TNF-α-857 and-1031 polymorphisms predict good therapeutic response to TNF-α blockers in Chinese Han patients with ankylosing spondylitis

被引:5
作者
Tong, Qiang [1 ]
Zhao, Dong-Bao [1 ]
Bajracharya, Punam [2 ]
Xu, Xia [1 ]
Kong, Rui-Na [1 ]
Zhang, Ju [1 ]
Dai, Sheng-Ming [1 ]
Cai, Qing [1 ]
机构
[1] Secoud Mil Med Univ, Changhai Hosp, Dept Rheumatol & Immunol, Shanghai 200433, Peoples R China
[2] Shree Birendra Hosp, Dept Internal Med, Kathmandu, Nepal
关键词
ankylosing spondylitis; polymorphism; therapeutic response; TNF-alpha; TNF-alpha blockers; TUMOR-NECROSIS-FACTOR; RHEUMATOID-ARTHRITIS; PROMOTER POLYMORPHISMS; GENE POLYMORPHISM; CLINICAL-RESPONSE; ASSOCIATION; SPONDYLOARTHRITIS; SUSCEPTIBILITY; RESPONSIVENESS; METAANALYSIS;
D O I
10.2217/PGS.12.133
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: To evaluate whether polymorphisms at -857, -1031, -308 and -238 positions of the TNF-alpha gene influence response to TNF-alpha-blocker therapy in Chinese Han patients with ankylosing spondylitis. Patients & methods: A total of 106 patients with ankylosing spondylitis were recruited and genotyped for -857, -1031, -308 and -238 TNF-alpha gene polymorphisms. In total, 32 received infliximab and 74 received a recombinant human TNF-alpha receptor II-IgG Fc fusion protein (rhTNFR-Fc). At the end of 12 weeks, patients were assessed using the Assessment of SpondyloArthritis International Society (ASAS) 20, 40, 50 and 70 criteria. Results: Polymorphisms at -308 and -238 did not affect therapeutic response. The -857 C/C genotype (p = 0.0021) responded better to therapy. The -1031 T/T genotype (p = 0.0004) showed better outcome. Conclusion: In Chinese Han ankylosing spondylitis patients, polymorphisms at the -308 and -238 positions of the TNF-alpha gene are unable to predict TNF-alpha-blocker response; however, -857 C/C and -1031 T/T genotypes have the ability to predict good response.
引用
收藏
页码:1459 / 1467
页数:9
相关论文
共 42 条
  • [1] Could single-nucleotide polymorphisms (SNPs) affecting the tumour necrosis factor promoter be considered as part of rheumatoid arthritis evolution?
    Aguillón, JC
    Cruzat, A
    Aravena, O
    Salazar, L
    Llanos, C
    Cuchacovich, M
    [J]. IMMUNOBIOLOGY, 2006, 211 (1-2) : 75 - 84
  • [2] Anderson JJ, 2001, ARTHRITIS RHEUM-US, V44, P1876, DOI 10.1002/1529-0131(200108)44:8<1876::AID-ART326>3.0.CO
  • [3] 2-F
  • [4] Investigation of the prognostic value of TNF-α gene polymorphism among patients treated with infliximab, and the effects of infliximab therapy on TNF-α production and apoptosis
    Balog, A
    Klausz, G
    Gál, J
    Molnár, T
    Nagy, F
    Ocsovszky, I
    Gyulai, Z
    Mándi, Y
    [J]. PATHOBIOLOGY, 2004, 71 (05) : 274 - 280
  • [5] Brown MA, 2008, ANN RHEUM DIS, V67, P434
  • [6] Chatzikyriakidou A, 2009, CLIN EXP RHEUMATOL, V27, P645
  • [7] Polymorphisms of tumor necrosis factor-α promoter region for susceptibility to HLA-B27-positive ankylosing spondylitis in Korean population
    Chung, Won-Tae
    Choe, Jung-Yoon
    Jang, Won Cheoul
    Park, Su Min
    Ahn, Young Chang
    Yoon, Il Kyu
    Kim, Tae-Hwan
    Nam, Youn-Hyoung
    Park, Sung-Hoon
    Lee, Sung-Won
    Kim, Seong-Kyu
    [J]. RHEUMATOLOGY INTERNATIONAL, 2011, 31 (09) : 1167 - 1175
  • [8] Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese
    Davidson, Stuart I.
    Liu, Yu
    Danoy, Patrick A.
    Wu, Xin
    Thomas, Gethin P.
    Jiang, Lei
    Sun, Linyun
    Wang, Niansong
    Han, Jun
    Han, Huanxing
    Visscher, Peter M.
    Brown, Matthew A.
    Xu, Huji
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2011, 70 (02) : 289 - 292
  • [9] Polymorphism at position-308 of the tumour necrosis factor α gene and rheumatoid arthritis pharmacogenetics
    Fonseca, JE
    Carvalho, T
    Cruz, M
    Nero, P
    Sobral, M
    Mourao, AF
    Cavaleiro, J
    Ligeiro, D
    Abreu, I
    Carmo-Fonseca, M
    Branco, JC
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (05) : 793 - 794
  • [10] GARRETT S, 1994, J RHEUMATOL, V21, P2286