Deighton C M, Cavanagh G, Rigby A S, Lloyd H L, Walker D J
Department of Rheumatology, Royal Victoria Infirmary, Newcastle upon Tyne.
Br J Rheumatol. 1993 Oct;32(10):893-8. doi: 10.1093/rheumatology/32.10.893.
The distribution of the HLA-DR allele frequencies of 105 RA patients has been compared with the expected distribution under recessive and dominant modes of inheritance using control data from 2041 controls and the antigen genotype frequency among patients methodology. The observed distribution was compatible with a recessive mode of HLA-linked inheritance in RA, with a dominant mode rejected, whether HLA-DR4 was considered alone, or HLA-DR4 and HLA-DR1 were combined as if they were behaving as a single predisposing gene. Mean sibship concordance rates (MSCRs) were calculated for categories of proband HLA-DR genotypes. The highest MSCR was for HLA-DR4 homozygous probands, and the lowest for HLA-DR2 or 7/non-4 genotypes. These combined observations suggest that interactions between both inherited HLA-haplotypes are important in the predisposition to RA.
运用来自2041名对照的控制数据以及患者中的抗原基因型频率方法,将105例类风湿关节炎(RA)患者的HLA - DR等位基因频率分布与隐性和显性遗传模式下的预期分布进行了比较。观察到的分布与RA中HLA连锁遗传的隐性模式相符,而显性模式被排除,无论单独考虑HLA - DR4,还是将HLA - DR4和HLA - DR1合并起来视为一个单一的易感基因。针对先证者HLA - DR基因型类别计算了平均同胞一致性率(MSCR)。MSCR最高的是HLA - DR4纯合先证者,最低的是HLA - DR2或7/非4基因型。这些综合观察结果表明,两种遗传的HLA单倍型之间的相互作用在RA易感性中很重要。