Deschamps I, Marcelli-Barge A, Poirier J C, Cohen-Haguenauer O, Abderrahim H, Cohen D, Lestradet H, Hors J
INSERM U.290, Hôpital Hérold, Paris, France.
Diabetologia. 1988 Dec;31(12):896-901. doi: 10.1007/BF00265374.
Heterogeneity between two haplotypes in linkage disequilibrium with DR3: B8, C4AQOB1,BfS,DR3 and B18,C4A3BQO,BfF1,DR3, with regard to age at onset of Type 1 (insulin-dependent) diabetes mellitus, was investigated in 325 unrelated French patients (146 males and 179 females, age at onset 1 month to 29 years) who were genotyped for HLA-A, B, C, DR and Bf and 225 of whom were typed for the C4A, B complement components. A subgroup of 82 patients and 75 control subjects were tested for DR beta and DQ beta DNA restriction fragment length polymorphism. The distribution according to age at onset and the mean ages at onset were compared between patients bearing B8, DR3 (n = 58), B18,DR3 (n = 62) or other DR3 haplotypes (Bx, DR3, n = 70), the haplotype segments C4AQOB1,DR3 (n = 41) or C4A3BQO,DR3 (n = 52) and the C4 null alleles C4AQO (N = 48) or C4BQO (n = 112) alone. The B8,DR3 haplotype, its smaller segment C4AQOB1,DR3 or C4AQO alone were associated with age at onset after 6 years (p less than 0.01, less than 0.08 and less than 0.02 respectively); on the other hand, the B18,DR3 haplotype, its segment C4A3BQO,DR3 or C4BQO alone were significantly more frequent in patients aged less than 6 years at onset (p less than 0.02, less than 0.01 and less than 0.01 respectively). Accordingly, the mean age of onset was significantly lower in the latter compared with the former patients (p less than 0.02, less than 0.02 and less than 0.01 respectively). No age-related variation was observed in BX,DR3 patients and their mean age of onset was intermediate.(ABSTRACT TRUNCATED AT 250 WORDS)
在325名无亲缘关系的法国患者(146名男性和179名女性,发病年龄为1个月至29岁)中,研究了与DR3处于连锁不平衡状态的两种单倍型之间的异质性:B8、C4AQOB1、BfS、DR3和B18、C4A3BQO、BfF1、DR3。这些患者进行了HLA - A、B、C、DR和Bf基因分型,其中225人还进行了C4A、B补体成分分型。对82名患者和75名对照受试者组成的亚组进行了DRβ和DQβDNA限制性片段长度多态性检测。比较了携带B8、DR3(n = 58)、B18、DR3(n = 62)或其他DR3单倍型(Bx、DR3,n = 70)的患者,单倍型片段C4AQOB1、DR3(n = 41)或C4A3BQO、DR3(n = 52)以及单独的C4无效等位基因C4AQO(N = 48)或C4BQO(n = 112)在发病年龄方面的分布及平均发病年龄。B8、DR3单倍型、其较小片段C4AQOB1、DR3或单独的C4AQO与6岁以后的发病年龄相关(p分别小于0.01、小于0.08和小于0.02);另一方面,B18、DR3单倍型、其片段C4A3BQO、DR3或单独的C4BQO在发病年龄小于6岁的患者中显著更常见(p分别小于0.02、小于0.01和小于0.01)。因此,与前一组患者相比,后一组患者的平均发病年龄显著更低(p分别小于0.02、小于0.02和小于0.01)。在Bx、DR3患者中未观察到与年龄相关的差异,其平均发病年龄处于中间水平。(摘要截短于250字)