Aristoteli Lina Panayiota, Møller Holger Jon, Bailey Brian, Moestrup Søren Kragh, Kritharides Leonard
Clinical Research Group, The Heart Research Institute, Sydney, Australia.
Atherosclerosis. 2006 Feb;184(2):342-7. doi: 10.1016/j.atherosclerosis.2005.05.004. Epub 2005 Jun 23.
CD163 is a monocyte-macrophage lineage specific scavenger receptor that mediates the uptake and clearance of haptoglobin-haemoglobin complexes, and soluble CD163 (sCD163) is also present in plasma. As atherosclerosis involves infiltration by monocyte-derived macrophages, we investigated whether sCD163 may act as a marker of coronary atherosclerosis (CAD).
Clinical features were identified and plasma was collected from 147 consecutive patients presenting for coronary angiography. Patients were classified as having CAD+, or being free of CAD- haemodynamically significant (>50% luminal diameter) coronary stenoses in one or more major coronary arteries (1, 2 or 3 vessel disease), and sCD163 concentration was measured by ELISA. Plasma sCD163 was non-parametrically distributed, being significantly higher in CAD+ patients (median 2.47 mg/L, 25th-75th percentile, 1.79-3.5mg/L) than in CAD- patients (2.09, 1.31-2.72 mg/L) (p=0.021, Mann-Whitney U-test). LogsCD163 increased significantly with increasing CAD extent (p=0.0036) and was significantly greater in patients with 3 vessel disease than in CAD- patients (p<0.001). Whereas logsCD163 correlated with CAD extent (Spearman r=0.22, p=0.008), logCRP did not, and sCD163 was only weakly correlated with CRP (r=0.19, p=0.039). Importantly, multivariate linear regression identified that sCD163 (p=0.0021) was a significant predictor of CAD extent and was independent of conventional risk factors age (p<0.0001), hypercholesterolemia (p=0.0023), hypertension (p=0.068), and current smoking (p=0.066).
The monocyte-specific marker sCD163 is a novel potential plasma marker of coronary atherosclerotic burden.
CD163是一种单核细胞-巨噬细胞谱系特异性清道夫受体,可介导结合珠蛋白-血红蛋白复合物的摄取和清除,可溶性CD163(sCD163)也存在于血浆中。由于动脉粥样硬化涉及单核细胞衍生的巨噬细胞浸润,我们研究了sCD163是否可作为冠状动脉粥样硬化(CAD)的标志物。
确定了147例连续接受冠状动脉造影患者的临床特征并采集了血浆。根据在一根或多根主要冠状动脉(1支、2支或3支血管病变)中是否存在血流动力学显著(管腔直径>50%)的冠状动脉狭窄,将患者分为CAD+组或无CAD-组,并通过酶联免疫吸附测定法测量sCD163浓度。血浆sCD163呈非参数分布,CAD+组患者(中位数2.47mg/L,第25-75百分位数,1.79-3.5mg/L)显著高于CAD-组患者(2.09,1.31-2.72mg/L)(p=0.021,曼-惠特尼U检验)。Log sCD163随CAD程度增加而显著升高(p=0.0036),且3支血管病变患者的Log sCD163显著高于CAD-组患者(p<0.001)。虽然Log sCD163与CAD程度相关(斯皮尔曼r=0.22,p=0.008),但Log CRP与CAD程度无关,且sCD163与CRP仅呈弱相关(r=0.19,p=0.039)。重要的是,多变量线性回归分析表明,sCD163(p=0.0021)是CAD程度的显著预测因子,且独立于传统危险因素年龄(p<0.0001)、高胆固醇血症(p=0.0023)、高血压(p=0.068)和当前吸烟情况(p=0.066)。
单核细胞特异性标志物sCD163是一种新型的潜在血浆冠状动脉粥样硬化负荷标志物。