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干扰素-γ基因多态性与系统性红斑狼疮易感性相关。

Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus.

机构信息

Department of Biological Sciences, KAIST, 335 Gwahangno, Yuseong-gu, Daejeon 305-701, Korea.

出版信息

Ann Rheum Dis. 2010 Jun;69(6):1247-50. doi: 10.1136/ard.2009.117572. Epub 2009 Nov 16.

Abstract

OBJECTIVE

Interferon-gamma (IFNG) is a type II interferon playing diverse roles in innate and adaptive immune systems. Elevated expression of IFNG has been associated with systemic lupus erythematosus (SLE). This study examined the association of IFNG polymorphisms with SLE susceptibility.

METHODS

Five tag single-nucleotide polymorphisms (SNP) and eight variations in all known regulatory sequences affecting IFNG expression within and around IFNG were genotyped in 1759 unrelated Korean subjects. SLE susceptibility association was assessed by comparing 742 SLE patients and 1017 unaffected controls using multivariate logistic regression analysis with adjustment for age and gender.

RESULTS

SLE susceptibility association was significant with rs2069705 in the promoter (adjusted OR 2.27, p=0.0024) and marginal with rs3181032 in the promoter (p=0.037), rs2430561 in intron 1 (p=0.022) and rs2069718 in intron 3 (p=0.026) in a recessive genetic model. Five other SNP showed no association and four other variations were not polymorphic.

CONCLUSION

Several SNP in IFNG are associated with SLE susceptibility, and the risk allele of an associated SNP (rs2430561) located in an NF-kappaB binding site has elevated IFNG expression versus the non-risk allele, supporting that elevated IFNG expression is associated with increased SLE susceptibility.

摘要

目的

干扰素-γ(IFNG)是一种 II 型干扰素,在先天和适应性免疫系统中发挥多种作用。IFNG 的表达升高与红斑狼疮(SLE)有关。本研究探讨了 IFNG 多态性与 SLE 易感性的关系。

方法

在 1759 名无关韩国个体中,对五个标签单核苷酸多态性(SNP)和所有已知影响 IFNG 表达的调节序列中的八个变异进行了基因分型,这些调节序列位于 IFNG 内及其周围。通过比较 742 例 SLE 患者和 1017 例无影响对照,使用多变量逻辑回归分析,调整年龄和性别,评估 SLE 易感性关联。

结果

启动子中的 rs2069705(调整后的 OR 2.27,p=0.0024)和启动子中的 rs3181032(p=0.037)、内含子 1 中的 rs2430561(p=0.022)和内含子 3 中的 rs2069718(p=0.026)在隐性遗传模型中与 SLE 易感性相关具有统计学意义。其他五个 SNP 没有关联,另外四个变异没有多态性。

结论

IFNG 中的几个 SNP 与 SLE 易感性相关,与相关 SNP(rs2430561)相关的风险等位基因位于 NF-κB 结合位点,其 IFNG 表达高于非风险等位基因,这支持了 IFNG 表达升高与 SLE 易感性增加相关。

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