Genetic structure of IDDM1: Two separate regions in the major histocompatibility complex contribute to susceptibility or protection

被引:72
作者
Moghaddam, PH
de Knijf, P
Roep, BO
Van der Auwera, B
Naipal, A
Gorus, F
Schuit, F
Giphart, MJ
机构
[1] Univ Leiden Hosp, Dept Immunohematol, NL-2300 RC Leiden, Netherlands
[2] Univ Leiden Hosp, Blood Bank, NL-2300 RC Leiden, Netherlands
[3] Leiden Univ, Dept Human Genet, NL-2300 RA Leiden, Netherlands
[4] Free Univ Brussels, Dept Endocrinol & Metab, Brussels, Belgium
[5] Free Univ Brussels, Dept Biochem, Brussels, Belgium
关键词
D O I
10.2337/diab.47.2.263
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-DQA1*0301-DQB1*0302/DQA1*0501-DQB1*0201 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 similar to 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.
引用
收藏
页码:263 / 269
页数:7
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