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急性冠状动脉综合征代谢组学分析的最新进展:一项叙述性综述

Recent progress in metabolomic analysis of acute coronary syndrome: a narrative review.

作者信息

Liu Jiaqi, Li Tingmiao, Qi Xin, He Chengyan

机构信息

Department of Laboratory Medicine, China-Japan Union Hospital of Jilin University, Changchun, China.

出版信息

Cardiovasc Diagn Ther. 2025 Apr 30;15(2):480-499. doi: 10.21037/cdt-24-431. Epub 2025 Apr 23.

Abstract

BACKGROUND AND OBJECTIVE

Acute coronary syndrome (ACS) is a common cardiovascular disease in clinical practice. It is caused mainly by vulnerable plaque rupture (PR) or surface plaque erosion (PE) caused by serious thrombotic events, and eventually leads to myocardial blood supply insufficiency or necrosis. The disease has high morbidity and mortality rates. In this study, we review the literature on biomarkers of ACS metabolites and modification of disease by altering related metabolic pathways through drugs, aiming to provide clarity on potential biomarkers of disease identified to date.

METHODS

PubMed was used for literature review. From January 1, 2014 to December 3, 2024, English articles on clinical trials, randomized controlled trials of metabolomics studies in ACS were included.

KEY CONTENT AND FINDINGS

In this review, we discuss the advantages and disadvantages of three techniques currently used for metabolomic analysis. In addition, the recent decade of metabolomic approaches to the discovery of potential diagnostic and prognostic biomarkers for ACS is reviewed. It was found that the metabolites changed in patients with ACS were mostly amino acids, lipids and carbohydrates. Tryptophan and glutamine can be used as potential diagnostic biomarkers. Mannitol and ceramide can be used as prognostic biomarkers. Drugs can improve disease by affecting changes in metabolites in the body.

CONCLUSIONS

ACS studies based on metabolomics have demonstrated great potential for identifying disease-related metabolomic features in the discovery of potential biomarkers for diagnosis and prognosis and mechanisms of drug therapy.

摘要

背景与目的

急性冠状动脉综合征(ACS)是临床常见的心血管疾病。它主要由易损斑块破裂(PR)或严重血栓事件导致的表面斑块侵蚀(PE)引起,最终导致心肌供血不足或坏死。该疾病具有较高的发病率和死亡率。在本研究中,我们回顾了关于ACS代谢物生物标志物以及通过药物改变相关代谢途径对疾病进行修饰的文献,旨在阐明迄今为止已确定的潜在疾病生物标志物。

方法

使用PubMed进行文献综述。纳入2014年1月1日至2024年12月3日期间关于ACS代谢组学研究的临床试验、随机对照试验的英文文章。

关键内容与发现

在本综述中,我们讨论了目前用于代谢组学分析的三种技术的优缺点。此外,还回顾了近十年来利用代谢组学方法发现ACS潜在诊断和预后生物标志物的情况。发现ACS患者体内发生变化的代谢物大多为氨基酸、脂质和碳水化合物。色氨酸和谷氨酰胺可用作潜在的诊断生物标志物。甘露醇和神经酰胺可用作预后生物标志物。药物可通过影响体内代谢物的变化来改善疾病。

结论

基于代谢组学的ACS研究在发现潜在诊断和预后生物标志物以及药物治疗机制方面,已显示出识别与疾病相关代谢组学特征的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5ba/12082212/150098c8961f/cdt-15-02-480-f1.jpg

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