Laboratory of Molecular Cardiology, Department of Cardiology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Med Sci Monit. 2019 Dec 22;25:9864-9874. doi: 10.12659/MSM.918913.
BACKGROUND Acute coronary syndrome (ACS) occurs approximately every 40 seconds, and was an underlying cause of death in 1 out of every 7 deaths. More accurate indicators are needed to distinguish patients with ACS from patients manifesting negative changes in electrocardiogram (ECG) and myocardial enzymes. This study aimed to investigate whether the expression of platelet carcinoembryonic antigen cell adhesion molecule-5 (CEACAM5/CEA/CD66e) could help predict ACS. MATERIAL AND METHODS We enrolled 82 participants (mean age 60 years, 33 females and 49 males). The expression of CEA on washed human platelets was assessed using two-color flow cytometry. The CEA levels on platelets and in serum of these 82 consecutive patients were detected using two-color whole-blood flow cytometry analysis and a custom-made Luminex multiplex assay, respectively. RESULTS CEA was expressed on the surface of human platelets. The expression of platelet CEA (P<0.01), but not serum CEA (P=0.30), was significantly higher in patients with ACS compared to patients with normal coronary artery. Increased platelet CEA levels could serve as a new independent indicator for ACS (P=0.0003). Platelet CEA testing (P=0.000002), as well as cardiac troponin I (cTnI) (P=0.0005), can diagnose ACS with high sensitivity and specificity, and, combined with cTnI (P<0.0001), can improve the diagnostic value. CONCLUSIONS Platelet CEA expression was higher in individuals presenting with ACS. Hence, platelet CEA might be a novel and reliable biomarker for ACS. Large-scale studies are needed to confirm this hypothesis.
急性冠状动脉综合征(ACS)每 40 秒发生一次,每 7 例死亡中就有 1 例是其根本原因。需要更准确的指标来区分 ACS 患者和心电图(ECG)和心肌酶谱出现负性改变的患者。本研究旨在探讨血小板癌胚抗原细胞黏附分子-5(CEACAM5/CEA/CD66e)的表达是否有助于预测 ACS。
我们纳入了 82 名参与者(平均年龄 60 岁,女性 33 名,男性 49 名)。使用双色流式细胞术评估洗涤后人血小板上 CEA 的表达。使用双色全血流式细胞术分析和定制的 Luminex 多重测定法分别检测 82 例连续患者血小板和血清中的 CEA 水平。
CEA 表达于人血小板表面。与正常冠状动脉患者相比,ACS 患者血小板 CEA(P<0.01),而非血清 CEA(P=0.30)的表达显著升高。血小板 CEA 水平升高可作为 ACS 的新独立指标(P=0.0003)。血小板 CEA 检测(P=0.000002)以及心肌肌钙蛋白 I(cTnI)(P=0.0005)均具有高灵敏度和特异性,与 cTnI 联合(P<0.0001)可提高诊断价值。
ACS 患者的血小板 CEA 表达升高。因此,血小板 CEA 可能是 ACS 的新型可靠生物标志物。需要进行大规模研究来验证这一假设。