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Soluble CD163 a Novel Marker of Activated Macrophages Is Elevated and Associated With Noncalcified Coronary Plaque in HIV-Infected Patients

机译:可溶性CD163一种活化的巨噬细胞的新标记在HIV感染患者中升高并与非钙化冠状动脉斑块相关

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>Background. Pro-inflammatory monocytes/macrophages may contribute to increased atherosclerosis in human immunodeficiency virus (HIV)–infected patients. We investigate—to our knowledge, for the first time—sCD163 and other markers of monocyte activation in relationship to atherosclerotic plaque in HIV-infected patients.>Methods. One hundred two HIV-infected and 41 HIV-seronegative men with equivalent cardiovascular risk factors and without history of coronary artery disease were prospectively recruited and underwent computed tomography coronary angiography.>Results. sCD163 levels and presence of plaque were significantly higher among antiretroviral-treated subjects with undetectable HIV RNA levels, compared with seronegative controls (1172 ± 646 vs. 883 ± 561 ng/mL [P = .02] for sCD163 and 61% vs. 39% [P = .03] for presence of plaque). After adjusting for age, race, lipids, blood pressure, glucose, smoking, sCD14, and HIV infection, sCD163 remained independently associated with noncalcified plaque (P = .008). Among HIV-infected patients, sCD163 was associated with coronary segments with noncalcified plaque (r = 0.21; P = .04), but not with calcium score. In contrast, markers of generalized inflammation, including C-reactive protein level, and D-dimer were not associated with sCD163 or plaque among HIV-infected patients.>Conclusions. sCD163, a monocyte/macrophage activation marker, is increased in association with noncalcified coronary plaque in men with chronic HIV infection and low or undetectable viremia. These data suggest a potentially important role of chronic monocyte/macrophage activation in the development of noncalcified vulnerable plaque.>Clinical Trial Registration. .
机译:>背景。促炎性单核细胞/巨噬细胞可能导致感染人类免疫缺陷病毒(HIV)的患者的动脉粥样硬化增加。我们首次调查了艾滋病毒感染患者中sCD163和单核细胞活化与动脉粥样硬化斑块的关系的其他标志物。>方法。 102名艾滋病毒感染者和41名艾滋病毒血清阴性者前瞻性征募了具有相同心血管危险因素且无冠心病病史的男性,并进行了计算机断层扫描冠状动脉造影。>结果。在未检测到HIV RNA的抗逆转录病毒治疗的受试者中,sCD163水平和斑块的存在显着增加与血清阴性对照相比(sCD163为1172±646 vs. 883±561 ng / mL [P = .02],斑块存在为61%vs. 39%[P = .03])。在调整了年龄,种族,脂质,血压,葡萄糖,吸烟,sCD14和HIV感染后,sCD163仍与未钙化斑块独立相关(P = 0.008)。在感染HIV的患者中,sCD163与冠状动脉节段伴有非钙化斑块相关(r = 0.21; P = .04),而与钙积分无关。相比之下,在HIV感染患者中,包括C反应蛋白水平和D-二聚体在内的全身性炎症标记与sCD163或斑块无关。>结论。 sCD163,单核细胞/巨噬细胞激活标记,慢性HIV感染和低或无法检测到病毒血症的男性中,与非钙化性冠状动脉斑块相关的血红蛋白增加。这些数据表明,慢性单核细胞/巨噬细胞活化在非钙化易损斑块形成中可能具有重要作用。>临床试验注册。

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