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HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk
Open accessAbstract
OBJECTIVE—The Type 1 Diabetes Genetics Consortium has collected type 1 diabetic families worldwide for genetic analysis. The major genetic determinants of type 1 diabetes are alleles at the HLA-DRB1 and DQB1 loci, with both susceptible and protective DR-DQ haplotypes present in all human populations. The aim of this study is to estimate the risk conferred by specific DR-DQ haplotypes and genotypes. RESEARCH DESIGN AND METHODS:—Six hundred and seven Caucasian families and 38 Asian families were typed at high resolution for the DRB1, DQA1, and DQB1 loci. The association analysis was performed by comparing the frequency of DR-DQ haplotypes among the chromosomes transmitted to an affected child with the frequency of chromosomes not transmitted to any affected child. RESULTS—A number of susceptible, neutral, and protective DR-DQ haplotypes have been identified, and a statistically significant hierarchy of type 1 diabetes risk has been established. The most susceptible haplotypes are the DRB1*0301-DQA1*0501-DQB1*0201 (odds ratio [OR] 3.64) and the DRB1*0405-DQA1*0301-DQB1*0302, DRB1*0401-DQA1*0301-DQB*0302, and DRB1*0402-DQA1*0301-DQB1*0302 haplotypes (ORs 11.37, 8.39, and 3.63), followed by the DRB1*0404-DQA1*0301-DQB1*0302 (OR 1.59) and the DRB1*0801-DQB1*0401-DQB1*0402 (OR 1.25) haplotypes. The most protective haplotypes are DRB1*1501-DQA1*0102-DQB1*0602 (OR 0.03), DRB1*1401-DQA1*0101-DQB1*0503 (OR 0.02), and DRB1*0701-DQA1*0201-DQB1*0303 (OR 0.02). CONCLUSIONS—Specific combinations of alleles at the DRB1, DQA1, and DQB1 loci determine the extent of haplotypic risk. The comparison of closely related DR-DQ haplotype pairs with different type 1 diabetes risks allowed identification of specific amino acid positions critical in determining disease susceptibility. These data also indicate that the risk associated with specific HLA haplotypes can be influenced by the genotype context and that the trans-complementing heterodimer encoded by DQA1*0501 and DQB1*0302 confers very high risk.
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“Of the many HLA types, HLA class II show the strongest association with type 1 diabetes, where haplotypes DRB1*0401-DQB1*0302 and DRB1*0301-DQB1*0201 confer the greatest susceptibility, and DRB1*1501 and DQA1*0102-DQB1*0602 provide disease resistance.74”
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“Both highly susceptibility and highly protective DR-DQ haplotypes and genotypes are found (Erlich et al., 2008).”
BackgroundImmune checkpoint inhibitor‐induced Type 1 diabetes: a systematic review and meta‐analysis
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“In the general population, children with the HLA DR3-DQ2/DR4-DQ8 genotype have 5% risk for islet autoimmunity and T1D [14 – 16].”
Immunogenetics of type 1 diabetes mellitus
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“The higher risk of this heterozygote compared with the two (DR3/DR3 and DR4/ DR4) homozygotes has been attributed to the two transcomplementing DQ heterodimers, including the a (DQA1*0501) and b (DQB1*0302) heterodimer, present only in this heterozygote (Erlich et al., 2008).”
BackgroundBesser, R. E. J., Bell, K. J., Couper, J., Ziegler, A., Wherrett, D. K., Knip, M., Speake, C., Casteels, K., Driscoll, K. A., Jacobsen, L. M., et al. (2022) · Pediatric Diabetes · doi:10.1111/pedi.13410 · Cited by 161
B cells in type 1 diabetes mellitus and diabetic kidney disease
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Recognition of Posttranslationally Modified GAD65 Epitopes in Subjects With Type 1 Diabetes
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Feature ranking of type 1 diabetes susceptibility genes improves prediction of type 1 diabetes
Winkler, C., Krumsiek, J., Buettner, F., Angermueller, C., Giannopoulou, E. Z., Theis, F. J., Ziegler, A., & Bonifacio, E. E. (2014) · Diabetologia · doi:10.1007/s00125-014-3362-1 · Cited by 143
“Genotyping Typing for HLA class II alleles at HLA-DRB1, HLA-DQA1 and HLA-DQB1, performed according to the T1DGC protocol with a sequence-specific olignonucleotidebased linear assay [16], was available for 1,814 individuals from the T1DGC set.”
