Cerná M, Vavrincová P, Havelka S
Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Acta Univ Carol Med (Praha). 1994;40(1-4):69-73.
HLA class II analysis in a group of 153 Czech children with juvenile rheumatoid arthritis by PCR and oligonucleotide hybridization demonstrated associations with several alleles. DRB10801 (RR = 5.3, p < 0.005) and DRB1 * 11 (RR = 2.2, p < 0.01) including all subtypes were shown to be increased in the rheumatoid factor-negative group (N = 137). The same results were observed in Italy, England and Norway. In patients with the pauciarticular onset with conversion to polyarticular within 3 years, a statistically significant increase in DR2 (RR = 10.1, p < 0.00005), mostly due to DRB11501, was found. In the iridocyclitis and antinuclear factor groups, susceptibility to DRB11201 was observed. There was a striking decrease in DRB10701 (RR = 0.3, p < 0.00005) in all groups. There was neither an increase in DRB11301 or DPB10301 nor a decrease in DRB104, as reported from other studies in Texas and Norway. The rheumatoid factor-positive group with polyarticular onset (N = 13) was associated with DRB104 (RR = 7.1, p < 0.005), as observed in adults. DPB10201 was increased in the persistent pauciarticular group (RR = 3.7, p < 0.0005). DPB10402 was decreased in all pauciarticular groups with or without conversion (RR = 0.3, p < 0.005). Taken together, there are not only genetic differences and clinical heterogeneity in juvenile rheumatoid arthritis patients but, also, common predisposing factors.
通过聚合酶链反应(PCR)和寡核苷酸杂交对153名捷克青少年类风湿性关节炎患儿进行的人类白细胞抗原(HLA)II类分析显示,该病与多个等位基因相关。类风湿因子阴性组(N = 137)中,包括所有亚型的DRB10801(相对风险率RR = 5.3,p < 0.005)和DRB111(RR = 2.2,p < 0.01)有所增加。在意大利、英国和挪威也观察到了相同的结果。在发病3年内从少关节型转变为多关节型的患者中,发现DR2(RR = 10.1,p < 0.00005)有统计学意义的增加,主要是由于DRB11501。在虹膜炎和抗核因子组中,观察到对DRB11201的易感性。所有组中DRB10701均显著降低(RR = 0.3,p < 0.00005)。与德克萨斯州和挪威的其他研究报告不同,DRB11301或DPB10301没有增加,DRB104也没有减少。多关节型发病的类风湿因子阳性组(N = 13)与DRB104相关(RR = 7.1,p < 0.005),这与成人情况相同。持续性少关节型组中DPB10201增加(RR = 3.7,p < 0.0005)。所有少关节型组,无论是否转变,DPB1*0402均降低(RR = 0.3,p < 0.005)。综上所述,青少年类风湿性关节炎患者不仅存在遗传差异和临床异质性,而且还有共同的易感因素。