Elgebaly Salwa A, Christenson Robert H, Kandil Hossam, Ibrahim Mohsen, Rizk Hussien, El-Khazragy Nashwa, Rashed Laila, Yacoub Beshoy, Eldeeb Heba, Ali Mahmoud M, Kreutzer Donald L
Research & Development, Nour Heart, Inc., Vienna, VA 22180, USA.
Department of Surgery, UConn Health, School of Medicine, Farmington, CT 06032, USA.
Diagnostics (Basel). 2021 Apr 14;11(4):703. doi: 10.3390/diagnostics11040703.
Although cardiovascular imaging techniques are widely used to diagnose myocardial ischemia in patients with suspected stable coronary artery disease (CAD), they have limitations related to lack of specificity, sensitivity and "late" diagnosis. Additionally, the absence of a simple laboratory test that can detect myocardial ischemia in CAD patients, has led to many patients being first diagnosed at the time of the development of myocardial infarction. Nourin is an early blood-based biomarker rapidly released within five minutes by "reversible" ischemic myocardium before progressing to necrosis. Recently, we demonstrated that the Nourin-dependent (marker of cell damage) and (marker of inflammation) can diagnose myocardial ischemia in patients with unstable angina (UA) and also stratify severity of ischemia, with higher expression in acute ST-segment elevation myocardial infarction (STEMI) patients compared to UA patients. Minimal baseline-gene expression levels of Nourin miRNAs were detected in healthy subjects.
To determine: (1) whether Nourin miRNAs are elevated in chest pain patients with myocardial ischemia suspected of CAD, who also underwent dobutamine stress echocardiography (DSE) or ECG/Treadmill stress test, and (2) whether the elevated levels of serum Nourin miRNAs correlate with results of ECHO/ECG stress test in diagnosing CAD patients.
Serum gene expression levels of , and their corresponding molecular pathway network were measured blindly in 70 enrolled subjects using quantitative real time PCR (qPCR). Blood samples were collected from: (1) patients with chest pain suspected of myocardial ischemia ( = 38) both immediately "pre-stress test" and "post-stress test" 30 min. after test termination; (2) patients with acute STEMI ( = 16) functioned as our positive control; and (3) healthy volunteers ( = 16) who, also, exercised on ECG/Treadmill stress test for Nourin baseline-gene expression levels.
(1) strong correlation was observed between Nourin miRNAs serum expression levels and results obtained from ECHO/ECG stress test in diagnosing myocardial ischemia in CAD patients; (2) positive "post-stress test" patients with CAD diagnosis showed upregulation of by 572-fold and by 122-fold, when compared to negative "post-stress test" patients ( < 0.001); (3) similarly, positive "pre-stress test" CAD patients showed upregulation of by 1198-fold and by 114-fold, when compared to negative "pre-stress test" patients ( < 0.001); and (4) healthy subjects had minimal baseline-gene expressions of Nourin miRNAs.
Nourin-dependent and are promising novel blood-based biomarkers for early diagnosis of myocardial ischemia in chest pain patients suspected of CAD in outpatient clinics. Early identification of CAD patients, while patients are in the stable state before progressing to infarction, is key to providing crucial diagnostic steps and therapy to limit adverse cardiac events, improve patients' health outcome and save lives.
尽管心血管成像技术被广泛用于诊断疑似稳定型冠状动脉疾病(CAD)患者的心肌缺血,但它们存在缺乏特异性、敏感性以及“延迟”诊断等局限性。此外,由于缺乏一种能够检测CAD患者心肌缺血的简单实验室检测方法,导致许多患者在心肌梗死发生时才首次被诊断出来。Nourin是一种早期血液生物标志物,在“可逆性”缺血心肌进展为坏死之前的五分钟内迅速释放。最近,我们证明了依赖Nourin的(细胞损伤标志物)和(炎症标志物)可以诊断不稳定型心绞痛(UA)患者的心肌缺血,还能对缺血严重程度进行分层,与UA患者相比,急性ST段抬高型心肌梗死(STEMI)患者中的表达更高。在健康受试者中检测到Nourin微小RNA的基线基因表达水平极低。
确定:(1)在疑似CAD且接受了多巴酚丁胺负荷超声心动图(DSE)或心电图/平板运动试验的胸痛心肌缺血患者中,Nourin微小RNA水平是否升高;(2)血清Nourin微小RNA水平升高是否与诊断CAD患者的超声心动图/心电图负荷试验结果相关。
使用定量实时聚合酶链反应(qPCR)对70名入组受试者的血清基因表达水平、及其相应的分子通路网络进行盲法检测。血液样本采集自:(1)疑似心肌缺血的胸痛患者(n = 38),在“负荷试验前”和试验结束后30分钟的“负荷试验后”立即采集;(2)急性STEMI患者(n = 16)作为我们的阳性对照;(3)健康志愿者(n = 16),他们也进行了心电图/平板运动试验以检测Nourin基线基因表达水平。
(1)在诊断CAD患者的心肌缺血时,观察到Nourin微小RNA血清表达水平与超声心动图/心电图负荷试验结果之间存在强烈相关性;(2)与“负荷试验后”阴性患者相比,CAD诊断阳性的“负荷试验后”患者的上调了572倍,上调了122倍(P < 0.001);(3)同样,与“负荷试验前”阴性患者相比,CAD诊断阳性的“负荷试验前”患者的上调了1198倍,上调了114倍(P < 0.001);(4)健康受试者的Nourin微小RNA基线基因表达水平极低。
依赖Nourin的和是有前景的新型血液生物标志物,可用于门诊疑似CAD的胸痛患者心肌缺血的早期诊断。在CAD患者进展为梗死之前处于稳定状态时尽早识别,是提供关键诊断步骤和治疗以限制不良心脏事件、改善患者健康结局和挽救生命的关键。