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中国系统性红斑狼疮患者白细胞介素-18启动子基因多态性:与-607位点CC基因型的关联

Interleukin-18 promoter gene polymorphisms in Chinese patients with systemic lupus erythematosus: association with CC genotype at position -607.

作者信息

Xu Qian, Tin Soe Kyaw, Sivalingam Suppiah Paramalingam, Thumboo Julian, Koh Dow Rhoon, Fong Kok Yong

机构信息

Department of Medicine, National University of Singapore, Singapore.

出版信息

Ann Acad Med Singap. 2007 Feb;36(2):91-5.

PMID:17364073
Abstract

INTRODUCTION

Interleukin-18 (IL-18) is a Th1 cytokine, which is postulated to play a role in systemic lupus erythematosus (SLE). Two single nucleotide polymorphisms (SNPs) in the IL-18 promoter gene region were found to influence the quantitative expression of the IL-18 protein. The aim of this study was to determine whether IL-18 promoter gene polymorphisms are associated with SLE.

MATERIALS AND METHODS

One hundred and thirteen Chinese SLE patients and 218 Chinese healthy individuals were recruited. Genomic DNA was extracted from peripheral venous blood. Sequence-specific primer PCR and restriction fragment length polymorphism (RFLP) analysis were used to genotype the DNA samples for SNP-137 and SNP- 607. The following genotypes were obtained: SNP(-607) AA, AC, CC and SNP(-137) GG, GC, CC. Plasma IL-18 concentrations of patients and control subjects were measured by enzyme-linked immunosorbent assay.

RESULTS

the frequency of SNP-607/CC genotype was significantly higher in SLE patients (Pc < 0.05) while genotype SNP-607/AC was significantly decreased in SLE patients compared to the control group (Pc <0.05). Plasma IL-18 concentrations were significantly higher in SLE patients than in control subjects (P <0.05). Both patients and control subjects with CC and AC genotypes have significantly higher IL-18 concentrations than those with AA genotype.

CONCLUSION

The IL-18 promoter gene polymorphism SNP-607 C allele is associated with SLE and may result in the enhanced production of IL-18 protein in SLE and normal individuals.

摘要

引言

白细胞介素-18(IL-18)是一种Th1细胞因子,据推测在系统性红斑狼疮(SLE)中发挥作用。已发现IL-18启动子基因区域的两个单核苷酸多态性(SNP)会影响IL-18蛋白的定量表达。本研究的目的是确定IL-18启动子基因多态性是否与SLE相关。

材料与方法

招募了113名中国SLE患者和218名中国健康个体。从外周静脉血中提取基因组DNA。采用序列特异性引物PCR和限制性片段长度多态性(RFLP)分析对DNA样本进行SNP-137和SNP-607基因分型。获得了以下基因型:SNP(-607)AA、AC、CC和SNP(-137)GG、GC、CC。通过酶联免疫吸附测定法测量患者和对照受试者的血浆IL-18浓度。

结果

SLE患者中SNP-607/CC基因型的频率显著更高(Pc<0.05),而与对照组相比,SLE患者中SNP-607/AC基因型显著降低(Pc<0.05)。SLE患者的血浆IL-18浓度显著高于对照受试者(P<0.05)。CC和AC基因型的患者和对照受试者的IL-18浓度均显著高于AA基因型的患者和对照受试者。

结论

IL-18启动子基因多态性SNP-607 C等位基因与SLE相关,可能导致SLE患者和正常个体中IL-18蛋白的产生增加。

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