Cavender D E, Wagener D K, Orchard T J, LaPorte R E, Becker D J, Kuller L H
Am J Epidemiol. 1984 Aug;120(2):315-27. doi: 10.1093/oxfordjournals.aje.a113894.
Multivariate models for the risk of insulin-dependent diabetes mellitus for siblings of patients with insulin-dependent diabetes were developed using logistic regression analysis. The individuals studied in this report are full siblings of the insulin-dependent diabetic patients diagnosed at Children's Hospital of Pittsburgh between 1964 and 1982. For all siblings considered together, the sharing of two (but not one) HLA haplotypes, the presence of insulin-dependent diabetes in a parent, and being relatively young at the time the proband in the family was diagnosed were significantly associated with increased risk. On the other hand, B7 + siblings had a significantly decreased risk compared to B7--siblings, indicating the presence of an HLA-linked protective gene for the development of the disease. There was a significant interaction between sharing two HLA haplotypes and maternal age at the time of birth; for non-HLA-identical siblings, risk increased with increased maternal age, but maternal age had little or no effect on the risk for HLA-identical siblings. When non-HLA-identical siblings (0 or 1 HLA haplotypes shared) were analyzed separately, only the presence of insulin-dependent diabetes in one of the parents and increased maternal age at the time of birth of the sibling were found to be significantly associated with increased risk. Both of the totally non-HLA-identical diabetic siblings (neither HLA haplotype shared) in this data set had a parent with insulin-dependent diabetes, indicating that at least one HLA haplotype must be inherited in common with an affected family member for diabetes to develop. For HLA-identical siblings, the significant variables were the age of the sibling when the proband was diagnosed, the possession of B7, and maternal age at the time of birth of the sibling, and all three were negatively associated with risk.
采用逻辑回归分析方法,建立了胰岛素依赖型糖尿病患者兄弟姐妹患胰岛素依赖型糖尿病风险的多变量模型。本报告中研究的个体是1964年至1982年期间在匹兹堡儿童医院被诊断为胰岛素依赖型糖尿病患者的全同胞。对于所有一起考虑的兄弟姐妹而言,共享两个(而非一个)HLA单倍型、父母一方患有胰岛素依赖型糖尿病以及在家族中先证者被诊断时年龄相对较小,均与风险增加显著相关。另一方面,与B7阴性的兄弟姐妹相比,B7阳性的兄弟姐妹风险显著降低,这表明存在一个与HLA相关的疾病发展保护基因。共享两个HLA单倍型与出生时母亲年龄之间存在显著交互作用;对于非HLA相同的兄弟姐妹,风险随母亲年龄增加而增加,但母亲年龄对HLA相同的兄弟姐妹的风险影响很小或没有影响。当分别分析非HLA相同的兄弟姐妹(共享0个或1个HLA单倍型)时,发现只有父母一方患有胰岛素依赖型糖尿病以及兄弟姐妹出生时母亲年龄增加与风险增加显著相关。该数据集中两个完全非HLA相同的糖尿病兄弟姐妹(未共享任何HLA单倍型)均有一位患有胰岛素依赖型糖尿病的父母,这表明糖尿病的发生至少必须与一名患病家庭成员共同遗传一个HLA单倍型。对于HLA相同的兄弟姐妹,显著变量是先证者被诊断时兄弟姐妹的年龄、拥有B7以及兄弟姐妹出生时母亲的年龄,且这三个变量均与风险呈负相关。