Islet cell antibody-positive relatives with human leukocyte antigen DQA1*0102, DQB1*0602: Identification by the diabetes prevention trial-type 1

被引:43
作者
Greenbaum, CJ [1 ]
Schatz, DK
Cuthbertson, D
Zeidler, A
Eisenbarth, GS
Krischer, JP
机构
[1] Puget Sound Hlth Care Syst, Dept Vet Affairs, Seattle, WA 98108 USA
[2] Univ Washington, Dept Med, Seattle, WA 98108 USA
[3] Univ Florida, Dept Pediat, Gainesville, FL 32610 USA
[4] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[5] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Denver, CO 80262 USA
[6] Univ So Calif, Dept Med Endocrinol & Diabet, Los Angeles, CA 90033 USA
关键词
D O I
10.1210/jc.85.3.1255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The presence of human leukocyte antigen (HLA) haplotype DQA1*0102, DQB1*0602 is associated with protection from type 1 diabetes. The Diabetes Prevention Trial-type 1 has identified 100 islet cell antibody (ICA)-positive relatives with this protective haplotype, far exceeding the number of such subjects reported in other studies worldwide. Comparisons between ICA(+) relatives with and without DQB1*0602 demonstrated no differences in gender or age; however, among racial groups, African-American ICA relatives were more likely to carry this haplotype than others. The ICA(+) DQB1*0602 individuals were less likely to have additional risk factors for diabetes [insulin autoantibody (IAA) positive or low first phase insulin release (FPIR)] than ICA(+) relatives without DQB1*0602. However, 29% of the ICA(+) DQB1*0602 relatives did have IAA or low FPIR, Although half of the ICA(+) DQB1*0602 relatives had a high risk second haplotype, this was not associated with the additional risk factors for diabetes. Hispanic ICA(+) individuals with DQB1*0602 were more likely to be IAA positive or to have low FPIR than other racial groups. In conclusion, the presence of ICA in the relatives described here suggests that whatever the mechanism that protects DQB1*0602 individuals from diabetes, it is likely to occur after the diabetes disease process has begun. In addition, there may be different effects of DQB1*0602 between ethnic groups.
引用
收藏
页码:1255 / 1260
页数:6
相关论文
共 39 条
[1]  
[Anonymous], 1995, TRANSPLANT P, V27, P3377
[2]   GENETIC-MARKERS FOR INSULIN-DEPENDENT DIABETES-MELLITUS IN JAPANESE [J].
AWATA, T ;
KANAZAWA, Y .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1994, 24 :S83-S87
[3]   ANALYSIS OF HLA-DQ GENOTYPES AND SUSCEPTIBILITY IN INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BAISCH, JM ;
WEEKS, T ;
GILES, R ;
HOOVER, M ;
STASTNY, P ;
CAPRA, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1836-1841
[4]   HLA-DQA1 AND HLA-DQB1 ALLELE AND GENOTYPE CONTRIBUTION TO IDDM SUSCEPTIBILITY IN AN ETHNICALLY MIXED POPULATION [J].
BALDUCCISILANO, PL ;
LAYRISSE, Z ;
DOMINGUEZ, E ;
AMARO, R ;
GUNCZLER, P ;
LANES, R ;
ZARO, R .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1994, 21 (06) :405-414
[5]  
BALDUCCISILANO PL, 1995, J AUTOIMMUN, V8, P425, DOI 10.1006/jaut.1995.0034
[7]   RAPID TYPING OF HLA-DQB1 DNA POLYMORPHISM USING NONRADIOACTIVE OLIGONUCLEOTIDE PROBES AND AMPLIFIED DNA [J].
BUGAWAN, TL ;
ERLICH, HA .
IMMUNOGENETICS, 1991, 33 (03) :163-170
[8]   AGE-DEPENDENT HLA GENETIC-HETEROGENEITY OF TYPE-1 INSULIN-DEPENDENT DIABETES-MELLITUS [J].
CAILLATZUCMAN, S ;
GARCHON, HJ ;
TIMSIT, J ;
ASSAN, R ;
BOITARD, C ;
DJILALISAIAH, I ;
BOUGNERES, P ;
BACH, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2242-2250
[9]   ETHNIC-DIFFERENCES IN HUMAN-LEUKOCYTE ANTIGEN MARKERS OF SUSCEPTIBILITY TO IDDM [J].
CRUICKSHANKS, KJ ;
JOBIM, LF ;
LAWLERHEAVNER, J ;
NEVILLE, TG ;
GAY, EC ;
CHASE, HP ;
KLINGENSMITH, G ;
TODD, JA ;
HAMMAN, RF .
DIABETES CARE, 1994, 17 (02) :132-137
[10]   IMPLICATION OF SPECIFIC DQB1 ALLELES IN GENETIC SUSCEPTIBILITY AND RESISTANCE BY IDENTIFICATION OF IDDM SIBLINGS WITH NOVEL HLA-DQB1 ALLELE AND UNUSUAL DR2 AND DR1 HAPLOTYPES [J].
ERLICH, HA ;
GRIFFITH, RL ;
BUGAWAN, TL ;
ZIEGLER, R ;
ALPER, C ;
EISENBARTH, G .
DIABETES, 1991, 40 (04) :478-481