Liu Meiling, Guo Siyi, Wang Liang
Department of Gastroenterology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Chongqing Medical University, Chongqing, China.
Therap Adv Gastroenterol. 2024 Mar 29;17:17562848241239580. doi: 10.1177/17562848241239580. eCollection 2024.
Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC.
This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data.
A systematic review.
We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways.
This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from 'lipids and lipid-like molecules' and 'organic acids and derivatives' superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types.
This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications.
尽管对溃疡性结肠炎(UC)进行了大量代谢组学研究,但结果差异很大,难以确定UC中的关键代谢异常。
本研究旨在通过分析现有的代谢组学数据,揭示UC中的关键代谢物和代谢途径。
系统评价。
我们在数据库(PubMed、Cochrane图书馆、Embase和Web of Science)以及相关研究参考文献中进行了全面检索,以获取截至2022年12月28日的UC代谢组学研究。确定了UC患者与对照组之间显著的代谢物差异,随后对相关代谢途径进行了分析。
本综述纳入了78项研究,确定了UC患者与对照组之间2868种差异表达的代谢物。这些代谢物主要来自“脂质和类脂质分子”以及“有机酸及其衍生物”超类。我们发现101种代谢物在同一样本类型的多个数据集中持续改变,78种代谢物在不同样本类型中共有。其中,62种代谢物在各种数据集或样本类型中表现出一致的调控趋势。通路分析揭示了22条显著改变 的代谢途径,其中6条途径在不同样本类型中反复富集。
本研究阐明了UC的关键代谢特征,为该疾病的分子机制和生物标志物发现提供了见解。未来的研究可以集中在验证这些发现并探索其临床应用。