Factors underlying the Long-term Efficacy of Faecal Microbiota Transplantation for Patients with Irritable Bowel Syndrome.

Alistipes Dysbiosis Holdemanella biformis Lactobacillus spp fatigue

Journal

Microbes and infection
ISSN: 1769-714X
Titre abrégé: Microbes Infect
Pays: France
ID NLM: 100883508

Informations de publication

Date de publication:
04 Jun 2024
Historique:
received: 17 01 2024
revised: 24 05 2024
accepted: 30 05 2024
medline: 7 6 2024
pubmed: 7 6 2024
entrez: 6 6 2024
Statut: aheadofprint

Résumé

The long-term effects of the transplant dose, its administration route and repeated faecal microbiota transplantation (FMT) on the outcomes of FMT for patients with irritable bowel syndrome (IBS) are unknown. This study included 171 patients (125 females and 46 males): 90 g of donor feces was administered into the large intestine (LI) in 58, into the small intestine (SI) in 57, and into the SI twice (repeated SI) in 56. The patients provided a fecal sample and completed five questionnaires at the baseline and at 2 years after FMT. Fecal bacteria and the dysbiosis index were analyzed using 16S rRNA gene PCR DNA amplification/probe. The response rates at 2 years after FMT were 47.2%, 80.9%, and 76.6% in the LI, SI, and repeated-SI groups, respectively. The response rate was significantly higher in the SI and repeated SI groups than in the LI group. IBS symptoms at 2 years after FMT were less severe in the SI and repeated-SI groups than in the LI group. Fluorescent signals of several bacteria were significantly correlated with IBS symptoms and fatigue after FMT. No long-term adverse events were observed. In conclusion, administering the transplant to the SI increased the long-term response rate and reduced IBS symptom severity compared with administering it to the LI, and led to the long-term colonization of beneficial bacteria. There was no long-term difference between one and two FMT procedures. (www.clinicaltrials.gov: NCT04236843).

Identifiants

pubmed: 38843950
pii: S1286-4579(24)00108-4
doi: 10.1016/j.micinf.2024.105372
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04236843']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105372

Informations de copyright

Copyright © 2024. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of Competing Interest M.E.S and JGH have nothing to disclose. OHG has received speaker honoraria from Bracco, GE Healthcare, Takeda AS, Ferring AS, Allergan, and Janssen-Cilag. He has served as consultant for Bracco, GE Healthcare, Takeda and Samsung.

Auteurs

Magdy El-Salhy (M)

Department of Medicine, Stord Hospital, Stord, Norway; Department of Clinical Medicine and Department of Gastroenterology, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway. Electronic address: magdy.elsalhy@sklbb.no.

Odd Helge Gilja (OH)

Department of Clinical Medicine and Department of Gastroenterology, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway.

Jan Gunnar Hatlebakk (JG)

Department of Clinical Medicine and Department of Gastroenterology, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway.

Classifications MeSH