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非靶向粪便代谢组学在炎症性肠病生物标志物和治疗靶点发现中的应用。

Untargeted faecal metabolomics for the discovery of biomarkers and treatment targets for inflammatory bowel diseases.

机构信息

Department of Gastroenterology and Hepatology, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands

Department of Genetics, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Gut. 2024 Oct 7;73(11):1909-1920. doi: 10.1136/gutjnl-2023-329969.

Abstract

The gut microbiome has been recognised as a key component in the pathogenesis of inflammatory bowel diseases (IBD), and the wide range of metabolites produced by gut bacteria are an important mechanism by which the human microbiome interacts with host immunity or host metabolism. High-throughput metabolomic profiling and novel computational approaches now allow for comprehensive assessment of thousands of metabolites in diverse biomaterials, including faecal samples. Several groups of metabolites, including short-chain fatty acids, tryptophan metabolites and bile acids, have been associated with IBD. In this article, we describe the contribution of metabolomics research to the field of IBD, with a focus on faecal metabolomics. We discuss the latest findings on the significance of these metabolites for IBD prognosis and therapeutic interventions and offer insights into the future directions of metabolomics research.

摘要

肠道微生物组已被认为是炎症性肠病 (IBD) 发病机制的关键组成部分,肠道细菌产生的广泛代谢物是微生物组与宿主免疫或宿主代谢相互作用的重要机制。高通量代谢组学分析和新的计算方法现在可以全面评估包括粪便样本在内的各种生物材料中的数千种代谢物。包括短链脂肪酸、色氨酸代谢物和胆汁酸在内的几类代谢物与 IBD 有关。在本文中,我们描述了代谢组学研究对 IBD 领域的贡献,重点介绍粪便代谢组学。我们讨论了这些代谢物对 IBD 预后和治疗干预的意义的最新发现,并提供了对代谢组学研究未来方向的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9657/11503092/d53d65f84c4d/gutjnl-73-11-g001.jpg

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