Cekmen M, Evereklioglu C, Er H, Inalöz H S, Doganay S, Türköz Y, Ozerol I H
Kocaeli University Medical Faculty, Research Hospital, Izmit, Turkey.
Int J Dermatol. 2003 Nov;42(11):870-5. doi: 10.1046/j.1365-4362.2003.01688.x.
BACKGROUND/AIMS: Vascular endothelial growth factor (VEGF) is a cytokine participating in inflammation with potent endothelial cell effects. It is produced by macrophages, neutrophils and vascular endothelial cells and can alter vessel permeability. Behçet's syndrome is a systemic inflammatory disorder with unknown etiology. Vascular endothelial dysfunction is one of the prominent features of the disease. We previously demonstrated the possible involvement of proinflammatory cytokines [tumor necrosis factor (TNF)-alpha, soluble interleukin-2 receptor (sIL-2R), interleukin (IL)-6 and IL-8], nitric oxide (NO) and adrenomedullin in the etiopathogenesis of Behçet's syndrome. Since VEGF expression is induced by these cytokines and VEGF itself is a potent stimulator of NO production with endothelial cell effects, this study aimed to investigate whether VEGF was affected during the course of Behçet's syndrome. We also assessed the possible involvement of VEGF in ocular Behçet's syndrome or in disease activity.
This multicenter case-control study included a total of 39 patients with active (n = 22) or inactive (n = 17) Behçet's syndrome (mean age, 38.1 +/- 10.4 years; 21 men and 18 women) satisfying International Study Group criteria, and 15 healthy hospital-based control volunteers (mean age, 39.2 +/- 9.3 years; eight men and seven women) matched for age and gender from a similar ethnic background. Patients were examined by a dermatologist and an ophthalmologist with an interest in Behçet's syndrome. Plasma VEGF concentrations were measured using a newly established enzyme-linked immunosorbent assay. Clinical findings and acute-phase reactant parameters such as erythrocyte sedimentation rate, alpha1-antitrypsin, alpha2-macroglobulin, and neutrophil count were used to classify the disease in Behçet's patients as active or inactive. The Wilcoxon test or the Mann-Whitney U-test was used for statistical analysis as indicated and the results were expressed as mean +/- SD, with range.
The mean plasma VEGF level in patients with Behçet's syndrome (291.9 +/- 97.1 pg/mL; range 121-532 pg/mL) was higher than that in control subjects (103.0 +/- 43.6 pg/mL; range 25-187 pg/mL) and the difference was significant (P < 0.001). Patients with active disease had significantly (P < 0.001) higher VEGF levels than patients with inactive disease (347.6 +/- 87.1 vs. 219.9 +/- 51.6 pg/mL). In addition, ocular Behçet's patients (n = 23) had higher VEGF levels (315.7 +/- 92.1 pg/mL) than nonocular patients (n = 16, 257.8 +/- 96.6 pg/mL) and the difference was of borderline significance (P = 0.041). The levels of all acute-phase reactant parameters were significantly higher in the active stage than in the inactive stage (for each, P < 0.01) or in control subjects (for each, P < 0.001).
VEGF may participate in the course of Behçet's syndrome, especially in the active stage, and elevated levels of VEGF may be an additional risk factor for the development of ocular disease, contributing to poor visual outcome.
背景/目的:血管内皮生长因子(VEGF)是一种参与炎症反应的细胞因子,对内皮细胞具有强大作用。它由巨噬细胞、中性粒细胞和血管内皮细胞产生,可改变血管通透性。白塞病是一种病因不明的全身性炎症性疾病。血管内皮功能障碍是该疾病的突出特征之一。我们之前证明促炎细胞因子[肿瘤坏死因子(TNF)-α、可溶性白细胞介素-2受体(sIL-2R)、白细胞介素(IL)-6和IL-8]、一氧化氮(NO)和肾上腺髓质素可能参与白塞病的发病机制。由于这些细胞因子可诱导VEGF表达,且VEGF本身是NO产生的强效刺激剂并对内皮细胞有作用,本研究旨在调查白塞病病程中VEGF是否受到影响。我们还评估了VEGF在眼部白塞病或疾病活动中的可能作用。
这项多中心病例对照研究共纳入39例符合国际研究组标准的活动期(n = 22)或非活动期(n = 17)白塞病患者(平均年龄38.1±10.4岁;男性21例,女性18例),以及15名来自相似种族背景、年龄和性别匹配的健康医院对照志愿者(平均年龄39.2±9.3岁;男性8例,女性7例)。患者由对白塞病感兴趣的皮肤科医生和眼科医生进行检查。使用新建立的酶联免疫吸附测定法测量血浆VEGF浓度。临床发现以及急性期反应物参数如红细胞沉降率、α1-抗胰蛋白酶、α2-巨球蛋白和中性粒细胞计数用于将白塞病患者的疾病分为活动期或非活动期。根据需要使用Wilcoxon检验或Mann-Whitney U检验进行统计分析,结果以平均值±标准差表示,并给出范围。
白塞病患者的平均血浆VEGF水平(291.9±97.1 pg/mL;范围121 - 532 pg/mL)高于对照组(103.0±43.6 pg/mL;范围25 - 187 pg/mL),差异有统计学意义(P < 0.001)。活动期疾病患者的VEGF水平显著高于非活动期疾病患者(P < 0.001)(347.6±87.1 vs. 219.9±51.6 pg/mL)。此外,眼部白塞病患者(n = 23)的VEGF水平(315.7±92.1 pg/mL)高于非眼部患者(n = 16,257.8±96.6 pg/mL),差异具有临界显著性(P = 0.041)。所有急性期反应物参数的水平在活动期均显著高于非活动期(每项P < 0.01)或对照组(每项P < 0.001)。
VEGF可能参与白塞病的病程,尤其是在活动期,VEGF水平升高可能是眼部疾病发生的另一个危险因素,导致视力预后不良。