Evidence map›Paper›PMID 33119074›Full record

ArticleJournal of Crohn's & colitis2021

The Impact of NOD2 Genetic Variants on the Gut Mycobiota in Crohn's Disease Patients in Remission and in Individuals Without Gastrointestinal Inflammation.

Andrew Nelson, Christopher J Stewart, Nicholas A Kennedy, John K Lodge, Mark Tremelling, UK IBD Genetics Consortium, Chris S Probert, Miles Parkes, John C Mansfield, Darren L Smith and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. Review
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  8. Review
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  12. Article
  13. The ProbioticFoods (Basel, Switzerland) · 2024
    Article
  14. A comprehensive guide to assess gut mycobiome and its role in pathogenesis and treatment of inflammatory bowel disease.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2024
    Review
  15. Article
  16. Article
  17. Metaproteomics of Gut Fungi in Gnotobiotic Mice.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  18. Review
  19. Metagenomic analysis of mycobiome in wild and captivity Sumatran orangutans (Journal of advanced veterinary and animal research · 2023
    Article
  20. 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

14 authors at 9 institutions in 2 countries.

Andrew NelsonFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.ORCID 0000-0001-6665-4929
Christopher J StewartTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-6033-338X
Nicholas A KennedyIBD Pharmacogenetics Group, University of Exeter, Exeter, UK.ORCID 0000-0003-4368-1961
John K LodgeFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.ORCID 0000-0001-6014-4952
Mark TremellingDepartment of Gastroenterology, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, UK.
UK IBD Genetics Consortium
Chris S ProbertInstitute of Translational Medicine, University of Liverpool, Liverpool, UK.ORCID 0000-0003-0477-6714
Miles ParkesDepartment of Gastroenterology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.ORCID 0000-0002-6467-0631
John C MansfieldTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0003-2490-7750
Darren L SmithFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.ORCID 0000-0003-4925-467X
Georgina L HoldGastrointestinal Research Group, University of Aberdeen, Aberdeen, UK.ORCID 0000-0001-7573-3397
Charlie W LeesInstitute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-0732-8215
Simon H BridgeFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.ORCID 0000-0002-6212-3255
Christopher A LambTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-7271-4956
Northumbria University · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBCambridge University Hospitals NHS Foundation Trust · GBNewcastle University · GBNorfolk and Norwich University Hospitals NHS Foundation Trust · GBUniversity of Aberdeen · GBUniversity of Exeter · GBUniversity of Liverpool · GBWestern General Hospital · GB

Funding

Medical Research Council MC_PC_19003Medical Research Council MR/M00533X/1Medical Research Council MR/S034919/1Wellcome Trust 097943
6 · The paper itself

Abstract

BACKGROUND AND

aimsHistorical and emerging data implicate fungi in Crohn's disease [CD] pathogenesis. However, a causal link between mycobiota, dysregulated immunity, and any impact of NOD2 variants remains elusive. This study aims to evaluate associations between NOD2 variants and faecal mycobiota in CD patients and non-CD subjects.

methodsFaecal samples were obtained from 34 CD patients [18 NOD2 mutant, 16 NOD2 wild-type] identified from the UK IBD Genetics Consortium. To avoid confounding influence of mucosal inflammation, CD patients were in clinical remission and had a faecal calprotectin <250 μg/g; 47 non-CD subjects were included as comparator groups, including 22 matched household [four NOD2 mutant] and 25 non-household subjects with known NOD2 genotype [14 NOD2 mutant] identified by the NIHR BioResource Cambridge. Faecal mycobiota composition was determined using internal transcribed spacer 1 [ITS1] sequencing and was compared with 16S rRNA gene sequences and volatile organic compounds.

resultsCD was associated with higher numbers of fungal observed taxonomic units [OTUs] [p = 0.033]. Principal coordinates analysis using Jaccard index [p = 0.018] and weighted Bray-Curtis dissimilarities [p = 0.01] showed Candida spp. clustered closer to CD patients whereas Cryptococcus spp. clustered closer to non-CD. In CD, we found higher relative abundance of Ascomycota [p = 0.001] and lower relative abundance Basidiomycota [p = 0.019] phyla. An inverse relationship was found between bacterial and fungal Shannon diversity in NOD2 wild-type which was independent of CD [r = -0.349; p = 0.029].

conclusionsThis study confirms compositional changes in the gut mycobiota in CD and provides evidence that fungi may play a role in CD pathogenesis. No NOD2 genotype-specific differences were observed in the faecal mycobiota.

Indexed as

AdultAgedCase-Control StudiesCrohn DiseaseFecesFemaleGastrointestinal MicrobiomeGenotypeHumansMaleMiddle AgedMutationMycosesNod2 Signaling Adaptor ProteinRemission InductionNod2 Signaling Adaptor ProteinCrohn’s diseasegut mycobiotaNOD2 genotype

Identifiers

PMID33119074
PMCPMC8095387
OpenAlexW3094829103

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.