Correlation between P2X7 receptor gene polymorphisms and gout

被引:21
|
作者
Gong, Qiong-yao [1 ,2 ]
Chen, Yong [1 ]
机构
[1] Ningbo 2 Hosp, Dept Rheumatol, Ningbo 315010, Zhejiang, Peoples R China
[2] Ningbo Univ, Sch Med, Ningbo 315211, Zhejiang, Peoples R China
关键词
Gout; P2X7; receptor; Single-nucleotide polymorphisms; HUMAN P2X(7) RECEPTOR; IL-1-BETA SECRETION; OF-FUNCTION; ARTHRITIS; INTERLEUKIN-1; INFLAMMASOME; LYMPHOCYTES; MECHANISMS; CHANNELS; RELEASE;
D O I
10.1007/s00296-015-3258-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Not all patients with hyperuricemia will develop acute gouty arthritis, indicating that other initiating factors need to be considered. The P2X7 receptor is an adenosine triphosphate-gated nonselective cation channel that has also been suggested to be a proinflammatory receptor. In the immune system, the P2X7 receptor is involved in the processing and release of various proinflammatory cytokines, including interleukin-1 beta (IL-1 beta), IL-18 and tumor necrosis factor-alpha (TNF-alpha). IL-1 beta is a central cytokine in the initiation of the acute inflammatory response, which plays a key role in the pathogenesis of gout and the pathology of acute gouty arthritis. This review will explore single-nucleotide polymorphisms in the P2X7R gene [including rs1718119 (Ala348Thr), rs208294 (His155Tyr), rs3751143 (Glu496Ala), rs28360457 (Arg307Gln) and rs2230911 (Thr357Ser)] and their correlation with the incidence of gout. We conclude that P2X7R gene polymorphisms impact the secretion of IL-1 beta and thus play a vital role in the pathogenesis of gout.
引用
收藏
页码:1307 / 1310
页数:4
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