Section of Rheumatology, Department of Medicine, School of Medicine, Vasculitis Center, Boston University, Boston, Massachusetts, United States of America.
PLoS One. 2012;7(1):e30197. doi: 10.1371/journal.pone.0030197. Epub 2012 Jan 18.
The endothelial-specific Angiopoietin-Tie2 ligand-receptor system is an important regulator of endothelial activation. Binding of angiopoietin-2 (Ang-2) to Tie2 receptor renders the endothelial barrier responsive to pro-inflammatory cytokines. We previously showed that circulating Ang-2 correlated with disease severity in a small cohort of critically ill patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis. The current study reassessed Ang-2 as a biomarker of disease activity and relapse in AAV. Circulating Ang-2 was measured in 162 patients with severe AAV (BVAS/WG≥3, with or without glomerulonephritis) in a clinical trial. Ang-2 levels during active AAV were compared to levels in the same patients during remission (BVAS/WG = 0). Levels in clinical subsets of AAV were compared, and association with future disease course was assessed. Ang-2 levels were elevated in severe disease (median 3.0 ng/ml, interquartile range 1.9-4.4) compared to healthy controls (1.2, 0.9-1.5). However, they did not reliably decline with successful treatment (median 2.6 ng/ml, interquartile range 1.9-3.8, median change -0.1). Ang-2 correlated weakly with BVAS/WG score (r = 0.17), moderately with markers of systemic inflammation (r = 0.25-0.41), and inversely with renal function (r = -0.36). Levels were higher in patients with glomerulonephritis, but levels adjusted for renal dysfunction were no different in patients with or without glomerulonephritis. Levels were higher in patients with newly diagnosed AAV and lower in patients in whom treatment had recently been started. Ang-2 levels during active disease did not predict response to treatment, and Ang-2 levels in remission did not predict time to flare. Thus, Ang-2 appears to have limited practical value in AAV as a biomarker of disease activity at time of measurement or for predicting future activity.
血管内皮细胞特异性血管生成素- Tie2 配体-受体系统是内皮细胞激活的重要调节因子。血管生成素-2(Ang-2)与 Tie2 受体结合使内皮屏障对促炎细胞因子产生反应。我们之前的研究表明,在一小部分患有抗中性粒细胞胞质抗体(ANCA)相关性血管炎的危重病患者中,循环 Ang-2 与疾病严重程度相关。本研究重新评估了 Ang-2 在 AAV 中的疾病活动和复发的生物标志物。在一项临床试验中,对 162 例严重 AAV(BVAS/WG≥3,伴有或不伴有肾小球肾炎)患者进行了循环 Ang-2 的测量。将活动期 AAV 患者的 Ang-2 水平与缓解期(BVAS/WG=0)患者的水平进行比较。比较了 AAV 的临床亚组的水平,并评估了与未来疾病过程的关联。与健康对照组(1.2,0.9-1.5)相比,严重疾病(中位数 3.0ng/ml,四分位距 1.9-4.4)的 Ang-2 水平升高。然而,随着成功治疗,它们并没有可靠地下降(中位数 2.6ng/ml,四分位距 1.9-3.8,中位数变化-0.1)。Ang-2 与 BVAS/WG 评分呈弱相关(r=0.17),与系统炎症标志物中度相关(r=0.25-0.41),与肾功能呈负相关(r=-0.36)。在有肾小球肾炎的患者中,Ang-2 水平较高,但调整肾功能障碍后的水平在有或没有肾小球肾炎的患者中无差异。在新诊断为 AAV 的患者中,Ang-2 水平较高,而在最近开始治疗的患者中,Ang-2 水平较低。活动期疾病期间的 Ang-2 水平不能预测治疗反应,缓解期的 Ang-2 水平不能预测复发时间。因此,Ang-2 作为一种测量时疾病活动的生物标志物或预测未来活动的标志物,在 AAV 中似乎具有有限的实际价值。