Evidence map›Paper›PMID 41791848›Full record

Observational studyGut2026

Gut microbiome signatures in colorectal neoplasia: a cross-sectional study across neoplasia stages and subtypes.

Panayiotis Louca, Sarah Manning, Eleanor Hackney, Linda Sharp, Mark A Hull, Sara Koo, Gregory R Young, Guy S Taylor, Yashvee Dunneram, Suparna Mitra and 8 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Gut, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Observational
  2. Article
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

18 authors.

Panayiotis Louca *Human Nutrition & Exercise Research Centre, Centre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Newcastle University, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0001-5956-1433
Sarah Manning *Department of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK.ORCID http://orcid.org/0000-0002-7105-8109
Eleanor HackneyDepartment of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK.
Linda SharpPopulation Health Sciences Institute, Newcastle University Centre for Cancer, Faculty of Medical Sciences, Newcastle University, Newcastle University Centre for Cancer, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0001-9515-1722
Mark A HullLeeds Institute of Medical Research, University of Leeds, St James's University Hospital, Leeds, UK.ORCID http://orcid.org/0000-0001-7414-1576
Sara KooDepartment of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK.
Gregory R YoungTranslational and Clinical Research Institute, Newcastle University, Newcastle University Faculty of Medical Sciences, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0001-5342-1421
Guy S TaylorPopulation Health Sciences Institute, Newcastle University Centre for Cancer, Faculty of Medical Sciences, Newcastle University, Newcastle University Centre for Cancer, Newcastle upon Tyne, UK.
Yashvee DunneramHuman Nutrition & Exercise Research Centre, Centre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Newcastle University, Newcastle upon Tyne, UK.
Suparna MitraLeeds Institute of Medical Research, University of Leeds, St James's University Hospital, Leeds, UK.ORCID http://orcid.org/0000-0002-9378-1496
James S HamptonDepartment of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK.
Christina DobsonHuman Nutrition & Exercise Research Centre, Centre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Newcastle University, Newcastle upon Tyne, UK.
Laura J NeilsonDepartment of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK.
Caroline AddisonNorth East Hub, Bowel Cancer Screening Programme, Gateshead, UK.
Emad M El-OmarMicrobiome Research Centre, St George & Sutherland Clinical Campuses, School of Clinical Medicine, Faculty of Medicine & Health, University of New South Wales, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0002-0011-3924
COLO-COHORT research team
Christopher J StewartTranslational and Clinical Research Institute, Newcastle University, Newcastle University Faculty of Medical Sciences, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0002-6033-338X
Colin J ReesDepartment of Gastroenterology, South Tyneside and Sunderland NHS Foundation Trust, South Tyneside District Hospital, South Tyneside and Sunderland NHS Foundation Trust, South Shields, UK Colin.Rees@newcastle.ac.uk.ORCID http://orcid.org/0000-0003-3050-8473

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile colorectal cancer (CRC) has been linked to the gut microbiome, it remains unclear whether specific microbial signatures are detectable in precursor lesions such as adenomatous polyps, serrated lesions or sessile serrated lesions.

objectiveTo assess gut microbiome taxonomic and functional associations with colorectal neoplasia presence, severity (non-advanced, advanced and CRC) and subtype and evaluate predictive potential in high-risk neoplasia.

designAnalysed cross-sectional stool metagenomes (pre-colonoscopy) from 1762 participants (97% White British) undergoing colonoscopy in the multicentre COLO-COHORT study. Neoplasia was classified per British Society of Gastroenterology surveillance guidelines. Linear mixed-effects models and random forest classifiers assessed taxonomic and functional associations, adjusting for dietary, clinical and lifestyle covariates.

resultsGut microbiome composition differences between individuals with and without neoplasia were statistically significant but minimal (R

conclusionThis large prospective cross-sectional study found weak and inconsistent associations between the gut microbiome and premalignant colorectal neoplasia, with no robust microbial signatures. Findings suggest that previously reported microbial shifts may emerge later in disease progression, potentially as a consequence rather than a cause of CRC. Longitudinal, multiomic studies disentangling temporal and causal pathways between the gut microbiome and neoplasia are required.

Indexed as

Colorectal NeoplasmsGastrointestinal MicrobiomeAgedColonoscopyCross-Sectional StudiesFecesFemaleHumansMaleMetagenomeMiddle AgedNeoplasm StagingCOLONIC ADENOMASCOLONOSCOPYCOLORECTAL NEOPLASIAMETAGENOMICS

Identifiers

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.