Evidence mapPaperPMID 38836628Full record

Trial reportJournal of Crohn's & colitis2024

Gut Microbial Species and Endotypes Associate with Remission in Ulcerative Colitis Patients Treated with Anti-TNF or Anti-integrin Therapy.

Fiona B Tamburini, Anupriya Tripathi, Maxwell P Gold, Julianne C Yang, Tommaso Biancalani, Jacqueline M McBride, Mary E Keir, Gardenia Study Group

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of Crohn's & colitis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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.

Fiona B TamburiniHuman Pathobiology & OMNI Reverse Translation, Genentech, South San Francisco, CA, USA.
Anupriya TripathiPrescient Design, Genentech, South San Francisco, CA, USA.
Maxwell P GoldBiological Research & AI Development, Genentech, South San Francisco, CA, USA.
Julianne C YangVatche and Tamar Manoukian Division of Digestive Diseases, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
Tommaso BiancalaniBiological Research & AI Development, Genentech, South San Francisco, CA, USA.
Jacqueline M McBrideTranslational Medicine OMNI-Biomarker Development, Genentech, South San Francisco, CA, USA.
Mary E KeirHuman Pathobiology & OMNI Reverse Translation, Genentech, South San Francisco, CA, USA.
Gardenia Study GroupHuman Pathobiology & OMNI Reverse Translation, Genentech, South San Francisco, CA, USA.

Funding

Genentech
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe gut microbiota contributes to aberrant inflammation in inflammatory bowel disease, but the bacterial factors causing or exacerbating inflammation are not fully understood. Further, the predictive or prognostic value of gut microbial biomarkers for remission in response to biologic therapy is unclear.

methodsWe perform whole metagenomic sequencing of 550 stool samples from 287 ulcerative colitis patients from a large, phase 3, head-to-head study of infliximab and etrolizumab.

resultsWe identify several bacterial species in baseline and/or post-treatment samples that associate with clinical remission. These include previously described associations [Faecalibacterium prausnitzii_F] as well as new associations with remission to biologic therapy [Flavonifractor plautii]. We build multivariate models and find that gut microbial species are better predictors for remission than clinical variables alone. Finally, we describe patient groups that differ in microbiome composition and remission rate after induction therapy, suggesting the potential utility of microbiome-based endotyping.

conclusionsIn this large study of ulcerative colitis patients, we show that few individual species associate strongly with clinical remission, but multivariate models including microbiome can predict clinical remission and have better predictive power compared with clinical data alone.

Indexed as

Antibodies, Monoclonal, HumanizedColitis, UlcerativeGastrointestinal MicrobiomeInfliximabRemission InductionTumor Necrosis Factor InhibitorsAdultFecesFemaleGastrointestinal AgentsHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedetrolizumabGastrointestinal AgentsInfliximabTumor Necrosis Factor Inhibitorsbiologic therapyinflammatory bowel diseaseMicrobiome

Identifiers

PMID38836628
PMCPMC11532613

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.