstruction. BAL specimens with BAs demonstrated higher bacterial biomass and lower diversity. Likewise, the odds of recovering bacterial cultures from BAL were higher if BAs were also detected. Detection of BAs in BAL was not associated with either inflammatory markers or clinical outcomes. We also observed different bacterial community types in BAL, which were associated with different clinical groups, levels of inflammatory markers and the degree of airway obstruction.

conclusionDetection of BAs in BAL was associated with alterations in the airway bacterial communities. Further studies are needed to evaluate whether BAs in BAL can be used to stratify patients and predict disease progression trajectories.

Indexed as

Bile Acids and SaltsBronchoalveolar Lavage FluidMicrobiotaPulmonary Disease, Chronic ObstructiveAgedCase-Control StudiesFemaleHumansLungMaleMiddle AgedRNA, Ribosomal, 16SBile Acids and SaltsRNA, Ribosomal, 16SCOPD PathologyPulmonary Disease, Chronic Obstructive

Identifiers

PMID39694676
PMCPMC11667286

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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.