Li Mengfan, Yang Lijiao, Mu Chenlu, Sun Yue, Gu Yu, Chen Danfeng, Liu Tianyu, Cao Hailong
Department of Gastroenterology and Hepatology, General Hospital, Tianjin Medical University, Tianjin Institute of Digestive Diseases, Tianjin Key Laboratory of Digestive Diseases, Tianjin, China.
Comput Struct Biotechnol J. 2022 Apr 4;20:2402-2414. doi: 10.1016/j.csbj.2022.03.038. eCollection 2022.
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.
炎症性肠病(IBD)包括克罗恩病(CD)和溃疡性结肠炎(UC),是一组临床慢性、复发性胃肠道炎症性疾病,且尚无根治方法。尽管确切病因尚不清楚,但高通量微生物基因组测序的发展显著揭示了IBD患者肠道微生物结构和功能的变化。微生物代谢组学的应用表明,微生物群可通过产生代谢产物影响IBD发病机制,这些代谢产物被认为是宿主-微生物相互作用的关键介质。本综述旨在阐述IBD中微生物组-代谢组界面紊乱的现有知识,描述肠道微生物群组成和代谢产物谱的改变。我们强调并阐述了IBD中几类潜在保护性代谢产物的最新发现,包括脂肪酸、氨基酸及其衍生物和胆汁酸。本文将有助于通过应用基于代谢组学的辅助治疗,更深入地理解IBD的新治疗方法。