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单核细胞谱系特异性可溶性CD163是冠状动脉粥样硬化的血浆标志物。

The monocytic lineage specific soluble CD163 is a plasma marker of coronary atherosclerosis.

作者信息

Aristoteli Lina Panayiota, Møller Holger Jon, Bailey Brian, Moestrup Søren Kragh, Kritharides Leonard

机构信息

Clinical Research Group, The Heart Research Institute, Sydney, Australia.

出版信息

Atherosclerosis. 2006 Feb;184(2):342-7. doi: 10.1016/j.atherosclerosis.2005.05.004. Epub 2005 Jun 23.

Abstract

BACKGROUND

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).

METHODS AND RESULTS

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).

CONCLUSIONS

The monocyte-specific marker sCD163 is a novel potential plasma marker of coronary atherosclerotic burden.

摘要

背景

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。

方法与结果

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)。

结论

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。

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