TIRAP C539T polymorphism contributes to tuberculosis susceptibility: Evidence from a meta-analysis

被引:14
作者
Liu, Qianqian [1 ]
Li, Wenzhang [2 ]
Li, Dongdong [1 ]
Feng, Yulin [3 ]
Tao, Chuanmin [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Lab Med, Chengdu 610041, Sichuan, Peoples R China
[2] Chengdu Med Coll, Affiliated Hosp 1, Dept Cardiol, Chengdu 610500, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Resp Med, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
TIRAP; MAL; Polymorphism; Tuberculosis; Meta-analysis; TOLL-LIKE RECEPTOR; S180L VARIANT; ASSOCIATION; TLR2;
D O I
10.1016/j.meegid.2014.06.025
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Toll-interleukin 1 receptor domain containing adaptor protein (TIRAP), an important adaptor protein downstream of the Toll-like receptor (TLR) 2 and 4 pathways, is highly involved in the activation and coordination of the anti-mycobacterial immune response. We performed a meta-analysis to assess the association between TIRAP C539T polymorphism and tuberculosis (TB) risk. Methods: A systematic literature search for relevant studies up to February 27, 2014 was conducted in PUBMED, EMBASE, Web of science, CNKI, VIP, and Wanfang database. The association between gene and disease was assessed using odds ratios (ORs) with 95% confidence intervals (95%CIs) based on five genetic models. Results: A total of 16 qualified studies were enrolled in this meta-analysis. The results of pooling all studies detected statistically resistance of TIRAP C539T mutants to TB risk (T vs. C: OR 0.80, 95%CI 0.65-0.97; TC vs. CC: OR 0.71, 95%Cl 0.55-0.92; TT + TC vs. CC: OR 0.74, 95% Cl 0.58-0.94). Further subgroup analyses by ethnicity also demonstrated reduced risk of TB in European population (T vs. C: OR 0.71, 95%CI 0.52-0.95; TC vs. CC: OR 0.56, 95%Cl 0.35-0.91; TT TC vs. CC: OR 0.61, 95%CI 0.40-0.92), whereas no such effects were observed in other ethnicities. Conclusion: This present meta-analysis suggests TIRAP C539T polymorphism is significantly correlated with reduced risk of TB infection, with stronger effect in European. Additional well-designed, larger-scale epidemiological studies among different ethnicities are needed. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
相关论文
共 33 条
[1]  
[Anonymous], FISHMANS PULMONARY D
[2]  
[Anonymous], GLOB TUB REP 2013
[3]   Mal, more than a bridge to MyD88 [J].
Bernard, Nicholas J. ;
O'Neill, Luke A. .
IUBMB LIFE, 2013, 65 (09) :777-786
[4]   Association between the PTPN22 1858C/T gene polymorphism and tuberculosis resistance [J].
Boechat, Antonio Luiz ;
Ogusku, Mauricio Morishi ;
Sadahiro, Aya ;
dos Santos, Maria Cristina .
INFECTION GENETICS AND EVOLUTION, 2013, 16 :310-313
[5]   Old and new selective pressures on Mycobacterium tuberculosis [J].
Brites, Daniela ;
Gagneux, Sebastien .
INFECTION GENETICS AND EVOLUTION, 2012, 12 (04) :678-685
[6]   The MyD88 rs6853 and TIRAP rs8177374 polymorphic sites are associated with resistance to human pulmonary tuberculosis [J].
Capparelli, R. ;
De Chiara, F. ;
Di Matteo, A. ;
Medaglia, C. ;
Iannelli, D. .
GENES AND IMMUNITY, 2013, 14 (08) :504-511
[7]   TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus [J].
Castiblanco, John ;
Varela, Diana-Cristina ;
Castano-Rodriguez, Natalia ;
Rojas-Villarraga, Adriana ;
Hincape, Maria-Eugenia ;
Anaya, Juan-Manuel .
INFECTION GENETICS AND EVOLUTION, 2008, 8 (05) :541-544
[8]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[9]   Polymorphic Variation in TIRAP Is Not Associated with Susceptibility to Childhood TB but May Determine Susceptibility to TBM in Some Ethnic Groups [J].
Dissanayeke, Shobana Rebecca ;
Levin, Samuel ;
Pienaar, Sandra ;
Wood, Kathryn ;
Eley, Brian ;
Beatty, David ;
Henderson, Howard ;
Anderson, Suzanne ;
Levin, Michael .
PLOS ONE, 2009, 4 (08)
[10]   Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis [J].
Duval, S ;
Tweedie, R .
BIOMETRICS, 2000, 56 (02) :455-463