Hanifi Moghaddam P, de Knijf P, Roep B O, Van der Auwera B, Naipal A, Gorus F, Schuit F, Giphart M J
Department of Immunohematology and Blood Bank, University Hospital, Leiden, The Netherlands.
Diabetes. 1998 Feb;47(2):263-9.
We analyzed 11 markers in the IDDM1 region in 120 IDDM patients and 83 healthy control subjects who were fully matched for the highest risk HLA-DQA10301-DQB1 0302/DQA10501-DQB10201 genotype. Our study provides strong evidence that two regions in the major histocompatibility complex contribute to IDDM susceptibility or protection. First, despite selection for highest IDDM-associated risk DQ genotypes, this region displays extensive linkage disequilibrium (LD) differences between IDDM patients and control subjects. A second critical region was mapped around the microsatellite locus D6S273 centromeric of TNF, and it is approximately 200 kb in size. LD analysis shows that "diabetogenic haplotypes" may have resulted from a recombination telomeric of D6S1014 in the region of D6S273 and TNFa. Haplotype analysis using HLA and microsatellite loci refines IDDM risk assessment in carriers of the HLA-DQ highest risk genotype.
我们对120例1型糖尿病患者和83名健康对照者的IDDM1区域中的11个标记物进行了分析,这些健康对照者与最高风险的HLA-DQA10301-DQB10302/DQA10501-DQB10201基因型完全匹配。我们的研究提供了强有力的证据,表明主要组织相容性复合体中的两个区域与1型糖尿病易感性或保护性有关。首先,尽管选择了与1型糖尿病相关风险最高的DQ基因型,但该区域在1型糖尿病患者和对照者之间显示出广泛的连锁不平衡(LD)差异。第二个关键区域定位在TNF着丝粒的微卫星位点D6S273周围,大小约为200 kb。LD分析表明,“致糖尿病单倍型”可能是由于D6S273和TNFα区域中D6S1014的端粒重组所致。使用HLA和微卫星位点的单倍型分析改进了HLA-DQ最高风险基因型携带者的1型糖尿病风险评估。