DPB1 Alleles are associated with type 1 diabetes susceptibility in multiple ethnic groups

被引:32
作者
Cruz, TD
Valdes, AM
Santiago, A
de Llado, TF
Raffel, LJ
Zeidler, A
Rotter, JI
Erlich, HA
Rewers, M
Bugawan, T
Noble, JA
机构
[1] Childrens Hosp Oakland, Res Inst, Oakland, CA 94609 USA
[2] Pontifical Catholic Univ, Dept Biol, Ponce, PR USA
[3] Ponce Sch Med, Ponce, PR USA
[4] Univ Calif Los Angeles, Cedars Sinai Med Ctr, Dept Pediat, Los Angeles, CA 90048 USA
[5] Univ Calif Los Angeles, Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
[6] Univ So Calif, Los Angeles Cty Hosp,Keck Sch Med, Div Endocrinol & Diabet, Sch Med,Med Ctr, Los Angeles, CA USA
[7] Roche Mol Syst, Alameda, CA USA
[8] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr, Denver, CO 80202 USA
关键词
D O I
10.2337/diabetes.53.8.2158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic associations between type 1 diabetes and alleles at the HLA class II locus DPB1 have been previously reported. Observed associations could be due to variation in the DPB1 locus itself or to linkage disequilibrium (LD) between DPB1 alleles and other susceptibility loci. One measure of whether the association of an allele with a disease reflects a true effect of the locus or is simply due to LD is the observation of that association in multiple ethnic groups. Previous type 1 diabetes associations have been reported for DPB1*0301 and DPB1*0202 (predisposing) and for DPB1*0402 (protective). In this study, results are reported from testing these associations in three different sample sets: 1) Puerto Rican case and control subjects, 2) Mexican-American simplex families, and 3) high-risk (DR3/DR4) individuals with and without an affected relative. DPB1*0301 was associated in all three groups, even after accounting for LD with DRB1-DQB1. DPB1*0202 and DPB1*0402 were positively and negatively associated, respectively, in two of the three populations. These results suggest that the observed DPB1 associations, especially that of the DPB1*0301 allele, with type 1 diabetes are likely to be true associations. This supports the concept that multiple genes in the HLA region can affect type 1 diabetes susceptibility.
引用
收藏
页码:2158 / 2163
页数:6
相关论文
共 22 条
[1]  
AFFEL LJ, 2002, GENETIC BASIS COMMON, P431
[2]  
BALDUCCISILANO PL, 1995, J AUTOIMMUN, V8, P425, DOI 10.1006/jaut.1995.0034
[3]   The association of specific BLA class I and II alleles with type 1 diabetes among Filipinos [J].
Bugawan, TL ;
Klitz, W ;
Alejandrino, M ;
Ching, J ;
Panelo, A ;
Solfelix, CM ;
Petrone, A ;
Buzzetti, R ;
Pozzilli, P ;
Erlich, HA .
TISSUE ANTIGENS, 2002, 59 (06) :452-469
[4]   A METHOD FOR TYPING POLYMORPHISM AT THE HLA-A LOCUS USING PCR AMPLIFICATION AND IMMOBILIZED OLIGONUCLEOTIDE PROBES [J].
BUGAWAN, TL ;
APPLE, R ;
ERLICH, HA .
TISSUE ANTIGENS, 1994, 44 (03) :137-147
[5]   The HLA-DPB1-associated component of the IDDM1 and its relationship to the major loci HLA-DQB1,-DQA1, and-DRB1 [J].
Cucca, F ;
Dudbridge, F ;
Loddo, M ;
Mulargia, AP ;
Lampis, R ;
Angius, E ;
De Virgiliis, S ;
Koeleman, BPC ;
Bain, SC ;
Barnett, AH ;
Gilchrist, F ;
Cordell, H ;
Welsh, K ;
Todd, JA .
DIABETES, 2001, 50 (05) :1200-1205
[6]   Incidence of IDDM in children living in Puerto Rico [J].
de Llado, TEF ;
de Pijem, LG ;
Hawk, B .
DIABETES CARE, 1998, 21 (05) :744-746
[7]   HLA CLASS-II ALLELES AND SUSCEPTIBILITY AND RESISTANCE TO INSULIN-DEPENDENT DIABETES-MELLITUS IN MEXICAN-AMERICAN FAMILIES [J].
ERLICH, HA ;
ZEIDLER, A ;
CHANG, J ;
SHAW, S ;
RAFFEL, LJ ;
KLITZ, W ;
BESHKOV, Y ;
COSTIN, G ;
PRESSMAN, S ;
BUGAWAN, T ;
ROTTER, JI .
NATURE GENETICS, 1993, 3 (04) :358-364
[8]   Association of HLA-DPB1(*)0301 with IDDM in Mexican-Americans [J].
Erlich, HA ;
Rotter, JI ;
Chang, JD ;
Shaw, SJ ;
Raffel, LJ ;
Klitz, W ;
Bugawan, TL ;
Zeidler, A .
DIABETES, 1996, 45 (05) :610-614
[9]  
EXCOFFIER L, 1995, MOL BIOL EVOL, V12, P921
[10]   HLA associations in type 1 diabetes: DPB1 alleles may act as markers of other HLA-complex susceptibility genes [J].
Johansson, S ;
Lie, BA ;
Pociot, F ;
Nerup, J ;
Cambon-Thomsen, A ;
Kockum, I ;
Thorsby, E ;
Undlien, DE .
TISSUE ANTIGENS, 2003, 61 (05) :344-351