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家族性类风湿关节炎:在先证者患青少年类风湿关节炎的四个家族中,HLA与疾病易感性位点的连锁关系。

Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis.

作者信息

Rossen R D, Brewer E J, Sharp R M, Ott J, Templeton J W

出版信息

J Clin Invest. 1980 Mar;65(3):629-42. doi: 10.1172/JCI109708.

Abstract

The occurrence of a chronic seronegative polyarthritis has been studied in four families in which the proband presented with some form of juvenile rheumatoid arthritis. In these families, histocompatibility testing suggested that susceptibility to arthritis was controlled by a dominant allele with variable penetrance and expressivity at the rheumatoid-like arthritis, first locus (RLA-1). The combined lod scores for the four families (2.70) indicated that the odds in favor of genetic linkage between the major histocompatibility complex and the postulated disease susceptibility gene, RLA-1, were 500:1. In one family, a recombinant event permitted localization of RLA-1 centromeric to HLA-D. Of major interest was the fact that there was significant pleomorphism in the clinical manifestations of arthritis in affected individuals. In some, symptoms first occurred in childhood and in others, in adult life. Even among those with childhood-onset arthritis, different types of juvenile rheumatoid arthritis were observed within the same family.

摘要

对四个家族中出现慢性血清阴性多关节炎的情况进行了研究,这些家族中的先证者患有某种形式的青少年类风湿性关节炎。在这些家族中,组织相容性检测表明,对关节炎的易感性由一个显性等位基因控制,该等位基因在类风湿样关节炎第一位点(RLA-1)具有可变的外显率和表达性。这四个家族的合并对数计分(2.70)表明,主要组织相容性复合体与假定的疾病易感基因RLA-1之间存在遗传连锁的几率为500:1。在一个家族中,一次重组事件使得RLA-1定位到HLA-D的着丝粒侧。最令人感兴趣的是,受影响个体的关节炎临床表现存在显著的多态性。在一些人中,症状首先出现在儿童期,而在另一些人中,则出现在成年期。即使在儿童期发病的关节炎患者中,同一个家族内也观察到了不同类型的青少年类风湿性关节炎。

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