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TLR4 多态性与活检证实的巨细胞动脉炎无关。

TLR4 polymorphism is not associated with biopsy proven giant cell arteritis.

机构信息

Rheumatology Department, The Queen Elizabeth Hospital, Woodville South, South Australia, Australia.

出版信息

Clin Exp Rheumatol. 2014 May-Jun;32(3 Suppl 82):S26-9. Epub 2014 Jan 20.

Abstract

OBJECTIVES

Giant cell arteritis (GCA) is a systemic inflammatory vasculitis affecting the elderly. It primarily affects medium and large arteries of the head and neck and can cause stroke and blindness. The cause of GCA is unknown; however both genetic and environmental factors are likely to be involved. TLR4 is implicated in the pathogenesis of GCA, however previous studies, examining the association between GCA and two TLR4 single nucleotide polymorphisms (SNPs), have reported conflicting results. The aim of this study was to determine the association between GCA and range of SNPs spanning the TLR4 gene sequence.

METHODS

A case-control genetic study was performed using DNA from Australian biopsy proven GCA patients (n=139) and population controls (n=130). Samples were genotyped for 8 SNPs tagging common variation across TLR4. These SNPs included rs4986790 (+896A/G, Asp299Gly) and rs4986791 (+1196C/T) which have been previously studied in GCA. Allelic and haplotypic variation was analysed by logistic regression assuming an additive genetic model. A random effects meta-analysis of the association between GCA and rs4986790 was performed utilising data from three previous studies.

RESULTS

rs4986790 and rs4986791 are in strong linkage disequilbrium and tag one of the five common TLR4 haplotypes identified. No associations were observed between TLR4 SNPs and/or haplotypes and GCA. A meta-analysis, comprising 577 GCA patients and 1153 controls, did not confirm an association between GCA and rs4986790 (OR 1.29, 95% CI 0.86, 1.92, p=0.22).

CONCLUSIONS

There is no evidence of an association between TLR4 polymorphism and susceptibility to GCA.

摘要

目的

巨细胞动脉炎(GCA)是一种影响老年人的系统性炎症性血管炎。它主要影响头颈部的大中动脉,可导致中风和失明。GCA 的病因尚不清楚;然而,遗传和环境因素都可能与之相关。TLR4 参与了 GCA 的发病机制,然而,先前研究检查了 GCA 与 TLR4 两个单核苷酸多态性(SNP)之间的关联,结果报告存在冲突。本研究旨在确定 GCA 与跨越 TLR4 基因序列的一系列 SNP 之间的关联。

方法

采用澳大利亚活检证实的 GCA 患者(n=139)和人群对照(n=130)的 DNA 进行病例对照遗传研究。对 8 个标记 TLR4 常见变异的 SNP 进行基因分型。这些 SNP 包括先前在 GCA 中研究过的 rs4986790(+896A/G,Asp299Gly)和 rs4986791(+1196C/T)。假设加性遗传模型,通过逻辑回归分析等位基因和单倍型变异。利用先前三项研究的数据,对 GCA 与 rs4986790 之间的关联进行了随机效应荟萃分析。

结果

rs4986790 和 rs4986791 紧密连锁,标记了五个常见 TLR4 单倍型之一。TLR4 SNP 与 GCA 之间没有观察到关联。荟萃分析包括 577 例 GCA 患者和 1153 例对照,未证实 GCA 与 rs4986790 之间存在关联(OR 1.29,95%CI 0.86,1.92,p=0.22)。

结论

TLR4 多态性与 GCA 易感性之间没有证据表明存在关联。

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