Evidence map›Paper›PMID 41392089›Full record

Trial reportNature communications2025

Encapsulated faecal microbiota transfer in young women with anorexia nervosa: an open-label feasibility pilot trial.

Brooke C Wilson, Ry Y Tweedie-Cullen, Benjamin B Albert, José G B Derraik, Daniel Ho, Marysia Depczynski, Christine Creagh, Taygen Edwards, Sucharita Gali, Hiran Thabrew and 2 more

Abstract readClinical Trial
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. 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

12 authors.

Brooke C WilsonLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0002-2213-542X
Ry Y Tweedie-CullenLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0003-0128-7181
Benjamin B AlbertLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0003-0498-3473
José G B DerraikDepartment of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0003-1226-1956
Daniel HoLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0002-3699-0419
Marysia DepczynskiLiggins Institute, University of Auckland, Auckland, New Zealand.
Christine CreaghLiggins Institute, University of Auckland, Auckland, New Zealand.
Taygen EdwardsLiggins Institute, University of Auckland, Auckland, New Zealand.
Sucharita GaliLiggins Institute, University of Auckland, Auckland, New Zealand.
Hiran ThabrewDepartment of Psychological Medicine, University of Auckland, Auckland, New Zealand.
Wayne S CutfieldLiggins Institute, University of Auckland, Auckland, New Zealand. w.cutfield@auckland.ac.nz.ORCID http://orcid.org/0000-0001-6107-3682
Justin M O'SullivanLiggins Institute, University of Auckland, Auckland, New Zealand. justin.osullivan@auckland.ac.nz.ORCID http://orcid.org/0000-0003-2927-450X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perturbations of the gut microbiome have been associated with anorexia nervosa (AN) suggesting microbiome-modulation treatments, like faecal microbiota transfer (FMT), may offer therapeutic benefits. This open-label feasibility pilot trial evaluated the tolerability and microbiological impact of encapsulated, multi-donor FMT in 18 young women with AN (Registration: ACTRN12621001504808). Participants completed clinical and microbiome assessments at enrolment (3 weeks pre-treatment), baseline, and 3, 6, and 12 weeks post-treatment. Fifteen participants completed FMT, and 11 completed the final follow-up. The primary outcome was the change in gut microbiome composition from baseline to 3 weeks compared with natural variation between enrolment and baseline. FMT produced a significantly greater shift post-treatment (mean ± SD Bray-Curtis dissimilarity 0.36 ± 0.11; p = 0.0007), with participants gaining 38 ± 16 new species. Donor-derived strains comprised 41 ± 12% of the microbiome at 3 weeks, with engraftment persisting at 6 and 12 weeks. FMT was generally well tolerated; adverse events were mostly mild to moderate and overlapped with typical AN symptomatology. Monitoring of clinical outcomes supported the safety profile and suggested potential improvements in anxiety and metabolic parameters; however, the small sample and absence of a control arm preclude safety and efficacy inference. Overall, these findings warrant further investigation through randomised controlled trials in AN.

Indexed as

Anorexia NervosaFecal Microbiota TransplantationGastrointestinal MicrobiomeAdolescentAdultFeasibility StudiesFecesFemaleHumansPilot ProjectsTreatment OutcomeYoung Adult

Identifiers

PMID41392089
PMCPMC12808231

What OpenQuestion holds

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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.