Evidence map›Paper›PMID 41918987›Full record

ArticleGut microbes reports2026

Comparison of microbiota profiles of fecal samples, rectal swabs and mucosal biopsies in patients with inflammatory bowel disease.

Tessel M van Rossen, Kim van den Hoek, Thomas Groot, Rob H Creemers, Maysa L M van Doorn-Schepens, Emma M van Andel, Matthijs E Grasman, Nanne K H de Boer, Gerd Bouma, Andries E Budding and 2 more

Abstract read
In one paragraph

Article in Gut microbes reports, 2026. 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. 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

12 authors.

Tessel M van RossenDepartment of Medical Microbiology & Infection Control, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-8945-134X
Kim van den HoekDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0009-0002-7520-5783
Thomas GrootInbiome, Amsterdam, The Netherlands.
Rob H CreemersDepartment of Gastroenterology & Hepatology, Zuyderland Medical Centre, Sittard, the Netherlands.ORCID https://orcid.org/0000-0002-5046-2030
Maysa L M van Doorn-SchepensDepartment of Medical Microbiology, OLVG Laboratory, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-1612-699X
Emma M van AndelDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-5462-1545
Matthijs E GrasmanDepartment of Gastroenterology & Hepatology, Northwest Clinics, Alkmaar, The Netherlands.ORCID https://orcid.org/0000-0001-5675-714X
Nanne K H de BoerDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-8357-9887
Gerd BoumaDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0084-5092
Andries E BuddingInbiome, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-5128-5411
Paul H M SavelkoulDepartment of Medical Microbiology & Infection Control, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-3527-6950
Adriaan A van BodegravenDepartment of Gastroenterology & Hepatology, Zuyderland Medical Centre, Sittard, the Netherlands.ORCID https://orcid.org/0000-0003-2636-303X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gut microbiota changes are associated with inflammatory bowel disease (IBD). In most microbiota studies, intestinal microbiota composition is examined in fecal samples, but their representativeness of mucosa-associated microbiota at inflammation sites remains unclear. This study aimed to explore microbiota composition in different IBD sample types and assess their interchangeability for research and clinical use. Multicentre, prospective, observational study including 200 IBD patients (518 samples). We compared microbiota profiles from faeces, rectal swabs and mucosal biopsies from different colon sites. Microbiota composition was analyzed by Molecular Culture™, a bacterial profiling technique based on species-specific differences in the 16S-23S interspace region of bacterial ribosomal DNA, with taxonomic classification by phylum-specific fluorescent PCR primers. Fecal samples and rectal swabs contained a higher microbial diversity and abundance than colonic biopsies. Microbiota compositions of different sample types within an individual happened to be quite dissimilar (median cosine similarities 0.43-0.53). Within individuals, biopsies from the same location in the colon were just as similar as biopsies from different locations (median cosine similarities 0.85 vs. 0.82, respectively). Fecal samples, rectal swabs and colonic biopsies of an individual show distinct microbiota profiles and should not be used interchangeably in microbiota studies or clinical applications.

Indexed as

inflammatory bowel diseaseMicrobiota compositionmicrobiota profilingsample typessampling methods

Identifiers

PMID41918987
PMCPMC13034629

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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.