MethodTissue distribution and clonal diversity of the T and B cell repertoire in type 1 diabetes
Seay, H. R., Yusko, E. C., Rothweiler, S., Zhang, L., Posgai, A. L., Campbell‐Thompson, M., Vignali, M., Emerson, R., Kaddis, J. S., Ko, D., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.88242 · Cited by 145
Immunologic endocrine disorders
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“J Clin Endocrinol Metab 1997;82(3):939–42.”
BackgroundInfluentialRother, K. I., Spain, L. M., Wesley, R. A., Digon, B. J., Baron, A., Chen, K., Nelson, P., Dosch, H.-M., Palmer, J. P., Brooks-Worrell, B., et al. (2009) · Diabetes Care · doi:10.2337/dc09-0773 · Cited by 133
Pathogenesis of Immunoglobulin A Nephropathy: Recent Insight from Genetic Studies
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“The same haplotype is highly protective from type 1 diabetes mellitus (58).”
BackgroundEvidence-based update on rosacea comorbidities and their common physiologic pathways
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Karnes, J. H., Bastarache, L., Shaffer, C. M., Gaudieri, S., Xu, Y., Glazer, A. M., Mosley, J. D., Zhao, S., Raychaudhuri, S., Mallal, S., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aai8708 · Cited by 126
Type 1 diabetes: A predictable disease
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Molecular Mechanisms in Autoimmune Type 1 Diabetes: a Critical Review
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“The highest risk of DR-DQ haplotypes for T1D are DRB1*0301-DQA1*0501DQB1*0201 and DRB1*0401-DQA1*0301-DQB1*0302 [77, 87].”
BackgroundThe molecular genetics of type 1 diabetes: new genes and emerging mechanisms
Ounissi‐Benkalha, H., & Polychronakos, C. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2008.04.002 · Cited by 117
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Self-citationGenetic and Epigenetic Factors in Etiology of Diabetes Mellitus Type 1
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Altered N‐glycosylation profiles as potential biomarkers and drug targets in diabetes
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Couper, J., Haller, M. J., Greenbaum, C. J., Ziegler, A., Wherrett, D. K., Knip, M., & Craig, M. E. (2018) · Pediatric Diabetes · doi:10.1111/pedi.12734 · Cited by 153
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Molecular mechanisms of HLA association with autoimmune diseases
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Multiple sclerosis and the major histocompatibility complex
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The landscape of host genetic factors involved in immune response to common viral infections
Kachuri, L., Francis, S. S., Morrison, M. L., Wendt, G. A., Bossé, Y., Cavazos, T. B., Rashkin, S. R., Ziv, E., & Witte, J. S. (2020) · Genome Medicine · doi:10.1186/s13073-020-00790-x · Cited by 127
“ive for type 1 diabetes [93], while DRB5*01:01-DRB15:01 confers the strongest risk for developing multiple sclerosis [86].”
Role of immune system in type 1 diabetes mellitus pathogenesis
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Definition, epidemiology and classification of diabetes in children and adolescents
Craig, M. E., Hattersley, A. T., & Donaghue, K. C. (2009) · Pediatric Diabetes · doi:10.1111/j.1399-5448.2009.00568.x · Cited by 463
“HLA genes having the strongest known association, there is linkage to specific combinations of alleles at the DRB1, DQA1 and DQB1 loci, with both susceptible or protective haplotypes (21; 45) (B).”
