Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.

Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
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6q23 上 TNFAIP3 附近的遗传变异与系统性红斑狼疮相关。

DOI:
10.1038/ng.200
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发表时间:
2008-09
期刊:
影响因子:
30.8
通讯作者:
Gaffney, Patrick M.
Gaffney, Patrick M.
中科院分区:
生物学1区
文献类型:
--
作者:
Graham, Robert R.;Cotsapas, Chris;Davies, Leela;Hackett, Rachel;Lessard, Christopher J.;Leon, Joanlise M.;Burtt, Noel P.;Guiducci, Candace;Parkin, Melissa;Gates, Casey;Plenge, Robert M.;Behrens, Timothy W.;Wither, Joan E.;Rioux, John D.;Fortin, Paul R.;Graham, Deborah Cunninghame;Wong, Andrew K.;Vyse, Timothy J.;Daly, Mark J.;Altshuler, David;Moser, Kathy L.;Gaffney, Patrick M.

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SLE是一种受遗传和环境因素影响的自身免疫性疾病。我们进行了全基因组关联扫描(GWAS),并观察到与变异inTNFAIP3(rs5029939, P = 2.89×10−12,OR = 2.29)相关的新证据。我们还发现了与SLE风险相关的两个独立信号的证据,其中一个在类风湿关节炎中被描述。这些结果表明,遗传变异intnfaip3有助于SLE和RA的不同风险。
SLE is an autoimmune disease influenced by genetic and environmental components. We performed a genome-wide association scan (GWAS) and observed novel association evidence with a variant inTNFAIP3(rs5029939, P = 2.89×10−12, OR = 2.29). We also found evidence of two independent signals of association to SLE risk, including one described in Rheumatoid Arthritis. These results establish that genetic variation inTNFAIP3contributes to differential risk for SLE and RA.
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