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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (5): 79-84.

• 论文 • 上一篇    下一篇

类风湿关节炎与肿瘤坏死因子受体Ⅱ196位点多态性相关性的Meta分析

葛勇鹏,杨清锐,张源潮   

  1. 山东大学附属省立医院风湿免疫科,  济南  250021
  • 收稿日期:2010-01-07 出版日期:2010-05-16 发布日期:2010-05-16
  • 通讯作者: 张源潮(1951- ),男,教授,博士生导师,主要从事风湿免疫病的基础和临床研究。 E-mail:qryang720@163.com
  • 作者简介:葛勇鹏(1983- ),男,硕士研究生,主要从事强直性脊柱炎和类风湿关节炎发病机制的研究。
  • 基金资助:

    山东省自然科学基金资助项目(Q2007C09);山东省医药卫生项目(2007AZ014);山东省科技攻关项目(2008GG10002009)

Association between rheumatoid arthritis and tumor necrosis factor receptor Ⅱ-196 site polymorphism: the Meta analysis

GE Yongpeng, YANG Qingrui, ZHANG Yuanchao   

  1. Department of Rheumatology and Immunology, Provincial Hospital Affiliated to  Shandong University, Jinan 250021,  China
  • Received:2010-01-07 Online:2010-05-16 Published:2010-05-16

摘要:

目的  探讨类风湿关节炎(RA)与肿瘤坏死因子受体Ⅱ196(TNFRⅡ196)基因位点多态性的关联情况。方法  检索已发表有关RA和TNFRⅡ196基因位点多态性的文献进行Meta分析。结果  有9篇文献入选,共纳入2140例RA患者(RA组)和1297例健康者(健康对照组)。综合分析显示RA与TNFRⅡ196位点等位基因及TG、GG基因型不存在关联,OR值、95%CI和P值分别为1.11,(0.91,1.34),P=0.32;1.38,(0.97,1.98),P=0.07;1.09,(0.93,1.27),P=0.31。家族性RA与TNFRⅡ196位点等位基因及GG基因型存在关联,OR值、95%CI和P值分别为1.43,(1.11,1.86),P=0.006;2.68,(1.39,5.17),P=0.003;家族性RA与TNFRⅡ196TG基因型不存在关联,OR=1.00,95%CI(0.71,1.39),P=0.98。散发性RA与TNFRⅡ196位点等位基因及GG、TG基因型不存在关联,OR值、95%CI和P值分别为1.13,(0.89,1.44),P=0.32;1.44,(0.75,2.76),P=0.27;1.03,(0.76,1.39),P=0.86。结论  Meta分析显示TNFRⅡ196基因位点多态性与RA患者不具有关联,TNFRⅡ196位点等位基因及GG基因型可能与家族性RA患者存在关联,与散发性RA无相关性。

关键词: 类风湿关节炎;多态现象(遗传学);肿瘤坏死因子受体Ⅱ;Meta分析

Abstract:

Objective  To investigate the association between the tumor necrosis factor receptor Ⅱposition 196 (TNFRⅡ196) gene polymorphism and patients with rheumatoid arthritis (RA).  Methods    We performed a metaanalysis of the published literatures on the TNFRⅡ position 196 gene polymorphism and RA. Results  A total of nine literatures involving 2140 cases and 1297 controls were included. Comprehensive analysis showed that there was no association between TNFRⅡ196 alleles, TNFRⅡ196TG, GG genotype and RA, (OR=1.11; 95% CI=0.91-1.34; P=0.32 for TNFRⅡ196 alleles;OR=1.38; 95% CI=0.97-1.98; P=0.07 for TNFRⅡ196TG genotype;and OR=1.09; 95% CI=0.93-1.27; P=0.31 for TNFRⅡ196GG genotype. However, an association between TNFRⅡ196 alleles and TNFRⅡ196GG genotype and familial RA was found (OR=1.43; 95% CI= 1.11-1.86; P=0.006 for TNFRⅡ196 alleles and OR=2.68; 95% CI=1.39-5.17; P=0.003 TNFRⅡ196GG genotype, respectively), but not between TNFRⅡ196TG genotype and familial RA (OR=1.00; 95% CI=0.71-1.39; P=0.98). Finally we found no association between the TNFRⅡ196 alleles, TNFRⅡ196GG, TG genotype and Sporadic RA (OR=1.13; 95% CI=0.891.44; P=0.32 for TNFRⅡ196 alleles; OR=1.44; 95% CI= 0.75-2.76; P=0.27 for TNFRⅡ196GG genotype; and OR=1.03; 95% CI=0.76-1.39; P=0.86 for TNFRⅡ196TG genotype). Conclusions  This Meta-analysis suggested that there was no association between the TNFR Ⅱposition 196 gene polymorphism and RA, but the TNFRⅡ196 alleles and the GG genotype might be associated with familial not sporadic RA.

Key words: arthritis, rheumatoid; Polymorphism(genetics); Tumor necrosis factor Receptor Ⅱ; Meta analysis

中图分类号: 

  • R593.22
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