A single-nucleotide polymorphism of the STAT4 gene is associated with systemic lupus erythematosus (SLE) in female Chinese population

被引:16
作者
Luan, Haixia [1 ,2 ]
Li, Ping [1 ,2 ]
Cao, Chunwei [3 ]
Li, Chaohua [3 ]
Hu, Chaojun [1 ,2 ]
Zhang, Shulan [1 ,2 ]
Zeng, Xiaofeng [1 ,2 ]
Zhang, Fengchun [1 ,2 ]
Zeng, Changqing [3 ]
Li, Yongzhe [1 ,2 ]
机构
[1] Peking Union Med Coll Hosp, Peking Union Med Coll, Dept Rheumatol & Clin Immunol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Beijing 100730, Peoples R China
[3] Chinese Acad Sci, Lab Canc Genom, Beijing Inst Genom, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
STAT4; SLE; Polymorphism; Genetic susceptibility; Female patients; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY; DISEASE; MECHANISMS; VARIANTS; ITGAM;
D O I
10.1007/s00296-010-1767-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. Genetic association of signal transducer and activator of transcription 4 (STAT4) with SLE susceptibility has been convincingly established in multiple populations including Asians, whereas studies of genetic relations between STAT4 polymorphisms and subphenotypes of SLE were rarely conducted. In this study, we selected Chinese female population and investigated genetic association between a polymorphism of STAT4 gene (rs7582694) and SLE. Furthermore, genetic association tests based on different subsets classified by 11 clinical manifestations were also performed. A total of 675 SLE female patients and 678 healthy controls were enrolled into this study, and SNP genotyping was performed using Sequenom's MassArray system (Sequenom iPLEX assay). Our study showed strong evidence for genetic predisposition of rs7582694 to SLE (X (2) = 23.7, OR = 0.68, 95% CI: 0.58-0.79, P = 1.13 x 10(-6)), while no association was observed between rs7582694 and any clinical presentations. The results of our study demonstrated that STAT4 rs7582694 SNP was significantly associated with SLE, and these results were in accordance with previous studies.
引用
收藏
页码:1251 / 1255
页数:5
相关论文
共 25 条
  • [21] A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5
    Sigurdsson, Snaevar
    Nordmark, Gunnel
    Garnier, Sophie
    Grundberg, Elin
    Kwan, Tony
    Nilsson, Olof
    Eloranta, Maija-Leena
    Gunnarsson, Iva
    Svenungsson, Elisabet
    Sturfelt, Gunnar
    Bengtsson, Anders A.
    Jonsen, Andreas
    Truedsson, Lennart
    Rantapaa-Dahlqvist, Solbritt
    Eriksson, Catharina
    Alm, Gunnar
    Goring, Harald H. H.
    Pastinen, Tomi
    Syvanen, Ann-Christine
    Ronnblom, Lars
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (18) : 2868 - 2876
  • [22] Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus
    Taylor, Kimberly E.
    Remmers, Elaine F.
    Lee, Annette T.
    Ortmann, Ward A.
    Plenge, Robert M.
    Tian, Chao
    Chung, Sharon A.
    Nititham, Joanne
    Hom, Geoffrey
    Kao, Amy H.
    Demirci, F. Yesim
    Kamboh, M. Ilyas
    Petri, Michelle
    Manzi, Susan
    Kastner, Daniel L.
    Seldin, Michael F.
    Gregersen, Peter K.
    Behrens, Timothy W.
    Criswell, Lindsey A.
    [J]. PLOS GENETICS, 2008, 4 (05):
  • [23] Medical sequencing of candidate genes for nonsyndromic cleft lip and palate
    Vieira, AR
    Avila, JR
    Daack-Hirsch, S
    Dragan, E
    Fèlix, TM
    Rahimov, F
    Harrington, J
    Schultz, RR
    Watanabe, Y
    Johnson, M
    Fang, J
    O'Brien, SE
    Orioli, IM
    Castilla, EE
    FitzPatrick, DR
    Jiang, RL
    Marazita, ML
    Murray, JC
    [J]. PLOS GENETICS, 2005, 1 (06) : 651 - 659
  • [24] Prevalence of rheumatic diseases and disability in China
    Xiang, Yao-Jun
    Dai, Sheng-Ming
    [J]. RHEUMATOLOGY INTERNATIONAL, 2009, 29 (05) : 481 - 490
  • [25] Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
    Yang, Wanling
    Shen, Nan
    Ye, Dong-Qing
    Liu, Qiji
    Zhang, Yan
    Qian, Xiao-Xia
    Hirankarn, Nattiya
    Ying, Dingge
    Pan, Hai-Feng
    Mok, Chi Chiu
    Chan, Tak Mao
    Wong, Raymond Woon Sing
    Lee, Ka Wing
    Mok, Mo Yin
    Wong, Sik Nin
    Leung, Alexander Moon Ho
    Li, Xiang-Pei
    Avihingsanon, Yingyos
    Wong, Chun-Ming
    Lee, Tsz Leung
    Ho, Marco Hok Kung
    Lee, Pamela Pui Wah
    Chang, Yuk Kwan
    Li, Philip H.
    Li, Ruo-Jie
    Zhang, Lu
    Wong, Wilfred Hing Sang
    Ng, Irene Oi Lin
    Lau, Chak Sing
    Sham, Pak Chung
    Lau, Yu Lung
    [J]. PLOS GENETICS, 2010, 6 (02):