Suppr超能文献

血浆代谢组学分析揭示腹主动脉瘤中能量、脂质和氨基酸代谢异常。

Plasma Metabolomics Analysis Identifies Abnormal Energy, Lipid, and Amino Acid Metabolism in Abdominal Aortic Aneurysms.

作者信息

Guo Yaming, Wan Shuwei, Han Mingli, Zhao Yubo, Li Chuang, Cai Gaopo, Zhang Shuai, Sun Zhi, Hu Xinhua, Cao Hui, Li Zhen

机构信息

Department of Endovascular Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China (mainland).

Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China (mainland).

出版信息

Med Sci Monit. 2020 Dec 1;26:e926766. doi: 10.12659/MSM.926766.

Abstract

BACKGROUND Abdominal aortic aneurysm (AAA) is a complicated aortic dilatation disease. Metabolomics is an emerging system biology method. This aim of this study was to identify abnormal metabolites and metabolic pathways associated with AAA and to discover potential biomarkers that could affect the size of AAAs. MATERIAL AND METHODS An untargeted metabolomic method was used to analyze the plasma metabolic profiles of 39 patients with AAAs and 30 controls. Multivariate analysis methods were used to perform differential metabolite screening and metabolic pathway analysis. Cluster analysis and univariate analysis were performed to identify potential metabolites that could affect the size of an AAA. RESULTS Forty-five different metabolites were identified with an orthogonal projection to latent squares-discriminant analysis model and the differences between them in the patients with AAAs and the control group were compared. A variable importance in the projection score >1 and P<0.05 were considered statistically significant. In patients with AAAs, the pathways involving metabolism of alanine, aspartate, glutamate, D-glutamine, D-glutamic acid, arginine, and proline; tricarboxylic acid cycling; and biosynthesis of arginine are abnormal. The progression of an AAA may be related to 13 metabolites: citric acid, 2-oxoglutarate, succinic acid, coenzyme Q1, pyruvic acid, sphingosine-1-phosphate, platelet-activating factor, LysoPC (16: 00), lysophosphatidylcholine (18: 2(9Z,12Z)/0: 0), arginine, D-aspartic acid, and L- and D-glutamine. CONCLUSIONS An untargeted metabolomic analysis using ultraperformance liquid chromatography-tandem mass spectrometry identified metabolites that indicate disordered metabolism of energy, lipids, and amino acids in AAAs.

摘要

背景

腹主动脉瘤(AAA)是一种复杂的主动脉扩张性疾病。代谢组学是一种新兴的系统生物学方法。本研究旨在识别与AAA相关的异常代谢物和代谢途径,并发现可能影响AAA大小的潜在生物标志物。

材料与方法

采用非靶向代谢组学方法分析39例AAA患者和30例对照者的血浆代谢谱。运用多变量分析方法进行差异代谢物筛选和代谢途径分析。进行聚类分析和单变量分析以识别可能影响AAA大小的潜在代谢物。

结果

通过正交投影到潜在变量判别分析模型鉴定出45种不同的代谢物,并比较了AAA患者与对照组之间它们的差异。投影得分变量重要性>1且P<0.05被认为具有统计学意义。在AAA患者中,涉及丙氨酸、天冬氨酸、谷氨酸、D-谷氨酰胺、D-谷氨酸、精氨酸和脯氨酸代谢的途径;三羧酸循环;以及精氨酸的生物合成均异常。AAA的进展可能与13种代谢物有关:柠檬酸、2-氧代戊二酸、琥珀酸、辅酶Q1、丙酮酸、鞘氨醇-1-磷酸、血小板活化因子、溶血磷脂酰胆碱(16:00)、溶血磷脂酰胆碱(18:2(9Z,12Z)/0:0)、精氨酸、D-天冬氨酸以及L-和D-谷氨酰胺。

结论

使用超高效液相色谱-串联质谱进行的非靶向代谢组学分析鉴定出了表明AAA中能量、脂质和氨基酸代谢紊乱的代谢物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9095/7718721/947e9f29ca48/medscimonit-26-e926766-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验