Hagag Adel A E, Abdel-Lateef Amal E, Aly Rabab
Department of Pediatrics, Tanta University Hospital, Tanta, Egypt
Department of Clinical Pathology, Tanta University, Egypt.
J Oncol Pharm Pract. 2014 Oct;20(5):356-61. doi: 10.1177/1078155213508439. Epub 2013 Nov 15.
Acute lymphoblastic leukemia is the most common childhood malignancies, representing nearly one-third of all pediatric cancers. Thrombomodulin is a membrane glycoprotein in the vascular endothelium. Its plasma level depends on the integrity of the endothelium. Soluble thrombomodulin is derived from injured endothelial cells or proteolytically cleaved from thrombomodulin by proteases. Von Willebrand factor is a blood glycoprotein involved in homeostasis. Its plasma level increases in neoplastic diseases and arises from adverse changes in the endothelium. Severe endothelial dysfunction is present during the acute phase of acute lymphoblastic leukemia. Plasma levels of von Willebrand factor and soluble thrombomodulin have been used as indexes of endothelial dysfunction.
The aim of this study was to assess serum soluble thrombomodulin and von Willebrand factor levels in children with acute lymphoblastic leukemia during acute phase of the disease to assess their potential prognostic value.
Forty patients with acute lymphoblastic leukemia included 26 males and 14 females with their ages ranged from 2 to 10 years and 20 healthy children of matched age and sex were included in this study. We analyzed serum soluble thrombomodulin and von Willebrand factor levels by enzyme-linked immunosorbent assay.
In children with acute lymphoblastic leukemia, there was a significant increase in soluble thrombomodulin, and von Willebrand factor levels during the acute phase of the disease. Children with an unfavorable outcome had higher levels of thrombomodulin and von Willebrand factor levels.
Serum thrombomodulin and von Willebrand factor levels as a parameter of endothelial dysfunction during the acute phase of acute lymphoblastic leukemia might represent an additional prognostic marker in childhood acute lymphoblastic leukemia.
急性淋巴细胞白血病是儿童最常见的恶性肿瘤,占所有儿童癌症的近三分之一。血栓调节蛋白是血管内皮中的一种膜糖蛋白。其血浆水平取决于内皮的完整性。可溶性血栓调节蛋白来源于受损的内皮细胞或由蛋白酶从血栓调节蛋白上蛋白水解切割而来。血管性血友病因子是一种参与体内平衡的血液糖蛋白。其血浆水平在肿瘤性疾病中升高,且源于内皮的不良变化。急性淋巴细胞白血病急性期存在严重的内皮功能障碍。血管性血友病因子和可溶性血栓调节蛋白的血浆水平已被用作内皮功能障碍的指标。
本研究旨在评估急性淋巴细胞白血病患儿疾病急性期血清可溶性血栓调节蛋白和血管性血友病因子水平,以评估其潜在的预后价值。
40例急性淋巴细胞白血病患者,其中男性26例,女性14例,年龄2至10岁,本研究纳入20例年龄和性别匹配的健康儿童。我们采用酶联免疫吸附测定法分析血清可溶性血栓调节蛋白和血管性血友病因子水平。
急性淋巴细胞白血病患儿在疾病急性期可溶性血栓调节蛋白和血管性血友病因子水平显著升高。预后不良的患儿血栓调节蛋白和血管性血友病因子水平较高。
血清血栓调节蛋白和血管性血友病因子水平作为急性淋巴细胞白血病急性期内皮功能障碍的参数,可能是儿童急性淋巴细胞白血病的一个额外预后标志物。