Evidence map›Paper›PMID 38736752›Full record

ArticleFrontiers in cellular and infection microbiology2024

Gut microbiota composition in travellers is associated with faecal lipocalin-2, a mediator of gut inflammation.

Javier Gandasegui, Andrea Vergara, Pedro Fleitas, Elisa Rubio, Mariana Fernandez-Pittol, Cristian Aylagas, Míriam Alvarez, Noelia Zancada, Daniel Camprubí-Ferrer, Jordi Vila and 3 more

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Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

13 authors.

Javier GandaseguiBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Andrea VergaraBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Pedro FleitasBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Elisa RubioBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Mariana Fernandez-PittolDepartment of Clinical Microbiology, Biomedical Diagnostic Center (CDB), Hospital Clínic of Barcelona, University of Barcelona, Barcelona, Spain.
Cristian AylagasDepartment of Clinical Microbiology, Biomedical Diagnostic Center (CDB), Hospital Clínic of Barcelona, University of Barcelona, Barcelona, Spain.
Míriam AlvarezBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Noelia ZancadaDepartment of Clinical Microbiology, Biomedical Diagnostic Center (CDB), Hospital Clínic of Barcelona, University of Barcelona, Barcelona, Spain.
Daniel Camprubí-FerrerBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Jordi VilaBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
José MuñozBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Paula PetroneBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.
Climent Casals-PascualBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: We examined the gut microbiota of travellers returning from tropical areas with and without traveller's diarrhoea (TD) and its association with faecal lipocalin-2 (LCN2) levels. Methods: Participants were recruited at the Hospital Clinic of Barcelona, Spain, and a single stool sample was collected from each individual to perform the diagnostic of the etiological agent causing gastrointestinal symptoms as well as to measure levels of faecal LCN2 as a biomarker of gut inflammation. We also characterised the composition of the gut microbiota by sequencing the region V3-V4 from the 16S rRNA gene, and assessed its relation with the clinical presentation of TD and LCN2 levels using a combination of conventional statistical tests and unsupervised machine learning approaches. Results: Among 61 participants, 45 had TD, with 40% having identifiable etiological agents. Surprisingly, LCN2 levels were similar across groups, suggesting gut inflammation occurs without clinical TD symptoms. Differential abundance (DA) testing highlighted a microbial profile tied to high LCN2 levels, marked by increased Discussion: The findings suggest a correlation between gut microbiome and LCN2 levels during travel, emphasising the need for further research to discern the nature of this relationship.

Indexed as

DiarrheaFecesGastrointestinal MicrobiomeLipocalin-2AdultBacteriaBiomarkersFemaleHumansInflammationMaleMiddle AgedRNA, Ribosomal, 16SSpainTravelYoung AdultBiomarkersLCN2 protein, humanLipocalin-2RNA, Ribosomal, 16Sdiarrhoeainflammationlipocalin-2machine learningmicrobiometravel

Identifiers

PMID38736752
PMCPMC11082338

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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.