Sanders P A, Grennan D M, Dyer P A, Thomson W, deLange G G
University of Manchester Rheumatic Diseases Centre, Hope Hospital, Salford, England.
J Rheumatol. 1987 Aug;14(4):718-22.
Clinical and immunogenetic factors were compared in 214 patients with sporadic rheumatoid arthritis (RA) and 117 patients from 52 multiplex families. Sex distribution, articular disease severity and seropositivity for rheumatoid and antinuclear factors were similar in familial and sporadic disease. There was a trend for Sjögren's and Felty's syndromes to be more frequent in familial RA but extraarticular disease features were otherwise similar in the 2 RA disease groups. Mean age of onset was 41.1 years in familial and 46.5 years in sporadic RA (p less than 0.0006); 67% of family probands, 74% of affected relatives and 57% of sporadic patients were HLA-DR4 positive (p less than 0.05 affected relatives vs sporadic). The similarity of clinical features found in familial and sporadic RA justifies the use of families with RA to study aspects of disease pathogenesis.
对214例散发性类风湿关节炎(RA)患者和来自52个多位点家庭的117例患者的临床和免疫遗传学因素进行了比较。在家族性和散发性疾病中,性别分布、关节疾病严重程度以及类风湿因子和抗核因子的血清阳性率相似。家族性RA中干燥综合征和费尔蒂综合征更为常见,但在这两组RA疾病中,关节外疾病特征在其他方面相似。家族性RA的平均发病年龄为41.1岁,散发性RA为46.5岁(p<0.0006);67%的家族先证者、74%的受累亲属和57%的散发性患者HLA-DR4阳性(受累亲属与散发性患者相比,p<0.05)。在家族性和散发性RA中发现的临床特征相似,这证明利用RA家族来研究疾病发病机制的各个方面是合理的。