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位于 TRAF1/C5 基因座的单核苷酸多态性与汉族人群的类风湿关节炎相关。

Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.

机构信息

Department of Rheumatology and Immunology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.

出版信息

BMC Med Genet. 2011 Apr 14;12:53. doi: 10.1186/1471-2350-12-53.

Abstract

BACKGROUND

Genetic variants in TRAF1C5 and PTPN22 genes have been shown to be significantly associated with arthritis rheumatoid in Caucasian populations. This study investigated the association between single nucleotide polymorphisms (SNPs) in TRAF1/C5 and PTPN22 genes and rheumatoid arthritis (RA) in a Han Chinese population. We genotyped SNPs rs3761847 and rs7021206 at the TRAF1/C5 locus and rs2476601 SNP in the PTPN22 gene in a Han Chinese cohort composed of 576 patients with RA and 689 controls. The concentrations of anti-cyclic citrullinated peptide antibodies (CCP) and rheumatoid factor (RF) were determined for all affected patients. The difference between the cases and the controls was compared using χ2 analysis.

RESULTS

Significant differences in SNPs rs3761847 and rs7021206 at TRAF1/C5 were observed between the case and control groups in this cohort; the allelic p-value was 0.0018 with an odds ratio of 1.28 for rs3761847 and 0.005 with an odds ratio of 1.27 for rs7021206. This significant association between rs3761847 and RA was independent of the concentrations of anti-CCP and RF. No polymorphism of rs2476601 was observed in this cohort.

CONCLUSIONS

We first demonstrated that genetic variants at the TRAF1/C5 locus are significantly associated with RA in Han Chinese, suggesting that TRAF1/C5 may play a role in the development of RA in this population, which expands the pathogenesis role of TRAF1/C5 in a different ethnicity.

摘要

背景

TRAF1C5 和 PTPN22 基因中的遗传变异已被证明与高加索人群中的关节炎类风湿显著相关。本研究调查了 TRAF1/C5 和 PTPN22 基因中的单核苷酸多态性(SNPs)与汉族人群中类风湿关节炎(RA)之间的关联。我们在由 576 例 RA 患者和 689 例对照组成的汉族队列中,对 TRAF1/C5 基因座的 rs3761847 和 rs7021206 以及 PTPN22 基因中的 rs2476601 SNP 进行了基因分型。对所有受影响的患者均测定了抗环瓜氨酸肽抗体(CCP)和类风湿因子(RF)的浓度。使用 χ2 分析比较病例组和对照组之间的差异。

结果

在该队列中,病例组和对照组之间的 TRAF1/C5 中的 rs3761847 和 rs7021206 SNP 存在显著差异;等位基因 p 值为 0.0018,OR 为 1.28,rs3761847 为 0.005,OR 为 1.27,rs7021206。rs3761847 与 RA 之间的这种显著关联与抗 CCP 和 RF 的浓度无关。在该队列中未观察到 rs2476601 的多态性。

结论

我们首次证明 TRAF1/C5 基因座的遗传变异与汉族人群中的 RA 显著相关,表明 TRAF1/C5 可能在该人群 RA 的发病机制中发挥作用,这扩展了 TRAF1/C5 在不同种族中的发病机制作用。

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