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CCL2/MCP-1 -2518A>G基因多态性在HLA-B27相关性葡萄膜炎中的作用

Role of the CCL2/MCP-1 -2518A>G gene polymorphism in HLA-B27 associated uveitis.

作者信息

Wegscheider Beate Julia, Weger Martin, Renner Wilfried, Posch Ursula, Ulrich Silvia, Hermann Josef, Ardjomand Navid, Haller-Schober Eva-Maria, El-Shabrawi Yosuf

机构信息

Department of Ophthalmology, Medical University Graz, Graz, Austria.

出版信息

Mol Vis. 2005 Nov 1;11:896-900.

Abstract

PURPOSE

Acute anterior uveitis (AAU) is the most common form of uveitis. Up to 50% of patients with AAU are HLA-B27 positive. Since HLA B27 itself plays only a minor role in the overall genetic background, other genetic variants are likely to contribute to the susceptibility to AAU. The chemokine (C-C motif) ligand 2 (CCL2) gene, coding for monocyte chemoattractant protein-1 (MCP-1), a chemotactic cytokine, is involved in the induction of uveitis. A CCL2 gene polymorphism, which is characterized by an A>G substitution at nucleotide -2518 in the promoter region of CCL2 has been previously shown to affect MCP-1 synthesis. The purpose of the present study was to investigate a hypothesized association between this genetic variant and the presence of HLA-B27 associated AAU.

METHODS

The study group comprised 114 patients with HLA-B27 associated AAU. One hundred and eleven healthy HLA-B27 positive individuals served as the HLA-B27 positive control group, whereas 81 healthy HLA-B27 negative individuals served as a HLA-B27 negative control group. Genotyping for the CCL2 -2518A>G polymorphism was performed by polymerase chain reaction.

RESULTS

Carriers of a CCL2 -2518G allele were found significantly more often in patients with HLA-B27 associated AAU than among HLA-B27 positive controls (49.2% and 31.5%, respectively; odds ratio 2.1; 95% confidence interval 1.2-3.6; p=0.007).

CONCLUSIONS

Our data suggest that the CCL2 -2518A>G polymorphism may play a role in HLA-B27 associated acute anterior uveitis.

摘要

目的

急性前葡萄膜炎(AAU)是葡萄膜炎最常见的形式。高达50%的AAU患者HLA - B27呈阳性。由于HLA - B27本身在整体遗传背景中仅起次要作用,其他基因变异可能导致AAU易感性。趋化因子(C - C基序)配体2(CCL2)基因编码单核细胞趋化蛋白 - 1(MCP - 1),一种趋化细胞因子,参与葡萄膜炎的诱导。先前已表明,CCL2基因多态性以CCL2启动子区域核苷酸 - 2518处的A>G替换为特征,可影响MCP - 1合成。本研究的目的是调查这种基因变异与HLA - B27相关AAU存在之间的假设关联。

方法

研究组包括114例HLA - B27相关AAU患者。111名健康的HLA - B27阳性个体作为HLA - B27阳性对照组,而81名健康的HLA - B27阴性个体作为HLA - B27阴性对照组。通过聚合酶链反应对CCL2 - 2518A>G多态性进行基因分型。

结果

在HLA - B27相关AAU患者中发现CCL2 - 2518G等位基因携带者的频率显著高于HLA - B27阳性对照组(分别为49.2%和31.5%;优势比2.1;95%置信区间1.2 - 3.6;p = 0.007)。

结论

我们的数据表明,CCL2 - 2518A>G多态性可能在HLA - B27相关急性前葡萄膜炎中起作用。

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