Kazanis Konstantinos, Dalamaga Maria, Nounopoulos Charalampos, Manolis Antonios S, Sakellaris Nikolaos, Jullien Gerard, Dionyssiou-Asteriou Amalia
Department of Clinical Biochemistry, Medical School, University of Athens, Greece.
Clin Chim Acta. 2009 Oct;408(1-2):65-9. doi: 10.1016/j.cca.2009.07.007. Epub 2009 Jul 19.
Ischemia modified albumin (IMA), is a new biomarker of oxidative processes involved with coronary artery disease (CAD). We determined serum IMA, high-sensitivity C-reactive protein (hsCRP), and natriuretic peptide (NT-proBNP), and evaluated their correlation with severity of coronary atherosclerosis in patients undergoing coronary angiography (CA). Cardiac troponin T (cTnT), CK-MB mass, albumin and Total Antioxidant Status (TAS) were also evaluated.
The study included 114 patients (88 men and 30 women) aged 43-80 years with documented CAD without evidence of acute coronary syndrome undergoing CA and 163 controls (131 men and 32 women) similarly aged.
IMA, hsCRP and NT-proBNP were higher (p<0.001 and p=0.008 for NT-proBNP) while TAS was lower (p<0.001) in patients than in controls. IMA and TAS were negatively correlated in all subjects (p<0.01). Among patients, there was no correlation between IMA and the number of diseased vessels. For CAD diagnosis the best cut-off point for IMA was 101.5 KU/L with a sensitivity and a specificity of 87.7% and a negative predictive value of 83.3%. IMA was associated with an increased risk for CAD (OR=1.23, 95% CI: 1.16-1.31; p<0.001).
IMA determination may provide earlier information of CAD presence before hsCRP or NT-proBNP elevation, contributing to early assessment of overall patient risk.
缺血修饰白蛋白(IMA)是一种与冠状动脉疾病(CAD)相关的氧化过程的新型生物标志物。我们测定了接受冠状动脉造影(CA)患者的血清IMA、高敏C反应蛋白(hsCRP)和利钠肽(NT-proBNP),并评估了它们与冠状动脉粥样硬化严重程度的相关性。还评估了心肌肌钙蛋白T(cTnT)、肌酸激酶同工酶质量(CK-MB mass)、白蛋白和总抗氧化状态(TAS)。
该研究纳入了114例年龄在43 - 80岁、确诊为CAD且无急性冠状动脉综合征证据并接受CA的患者(88例男性和30例女性)以及163例年龄相仿的对照组(131例男性和32例女性)。
患者的IMA、hsCRP和NT-proBNP水平较高(NT-proBNP的p<0.001和p = 0.008),而TAS水平较低(p<0.001)。所有受试者中IMA与TAS呈负相关(p<0.01)。在患者中,IMA与病变血管数量之间无相关性。对于CAD诊断,IMA的最佳截断值为101.5 KU/L,敏感性和特异性分别为87.7%和阴性预测值为83.3%。IMA与CAD风险增加相关(OR = 1.23,95%CI:[1.16 - 1.31];p<0.001)。
测定IMA可能在hsCRP或NT-proBNP升高之前提供CAD存在的早期信息,有助于对患者总体风险进行早期评估。