Pile K D, Wordsworth B P, Bell J I
Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom.
Ann Rheum Dis. 1992 Nov;51(11):1250-1. doi: 10.1136/ard.51.11.1250.
There is a polygenic component to rheumatoid arthritis (RA) in addition to the known association with HLA-DR4. It has previously been shown in another autoimmune disease (type I diabetes mellitus) that a gene on chromosome 11p can act with HLA-DR4 to enhance susceptibility (relative risk 5-6). It is therefore possible that this locus may also affect the development of RA. Genotype frequencies at this locus, defined by a dimorphic Fok 1 restriction site, were compared in 139 healthy controls and 213 patients with classical/definite RA. In contrast with diabetes there was no increase in genotypes lacking the Fok 1 site, either in the rheumatoid group overall (125/211 compared with 86/139 controls) or in the DR4 positive rheumatoid group (76/140 compared with controls). These results indicate that the interaction between DR4 and a locus on chromosome 11p is not common to all DR4 associated autoimmune diseases.
除了已知的与HLA - DR4的关联外,类风湿性关节炎(RA)还存在多基因成分。此前在另一种自身免疫性疾病(I型糖尿病)中已表明,11号染色体p上的一个基因可与HLA - DR4共同作用以增强易感性(相对风险为5 - 6)。因此,该基因座也有可能影响RA的发展。在139名健康对照者和213名患有典型/确诊RA的患者中,比较了由双态性Fok 1限制性位点定义的该基因座的基因型频率。与糖尿病不同,在整个类风湿性关节炎组(125/211,对照组为86/139)或DR4阳性类风湿性关节炎组(76/140,与对照组相比)中,缺乏Fok 1位点的基因型均未增加。这些结果表明,DR4与11号染色体p上的一个基因座之间的相互作用并非所有与DR4相关的自身免疫性疾病所共有。