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白细胞介素-23 受体基因赋予汉族人群易患白塞病的易感性。

IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population.

机构信息

The First Affiliated Hospital, Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, and Chongqing Eye Institute, Chongqing 400016, PR China.

出版信息

Ann Rheum Dis. 2010 Jul;69(7):1325-8. doi: 10.1136/ard.2009.119420. Epub 2010 Apr 7.

Abstract

PURPOSE

IL-23 has been shown to be involved in the pathogenesis of Behcet's disease (BD) through promoting IL-17 production. This study examined whether IL-23R polymorphisms were associated with susceptibility to this disease in a Chinese Han population.

METHODS

Four single-nucleotide polymorphisms (SNP), rs7517847, rs11209032, rs 1343151 and rs17375018 were genotyped in 338 BD patients and 407 age, sex and ethnically matched healthy controls using a PCR restriction fragment length polymorphism assay.

RESULTS

A significantly increased prevalence of the homozygous rs17375018 GG genotype and G allele was found in BD patients compared with controls (corrected p (p(c))<0.001,odds ratio (OR) 1.86, 95% CI 1.39 to 2.49; p(c)<0.001, OR 1.57, 95% CI 1.25 to 1.98, respectively). The frequencies of the AA genotype and A allele of the SNP rs11209032 were significantly higher in BD patients compared with controls (p(c)=0.024, OR 1.69, 95% CI 1.21 to 2.35; p(c)<0.001, OR 1.48, 95% CI 1.21 to 1.82, respectively). In addition, the results showed a significantly decreased frequency of the AGCG haplotype in BD patients compared with controls (p(c)=0.0016, OR 0.59, 95% CI 0.45 to 0.77).

CONCLUSIONS

This study, for the first time, identified a strong association of an SNP of IL-23R, rs17375018, with BD. The results also suggested that both rs11209032 AA and rs17375018 GG of IL-23R are predisposing genotypes for BD and that the AGCG haplotype may provide protection against BD.

摘要

目的

白细胞介素-23(IL-23)已被证明通过促进白细胞介素-17(IL-17)的产生而参与白塞病(BD)的发病机制。本研究旨在探讨 IL-23R 多态性是否与中国汉族人群易患该病有关。

方法

采用 PCR 限制性片段长度多态性分析方法,对 338 例 BD 患者和 407 例年龄、性别和种族匹配的健康对照者的 4 个单核苷酸多态性(SNP)rs7517847、rs11209032、rs1343151 和 rs17375018 进行基因分型。

结果

与对照组相比,BD 患者中 rs17375018 纯合 GG 基因型和 G 等位基因的患病率显著升高(校正 p(p(c))<0.001,优势比(OR)1.86,95%可信区间(CI)1.39 至 2.49;p(c)<0.001,OR 1.57,95% CI 1.25 至 1.98)。与对照组相比,SNP rs11209032 的 AA 基因型和 A 等位基因在 BD 患者中的频率显著升高(p(c)=0.024,OR 1.69,95% CI 1.21 至 2.35;p(c)<0.001,OR 1.48,95% CI 1.21 至 1.82)。此外,结果显示 BD 患者中 rs17375018 与 rs11209032 联合的 AGCG 单倍型频率显著降低(p(c)=0.0016,OR 0.59,95% CI 0.45 至 0.77)。

结论

本研究首次发现白细胞介素-23R 上的 SNP rs17375018 与 BD 存在强关联。结果还表明,IL-23R 的 rs11209032AA 和 rs17375018GG 均为 BD 的易感基因型,而 AGCG 单倍型可能对 BD 有保护作用。

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