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粪便微生物群移植对散发性肌萎缩侧索硬化症患者的影响:一项随机、双盲、安慰剂对照试验。

Effect of fecal microbiota transplantation on patients with sporadic amyotrophic lateral sclerosis: a randomized, double-blind, placebo-controlled trial.

作者信息

Feng Renyi, Zhu Qingyong, Wang Ao, Wang Hanzhen, Wang Jiuqi, Chen Pei, Zhang Rui, Liang Dongxiao, Teng Junfang, Ma Mingming, Ding Xuebing, Wang Xuejing

机构信息

Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Institute of Parkinson and Movement Disorder, Zhengzhou University, Zhengzhou, Henan, China.

出版信息

BMC Med. 2024 Dec 2;22(1):566. doi: 10.1186/s12916-024-03781-6.

Abstract

BACKGROUND

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder marked by the progressive loss of motor neurons. Recent insights into ALS pathogenesis underscore the pivotal role of the gut microbiome, prompting an investigation into the potential therapeutic impact of fecal microbiota transplantation (FMT) on sporadic ALS patients.

METHODS

Conducted as a double-blind, placebo-controlled, parallel-group, randomized clinical trial, the study enrolled 27 participants from October 2022 to April 2023. The participants were followed up for 6 months from February 2023 to October 2023, during in-person visits at baseline, week 15, week 23, and week 35. The participants, evenly randomized, received either healthy donor FMT (FMT, n = 14) or a mixture of 0.9% saline and food coloring (E150c) as sham transplantation (placebo, n = 13). The primary outcome measured the change in the ALS Functional Rating Scale-Revised (ALSFRS-R) total score from baseline to week 35. Secondary outcomes included changes in gastrointestinal and respiratory functions, muscle strength, autonomic function, cognition, quality of life, intestinal microbiome composition, and plasm neurofilament light chain protein (NFL). Efficacy and safety outcomes were assessed in the intention-to-treat population.

RESULTS

A total of 27 randomized patients (47% women; mean age, 67.2 years), 24 participants completed the entire study. Notably, ALSFRS-R score changes exhibited no significant differences between FMT (6.1 [SD, 3.11]) and placebo (6.41[SD, 2.73]) groups from baseline to week 35. Secondary efficacy outcomes, encompassing respiratory function, muscle strength, autonomic function, cognition, quality of life, and plasm NFL, showed no significant differences. Nevertheless, the FMT group exhibited improvements in constipation, depression, and anxiety symptoms. FMT induced a shift in gut microbiome community composition, marked by increased abundance of Bifidobacterium, which persisted until week 15 (95% CI, 0.04 to 0.28; p = 0.01). Gastrointestinal adverse events were the primary manifestations of FMT-related side effects.

CONCLUSIONS

In this clinical trial involving 27 sporadic ALS patients, FMT did not significantly slow the decline in ALSFRS-R score. Larger multicenter trials are needed to confirm the efficacy of FMT in sporadic ALS patients and to explore the underlying biological mechanisms.

TRIAL REGISTRATION

Chinese Clinical Trial Registry Identifier: ChiCTR 2200064504.

摘要

背景

肌萎缩侧索硬化症(ALS)是一种毁灭性的神经退行性疾病,其特征是运动神经元逐渐丧失。最近对ALS发病机制的深入了解突出了肠道微生物群的关键作用,促使人们对粪便微生物群移植(FMT)对散发性ALS患者的潜在治疗影响进行研究。

方法

该研究作为一项双盲、安慰剂对照、平行组、随机临床试验进行,于2022年10月至2023年4月招募了27名参与者。从2023年2月至2023年10月对参与者进行了6个月的随访,在基线、第15周、第23周和第35周进行现场访视。参与者被均匀随机分组,分别接受健康供体FMT(FMT组,n = 14)或0.9%生理盐水与食用色素(E150c)的混合物作为假移植(安慰剂组,n = 13)。主要结局指标为从基线到第35周ALS功能评定量表修订版(ALSFRS-R)总分的变化。次要结局指标包括胃肠和呼吸功能、肌肉力量、自主神经功能、认知、生活质量、肠道微生物群组成以及血浆神经丝轻链蛋白(NFL)的变化。在意向性治疗人群中评估疗效和安全性结局。

结果

共有27名随机分组患者(47%为女性;平均年龄67.2岁),24名参与者完成了整个研究。值得注意的是,从基线到第35周,FMT组(6.1[标准差,3.11])和安慰剂组(6.41[标准差,2.73])的ALSFRS-R评分变化无显著差异。包括呼吸功能、肌肉力量、自主神经功能、认知、生活质量和血浆NFL在内的次要疗效结局指标也无显著差异。然而,FMT组在便秘、抑郁和焦虑症状方面有所改善。FMT导致肠道微生物群群落组成发生变化,其特征是双歧杆菌丰度增加,这种变化一直持续到第15周(95%置信区间,0.04至0.28;p = 0.01)。胃肠道不良事件是FMT相关副作用的主要表现。

结论

在这项涉及27名散发性ALS患者的临床试验中,FMT并未显著减缓ALSFRS-R评分的下降。需要更大规模的多中心试验来证实FMT对散发性ALS患者的疗效,并探索其潜在的生物学机制。

试验注册

中国临床试验注册中心标识符:ChiCTR 2200064504。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef9/11610222/050173c994c6/12916_2024_3781_Fig1_HTML.jpg

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