Paganelli Franck, Cappiello Gabriel, Aliouane Soumeya, Kipson Nathalie, Criado Christine, Hamou Khadidja, Ntawanga Jehuel, Peroni Erika, Carreno Maria, Methlin Lucas, Mottola Giovanna, Fromonot Julien, Deharo Pierre, Gaudry Marine, Marlinge Marion, Guieu Régis, Ruf Jean
Department of Cardiology, North Hospital, 13015 Marseille, France.
Center for Cardio-Vascular and Nutrition Research (C2VN), INSERM, INRAE and Aix-Marseille University, 13005 Marseille, France.
Biomedicines. 2022 Aug 1;10(8):1849. doi: 10.3390/biomedicines10081849.
The evaluation of suspected coronary artery disease (CAD) in the medical community is challenging. Patients with suspected coronary chronic syndrome (CCS) are referred by the medical community to be assessed by specialists for the performance of noninvasive tests that have high rates of false positives and false negatives. While troponins are the gold standard for evaluate myocardial injuries, there is no biomarker to assess myocardial ischemia in patient populations with negative electrocardiography or without an increase in troponin level. A2A adenosine receptors control the coronary blood flow through its vasodilating properties. It has been shown that patients with CAD have a lower A2AR expression on peripheral blood mononuclear cells, suggesting a link between A2AR production and the severity of CAD. Herein, we present a new and innovative method of inhibition ELISA for A2AR in the plasma of patients who permit the evaluation of the amount of soluble A2AR. For this analysis, the total study sample was 54, including 31 patients with CAD with stenosis > 50% and a significant fractional flow reserve (FFR < 0.8) (Group 1) and 23 patients with normal or non-obstructive coronary arteries (stenosis < 50% and nonsignificant FFR > 0.8) (Group 2). The % inhibition (which is linked to the presence of soluble receptors) with the plasma of patients with FFR < 0.8 was significantly lower than that of patients with FFR > 0.8 (median [range]: 68% [20.7−86.9] vs. 83% [67−88.4]; p < 0.001). The ROC curve indicated a good sensitivity/specificity ratio with a cut off of 72.5% and an area under the curve of 0.87. In conclusion, a rapid ELISA to assess soluble A2AR in the plasma shows promise to screen patients suspected of having CAD.
医学界对疑似冠状动脉疾病(CAD)的评估具有挑战性。疑似冠状动脉慢性综合征(CCS)的患者被医学界转介给专科医生,以进行无创检查,而这些检查的假阳性和假阴性率很高。虽然肌钙蛋白是评估心肌损伤的金标准,但对于心电图阴性或肌钙蛋白水平未升高的患者群体,尚无生物标志物可用于评估心肌缺血。A2A腺苷受体通过其血管舒张特性控制冠状动脉血流。研究表明,CAD患者外周血单核细胞上的A2AR表达较低,这表明A2AR产生与CAD严重程度之间存在联系。在此,我们提出了一种新的创新方法,即抑制ELISA法,用于检测允许评估可溶性A2AR量的患者血浆中的A2AR。本分析的总研究样本为54例,其中包括31例CAD患者,其狭窄程度>50%且血流储备分数明显降低(FFR<0.8)(第1组),以及23例冠状动脉正常或无阻塞的患者(狭窄程度<50%且FFR>0.8无显著意义)(第2组)。FFR<0.8的患者血浆的抑制百分比(与可溶性受体的存在相关)显著低于FFR>0.8的患者(中位数[范围]:68%[20.7−86.9]对83%[67−88.4];p<0.001)。ROC曲线显示,截断值为72.5%时,灵敏度/特异性比良好,曲线下面积为0.87。总之,一种用于评估血浆中可溶性A2AR的快速ELISA法有望用于筛查疑似CAD的患者。