Kilding Rachael, Wilson Anthony G
Division of Genomic Medicine, The University of Sheffield, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, United Kingdom.
Cytokine. 2005 Oct 21;32(2):71-5. doi: 10.1016/j.cyto.2005.07.015. Epub 2005 Sep 30.
Rheumatoid arthritis (RA) is a complex heterogeneous disease with an estimated genetic contribution to of 30-50%. Approximately one third arises from the major histocompatibility complex (MHC) at 6p21.3. The contribution of specific DRB1 alleles encoding the shared epitope has been well described, however, several recent studies have suggested that additional telomeric genetic influences may exist. This region is difficult to study as a result of the presence of strong linkage disequilibrium (LD) within the MHC and high gene density particularly in the central class III region. In this article we review the current data supporting the existence of a non-DRB1 susceptibility gene for rheumatoid arthritis, in particular within the class III region.
类风湿关节炎(RA)是一种复杂的异质性疾病,估计遗传因素占30%-50%。约三分之一源于位于6p21.3的主要组织相容性复合体(MHC)。编码共享表位的特定DRB1等位基因的作用已得到充分描述,然而,最近的几项研究表明可能存在其他端粒遗传影响。由于MHC内存在强连锁不平衡(LD)以及基因密度高,尤其是在中央III类区域,该区域难以研究。在本文中,我们综述了支持类风湿关节炎存在非DRB1易感基因的现有数据,特别是在III类区域内。