Association of HLA-DPB1(*)0301 with IDDM in Mexican-Americans

被引:65
作者
Erlich, HA
Rotter, JI
Chang, JD
Shaw, SJ
Raffel, LJ
Klitz, W
Bugawan, TL
Zeidler, A
机构
[1] CEDARS SINAI RES INST,DEPT MED,LOS ANGELES,CA
[2] CEDARS SINAI RES INST,DEPT PEDIAT,LOS ANGELES,CA
[3] RANCHO LOS AMIGOS MED CTR,DOWNEY,CA
[4] UNIV CALIF BERKELEY,DEPT INTEGRAT BIOL,BERKELEY,CA
[5] UNIV SO CALIF,LOS ANGELES CTY MED CTR,LOS ANGELES,CA 90033
关键词
D O I
10.2337/diabetes.45.5.610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Susceptibility to IDDM has been associated with specific alleles at the HLA class II loci in a variety of human populations. Previous studies among Mexican-Americans, a group ancestrally derived from Native Americans and Hispanic whites, showed that the DR4 haplotypes (DRB1*0405-DQB1*0302 and DBB1*0402-DQB1*0302) and the DR3 haplotype (DRB1*0301-DQB1*0201) were increased among patients and suggested a role for both DR and DQ alleles in susceptibility and resistance. Based on the analysis of 42 Mexican-American IDDM families and ethnically matched control subjects by polymerase chain reaction/sequence-specific oligonucleotide probe typing, we report an association of IDDM with the DPB1 allele, *0301 (relative risk = 6.6; P = 0.0012) in this population. The analysis of linkage disequilibrium patterns in this population indicates that the observed increased frequency in DPB1*0301 among patients cannot be attributed simply to linkage disequilibrium with highrisk DR-DQ haplotypes. These data suggest that in addition to alleles at the DRB1 and DQB1 loci, polymorphism at the DPB1 locus may also influence IDDM risk.
引用
收藏
页码:610 / 614
页数:5
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