Payami H, Khan M H, Grennan D M, Sanders P A, Dyer P A, Thomson G
Am J Hum Genet. 1987 Sep;41(3):331-49.
We have developed a method to study the genetic relationship between any two HLA-associated diseases. We have considered the following hypotheses: (1) both diseases are caused by a common allele; (2) different alleles at the same locus predispose to the two diseases; (3) one disease is predisposed by two alleles, one of which can also lead to the second disease; and (4) different HLA-linked loci are involved in the etiology of each disease. For each hypothesis, we have derived the expected HLA haplotype-sharing distribution in sib pairs who are affected with two diseases. The comparison of the expectations indicate that, in many cases, the alternate hypotheses can be distinguished, if the sample size is appropriately large. The knowledge of the mode of inheritance of each disease is not usually necessary; however, it can greatly increase the power of the test. Analyses of data on pairwise combinations of rheumatoid arthritis (RA), autoimmune thyroid disease (ATD), and insulin-dependent (type I) diabetes mellitus (IDDM) suggest that (a) IDDM is predisposed by two HLA-linked alleles, one of which also predisposes to ATD, (b) one of the IDDM alleles also confers susceptibility to RA, and (c) although the HLA-linked susceptibilities to RA and ATD appear to be primarily due to distinct alleles, the ATD allele may also have a minor role in predisposition to RA.
我们已经开发出一种方法来研究任意两种与HLA相关疾病之间的遗传关系。我们考虑了以下几种假设:(1)两种疾病由一个共同的等位基因引起;(2)同一基因座上的不同等位基因使个体易患这两种疾病;(3)一种疾病由两个等位基因引起,其中一个等位基因也可导致第二种疾病;(4)每种疾病的病因涉及不同的HLA连锁基因座。对于每种假设,我们推导出了患两种疾病的同胞对中预期的HLA单倍型共享分布。预期结果的比较表明,在许多情况下,如果样本量足够大,就可以区分这些替代假设。通常不需要了解每种疾病的遗传模式;然而,这极大地增强了检验效能。对类风湿性关节炎(RA)、自身免疫性甲状腺疾病(ATD)和胰岛素依赖型(I型)糖尿病(IDDM)的成对组合数据进行分析,结果表明:(a)IDDM由两个与HLA连锁的等位基因引起,其中一个也使个体易患ATD;(b)IDDM的一个等位基因也使个体易患RA;(c)虽然与HLA连锁的对RA和ATD的易感性似乎主要是由不同的等位基因引起的,但ATD等位基因在RA易感性方面可能也起次要作用。