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肠道宏基因组作为慢传输型便秘潜在的诊断和预测生物标志物

Gut Metagenome as a Potential Diagnostic and Predictive Biomarker in Slow Transit Constipation.

作者信息

Tian Hongliang, Ye Chen, Yang Bo, Cui Jiaqu, Zheng Zhijun, Wu Chunyan, Zhou Shailan, Lv Xiaoqiong, Qin Nan, Qin Huanlong, Li Ning, Chen Qiyi

机构信息

Intestinal Microenvironment Treatment Center of General Surgery, Tenth People's Hospital of Tongji University, Shanghai, China.

Clinical Research Center for Digestive Diseases of Tongji University, Shanghai, China.

出版信息

Front Med (Lausanne). 2022 Feb 8;8:777961. doi: 10.3389/fmed.2021.777961. eCollection 2021.

Abstract

Slow transit constipation (STC) is one of the most frequent gastrointestinal diagnoses. In this study, we conducted a quantitative metagenomics study in 118 Chinese individuals. These participants were divided into the discovery cohort of 50 patients with STC and 40 healthy controls as well as a validation cohort of 16 patients and 12 healthy controls. We found that the intestinal microbiome of patients with STC was significantly different from that of healthy individuals at the phylum, genus, and species level. Patients with STC had markedly higher levels of Alistipes and Eubacterium and lower abundance of multiple species belonging to the genus. Patients with STC gene expression levels and the Kyoto Encyclopedia of Genes and Genomes (KEGG) orthology pathway (such as fatty acid biosynthesis, butanoate metabolism, and methane metabolism pathways) enrichment were also substantially different from those of healthy controls. These microbiome and metabolite differences may be valuable biomarkers for STC. Our findings suggest that alteration of the microbiome may lead to constipation by changing the levels of microbial-derived metabolites in the gut. Above findings may help us in the development of microbial drugs.

摘要

慢传输型便秘(STC)是最常见的胃肠道诊断疾病之一。在本研究中,我们对118名中国个体进行了定量宏基因组学研究。这些参与者被分为发现队列,包括50例STC患者和40名健康对照,以及验证队列,包括16例患者和12名健康对照。我们发现,STC患者的肠道微生物群在门、属和种水平上与健康个体存在显著差异。STC患者的阿利斯杆菌属和真杆菌属水平明显较高,而属于该属的多个物种的丰度较低。STC患者的基因表达水平以及京都基因与基因组百科全书(KEGG)直系同源途径(如脂肪酸生物合成、丁酸代谢和甲烷代谢途径)的富集情况也与健康对照有很大不同。这些微生物群和代谢物差异可能是STC的有价值生物标志物。我们的研究结果表明,微生物群的改变可能通过改变肠道中微生物衍生代谢物的水平导致便秘。上述发现可能有助于我们开发微生物药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/870e/8862142/307939e62b7f/fmed-08-777961-g0001.jpg

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