缺血修饰白蛋白在缺血性疾病中的生化应用和临床应用

Nimesha N. Senadeera, C. Ranaweera, Inoka C. Perera, D. U. Kottahachchi
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摘要

动脉粥样硬化性冠状动脉疾病是对全球健康的重大威胁,每年影响数百万人。随着时间的推移,斑块堆积会使冠状动脉变窄,减少流向心肌的血液,导致心肌缺血。及时诊断和干预是恢复心肌血流和预防心肌梗死的关键。由于筛查和诊断测试手段有限,心肌缺血的早期诊断仍具有挑战性。虽然心肌肌钙蛋白被认为是检测心肌损伤的金标准,但它在识别心肌缺血方面的效果有限。缺血修饰白蛋白(IMA)是一种修饰白蛋白变体,可作为缺血的早期敏感标记物。尽管对 IMA 作为缺血生物标志物的诊断应用进行了广泛的研究,但在了解其形成、灵敏和特异性检测以及精确的临床实用性方面仍存在很大的差距。本综述旨在通过汇编有关 IMA 的文献,讨论有关其结构、形成和检测方法的最新发现,弥补这些不足。需要进一步开展研究,加深对 IMA 结构和形成的了解,以开发新型检测技术或改进现有技术。然而,目前可用的复杂方法费用较高,需要专业设备和合格人员。
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Biochemical Insights and Clinical Applications of Ischemia-Modified Albumin in Ischemic Conditions
Atherosclerotic coronary artery disease is a significant global health threat, impacting millions annually. Over time, plaque buildup narrows the coronary arteries, reducing blood flow to the heart muscle and resulting in myocardial ischemia. Timely diagnosis and intervention are crucial for restoring the blood flow to the heart muscle and preventing myocardial infarction. Given the limited availability of screening and diagnostic tests, the early diagnosis of myocardial ischemia remains challenging. While cardiac troponin is considered the gold standard for detecting myocardial injury, its effectiveness in identifying myocardial ischemia is limited. Ischemia-modified albumin (IMA) is a modified albumin variant that serves as a sensitive and early marker for ischemia. Despite extensive research on diagnostic applications of IMA as a biomarker for ischemia, significant gaps remain in understanding its formation, sensitive and specific detection, and precise clinical utility. This review aims to address these gaps by compiling literature on IMA discussing the latest findings on structure and formation, and detection methods. Further research is required to enhance understanding of the structure and formation of IMA, aiming to develop novel detection techniques or improve existing ones. However, currently, available sophisticated methods are associated with higher expenses and require specialized equipment and qualified personnel.
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