Premnath Sujatha Mahadevarao, Nanda Sunil Kumar, Ray Lopamudra, Arokiaraj Mark Christopher, Ravichandran Kandasamy
Department of Biochemistry, Pondicherry Institute of Medical Science, Pondicherry University, Puducherry, India.
Department of Biochemistry, Shri Balaji Institute of Medical Sciences, Raipur, Chhattisgarh, India.
Int J Appl Basic Med Res. 2022 Oct-Dec;12(4):249-253. doi: 10.4103/ijabmr.ijabmr_203_22. Epub 2022 Dec 19.
Atherosclerosis being the keystone in the pathology of coronary artery disease (CAD) is a chronic inflammation of arterial intima mediated by various inflammatory markers. Pentraxin 3 (PTX3) and high-sensitivity C-reactive protein (hs-CRP) are the two important biomarkers of chronic inflammation that causes atherosclerosis.
This study aims to investigate the association of serum PTX3 and hs-CRP with the severity of coronary stenosis in patients undergoing coronary angiogram.
A total of 80 patients who underwent elective coronary angiogram were included. Their blood sample was collected for PTX3 and hs-CRP estimation prior to angiogram. Based on the angiogram, the participants were divided into four groups based on the number of arteries affected. PTX3 was estimated using enzyme-linked immunosorbent assay and hs-CRP was assayed using latex-enhanced immunosorbent assay.
Kruskal-Wallis test was used to find the association of PTX3 and hs-CRP in each group and Pearson's correlation was used to correlate PTX3 and hs-CRP with the extent of stenosis.
The mean PTX3 and hs-CRP levels in patients with some lesions in the coronary artery were 231.5 ± 129.9 pg/mL and 2.4 ± 0.4 mg/mL, respectively. The PTX3 levels elevate gradually with the severity of stenosis with = 0.000 which is highly significant. A strong positive correlation was observed ( = 0.7929, < 0.00001) with PTX3 and severity of stenosis. Whereas, for hs-CRP, the correlation was weaker ( = 0.3011, = 0.006).
PTX3 and hs-CRP can not only predict the number of arteries affected but also can differentiate between normal coronaries and CAD which can minimize the use of angiography.
动脉粥样硬化是冠状动脉疾病(CAD)病理的关键因素,是由多种炎症标志物介导的动脉内膜慢性炎症。五聚体3(PTX3)和高敏C反应蛋白(hs-CRP)是导致动脉粥样硬化的慢性炎症的两个重要生物标志物。
本研究旨在探讨接受冠状动脉造影的患者血清PTX3和hs-CRP与冠状动脉狭窄严重程度的相关性。
共纳入80例行择期冠状动脉造影的患者。在造影前采集他们的血样以检测PTX3和hs-CRP。根据造影结果,根据受累动脉数量将参与者分为四组。采用酶联免疫吸附测定法检测PTX3,采用乳胶增强免疫吸附测定法检测hs-CRP。
采用Kruskal-Wallis检验来发现每组中PTX3和hs-CRP的相关性,并采用Pearson相关性分析来分析PTX3和hs-CRP与狭窄程度的相关性。
冠状动脉有一些病变的患者中,PTX3和hs-CRP的平均水平分别为231.5±129.9 pg/mL和2.4±0.4 mg/mL。PTX3水平随狭窄严重程度逐渐升高,P = 0.000,具有高度显著性。观察到PTX3与狭窄严重程度呈强正相关(r = 0.7929,P < 0.00001)。而对于hs-CRP,相关性较弱(r = 0.3011,P = 0.006)。
PTX3和hs-CRP不仅可以预测受累动脉的数量,还可以区分正常冠状动脉和CAD,从而可减少血管造影的使用。