<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>71</volume><submitter>Bruggeman A</submitter><funding>Biocodex Microbiota Foundation</funding><funding>FWO</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Dysregulation of the gut microbiome has been implicated in Parkinson's disease (PD). This study aimed to evaluate the clinical effects and safety of a single faecal microbiota transplantation (FMT) in patients with early-stage PD.&lt;h4>Methods&lt;/h4>The GUT-PARFECT trial, a single-centre randomised, double-blind, placebo-controlled trial was conducted at Ghent University Hospital between December 01, 2020 and December 12, 2022. Participants (aged 50-65 years, Hoehn and Yahr stage 2) were randomly assigned to receive nasojejunal FMT with either healthy donor stool or their own stool. Computer-generated randomisation was done in a 1:1 ratio through permutated-block scheduling. Treatment allocation was concealed for participants and investigators. The primary outcome measure at 12 months was the change in the Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) motor score obtained during off-medication evaluations. Intention-to-treat analysis was performed using a mixed model for repeated measures analysis. This completed trial is registered on ClinicalTrials.gov (NCT03808389).&lt;h4>Findings&lt;/h4>Between December 2020 and December 2021, FMT procedures were conducted on 46 patients with PD: 22 in the healthy donor group and 24 in the placebo group. Clinical evaluations were performed at baseline, 3, 6, and 12 months post-FMT. Full data analysis was possible for 21 participants in the healthy donor group and 22 in the placebo group. After 12 months, the MDS-UPDRS motor score significantly improved by a mean of 5.8 points (95% CI -11.4 to -0.2) in the healthy donor group and by 2.7 points (-8.3 to 2.9) in the placebo group (p = 0.0235). Adverse events were limited to temporary abdominal discomfort.&lt;h4>Interpretation&lt;/h4>Our findings suggested a single FMT induced mild, but long-lasting beneficial effects on motor symptoms in patients with early-stage PD. These findings highlight the potential of modulating the gut microbiome as a therapeutic approach and warrant a further exploration of FMT in larger cohorts of patients with PD in various disease stages.&lt;h4>Funding&lt;/h4>Flemish PD patient organizations (VPL and Parkili), Research Foundation Flanders (FWO), Biocodex Microbiota Foundation.</pubmed_abstract><journal>EClinicalMedicine</journal><pagination>102563</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11056595</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety and efficacy of faecal microbiota transplantation in patients with mild to moderate Parkinson's disease (GUT-PARFECT): a double-blind, placebo-controlled, randomised, phase 2 trial.</pubmed_title><pmcid>PMC11056595</pmcid><pubmed_authors>Santens P</pubmed_authors><pubmed_authors>Vuylsteke M</pubmed_authors><pubmed_authors>Bruggeman A</pubmed_authors><pubmed_authors>Vandendriessche C</pubmed_authors><pubmed_authors>Tate DJ</pubmed_authors><pubmed_authors>Hamerlinck H</pubmed_authors><pubmed_authors>Raes J</pubmed_authors><pubmed_authors>Verhasselt B</pubmed_authors><pubmed_authors>Laukens D</pubmed_authors><pubmed_authors>Devolder L</pubmed_authors><pubmed_authors>Vandenbroucke RE</pubmed_authors><pubmed_authors>De Looze D</pubmed_authors><pubmed_authors>De Commer L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and efficacy of faecal microbiota transplantation in patients with mild to moderate Parkinson's disease (GUT-PARFECT): a double-blind, placebo-controlled, randomised, phase 2 trial.</name><description>&lt;h4>Background&lt;/h4>Dysregulation of the gut microbiome has been implicated in Parkinson's disease (PD). This study aimed to evaluate the clinical effects and safety of a single faecal microbiota transplantation (FMT) in patients with early-stage PD.&lt;h4>Methods&lt;/h4>The GUT-PARFECT trial, a single-centre randomised, double-blind, placebo-controlled trial was conducted at Ghent University Hospital between December 01, 2020 and December 12, 2022. Participants (aged 50-65 years, Hoehn and Yahr stage 2) were randomly assigned to receive nasojejunal FMT with either healthy donor stool or their own stool. Computer-generated randomisation was done in a 1:1 ratio through permutated-block scheduling. Treatment allocation was concealed for participants and investigators. The primary outcome measure at 12 months was the change in the Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) motor score obtained during off-medication evaluations. Intention-to-treat analysis was performed using a mixed model for repeated measures analysis. This completed trial is registered on ClinicalTrials.gov (NCT03808389).&lt;h4>Findings&lt;/h4>Between December 2020 and December 2021, FMT procedures were conducted on 46 patients with PD: 22 in the healthy donor group and 24 in the placebo group. Clinical evaluations were performed at baseline, 3, 6, and 12 months post-FMT. Full data analysis was possible for 21 participants in the healthy donor group and 22 in the placebo group. After 12 months, the MDS-UPDRS motor score significantly improved by a mean of 5.8 points (95% CI -11.4 to -0.2) in the healthy donor group and by 2.7 points (-8.3 to 2.9) in the placebo group (p = 0.0235). Adverse events were limited to temporary abdominal discomfort.&lt;h4>Interpretation&lt;/h4>Our findings suggested a single FMT induced mild, but long-lasting beneficial effects on motor symptoms in patients with early-stage PD. These findings highlight the potential of modulating the gut microbiome as a therapeutic approach and warrant a further exploration of FMT in larger cohorts of patients with PD in various disease stages.&lt;h4>Funding&lt;/h4>Flemish PD patient organizations (VPL and Parkili), Research Foundation Flanders (FWO), Biocodex Microbiota Foundation.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-04-30T21:21:56.423Z</modification><creation>2026-04-07T16:21:23.963Z</creation></dates><accession>S-EPMC11056595</accession><cross_references><pubmed>38686220</pubmed><doi>10.1016/j.eclinm.2024.102563</doi></cross_references></HashMap>