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差异网络分析揭示了与急性心肌梗死患者死亡率相关的代谢决定因素,并提出了用于预测死亡的不同临床评分所依据的潜在机制。

Differential Network Analysis Reveals Metabolic Determinants Associated with Mortality in Acute Myocardial Infarction Patients and Suggests Potential Mechanisms Underlying Different Clinical Scores Used To Predict Death.

机构信息

Magnetic Resonance Center (CERM) , University of Florence , Sesto Fiorentino 50019 , Italy.

Consorzio Interuniversitario Risonanze Magnetiche di Metallo Proteine (C.I.R.M.M.P.) , Sesto Fiorentino 50019 , Italy.

出版信息

J Proteome Res. 2020 Feb 7;19(2):949-961. doi: 10.1021/acs.jproteome.9b00779. Epub 2020 Jan 17.

Abstract

We present here the differential analysis of metabolite-metabolite association networks constructed from an array of 24 serum metabolites identified and quantified via nuclear magnetic resonance spectroscopy in a cohort of 825 patients of which 123 died within 2 years from acute myocardial infarction (AMI). We investigated differences in metabolite connectivity of patients who survived, at 2 years, the AMI event, and we characterized metabolite-metabolite association networks specific to high and low risks of death according to four different risk parameters, namely, acute coronary syndrome classification, Killip, Global Registry of Acute Coronary Events risk score, and metabolomics NOESY RF risk score. We show significant differences in the connectivity patterns of several low-molecular-weight molecules, implying variations in the regulation of several metabolic pathways regarding branched-chain amino acids, alanine, creatinine, mannose, ketone bodies, and energetic metabolism. Our results demonstrate that the characterization of metabolite-metabolite association networks is a promising and powerful tool to investigate AMI patients according to their outcomes at a molecular level.

摘要

我们在此介绍了通过核磁共振光谱技术鉴定和定量分析 825 名急性心肌梗死(AMI)患者的 24 种血清代谢物,并构建了代谢物-代谢物关联网络的差异分析。我们研究了在 AMI 事件发生后 2 年内存活的患者的代谢物连接性差异,并根据急性冠状动脉综合征分类、Killip 分级、全球急性冠状动脉事件注册风险评分和代谢组学 NOESY RF 风险评分这四个不同的风险参数,对与死亡风险高低相关的代谢物-代谢物关联网络进行了特征描述。我们发现了一些低分子量分子连接模式的显著差异,这意味着在支链氨基酸、丙氨酸、肌酸、甘露糖、酮体和能量代谢等代谢途径的调控方面存在差异。我们的研究结果表明,代谢物-代谢物关联网络的特征描述是一种有前途的、强大的工具,可以在分子水平上根据 AMI 患者的结局对其进行研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67c/7011173/6847fe1920fa/pr9b00779_0006.jpg

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