Clerget-Darpoux F, Babron M C, Deschamps I, Hors J
Unité de Recherches de Génétique Epidémiologique (INSERM U. 155), Château de Longchamp, Paris, France.
Am J Hum Genet. 1991 Jul;49(1):42-8.
The marker association segregation chi-square (MASC) method was applied to a sample of 416 Caucasians affected with insulin-dependent diabetes mellitus (IDDM), for which information on the parental and sibship status was available, as well as HLA typing. We show that the model which best explains all the observations assumes a cis or trans complementation of two tightly linked genes within the HLA region, an additional maternal effect, and other familial factors. The HLA molecule corresponding to the complementation of Arg52(+) and Asp57(-) has been recently proposed as explaining susceptibility to IDDM. However, this hypothesis does not account for the overall observations made on the HLA marker in IDDM patients and their relatives. The MASC method may also be applied to evaluate the risk for relatives of an affected individual (the "index"). For example, the risk for a sib depends not only on the parental status and on the number of HLA haplotypes he shares with the index, but also on which haplotype the index himself inherited from his mother and father.
标记关联分离卡方(MASC)方法应用于416名患有胰岛素依赖型糖尿病(IDDM)的高加索人样本,这些样本可获取有关父母和同胞关系的信息以及HLA分型。我们表明,最能解释所有观察结果的模型假定HLA区域内两个紧密连锁基因的顺式或反式互补、额外的母体效应以及其他家族因素。最近有人提出,对应于Arg52(+)和Asp57(-)互补的HLA分子可解释对IDDM的易感性。然而,这一假设无法解释对IDDM患者及其亲属的HLA标记所做的总体观察结果。MASC方法也可用于评估受影响个体(“索引病例”)亲属的风险。例如,同胞的风险不仅取决于父母的状态以及他与索引病例共享的HLA单倍型数量,还取决于索引病例自身从其母亲和父亲那里继承的是哪种单倍型。