Runstadler J A, Säilä H, Savolainen A, Leirisalo-Repo M, Aho K, Tuomilehto-Wolf E, Tuomilehto J, Seldin M F
Rowe Program in Human Genetics and Molecular Medicine, Department of Biological Chemistry, University of California, Davis, USA.
Genes Immun. 2003 Jul;4(5):326-35. doi: 10.1038/sj.gene.6364002.
This study used Finnish juvenile idiopathic arthritis (JIA) probands with pauciarticular and rheumatoid factor (RF) negative polyarticular subtypes of JIA to further define the genetic susceptibility to JIA. We examined 16 markers spanning an 18 cM region of chromosome 6 encompassing the MHC and surrounding genomic region in a set of 235 Finnish JIA nuclear families and 639 Finnish control individuals. Analysis by case/control association and transmission disequilibrium test (TDT) methods each demonstrated strong evidence for a susceptibility locus near the D6S2447 microsatellite (P<10(-6) for both methods) that is flanked by DQB1 and DRB1. Analysis of the DRB1 locus suggested that DRB10801 and DRB11101 rather than DQA1 or other HLA alleles may be responsible for conferring susceptibility to disease. These findings are consistent with the most compelling results of previous reports on HLA associations and suggest a JIA DRB1 shared epitope encompassing critical amino-acid residues in the third hypervariable region of this molecule. Most importantly, in pauciarticular patients, the strong association does not extend to proximal markers as it does in polyarticular patients (P<0.00001). Analysis strongly suggests that the difference is because of additional JIA susceptibility loci within the MHC being present in polyarticular RF negative patients.
本研究使用芬兰青少年特发性关节炎(JIA)先证者,这些先证者患有少关节型和类风湿因子(RF)阴性多关节型JIA亚型,以进一步确定JIA的遗传易感性。我们在一组235个芬兰JIA核心家庭和639名芬兰对照个体中,检测了跨越6号染色体上一个18 cM区域的16个标记,该区域包含主要组织相容性复合体(MHC)和周围的基因组区域。通过病例/对照关联分析和传递不平衡检验(TDT)方法进行的分析均显示,在D6S2447微卫星附近存在一个易感性位点的有力证据(两种方法的P值均<10⁻⁶),该位点两侧是DQB1和DRB1。对DRB1位点的分析表明,可能是DRB10801和DRB11101而非DQA1或其他HLA等位基因赋予了疾病易感性。这些发现与先前关于HLA关联的最令人信服的结果一致,并提示存在一个JIA DRB1共享表位,其包含该分子第三高变区中的关键氨基酸残基。最重要的是,在少关节型患者中,这种强关联并不像在多关节型患者中那样延伸至近端标记(P<0.00001)。分析强烈提示,这种差异是由于多关节型RF阴性患者的MHC内存在额外的JIA易感性位点。