Literature DB >> 12750767

IDDM2/insulin VNTR modifies risk conferred by IDDM1/HLA for development of Type 1 diabetes and associated autoimmunity.

M Walter1, E Albert, M Conrad, E Keller, M Hummel, K Ferber, B J Barratt, J A Todd, A-G Ziegler, E Bonifacio.   

Abstract

AIM/HYPOTHESIS: Type 1 diabetes (T1D) is an autoimmune disease with multiple susceptibility genes. The aim of this study was to determine whether combining IDDM1/HLA and IDDM2/ insulin( INS) 5' variable number of tandem repeat locus (VNTR) genotypes improves T1D risk assessment.
METHODS: Patients with T1D (n=488), control subjects (n=846), and offspring of parents with T1D (n=1122) were IDDM1 and IDDM2 genotyped. Offspring were followed for islet autoantibodies and T1D from birth until the age of 2 to 12 years.
RESULTS: Compared to the I/I INS VNTR genotype, the I/III and III/III genotypes reduced T1D risk conferred by IDDM1/HLA in all HLA genotype categories of the case-control cohort by 1.6-fold to three-fold. The highest T1D risk was associated with INS VNTR class I/I plus HLA DR3/DR4-DQ8 (20.4% in patients, 0.6% in control subjects) or HLA DR4-DQ8/DR4-DQ8 (6.3% in patients, 0.2% in control subjects). In the offspring, HLA DR3/DR4-DQ8 and DR4-DQ8/DR4-DQ8 conferred increased risk for early development of islet autoantibodies (14.6% and 12.9% by age 2 years). Offspring with these high risk IDDM1 genotypes plus the INS VNTR class I/I genotype (n=71; 6.3%) had the highest risk of developing islet autoantibodies (21.8% by age 2 years vs 8.9% in offspring with high risk IDDM1 plus INS VNTR class I/III or III/III genotypes, p<0.05) and T1D (8.5% by age 6 years vs 4.3%). Offspring who developed autoantibodies to multiple antigens had increased frequencies of both high risk IDDM1 and IDDM2 genotypes (p<0.0001), whereas offspring who developed autoantibodies to GAD only had increased frequencies of high risk IDDM1 and protective IDDM2 genotypes, suggesting that IDDM2 influences the autoimmune target specificity. CONCLUSION/
INTERPRETATION: Combining IDDM1 and IDDM2 genotyping identifies a minority of children with an increased T1D risk.

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Year:  2003        PMID: 12750767     DOI: 10.1007/s00125-003-1082-z

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  22 in total

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2.  Early expression and high prevalence of islet autoantibodies for DR3/4 heterozygous and DR4/4 homozygous offspring of parents with Type I diabetes: the German BABYDIAB study.

Authors:  M Schenker; M Hummel; K Ferber; M Walter; E Keller; E D Albert; H U Janka; C Kastendiek; M Sorger; F Louwen; A G Ziegler
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3.  Autoantibody appearance and risk for development of childhood diabetes in offspring of parents with type 1 diabetes: the 2-year analysis of the German BABYDIAB Study.

Authors:  A G Ziegler; M Hummel; M Schenker; E Bonifacio
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4.  Prevalence, characteristics and diabetes risk associated with transient maternally acquired islet antibodies and persistent islet antibodies in offspring of parents with type 1 diabetes.

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5.  Analysis of HLA-DQ genotypes and susceptibility in insulin-dependent diabetes mellitus.

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7.  A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus.

Authors:  G I Bell; S Horita; J H Karam
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8.  Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes.

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9.  A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins.

Authors:  F Cucca; R Lampis; M Congia; E Angius; S Nutland; S C Bain; A H Barnett; J A Todd
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10.  Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1, -DRB1 disease loci.

Authors:  P Zavattari; R Lampis; C Motzo; M Loddo; A Mulargia; M Whalen; M Maioli; E Angius; J A Todd; F Cucca
Journal:  Hum Mol Genet       Date:  2001-04-01       Impact factor: 6.150

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2.  Novel gene associations in type 1 diabetes.

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4.  A novel approach for the analysis of longitudinal profiles reveals delayed progression to type 1 diabetes in a subgroup of multiple-islet-autoantibody-positive children.

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Review 6.  Predicting type 1 diabetes.

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7.  Characteristics of rapid vs slow progression to type 1 diabetes in multiple islet autoantibody-positive children.

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Review 8.  A functional framework for interpretation of genetic associations in T1D.

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9.  Mature high-affinity immune responses to (pro)insulin anticipate the autoimmune cascade that leads to type 1 diabetes.

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10.  Insulin gene VNTR genotype associates with frequency and phenotype of the autoimmune response to proinsulin.

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