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Consecutive fecal microbiota transplantation for metabolic dysfunction-associated steatotic liver disease: a randomized controlled trial

  • Bas Groenewegen*
  • , Merel M. Ruissen
  • , Emily Crossette
  • , Rajita Menon
  • , Amanda L. Prince
  • , Jason M. Norman
  • , Bart E. P. B. Ballieux
  • , Hildo J. Lamb
  • , Elisabeth M. Terveer
  • , Josbert J. Keller
  • , Maarten E. Tushuizen
  • *Corresponding author for this work
  • Leiden University
  • Vedanta Biosciences, Inc.
  • Haaglanden Medisch Centrum

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The gut microbiota is increasingly considered a contributory factor in metabolic dysfunction-associated steatotic liver disease (MASLD). This double-blind RCT evaluated the effect of three consecutive fecal microbiota transplantations (FMT) on hepatic steatosis in MASLD. Twenty patients with MASLD were randomized (1:1) to receive allogeneic or autologous FMTs at weeks 0, 3, and 6, with follow-up through week 12. FMT material was derived from two donors. We assessed changes in hepatic steatosis (magnetic resonance imaging-derived proton density fat fraction (MRI-PDFF)), glucose tolerance (oral glucose tolerance test), liver biochemistry, and gut microbiota composition/engraftment. Change in MRI-PDFF from baseline to week 12 was not significantly different between groups (p = 0.50). Liver biochemistry and glucose tolerance also showed no significant overall changes. Patients’ stool microbiota exhibited high baseline alpha diversity and similar composition across treatment groups, diverging by week 12 (p = 0.02). Two microbial taxa belonging to the families Gastranaerophilaceae and Rikenellaceae were associated with triglyceride levels after FMT. No further microbiota signatures were associated with FMT-treatment or response. Donor microbiota engraftment appeared donor-specific, but not treatment- or response-specific. In conclusion, FMT did not significantly affect hepatic steatosis, glucose tolerance, liver biochemistry, or gut microbiota signatures. Future studies should consider including patients with low microbiota diversity. Dutch Trial Register: NL-OMON48776; Central Committee on Research Involving Human Subjects: NL66705.058.18; Clinicaltrials.gov: NCT04465032.
Original languageEnglish
Article number2541035
JournalGut microbes
Volume17
Issue number1
DOIs
Publication statusPublished - 31 Dec 2025
Externally publishedYes

Keywords

  • Fecal microbiota transplantation (FMT)
  • MRI-PDFF
  • NAFLD
  • glucose tolerance
  • gut microbiota
  • hepatic steatosis
  • insulin resistance
  • metabolic dysfunction-associated steatotic liver disease (MASLD)
  • microbiota diversity
  • microbiota engraftment

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