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作为人类急性心肌梗死预后标志物的铜还原抗氧化能力反应性晚期糖基化终产物

CUPRAC-Reactive Advanced Glycation End Products as Prognostic Markers of Human Acute Myocardial Infarction.

作者信息

Bayarsaikhan Govigerel, Bayarsaikhan Delger, Oh Pyung Chun, Kang Woong Chol, Lee Bonghee

机构信息

Center for Genomics and Proteomics, Lee Gil Ya Cancer and Diabetes Institute, School of Medicine, Gachon University, Incheon City 406-840, Korea.

Gil Medical Center, Department of Cardiology, Gachon University of Medicine and Science, Incheon City 405-760, Korea.

出版信息

Antioxidants (Basel). 2021 Mar 11;10(3):434. doi: 10.3390/antiox10030434.

Abstract

Cardiovascular disorders, especially acute coronary syndromes, are among the leading causes of mortality worldwide, and advanced glycation end products (AGEs) are associated with cardiovascular disease and serve as biomarkers for diagnosis and prediction. In this study, we investigated the utility of AGEs as prognostic biomarkers for acute myocardial infarction (AMI). We measured AGEs in serum samples of AMI patients ( = 27) using the cupric ion reducing antioxidant capacity (CUPRAC) method on days 0, 2, 14, 30, and 90 after AMI, and the correlation of serum AGE concentration and post-AMI duration was determined using Spearman's correlation analysis. Compared to total serum protein, the level of CUPRAC reactive AGEs was increased from 0.9 to 2.1 times between 0-90 days after AMI incident. Furthermore, the glycation pattern and Spearman's correlation analysis revealed four dominant patterns of AGE concentration changes in AMI patients: stable AGE levels (straight line with no peak), continuous increase, single peak pattern, and multimodal pattern (two or more peaks). In conclusion, CUPRAC-reactive AGEs can be developed as a potential prognostic biomarker for AMI through long-term clinical studies.

摘要

心血管疾病,尤其是急性冠状动脉综合征,是全球主要的死亡原因之一,而晚期糖基化终产物(AGEs)与心血管疾病相关,并可作为诊断和预测的生物标志物。在本研究中,我们调查了AGEs作为急性心肌梗死(AMI)预后生物标志物的效用。我们在AMI患者(n = 27)的血清样本中,于AMI发生后的第0、2、14、30和90天,使用铜离子还原抗氧化能力(CUPRAC)方法测量AGEs,并使用Spearman相关分析确定血清AGE浓度与AMI后病程的相关性。与总血清蛋白相比,AMI发病后0 - 90天内,CUPRAC反应性AGEs水平从0.9倍增加到2.1倍。此外,糖基化模式和Spearman相关分析揭示了AMI患者AGE浓度变化的四种主要模式:稳定的AGE水平(无峰值的直线)、持续增加、单峰模式和多峰模式(两个或更多峰值)。总之,通过长期临床研究,CUPRAC反应性AGEs可被开发为AMI潜在的预后生物标志物。

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