Division of Nephrology, Department of Internal Medicine, Ewha Womans University School of Medicine, Seoul, Korea.
Korean J Intern Med. 2012 Sep;27(3):327-37. doi: 10.3904/kjim.2012.27.3.327. Epub 2012 Sep 1.
BACKGROUND/AIMS: Chronic inflammatory status is a possible risk factor for vascular access dysfunction in hemodialysis (HD) patients, but susceptibility differences appear among individuals. Interleukin (IL)-6 is a well-known inflammatory cytokine with various polymorphisms. We examined whether IL-6 polymorphisms are associated with vascular access dysfunction in HD patients.
A total of 80 HD patients (including 42 diabetic patients) were enrolled. Polymorphisms in the IL-6 gene promoter (-634 C/G and -174 G/C) were studied using restriction length polymorphism polymerase chain reaction analysis. Vascular access patency was compared between the patient groups with respect to IL-6 polymorphisms. An additional 89 healthy individuals were enrolled in the control group. Plasma IL-6 levels were determined by enzyme-linked immunosorbent assay.
The GG genotype and G allele at position -634 in the IL-6 promoter were more frequently observed in HD patients than in controls. Furthermore, the distribution of the -634 polymorphism differed according to vascular access patency in non-diabetic HD patients. However, the G allele was not a significant risk factor for early access failure. No significant association appeared between the IL-6 -634 C/G polymorphism and plasma IL-6 levels. The C allele of the IL-6 -174 G/C polymorphism was not detected in our study population.
The IL-6 -634 G allele appears with greater frequently in patients with end-stage renal disease and may be associated with vascular access dysfunction in non-diabetic HD patients.
背景/目的:慢性炎症状态是血液透析(HD)患者血管通路功能障碍的一个可能的危险因素,但个体之间存在易感性差异。白细胞介素(IL)-6 是一种众所周知的具有多种多态性的炎症细胞因子。我们研究了 IL-6 多态性是否与 HD 患者的血管通路功能障碍有关。
共纳入 80 例 HD 患者(包括 42 例糖尿病患者)。采用限制性长度多态性聚合酶链反应分析研究了 IL-6 基因启动子(-634C/G 和-174G/C)的多态性。根据 IL-6 多态性比较了血管通路通畅性在患者组之间的差异。另外还纳入了 89 名健康个体作为对照组。通过酶联免疫吸附试验测定血浆 IL-6 水平。
HD 患者 IL-6 启动子位置-634 的 GG 基因型和 G 等位基因比对照组更常见。此外,非糖尿病 HD 患者的血管通路通畅性与-634 多态性的分布有关。然而,G 等位基因不是早期通路失败的显著危险因素。IL-6-634C/G 多态性与血浆 IL-6 水平之间没有明显的关联。在我们的研究人群中未检测到 IL-6-174G/C 多态性的 C 等位基因。
IL-6-634G 等位基因在终末期肾病患者中更为常见,可能与非糖尿病 HD 患者的血管通路功能障碍有关。