期刊文献+

尿酸转运蛋白相关基因多态性与原发性痛风遗传易感性关系的荟萃分析 被引量:5

Association of single nucleotide polymorphisms of uric acid transporter protein gene with risk of primary gout: a meta-analysis
下载PDF
导出
摘要 目的探讨尿酸转运蛋白相关基因单核苷酸多态性与原发性痛风的相关性。方法检索Pub Med数据库、EMBASE数据库、中国知网数据库和万方数据库的相关中英文文献,收集尿酸转运蛋白相关基因多态性与原发性痛风易感性的相关研究,按纳入与排除标准筛选文献,提取资料。使用Rev Man 5.3软件进行荟萃统计分析,敏感性分析及发表偏倚分析。结果共10 386例原发性痛风患者和21 076例对照者纳入分析,荟萃分析结果显示,SLC2A9 rs3733591[OR(95%CI)=0.76(0.66,0.89),P<0.05]、SLC2A9rs16890979[OR(95%CI)=0.33(0.18,0.58),P<0.05]、SLC2A9 rs6855911[OR(95%CI)=0.66(0.56,0.77),P<0.05]、SLC2A9rs13124007[OR(95%CI)=1.49(1.17,1.91),P<0.05]、SLC2A9 rs1014290[OR(95%CI)=0.69(0.53,0.89),P<0.05]和ABCG2rs2231142[OR(95%CI)=2.13(1.81,2.50),P<0.05]这六个位点的多态性与原发性痛风易感性相关。结论 SLC2A9(rs3733591、rs16890979、rs6855911、rs13124007和rs1014290)和ABCG2(rs2231142)的多态性与原发性痛风易感性相关。 Objective To assess the association of uric acid transporter protein gene single nucleotide polymorphisms with the risk of primary gout. Methods Studies on uric acid transporter-related gene polymorphisms with primary gout were searched in PubMed, EMBASE, CNKI and China Wanfang literature databases. Information was extracted according to inclusion and exclusion criteria. REVMAN 5.3 software was applied to perform meta-analysis, sensitivity analysis and publication bias analysis. Results Total 10,386 cases and 21,076 controls were included for the current meta-analyses. The results showed that SLC2A9 rs3733591 (OR=0.76, 95%C/: 0.66, 0.89, P〈0.05), SLC2A9 rs16890979 (OR = 0.33, 95%C/: 0.18, 0.58, P〈0.05), SLC2A9 rs6855911(OR=0.66, 95%C/: 0.56, 0.77, P〈0.05), SLC2A9 rs13124007(OR=1.49, 95%C/: 1.17, 1.91, P〈0.05), SLC2A9 rs1014290 (OR=0.69, 95%C/: 0.53, 0.89, P〈0.05) and ABCG2 rs2231142(OR=2.13, 95%C/: 1.81, 2.50, P〈0.05) were significantly associated with the risk of primary gout. Conclusion Our results showed six genetic variants SLC2A9 rs3733591, rs16890979, rs6855911, rs13124007, rs1014290 and ABCG2 rs2231142 are significantly associated with primary gout.
作者 应颖 黄海燕 邹荣鑫 李晓可 陈勇 YING Ying HUANG Haiyan ZOU Rongxirt et al(Department of Rheumatology, Ningbo Second Municipal Hospital, Ningbo 315010, China)
出处 《浙江医学》 CAS 2017年第20期1763-1770,1777,共9页 Zhejiang Medical Journal
基金 浙江省医药卫生基金项目(2015KYB346 2017KY589)
关键词 痛风 SLC2A9 ABCG2 SLC17A3 LRRC16A 荟萃分析 单核苷酸多态性 Gout SLC2A9 ABCG2 SLC17A3 LRRC16A Meta-analysis Singlenucleotidepolymorphism
  • 相关文献

参考文献11

二级参考文献36

  • 1罗宇成,谭光林.痛风患者血尿酸正常原因分析[J].川北医学院学报,2005,20(3):351-352. 被引量:5
  • 2Ea HK, Bardin T, Jinnah HA, et al. Severe gouty arthritis and mild neurologic symptoms due to F199C, a newly identified variant of the hypoxanthine guanine phosphoribosyl transferase [J]. Arthritis Rheum,2009,60(7):2201-2204. 被引量:1
  • 3Yang Q, Dehqhan A, Smith AV, et al. Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors[J]. Circ Cardiovasc Genet,2008,3(6):523-530. 被引量:1
  • 4Caulfield M J, Munroe P B, O'Neill D, et al. SLC2A9 is a high-capacity urate transporter in humans [J]. PLoS Med,2008,5(10): e197-201. 被引量:1
  • 5Hart TC, Gorry MC, Hart PS, et al. Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy [J]. J Med Genet,2002,39(12): 882-892. 被引量:1
  • 6Yamada Y, Nomura N, Yamada K, et al. Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) deficien?cies: novel mutations and the spectrum of Japanese mutations [J]. Nucleosides Nucleotides Nucleic Acids,2008,27(6):570-574. 被引量:1
  • 7Yamada Y, Yamada K, Nomura N, et al. Molecular analysis of two enzyme genes, HPRTl and PRPSI, causing X-linked inborn errors of purine metabolism [J]. Nucleosides Nucleotides Nucleic Acids, 2004,29(6):291-294. 被引量:1
  • 8Vitart V, Rudan I, Hayward C, et al. SLC2A9 is a newly identified orate transporter influencing serum wale concentration, orate excretion and gout[J]. Nat Genet,2008,40(4):437-442. 被引量:1
  • 9Doring A, Gieger C, Mehta D, et al. SLC2A9 influences uric acid concentrations with pronounces sex-specific effects [J]. Nat Genet, 2008,40(4):430-436. 被引量:1
  • 10McArdle PF, Parsa A, Chang YP, et al. Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish[J]. Arthritis Rheum,2008,58(9):2874-2881. 被引量:1

共引文献13

同被引文献41

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部