类风湿性关节炎
医学
单核苷酸多态性
单倍型
免疫学
优势比
SNP公司
内科学
关节炎
等位基因
病例对照研究
基因型
遗传学
生物
基因
作者
Elaine F. Remmers,Robert M. Plenge,Annette Lee,Robert R. Graham,Geoffrey Hom,Timothy W. Behrens,Paul I.W. de Bakker,Julie M. Le,Hye Soon Lee,Franak Batliwalla,Wentian Li,Seth L. Masters,Matthew G. Booty,John P. Carulli,Leonid Padyukov,Lars Alfredsson,Lars Klareskog,Wei V. Chen,Christopher I. Amos,Lindsey A. Criswell,Michael F. Seldin,Daniel L. Kastner,Peter K. Gregersen
摘要
Rheumatoid arthritis is a chronic inflammatory disease with a substantial genetic component. Susceptibility to disease has been linked with a region on chromosome 2q.We tested single-nucleotide polymorphisms (SNPs) in and around 13 candidate genes within the previously linked chromosome 2q region for association with rheumatoid arthritis. We then performed fine mapping of the STAT1-STAT4 region in a total of 1620 case patients with established rheumatoid arthritis and 2635 controls, all from North America. Implicated SNPs were further tested in an independent case-control series of 1529 patients with early rheumatoid arthritis and 881 controls, all from Sweden, and in a total of 1039 case patients and 1248 controls from three series of patients with systemic lupus erythematosus.A SNP haplotype in the third intron of STAT4 was associated with susceptibility to both rheumatoid arthritis and systemic lupus erythematosus. The minor alleles of the haplotype-defining SNPs were present in 27% of chromosomes of patients with established rheumatoid arthritis, as compared with 22% of those of controls (for the SNP rs7574865, P=2.81x10(-7); odds ratio for having the risk allele in chromosomes of patients vs. those of controls, 1.32). The association was replicated in Swedish patients with recent-onset rheumatoid arthritis (P=0.02) and matched controls. The haplotype marked by rs7574865 was strongly associated with lupus, being present on 31% of chromosomes of case patients and 22% of those of controls (P=1.87x10(-9); odds ratio for having the risk allele in chromosomes of patients vs. those of controls, 1.55). Homozygosity of the risk allele, as compared with absence of the allele, was associated with a more than doubled risk for lupus and a 60% increased risk for rheumatoid arthritis.A haplotype of STAT4 is associated with increased risk for both rheumatoid arthritis and systemic lupus erythematosus, suggesting a shared pathway for these illnesses.
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