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本文引用的文献

1
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.全基因组关联研究荟萃分析确定了七个新的类风湿关节炎风险位点。
Nat Genet. 2010 Jun;42(6):508-14. doi: 10.1038/ng.582. Epub 2010 May 9.
2
A haplotype in STAT4 gene associated with rheumatoid arthritis in Caucasians is not associated in the Han Chinese population, but with the presence of rheumatoid factor.与白种人类风湿关节炎相关的STAT4基因单倍型在汉族人群中不相关,但与类风湿因子的存在相关。
Rheumatology (Oxford). 2009 Nov;48(11):1363-8. doi: 10.1093/rheumatology/kep207. Epub 2009 Sep 8.
3
TRAF1 polymorphisms associated with rheumatoid arthritis susceptibility in Asians and in Caucasians.与亚洲人和高加索人类风湿关节炎易感性相关的TRAF1基因多态性。
Arthritis Rheum. 2009 Sep;60(9):2577-84. doi: 10.1002/art.24759.
4
Overlap of disease susceptibility loci for rheumatoid arthritis and juvenile idiopathic arthritis.类风湿关节炎和幼年特发性关节炎疾病易感性基因座的重叠。
Ann Rheum Dis. 2010 Jun;69(6):1049-53. doi: 10.1136/ard.2009.110650. Epub 2009 Aug 11.
5
The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases.9q33 染色体上的 TRAF1-C5 区域与多种自身免疫性疾病有关。
Ann Rheum Dis. 2010 Apr;69(4):696-9. doi: 10.1136/ard.2008.106567. Epub 2009 May 10.
6
Susceptibility variants for rheumatoid arthritis in the TRAF1-C5 and 6q23 loci: a meta-analysis.TRAF1-C5 和 6q23 基因座中类风湿关节炎的易感性变异:一项荟萃分析。
Ann Rheum Dis. 2010 Mar;69(3):561-6. doi: 10.1136/ard.2009.109447. Epub 2009 Apr 27.
7
Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese.TRAF1-C5 多态性与日本人群类风湿关节炎和系统性红斑狼疮易感性的关联研究。
Ann Rheum Dis. 2010 Feb;69(2):368-73. doi: 10.1136/ard.2008.104315. Epub 2009 Mar 30.
8
Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.类风湿关节炎的遗传风险因素在白种人和韩国人群中存在差异。
Arthritis Rheum. 2009 Feb;60(2):364-71. doi: 10.1002/art.24245.
9
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.位于6号染色体23区带的TNFAIP3基因附近的遗传变异与系统性红斑狼疮相关。
Nat Genet. 2008 Sep;40(9):1059-61. doi: 10.1038/ng.200.
10
Prevalence of rheumatic diseases and disability in China.中国风湿性疾病的患病率与残疾情况
Rheumatol Int. 2009 Mar;29(5):481-90. doi: 10.1007/s00296-008-0809-z. Epub 2008 Dec 6.

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.

DOI:10.1186/1471-2350-12-53
PMID:21492465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3094270/
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。