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结肠镜下粪便微生物群移植治疗轻至中度帕金森病:一项随机对照试验。

Colonoscopic fecal microbiota transplantation for Mild-to-Moderate Parkinson's Disease: A randomized controlled trial.

作者信息

Wang Jingyi, Xue Liujun, Zhang Minna, Shen Peng, Zhao Wenzhuo, Tong Qiang, Wu Shangnong, Dai Weijie, Yang Xiaozhong, Wang Honggang

机构信息

Department of Gastroenterology, the Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian 223301, China.

Department of Neurology, the Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, No.1 Huanghe West Road, Huaian, China.

出版信息

Brain Behav Immun. 2025 Aug 21;130:106086. doi: 10.1016/j.bbi.2025.106086.

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.

摘要

目的

越来越多的证据支持粪便微生物群移植(FMT)治疗帕金森病(PD)的有效性和安全性。粪便微生物群通常通过口服胶囊、鼻空肠管或结肠镜进行移植,但冷冻常常会降低移植微生物群的多样性和活力。这项单中心、双盲、随机、安慰剂对照试验旨在探讨通过结肠镜进行新鲜FMT治疗PD的有效性和安全性。

方法

30例轻度至中度PD患者(Hoehn-Yahr分期I-III)按1:1比例随机分为FMT组(通过结肠镜进行新鲜FMT)和安慰剂组(通过结肠镜注射生理盐水)。使用相关量表评估运动和非运动症状、便秘、生活质量、认知功能、情绪状态和睡眠质量。在治疗前以及治疗后4周、8周和12周采集粪便样本进行宏基因组学和代谢组学分析。

结果

本研究共纳入30例轻度至中度PD患者,其中男性18例,女性12例,中位年龄68岁,中位发病年龄63.5岁,中位病程3年。在12周时,FMT组的帕金森病统一评分量表Ⅲ(UPDRSⅢ)(组×时间效应,B = -8.80[-13.79,-3.81])、帕金森病生活质量问卷(PAC-QOL)(组×时间效应,B = -29.67[-45.35,-13.98])、UPDRSⅡ(组×时间效应,B = -5.07[-8.85,-1.28])、非运动症状评分量表(NMSS)(组×时间效应,B = -35.60[-53.59,-17.61])、帕金森病问卷-39(PDQ-39)(组×时间效应,B = -17.80[-28.21,-7.39])、汉密尔顿焦虑量表(HAMA)(组×时间效应,B = -1.66[-2.92,-0.40])和汉密尔顿抑郁量表(HAMD)(组×时间效应,B = -1.33[-2.49,-0.16])评分显著降低,而每周完全自主排便次数(CSBM)(组×时间效应,B = 3.03[1.42,4.63])和布里斯托大便分类法评分(组×时间效应,B = 1.95[0.12,3.79])显著增加(均P<0.05)。FMT组的肠道微生物群和粪便代谢产物出现显著变化。随访期间未观察到不良事件。

结论

通过结肠镜进行新鲜FMT是一种治疗轻度至中度PD安全且耐受性良好的方法。它能有效缓解运动和非运动症状,从而促进排便并改善生活质量。这些效果至少可维持12周,可能归因于肠道微生物群和粪便代谢产物的优化。

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