Gweon Tae-Geun, Kang Sang-Bum, Na Soo-Young, Oh Dong Jun, Kim Sang Wook, Seo Geom Seog, Cho Joo Young
Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul 02812, Republic of Korea.
Department of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon 14662, Republic of Korea.
Nutrients. 2025 Feb 11;17(4):641. doi: 10.3390/nu17040641.
infection (CDI) is an important nosocomial diarrheal disease. The benefits of the probiotic () in the preservation of intestinal microbiota have not been studied in patients with CDI to date. Therefore, we aimed to investigate the efficacy of in preserving the intestinal microbiota in patients with CDI. A multicenter, randomized, placebo-controlled trial was carried out at six academic centers in Korea. Individuals diagnosed with mild to moderate CDI were included in this trial. CDI was treated with vancomycin 125 mg four times daily for two weeks. Along with vancomycin, was administered for five days in this study, while a placebo was given to the placebo group. Microbiome analysis was performed before and five days after administering vancomycin and or placebo, using 16S rRNA amplicon sequencing. Alpha and beta diversity was compared between the two groups. A total of 35 participants were finally included in this study, with 16 in the study group and 19 in the placebo group. The alpha diversity was similar in both groups before CDI treatment. After five days of the administration of vancomycin and or placebo, alpha diversity did not decrease in the study group (Chao1 index, = 0.665; observed features, = 0.692). In contrast, alpha diversity decreased in the placebo group (Chao1 index, = 0.011; observed features, = 0.011). Beta diversity did not differ between the two groups. The addition of to vancomycin was effective in preserving gut microbiota in patients with CDI.
艰难梭菌感染(CDI)是一种重要的医院获得性腹泻疾病。迄今为止,益生菌()在保护肠道微生物群方面的益处尚未在CDI患者中进行研究。因此,我们旨在研究()在保护CDI患者肠道微生物群方面的疗效。在韩国的六个学术中心进行了一项多中心、随机、安慰剂对照试验。该试验纳入了诊断为轻度至中度CDI的个体。CDI采用万古霉素125毫克每日四次治疗两周。在本研究中,除万古霉素外,()给药五天,而安慰剂组给予安慰剂。在给予万古霉素和()或安慰剂之前及之后五天,使用16S rRNA扩增子测序进行微生物组分析。比较两组之间的α和β多样性。本研究最终共纳入35名参与者,研究组16名,安慰剂组19名。CDI治疗前两组的α多样性相似。在给予万古霉素和()或安慰剂五天后,研究组的α多样性没有下降(Chao1指数,=0.665;观察到的特征,=0.692)。相比之下,安慰剂组的α多样性下降(Chao1指数,=0.011;观察到的特征,=0.011)。两组之间的β多样性没有差异。在万古霉素治疗中添加()对保护CDI患者的肠道微生物群有效。