Evidence map›Paper›PMID 36963782›Full record

ArticleRMD open2023

Characterisation of gut microbiota composition in patients with axial spondyloarthritis and its modulation by TNF inhibitor treatment.

Marie Vallier, Béatrice Segurens, Elise Larsonneur, Vincent Meyer, Stephanie Ferreira, Christophe Caloustian, Jean-François Deleuze, Maxime Dougados, Mathias Chamaillard, Corinne Miceli-Richard

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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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

10 authors at 5 institutions in 2 countries.

Marie Vallier *Max Planck Institute for Evolutionary Biology, Plon, Germany.
Béatrice Segurens *CEA CNRGH, Evry, France.
Elise LarsonneurCEA CNRGH, Evry, France.
Vincent MeyerCEA CNRGH, Evry, France.
Stephanie FerreiraGenoscreen, Lille, France.
Christophe CaloustianCEA CNRGH, Evry, France.
Jean-François DeleuzeCEA CNRGH, Evry, France.
Maxime DougadosHopital Cochin, Rheumatology, Université Paris Descartes Faculté de Médecine, Paris, France.ORCID 0000-0003-3009-6229
Mathias ChamaillardINSERM U1003, Laboratory of Cell Physiology, Villeneuve-d'Ascq, France.
Corinne Miceli-RichardRheumatology, Universite Paris Descartes, Paris, France corinne.miceli@aphp.fr.ORCID 0000-0002-3009-3637
Commissariat à l'Énergie Atomique et aux Énergies Alternatives · FRDélégation Paris 5 · FRInserm · FRMax Planck Institute for Evolutionary Biology · DEUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess whether gut microbiota composition is associated with patient characteristics and may have predictive value on the response to TNF inhibitor (TNFi) treatment in axial spondyloarthritis (AxSpA).

methodsThe study involved 61 patients fulfilling the Assessment of SpondyloArthritis International Society classification criteria for AxSpA. All patients had active disease despite non-steroidal anti-inflammatory drugs intake and were eligible for treatment with a TNFi. At baseline, the mean Ankylosing Spondylitis Disease Activity Score was 2.9±1 and mean C reactive protein (CRP) level 9.7±11.4 mg/L. Bacterial 16S ribosomal RNA gene sequencing was performed on stool samples collected at baseline (month 0 (M0)) and 3 months after TNFi initiation (month 3 (M3)). Alpha and beta diversity metrics were calculated on the relative abundance of core operational taxonomic units (OTUs).

resultsThe HLA-B27 status affected at least in part the global composition of faecal microbiota at M0 as well as the abundance/prevalence of several anaerobic bacteria in the families

conclusionsSeveral SpA patients' characteristics modulate the composition of gut microbiota as did TNFi treatment. Moreover, the abundance/prevalence of seven OTUs at baseline may be used as a novel non-invasive index that predicts the response to TNFi with greater accuracy than HLA-B27 status, CRP level and measures of disease activity.

Indexed as

Gastrointestinal MicrobiomeSpondylitis, AnkylosingHLA-B27 AntigenHumansTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsHLA-B27 AntigenTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorsinflammationspondylitis, ankylosingtherapeuticstumor necrosis factor inhibitors

Identifiers

PMID36963782
PMCPMC10040062
OpenAlexW4360843953

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Registered trials

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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.