Park Gregory S, Ireland Kathleen F, Opoka Robert O, John Chandy C
Department of Pediatrics, University of Minnesota Medical School, Minneapolis.
Makerere University Faculty of Medicine, Kampala, Uganda.
J Pediatric Infect Dis Soc. 2012 Mar;1(1):16-25. doi: 10.1093/jpids/pis010. Epub 2012 Mar 1.
Endothelial activation may contribute to development of severe disease from Plasmodium falciparum infection, but optimal markers of endothelial activation in severe malaria, the extent of endothelial activation in asymptomatic infection, and the effect of blood group O on endothelial activation have not been defined.
Serum levels of 3 markers of endothelial activation-von Willebrand factor (VWF), soluble intercellular adhesion molecule-1 (sICAM-1), and soluble vascular cell adhesion molecule-1 (sVCAM-1)-were assessed in Ugandan children with cerebral malaria (CM) (n = 86), children with uncomplicated malaria (UM) (n = 81), and community children (CC) (n = 90).
Serum VWF, sICAM-1, and sVCAM-1 levels were all elevated in asymptomatic community children with microscopy-confirmed parasitemia when compared with children without parasitemia by microscopy or polymerase chain reaction (all, P ≤ .05). Levels of VWF, sICAM-1, and sVCAM-1 were higher in children with UM than in CC (all, P < 0.001), but only VWF levels effectively distinguished CM from UM (P < 0.001), a finding confirmed by receiver operating characteristic analyses (area under the curve = 0.67; 95% confidence interval, .58-.75). Von Willebrand factor levels were lower in children with blood group O versus non-O blood groups across the disease spectrum, but VWF levels remained higher in CM versus UM, even after controlling for blood group.
Endothelial activation, as assessed by serum levels of VWF, sICAM-1, and sVCAM-1, occurs even in subclinical P. falciparum parasitemia. Von Willebrand factor levels increase with greater malaria disease severity. Blood group O is associated with lower VWF levels, but presence of blood group O alone does not explain the higher VWF levels seen in children with CM.
内皮细胞激活可能促使恶性疟原虫感染发展为严重疾病,但严重疟疾中内皮细胞激活的最佳标志物、无症状感染时内皮细胞激活的程度以及O血型对内皮细胞激活的影响尚未明确。
对乌干达患有脑型疟疾(CM)的儿童(n = 86)、患有非重症疟疾(UM)的儿童(n = 81)和社区儿童(CC)(n = 90),评估血清中3种内皮细胞激活标志物——血管性血友病因子(VWF)、可溶性细胞间黏附分子-1(sICAM-1)和可溶性血管细胞黏附分子-1(sVCAM-1)的水平。
与通过显微镜或聚合酶链反应检测无寄生虫血症的儿童相比,显微镜确诊有寄生虫血症的无症状社区儿童血清VWF、sICAM-1和sVCAM-1水平均升高(均P≤0.05)。UM儿童的VWF、sICAM-1和sVCAM-1水平高于CC儿童(均P<0.001),但只有VWF水平能有效区分CM和UM(P<0.001),这一发现经受试者工作特征分析得到证实(曲线下面积=0.67;95%置信区间,0.58 - 0.75)。在整个疾病谱中,O血型儿童的血管性血友病因子水平低于非O血型儿童,但即使在控制血型因素后,CM儿童的VWF水平仍高于UM儿童。
通过血清VWF、sICAM-1和sVCAM-1水平评估,即使在亚临床恶性疟原虫寄生虫血症中也会发生内皮细胞激活。血管性血友病因子水平随疟疾疾病严重程度增加而升高。O血型与较低的VWF水平相关,但仅O血型的存在并不能解释CM儿童中较高的VWF水平。