Cox N J, Baker L, Spielman R S
Department of Human Genetics, University of Pennsylvania School of Medicine, Philadelphia 19104-6072.
Am J Hum Genet. 1988 Jan;42(1):167-72.
An association between insulin-dependent diabetes mellitus (IDDM) and an RFLP adjacent to the insulin gene has been consistently observed, but its etiological significance is unclear. We studied unrelated IDDM patients (N = 45) and controls (N = 65) to confirm the association--and assessed evidence for linkage in 22 families with at least two affected (IDDM) sibs--to determine whether the insulin-gene region actually contributes to susceptibility to IDDM. All individuals were typed for the RFLP in the 5'-flanking region of the insulin gene (5'FP) used in the previous studies, and the 12 families not fully informative for linkage with the 5'FP were typed for additional closely linked RFLPs. We found a higher frequency of class 1 alleles of the 5'FP in IDDM patients (.83) than in controls (.75), which is consistent with the reported association, but the difference was not statistically significant in our sample. Among the 33 affected sib pairs (ASPs) in 22 families, if maximum possible sharing is assumed when sharing is ambiguous, 10 pairs share both parental insulin genes, 17 pairs share one, and six share neither. This distribution is incompatible with close linkage. In contrast, for the HLA region, for which all 22 families are fully informative, 19 of the 33 ASPs share two haplotypes and the remaining 14 share one. There are no pairs that share neither HLA haplotype. Thus, although these data clearly illustrate the contribution of HLA-linked susceptibility to IDDM, they argue strongly against a contribution of similar magnitude by the insulin-gene region.
胰岛素依赖型糖尿病(IDDM)与胰岛素基因附近的一个限制性片段长度多态性(RFLP)之间的关联一直以来都有观察到,但其病因学意义尚不清楚。我们研究了无亲缘关系的IDDM患者(N = 45)和对照组(N = 65)以确认这种关联,并评估了22个至少有两个患病(IDDM)同胞的家庭中的连锁证据,以确定胰岛素基因区域是否真的对IDDM易感性有影响。所有个体都针对先前研究中使用的胰岛素基因5'侧翼区域(5'FP)的RFLP进行了分型,并且对12个与5'FP连锁信息不完全的家庭进行了另外紧密连锁的RFLP分型。我们发现IDDM患者中5'FP的1类等位基因频率(.83)高于对照组(.75),这与报道的关联一致,但在我们的样本中差异无统计学意义。在22个家庭中的33对患病同胞对(ASP)中,如果在共享情况不明确时假设最大可能共享,10对共享双亲的胰岛素基因,17对共享一个,6对都不共享。这种分布与紧密连锁不相容。相比之下,对于HLA区域,所有22个家庭的信息都完全明确,33个ASP中有19个共享两个单倍型,其余14个共享一个。没有一对不共享任何HLA单倍型。因此,尽管这些数据清楚地说明了HLA连锁易感性对IDDM的影响,但它们有力地反驳了胰岛素基因区域有类似程度影响的观点。