Michael Harrop
Well-known member
https://www.sciencedirect.com/science/article/pii/S0889159125003216
Donor:
Highlights
- The study was a single-center, randomized, placebo-controlled, double-blind clinical trial.
- All colonoscopy procedures were performed by an expert endoscopist, all scale assessments were performed by an expert dyskinesia physician, and medication doses for all patients were not adjusted throughout the trial.
- Fresh fecal microbiota was transplanted via colonoscopy within 5 h of collection, preserving the maximum diversity and activity of the microbiota.
- In addition to the improvement of motor symptoms in patients of Parkinson’s disease, we also found that FMT was beneficial on non-motor symptoms, including quality of life, defecation and mood.
- In addition to assessing PD symptom scales and changes in gut microbiota before and after FMT, we also examined fecal metabolomics and conducted correlation analyses.
Abstract
Objective
Growing evidence supports the efficacy and safety of fecal microbiota transplantation (FMT) in treating Parkinson’s disease (PD). Fecal microbiota are commonly transplanted via oral capsules, a nasojejunal tube, or colonoscopy, but freezing often decreases the diversity and viability of transplanted microbiota. This single-center, double-blind, randomized, placebo-controlled trial aims to explore the efficacy and safety of fresh FMT via colonoscopy in dealing with PD.
Methods
Thirty patients with mild-to-moderate PD (Hoehn-Yahr stage I-III) were randomly assigned into the FMT group (fresh FMT via colonoscopy) and placebo group (saline injection via colonoscopy) in a 1:1 ratio. Motor and non-motor symptoms, constipation, quality of life, cognitive function, emotional state and sleep quality were assessed using relevant scales. Fecal samples were harvested before and at 4, 8 and 12 weeks after treatment for metagenomic and metabolomics analyses.
Results
A total of 30 patients with mild-to-moderate PD were enrolled in the present study, involving 18 males and 12 females with a median age of 68 years, a median age of onset of 63.5 years, and a median disease duration of 3 years. At 12 weeks, scores of the UPDRS Ⅲ (group × time effect, B = − 8.80 [−13.79, −3.81]), PAC-QOL (group × time effect, B = − 29.67 [−45.35, −13.98]), UPDRS Ⅱ (group × time effect, B = − 5.07 [−8.85, −1.28]), NMSS (group × time effect, B = − 35.60 [−53.59, −17.61]), PDQ-39 (group × time effect, B = − 17.80 [−28.21, −7.39]), HAMA (group × time effect, B = − 1.66 [−2.92, −0.40]), and HAMD (group × time effect, B = − 1.33 [−2.49, −0.16]) were significantly reduced in the FMT group, while CSBM per week (group × time effect, B = 3.03 [1.42, 4.63]) and the Bristol Stool Scale score (group × time effect, B = 1.95 [0.12, 3.79]) significantly increased (all P < 0.05). Significant alterations were seen in the gut microbiota and fecal metabolites in the FMT group. No adverse events were observed during the follow-up period.
Conclusion
Fresh FMT via colonoscopy is a safe and well-tolerated procedure for treating mild-to-moderate PD. It effectively alleviates motor and non-motor symptoms, thus facilitating defecation and improving the quality of life. These effects can be maintained for a minimum of 12 weeks and may be attributed to the optimization of gut microbiota and fecal metabolites.
Donor:
Following the guidelines for FMT proposed at the European Consensus Conference (Cammarota G et al., 2017), a healthy 18-year-old male volunteer, without familial relationship with any of the enrolled PD patients, and a history of gastrointestinal/neurological diseases or surgeries, was selected as a stool donor. He was not medicated with antibiotics, immunosuppressants, or other drugs in the month earlier. The Hamilton Anxiety Scale (HAMA), Hamilton Depression Scale (HAMD), and Pittsburgh Sleep Quality Index (PSQI) were graded within normal ranges. Laboratory testing, including blood routine test, urinalysis, stool tests, liver and kidney function tests, and serological tests for HIV, syphilis, hepatitis C, and hepatitis B surface antigen, were all normal.
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