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IL-21 基因的单核苷酸多态性与中国人群的系统性红斑狼疮有关。

A single nucleotide polymorphism of IL-21 gene is associated with systemic lupus erythematosus in a Chinese population.

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 81 Meishan Road, Hefei, Anhui 230032, People's Republic of China.

出版信息

Inflammation. 2012 Dec;35(6):1781-5. doi: 10.1007/s10753-012-9497-7.

DOI:10.1007/s10753-012-9497-7
PMID:22752563
Abstract

The aim of this study was to examine the association of single-nucleotide polymorphisms (SNPs) in IL-21 gene with susceptibility to systemic lupus erythematosus (SLE) in a Chinese population. A total of 605 independent SLE patients and 666 unrelated healthy controls were recruited for the case-control association study. Two SNPs (rs2221903 and rs907715) within the IL-21 gene intronic region were genotyped by TaqMan SNP allelic discrimination methods. The allele T frequency of SNP rs2221903 in patients and healthy controls was 89.4 % and 86.8 %, respectively [T versus C, odds ratio (OR) = 1.287, 95 % confidence interval (CI) = 1.010-1.640]. No significant differences in genotype frequencies were shown between SLE patients and healthy controls (P value = 0.705, 0.406, respectively). However, the effect of recessive model (TT versus CC + CT, OR = 1.368, 95 % CI = 1.050-1.781) was observed. Distributions of allele and genotype frequencies of the SNP rs907715 showed no significant differences between SLE patients and controls. Analysis of the haplotypes revealed that CC haplotype was significantly associated with SLE (OR = 0.734, 95 % CI = 0.573-0.941). In conclusion, our findings suggest that a SNP (rs2221903) and CC haplotype (rs2221903 and rs907715) of the IL-21 gene is associated with SLE in the Chinese population. However, further studies are needed to determine the functional consequences of this polymorphism with SLE susceptibility.

摘要

本研究旨在探讨白细胞介素 21(IL-21)基因单核苷酸多态性(SNP)与中国人群系统性红斑狼疮(SLE)易感性的关联。共纳入 605 例独立的 SLE 患者和 666 例无关的健康对照进行病例对照关联研究。采用 TaqMan SNP 等位基因鉴别方法对 IL-21 基因内含子区的两个 SNP(rs2221903 和 rs907715)进行基因分型。患者和健康对照组 SNP rs2221903 的等位基因 T 频率分别为 89.4%和 86.8%[T 与 C,比值比(OR)=1.287,95%置信区间(CI)=1.010-1.640]。SLE 患者和健康对照组的基因型频率无显著差异(P 值分别为 0.705、0.406)。然而,隐性模型(TT 与 CC+CT,OR=1.368,95%CI=1.050-1.781)的作用是观察到的。SNP rs907715 的等位基因和基因型频率分布在 SLE 患者和对照组之间无显著差异。单倍型分析显示 CC 单倍型与 SLE 显著相关(OR=0.734,95%CI=0.573-0.941)。总之,我们的研究结果表明,IL-21 基因的 SNP(rs2221903)和 CC 单倍型(rs2221903 和 rs907715)与中国人群的 SLE 相关。然而,需要进一步的研究来确定这种多态性与 SLE 易感性的功能后果。

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