Evidence map›Paper›PMID 32060060›Full record

ArticleThe European respiratory journal2020

Dissimilarity of the gut-lung axis and dysbiosis of the lower airways in ventilated preterm infants.

David Gallacher, Emma Mitchell, Dagmar Alber, Richard Wach, Nigel Klein, Julian R Marchesi, Sailesh Kotecha

Open access · hybridAbstract read
In one paragraph

Article in The European respiratory journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 5% of its field
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

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Trial
  3. The gut-lung axis in early life: microbiome-associated mechanisms and clinical relevance.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  4. Article
  5. [A prospective cohort study of gut microbiota changes in very preterm infants with bronchopulmonary dysplasia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Observational
  10. Gut-X axis.iMeta · 2025
    Review
  11. The neonate respiratory microbiome.Acta physiologica (Oxford, England) · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. The impact of gut microbiota on morbidities in preterm infants.The Kaohsiung journal of medical sciences · 2024
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

David GallacherDept of Child Health, School of Medicine, Cardiff University, Cardiff, UK.
Emma MitchellDept of Child Health, School of Medicine, Cardiff University, Cardiff, UK.
Dagmar AlberInstitute of Child Health, University College London, London, UK.
Richard WachNeonatal Unit, North Bristol NHS Trust, Bristol, UK.
Nigel KleinInstitute of Child Health, University College London, London, UK.
Julian R MarchesiSchool of Biosciences, Cardiff University, Cardiff, UK.
Sailesh KotechaDept of Child Health, School of Medicine, Cardiff University, Cardiff, UK kotechaS@cardiff.ac.uk.
Cardiff University · GBUniversity College London · GBImperial College London · GBNorth Bristol NHS Trust · GB

Funding

Medical Research Council MR/M022552/1
6 · The paper itself

Abstract

backgroundChronic lung disease of prematurity (CLD), also called bronchopulmonary dysplasia, is a major consequence of preterm birth, but the role of the microbiome in its development remains unclear. Therefore, we assessed the progression of the bacterial community in ventilated preterm infants over time in the upper and lower airways, and assessed the gut-lung axis by comparing bacterial communities in the upper and lower airways with stool findings. Finally, we assessed whether the bacterial communities were associated with lung inflammation to suggest dysbiosis.

methodsWe serially sampled multiple anatomical sites including the upper airway (nasopharyngeal aspirates), lower airways (tracheal aspirate fluid and bronchoalveolar lavage fluid) and the gut (stool) of ventilated preterm-born infants. Bacterial DNA load was measured in all samples and sequenced using the V3-V4 region of the 16S rRNA gene.

resultsFrom 1102 (539 nasopharyngeal aspirates, 276 tracheal aspirate fluid, 89 bronchoalveolar lavage, 198 stool) samples from 55 preterm infants, 352 (32%) amplified suitably for 16S RNA gene sequencing. Bacterial load was low at birth and quickly increased with time, but was associated with predominant operational taxonomic units (OTUs) in all sample types. There was dissimilarity in bacterial communities between the upper and lower airways and the gut, with a separate dysbiotic inflammatory process occurring in the lower airways of infants. Individual OTUs were associated with increased inflammatory markers.

conclusionsTaken together, these findings suggest that targeted treatment of the predominant organisms, including those not routinely treated, such as

Indexed as

DysbiosisBacteriaBronchoalveolar Lavage FluidBronchopulmonary DysplasiaDNA, BacterialFecesFemaleGastrointestinal MicrobiomeHumansInfant, NewbornInfant, PrematureLungMaleRNA, Ribosomal, 16STracheaDNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID32060060
PMCPMC7236867
OpenAlexW3006626248

What OpenQuestion holds

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LicenceCC BY
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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.