代谢组
炎症性肠病
代谢组学
微生物群
溃疡性结肠炎
肠道菌群
疾病
串扰
代谢物
生物
发病机制
计算生物学
生物信息学
医学
免疫学
内科学
生物化学
物理
光学
作者
Mengfan Li,Lijiao Yang,Chenlu Mu,Yue Sun,Yu Gu,Danfeng Chen,Tianyu Liu,Hailong Cao
标识
DOI:10.1016/j.csbj.2022.03.038
摘要
Inflammatory bowel disease (IBD), comprising Crohn's disease (CD) and ulcerative colitis (UC), is a set of clinically chronic, relapsing gastrointestinal inflammatory disease and lacks of an absolute cure. Although the precise etiology is unknown, developments in high-throughput microbial genomic sequencing significantly illuminate the changes in the intestinal microbial structure and functions in patients with IBD. The application of microbial metabolomics suggests that the microbiota can influence IBD pathogenesis by producing metabolites, which are implicated as crucial mediators of host-microbial crosstalk. This review aims to elaborate the current knowledge of perturbations of the microbiome-metabolome interface in IBD with description of altered composition and metabolite profiles of gut microbiota. We emphasized and elaborated recent findings of several potentially protective metabolite classes in IBD, including fatty acids, amino acids and derivatives and bile acids. This article will facilitate a deeper understanding of the new therapeutic approach for IBD by applying metabolome-based adjunctive treatment.
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