P424 利用内镜刷分析溃疡性结肠炎患者的肠道微生物群

B Lee, B Keum, S Kim, H Jeon, Y Jeen, C Hoonjai
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摘要

背景 溃疡性结肠炎的确切发病机制尚不清楚,但已知其病因之一是微生物菌群失调。粘膜相关微生物群与溃疡性结肠炎的发病机制关系更为密切。然而,粘膜相关微生物群的最佳取样方法仍有待研究。在这项研究中,我们使用内镜刷取样研究了溃疡性结肠炎患者的粘膜相关微生物群。我们假设内镜刷取样本是获取粘膜相关微生物组样本的精确且无创的方法。方法 本研究筛选了在韩国大学安南医院消化内科就诊的 UC 患者。研究人员审查了病历、结肠镜检查和粪便样本等临床数据。受试者分别使用粪便和唾液样本采集器提供粪便和唾液样本。在乙状结肠镜检查过程中,使用细胞学刷子在结肠粘膜上刷3-4下,收集刷子样本。样本在韩国大学医学中心进行微生物组分析。结果 从 2022 年 7 月到 2023 年 1 月,我们对 19 名 UC 患者进行了前瞻性研究。在刷子、粪便和唾液的微生物群中,固着菌、类杆菌、蛋白菌和放线菌是最常见的菌种。(图 1-1)粪便和刷子的微生物群在α和β多样性方面没有显著差异。(图 1-2)但是,口腔微生物群在β多样性方面与粪便和刷子不同。图 1-4 结论 粪便和刷子中的微生物组没有明显差异。不过,与目前使用的粪便取样相比,内窥镜刷取样粘膜相关微生物群的新方法并不逊色。此外,对口腔微生物群的分析表明,固形菌可被视为评估疾病严重程度的有用生物标志物。因此,有必要通过增加研究对象的数量来开展后续研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P424 Analysis of the intestinal microbiome using an Endoscopic Brush in Ulcerative colitis
Background The precise pathogenesis of the Ulcerative colitis is still yet unknown, but one of its cause is known to be microbial dysbiosis. The mucosa-associated microbiota are more deeply involved in the pathogenesis of UC. However, the optimal sampling of mucosa-associated microbiome has yet to be investigated. In this study, we investigated the mucosa-associated microbiome in patients with ulcerative colitis, using endoscopic brush samples. We hypothesized that endoscopic brushing is precise and noninvasive method to get sample of mucosa-associated microbiome. Methods Patients with UC who visited the gastroenterology department of Korea University Anam hospital were screened for this study. Clinical data such as medical records, colonoscopy and fecal samples were reviewed. Using a stool and saliva sample collector kit respectively, the subjects provided stool and saliva samples. Brushing samples were collected during the sigmoidoscopy procedure with 3-4 brush strokes on the colon mucosa using the cytology brush. The samples were analyzed for microbiome in the Korea University Medical Center. Results From July 2022 to January 2023, we prospectively enrolled 19 patients with UC. Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria were the most common species in microbiota of brush, stool and saliva.(Fig.1-1) The microbiome between stool and brush was no significant difference in alpha and beta diversities.(Fig.1-2) However, Oral microbiome was different from stool and brush in beta diversities.(Fig.1-3) Patients were categorized into to analyze the oral microbiome. A trend was observed where increased disease severity was associated with an increase in Firmicutes.(Fig.1-4) Conclusion The microbiome of stool and brush was no significantly different. However, the novel sampling of mucosa-associated microbiome, endoscopic brush, is not inferior compared to currently used sampling of stool. Also the analysis of the oral microbiome suggested that Firmicutes could be considered a useful biomarker for assessing disease severity. Therefore, it is necessary to conduct followup research by increasing the number of subjects.
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