Hassan Jabbar Auda, Ali Mohammed Barakat, Hassan Sarhan Sachet, Raed Fanoukh Aboqader, Adnan Taan Thamer
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Serum levels of TNF-α and E-selectin were measured using enzyme-linked immunosorbent assay (ELISA). Results showed significant differences in lipid profiles between ACS patients and controls, supporting the impact of dyslipidemia on ACS development. E-selectin levels were significantly elevated in ACS patients (213.26 ± 2.72 pg/mL) compared to controls (175.11 ± 2.71 pg/mL), with P < 0.0001. Similarly, TNF-α levels were higher in patients (83.20 ± 3.88 pg/mL) than controls (45.65 ± 1.79 pg/mL), also with P < 0.0001. ROC curve analysis demonstrated that E-selectin had 96% sensitivity and specificity at a cutoff of 73.44 pg/mL, while TNF-α had 93% sensitivity and 86% specificity at a cutoff of 188.65 pg/mL. 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引用次数: 0
摘要
冠状动脉疾病(CAD)仍然是世界范围内死亡的主要原因,特别是在发展中国家,血脂异常是一个主要的危险因素。本研究旨在评估脂质参数和炎症生物标志物- e -选择素和肿瘤坏死因子-α (TNF-α),以了解它们在急性冠脉综合征(ACS)发病中的作用。采用病例对照设计,涉及120名参与者:60名诊断为ACS的患者和60名健康对照者,于2024年1月至12月登记。使用SMART-120化学分析仪分析血液样本以评估脂质谱,包括总胆固醇、甘油三酯、HDL、LDL和VLDL。采用酶联免疫吸附法(ELISA)检测血清TNF-α和e-选择素水平。结果显示ACS患者和对照组之间的脂质谱存在显著差异,支持血脂异常对ACS发展的影响。ACS患者E-selectin水平(213.26±2.72 pg/mL)显著高于对照组(175.11±2.71 pg/mL),差异有统计学意义(P < 0.0001)。同样,患者的TNF-α水平(83.20±3.88 pg/mL)高于对照组(45.65±1.79 pg/mL), P < 0.0001。ROC曲线分析表明,E-selectin在73.44 pg/mL的临界值下具有96%的敏感性和特异性,TNF-α在188.65 pg/mL的临界值下具有93%的敏感性和86%的特异性。两种生物标志物均与体重指数呈正相关(r = 0.572, P < 0.0001)。研究结果表明,TNF-α和E-selectin是ACS的潜在诊断生物标志物,并发挥关键作用。
TNF-α and E-Selectin as Valuable Biomarkers in Patients with Acute Coronary Artery Syndrome.
Coronary artery disease (CAD) remains the leading cause of mortality worldwide, especially in developing countries, with dyslipidemia being a major risk factor. This study aimed to evaluate lipid parameters and inflammatory biomarkers-E-selectin and tumor necrosis factor-alpha (TNF-α)-to understand their roles in the pathogenesis of acute coronary syndrome (ACS). A case-control design was used, involving 120 participants: 60 patients diagnosed with ACS and 60 healthy controls, enrolled between January and December 2024. Blood samples were analyzed to assess lipid profiles, including total cholesterol, triglycerides, HDL, LDL, and VLDL, using a SMART-120 chemistry analyzer. Serum levels of TNF-α and E-selectin were measured using enzyme-linked immunosorbent assay (ELISA). Results showed significant differences in lipid profiles between ACS patients and controls, supporting the impact of dyslipidemia on ACS development. E-selectin levels were significantly elevated in ACS patients (213.26 ± 2.72 pg/mL) compared to controls (175.11 ± 2.71 pg/mL), with P < 0.0001. Similarly, TNF-α levels were higher in patients (83.20 ± 3.88 pg/mL) than controls (45.65 ± 1.79 pg/mL), also with P < 0.0001. ROC curve analysis demonstrated that E-selectin had 96% sensitivity and specificity at a cutoff of 73.44 pg/mL, while TNF-α had 93% sensitivity and 86% specificity at a cutoff of 188.65 pg/mL. Both biomarkers positively correlated with body mass index (r = 0.572, P < 0.0001).The findings suggest that TNF-α and E-selectin are potential diagnostic biomarkers for ACS and play key .
期刊介绍:
The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).