Department of Medicine, Stord Hospital, Stord, Norway.
Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Scand J Gastroenterol. 2022 Sep;57(9):1036-1045. doi: 10.1080/00365521.2022.2064725. Epub 2022 Apr 29.
Fecal microbiota transplantation (FMT) is a promising intervention for patients with irritable bowel syndrome (IBS). The present study aimed to identify any differences in FMT response between patients with severe and moderate IBS symptoms.
The study included the 164 patients who participated in our previous study, of which 96 (58.5%) and 68 (41.5%) had severe (S-IBS-S) and moderate (Mo-IBS-S) IBS, respectively. The patients were randomly divided into a placebo group (own feces) and 30-g and 60-g (donor feces) FMT groups. Patients completed three questionnaires that assessed their symptoms and quality of life at baseline and at 2 weeks, 1 month, and 3 months after FMT, and provided fecal samples before and 1 month after FMT. The fecal bacteria were analyzed using the 16S rRNA gene in PCR DNA amplification covering the V3-V9 variable genes.
Response rates of the placebo group did not differ between S-IBS-S and Mo-IBS-S patients at 2 weeks, 1 month and 3 months after FMT. The response rates in the active treatment group were higher in S-IBS-S patients than in Mo-IBS-S patients at each observation time. FMT reduced abdominal symptoms and fatigue and improved the quality of life in patients with both severe and moderate IBS. Patients with S-IBS-S had higher levels of , and lower levels of than Mo-IBS-S,
Patients with S-IBS-S have a higher response rate to FMT and a marked improvement in fatigue and in quality of life compared with those with Mo-IBS-S. The clinical trial registration number is NCT03822299 and is available at www.clinicaltrials.gov.
粪便微生物群移植(FMT)是治疗肠易激综合征(IBS)患者的一种很有前途的干预措施。本研究旨在确定严重和中度 IBS 症状患者对 FMT 反应的任何差异。
该研究纳入了参加我们之前研究的 164 名患者,其中 96 名(58.5%)和 68 名(41.5%)患有严重(S-IBS-S)和中度(Mo-IBS-S)IBS。患者被随机分为安慰剂组(自身粪便)和 30 克和 60 克(供体粪便)FMT 组。患者在 FMT 前和 1 个月后完成了三个评估症状和生活质量的问卷,并在 FMT 后 2 周、1 个月和 3 个月进行了评估,并提供了粪便样本。使用 PCR DNA 扩增覆盖 V3-V9 可变基因的 16S rRNA 基因分析粪便细菌。
FMT 后 2 周、1 个月和 3 个月,安慰剂组的 S-IBS-S 和 Mo-IBS-S 患者的反应率没有差异。在每个观察时间,活跃治疗组的 S-IBS-S 患者的反应率均高于 Mo-IBS-S 患者。FMT 减轻了腹部症状和疲劳,改善了严重和中度 IBS 患者的生活质量。S-IBS-S 患者的 水平较高, 水平较低。
与 Mo-IBS-S 相比,S-IBS-S 患者对 FMT 的反应率更高,疲劳和生活质量改善更为明显。临床试验注册号为 NCT03822299,可在 www.clinicaltrials.gov 上查询。