Evidence map›Paper›PMID 42832303›Full record

Trial reportRheumatology (Oxford, England)2026

Efficacy and safety of probiotic supplementation in PsA-a randomized controlled trial.

Philipp Bosch, Angelika Lackner, Barbara Dreo, Johannes Fessler, Florentine Moazedi-Fürst, Rusmir Husic, Joana Séneca, Andreas Haidmayer, Vanessa Stadlbauer, Anirudh Subramanian Muralikrishnan and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Philipp BoschDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0002-6783-6422
Angelika LacknerDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0002-2036-9564
Barbara DreoDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0003-3937-9030
Johannes FesslerDivision of Immunology, Otto Loewi research Center, Medical University of Graz, Graz, Austria.ORCID 0000-0002-8841-3795
Florentine Moazedi-FürstDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0002-2720-8261
Rusmir HusicDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0001-5435-6967
Joana SénecaJoint Microbiome Facility, University of Vienna, Vienna, Austria.ORCID 0000-0003-3951-3674
Andreas HaidmayerDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.
Vanessa StadlbauerDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0001-5508-8271
Anirudh Subramanian MuralikrishnanDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0001-7102-9968
Jens ThielDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0001-7582-1514
Martin StradnerDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID 0000-0002-7884-6626

Funding

Austrian Research Promotion Agency (FFG)Federal Ministry of Science, Research and Economy (BMWFW)Federal Ministry of Transport, Innovation and Technology (BMVIT)K1 COMET Competence Center CBmedLand Steiermark
6 · The paper itself

Abstract

objectivesTo evaluate the clinical efficacy and safety of a multispecies probiotic in patients with PsA in moderate disease activity.

methodsIn this single-centre, randomized, double-blind, placebo-controlled trial (RCT), 66 PsA patients with moderate disease activity (Psoriatic Arthritis Disease Activity Score [PASDAS] > 3.2 to <5.4) on stable immunomodulatory therapy were randomized 1:1 to receive either a multispecies (Lactobacillus, Bifidobacterium) probiotic or placebo for 12 weeks. The primary outcome was treatment response at week 12, defined as achieving low disease activity or remission (PASDAS ≤3.2) without treatment change. Secondary outcomes included gut permeability markers, immune cell and microbiome composition. Analyses were conducted per a modified intention-to-treat (only complete cases for primary outcome), with sensitivity analyses using multiple imputation, per-protocol datasets and qPCR-based detection of the probiotic strains in stool (adherence).

resultsFifty-six participants were included in the main analysis. Thirteen (43%) participants in the probiotic group and 17 (65%) in the placebo group achieved the primary outcome (P = 0.167). The corresponding odds ratio was 0.4 (95% CI 0.13-1.18). Patient-reported pain and global assessment were the main PASDAS components improving over time, with no between-group differences. No differences were observed in secondary clinical outcomes, gut permeability markers (zonulin, calprotectin, alpha-1-antitrypsin), immune cell profiles or stool microbiome composition between the groups at week 12. No serious adverse events related to the study product were reported.

conclusionIn this first RCT investigating probiotic supplementation in PsA, probiotic treatment did not show superiority over placebo in achieving treatment response, or altering gut microbiome, or permeability.

Indexed as

Arthritis, PsoriaticProbioticsAdultBifidobacteriumDouble-Blind MethodFecesFemaleGastrointestinal MicrobiomeHumansLactobacillusMaleMiddle AgedSeverity of Illness IndexTreatment Outcomedisease activitymicrobiomeprobioticsPsArandomized controlled trials

Identifiers

PMID42832303
PMCPMC13656753

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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.