Evidence map›Paper›PMID 35459927›Full record

ArticleScientific reports2022

The gut fungal and bacterial microbiota in pediatric patients with inflammatory bowel disease introduced to treatment with anti-tumor necrosis factor-α.

Rebecka Ventin-Holmberg, Miikka Höyhtyä, Schahzad Saqib, Katri Korpela, Anne Nikkonen, Anne Salonen, Willem M de Vos, Kaija-Leena Kolho

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Increased gutThe journal of allergy and clinical immunology. Global · 2026
    Article
  5. [Research progress on biologics and therapeutic drug monitoring in pediatric inflammatory bowel disease].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Role ofWorld journal of gastroenterology · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Human microbiome collection.Scientific reports · 2023
    Article
  18. Review
  19. 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

8 authors at 2 institutions in 2 countries.

Rebecka Ventin-Holmberg *Translational Immunology Research Program, University of Helsinki, Helsinki, Finland.
Miikka Höyhtyä *Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Schahzad SaqibFaculty of Medicine, Human Microbiome Research Program, University of Helsinki, Helsinki, Finland.
Katri KorpelaFaculty of Medicine, Human Microbiome Research Program, University of Helsinki, Helsinki, Finland.
Anne NikkonenUniversity of Helsinki and Children's Hospital, Helsinki University Hospital, University of Helsinki, Helsinki, Finland, Stenbäckinkatu 11 (Skidicum).
Anne SalonenFaculty of Medicine, Human Microbiome Research Program, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-6960-7447
Willem M de VosFaculty of Medicine, Human Microbiome Research Program, University of Helsinki, Helsinki, Finland.
Kaija-Leena KolhoTranslational Immunology Research Program, University of Helsinki, Helsinki, Finland. kaija-leena.kolho@helsinki.fi.
University of Helsinki · FITampere University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric inflammatory bowel disease (PIBD) is a globally increasing chronic inflammatory disease associated with an imbalanced intestinal microbiota and treated with several treatment options, including anti-tumor necrosis factor alpha (TNF-α), such as infliximab (IFX). Up to half of the patients do not respond to the drug and there are no methods for response prediction. Our aim was to predict IFX response from the gut microbiota composition since this is largely unexplored in PIBD. The gut microbiota of 30 PIBD patients receiving IFX was studied by MiSeq sequencing targeting 16S and ITS region from fecal samples collected before IFX and two and six weeks after the start of treatment. The response to IFX induction was determined by fecal calprotectin value < 100 µg/g at week six. The bacterial microbiota differed significantly between response groups, with higher relative abundance of butyrate-producing bacteria in responders compared to non-responders at baseline, validated by high predictive power (area under curve = 0.892) for baseline Ruminococcus and calprotectin. Additionally, non-responders had higher abundance of Candida, while responders had higher abundance of Saccharomyces at the end of the study. The gut microbiota composition in PIBD patients could predict response to IFX treatment in the future.

Indexed as

Crohn DiseaseGastrointestinal MicrobiomeInflammatory Bowel DiseasesTumor Necrosis Factor-alphaBacteriaChildHumansInfliximabLeukocyte L1 Antigen ComplexInfliximabLeukocyte L1 Antigen ComplexTumor Necrosis Factor-alpha

Identifiers

PMID35459927
PMCPMC9033777
OpenAlexW4224293549

What Socratic 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 Socratic graph.