A NEW MARKER IN THE HLA CLASS-I REGION IS ASSOCIATED WITH THE AGE AT ONSET OF IDDM

被引:44
作者
DEMAINE, AG
HIBBERD, ML
MANGLES, D
MILLWARD, BA
机构
关键词
IDDM; MAJOR HISTOCOMPATIBILITY COMPLEX; IMMUNOGENETICS; AUTOIMMUNITY; HLA AND DISEASE;
D O I
10.1007/s001250050329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The (MHC) class II association with insulin-dependent diabetes mellitus (IDDM) is well documented. However, it is likely that genes within the MHC class III and the class I region also play a role in determining susceptibility to IDDM. In this study we have used a novel molecular probe to investigate the class I P3A and P3B loci of 179 patients with IDDM and 142 normal control subjects. A highly significant increase in the frequency of the class I P3 4.0;1.5 kilobase (kb) and 4.0;1.8;1.5 kb genotypes was found in patients compared to the control subjects ((2)(chi) 46.8, 6 df, p < 0.0001). The association with the P3B 1.5 kb allele was strongly associated with the age at onset of diabetes, being present in 96.2% of subjects who developed diabetes between the age of 10-20 years compared to 55.0 and 74.6% who developed diabetes before 10 years or after 20 years, respectively ((2)(chi) 31.4, p < 0.0001). There was no evidence for linkage disequilibrium between the DQA1 and DQB1 loci and P3B suggesting that this is an independent association. In conclusion, these results suggest that genes in both the MHC class I and II regions confer susceptibility to IDDM and are related to the age at onset of the disease.
引用
收藏
页码:623 / 628
页数:6
相关论文
共 30 条
[1]  
ABDERRAHIM H, 1994, GENOMICS, V23, P526
[2]   INSITU CHARACTERIZATION OF AUTOIMMUNE PHENOMENA AND EXPRESSION OF HLA MOLECULES IN THE PANCREAS IN DIABETIC INSULITIS [J].
BOTTAZZO, GF ;
DEAN, BM ;
MCNALLY, JM ;
MACKAY, EH ;
SWIFT, PGF ;
GAMBLE, DR .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (06) :353-360
[3]   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
[4]  
CAPLEN NJ, 1990, IMMUNOGENETICS, V32, P427
[5]  
CHIMINI G, 1990, IMMUNOGENETICS, V32, P419
[6]   GENETIC SUSCEPTIBILITY IN DIABETES-MELLITUS - ANALYSIS OF HLA ASSOCIATION [J].
CUDWORTH, AG ;
WOODROW, JC .
BRITISH MEDICAL JOURNAL, 1976, 2 (6040) :846-848
[7]   2 POLYMORPHISMS AT THE LOCUS D698 DEFINED BY A YAC [J].
DAVID, V ;
BORETTO, J ;
JOUANOLLE, AM ;
MAUVIEUX, V ;
ELKHALOUN, A ;
PERICHON, M ;
BLAYAU, M ;
PONTAROTTI, P .
NUCLEIC ACIDS RESEARCH, 1990, 18 (18) :5582-5582
[8]  
DEGLIESPOSTI MA, 1992, IMMUNOGENETICS, V35, P355
[9]   HLA DQA, DQB, AND DRB GENOTYPING BY OLIGONUCLEOTIDE ANALYSIS - DISTRIBUTION OF ALLELES AND HAPLOTYPES IN BRITISH CAUCASOIDS [J].
DOHERTY, DG ;
VAUGHAN, RW ;
DONALDSON, PT ;
MOWAT, AP .
HUMAN IMMUNOLOGY, 1992, 34 (01) :53-63
[10]   A GENE IN THE HLA CLASS-I REGION CONTRIBUTES TO SUSCEPTIBILITY TO IDDM IN THE FINNISH POPULATION [J].
FENNESSY, M ;
METCALFE, K ;
HITMAN, GA ;
NIVEN, M ;
BIRO, PA ;
TUOMILEHTO, J ;
TUOMILEHTOWOLF, E ;
AKERBLOM, HK ;
LOUNAMAA, R ;
TOIVANEN, L ;
FAGERLUND, A ;
FLITTNER, M ;
GUSTAFSSON, B ;
HAGGQVIST, C ;
HAKULINEN, A ;
HERVA, L ;
HILTUNEN, P ;
HUHTAMAKI, T ;
HUTTUNEN, NP ;
HYTTINEN, M ;
JOKI, T ;
JOKISALO, R ;
KAAR, ML ;
KALLIO, S ;
KAPRIO, EA ;
KASKI, U ;
KNIP, M ;
LAINE, L ;
LAPPALAINEN, J ;
MAENPAA, J ;
MAKELA, AL ;
NIEMI, K ;
NIIRANEN, A ;
NUUJA, A ;
OJAJARVI, P ;
OTONKOSKI, T ;
PIHLAJAMAKI, K ;
PONTYNEN, S ;
RAJANTIE, J ;
SANKALA, J ;
SCHUMACHER, J ;
SILLANPAA, M ;
STAHLBERG, MR ;
STRAHLMANN, CH ;
UOTILA, T ;
VARE, M ;
VARIMO, P ;
WETTENSTRAND, G .
DIABETOLOGIA, 1994, 37 (09) :937-944