Lv Miwei, Zhang Jiawei, Deng Jiaxin, Hu Jiancong, Zhong Qinghua, Su Mingli, Lin Dezheng, Xu Tian, Bai Xuhao, Li Juan, Guo Xuefeng
Department of Endoscopic Surgery, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Front Microbiol. 2023 Apr 4;14:1097892. doi: 10.3389/fmicb.2023.1097892. eCollection 2023.
The essence of enterotypes is to stratify the entire human gut microbiota, and dysregulation of gut microbiota is closely related to the development of colorectal adenoma. Enterotypes may therefore be a useful target for the prevention of colorectal adenoma. However, the relationship between gut microbiota and colorectal adenoma has not been fully elucidated. In this study, we aimed to analyze the differences in gut microbiome composition between adenoma and control populations.
We recruited 31 patients with colorectal adenoma and 71 non-adenoma controls. Patient demographics, risk factors, fecal samples from each subject were collected and metagenomic sequencing was performed. LEfSe analysis was used to reveal differences in intestinal microbiome composition. Multiple logistic regression analysis was used to determine the association between enterotypes and colorectal adenoma.
The results showed that enterotype (enterotype 4) is only present in adenoma group. Logistic regression analysis showed that enterotype was an independent risk factor for colorectal adenoma.
The enterotype may increase the occurrence of colorectal adenoma through inflammatory association and interference with glucose and lipid metabolism in human body. In conclusion, the differences we observed between different enterotypes add a new potential factor to the development of colorectal adenoma.
肠型的本质是对整个人体肠道微生物群进行分层,而肠道微生物群的失调与结直肠腺瘤的发生密切相关。因此,肠型可能是预防结直肠腺瘤的一个有用靶点。然而,肠道微生物群与结直肠腺瘤之间的关系尚未完全阐明。在本研究中,我们旨在分析腺瘤人群与对照人群肠道微生物组组成的差异。
我们招募了31例结直肠腺瘤患者和71例非腺瘤对照。收集患者的人口统计学资料、危险因素以及每个受试者的粪便样本,并进行宏基因组测序。采用线性判别分析效应大小(LEfSe)分析来揭示肠道微生物组组成的差异。采用多因素logistic回归分析来确定肠型与结直肠腺瘤之间的关联。
结果显示,肠型(肠型4)仅存在于腺瘤组。logistic回归分析表明,肠型是结直肠腺瘤的独立危险因素。
该肠型可能通过炎症关联以及对人体葡萄糖和脂质代谢的干扰增加结直肠腺瘤的发生。总之,我们在不同肠型之间观察到的差异为结直肠腺瘤的发生增添了一个新的潜在因素。