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Co-occurrence of Type 1 Diabetes and Celiac Disease Autoimmunity
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“In addition, rs689 (−23 Hph I) was genotyped in all cohorts except the Danish using a reverse dot-plot method”
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Self-citationType 1 diabetes genome‐wide association studies: not to be lost in translation
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Immunomodulatory therapy to preserve pancreatic β-cell function in type 1 diabetes
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“Genetic susceptibility to type 1 diabetes is largely conferred by the inheritance of the human leukocyte antigen (HLA) class II haplotypes of HLA-DR and HLA-DQ located within the major histocompatibility complex (MHC) on chromosome 6p21 (Ref”
BackgroundThe environment and the origins of islet autoimmunity and Type 1 diabetes
Regnell, S. E., & Lernmark, Å. (2012) · Diabetic Medicine · doi:10.1111/dme.12099 · Cited by 86
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Type 1 Diabetes-associated HLA-DQ8 Transdimer Accommodates a Unique Peptide Repertoire
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Type 1 Diabetes Mellitus: Cellular and Molecular Pathophysiology at A Glance.
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Shared genetics in coeliac disease and other immune-mediated diseases
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The immunopathology of ANCA-associated vasculitis
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“eases, including type 1 diabetes [51] and SLE [52].”
BackgroundHLA DPA1, DPB1 Alleles and Haplotypes Contribute to the Risk Associated With Type 1 Diabetes
Varney, M., Valdés, A., Carlson, J., Noble, J., Tait, B., Bonella, P., Lavant, E., Fear, A. L., Louey, A., Moonsamy, P., et al. (2010) · Diabetes · doi:10.2337/db09-0680 · Cited by 82
Self-citationAnand, V., Li, Y., Liu, B., Ghalwash, M., Koski, E., Ng, K., Dunne, J. L., Jönsson, J., Winkler, C., Knip, M., et al. (2021) · Diabetes Care · doi:10.2337/dc20-1836 · Cited by 83
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Cell-surface MHC density profiling reveals instability of autoimmunity-associated HLA
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Interferon alpha: The key trigger of type 1 diabetes
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A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes
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“Erlich (Roche Molecular Systems, Pleasanton, CA, USA) on all consenting participants [16].”
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“Although the impact of HLA genes on T1D susceptibility has been extensively studied, most of the related data, however, were from Caucasian populations (24) and notably from the T1DGC studies (9).”
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“In a Swedish population of diabetic dogs, there was an overrepresentation of some Scandinavian breeds, including the Swedish elkhound and Lapphund, with the majority reported to be female entire and thus likely to be suffering from dioestrus diabetes (Fall et al., 2007).”
BackgroundUpdate on diagnosis, pathogenesis and management of ketosis-prone Type 2 diabetes mellitus
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“These class II molecules play a role in the presentation of antigenic peptides to helper T cells, whereas class I molecules present to cytotoxic T cells.”
BackgroundTissue-Specific Methylation of Human Insulin Gene and PCR Assay for Monitoring Beta Cell Death
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Metadata
- Authors
- Erlich, H., Valdes, A. M., Noble, J., Carlson, J. A., Varney, M., Concannon, P., Mychaleckyj, J. C., Todd, J. A., Bonella, P., Fear, A. L., Lavant, E., Louey, A., Moonsamy, P., & for the Type 1 Diabetes Genetics Consortium
- Affiliations
- Roche Molecular Systems, Alameda, California
- Children's Hospital Oakland Research Institute, Oakland, California
- Skåne University Hospital (SE)
- Australian Red Cross Lifeblood (AU)
- Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia
- University of Virginia (US)
- University of Cambridge (GB)
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2008-04-01
- Volume
- 57
- Issue
- 4
- Pages
- 1084-1092
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- PMC
- PMC4103420
- OpenAlex
- W2157754662
- Cited by
- 790
- References
- 0
- Citations by year
- 2026: 31 · 2025: 43 · 2024: 56 · 2023: 46 · 2022: 41 · 2021: 54 · 2020: 58 · 2019: 48 · 2018: 33 · 2017: 41 · 2016: 40 · 2015: 38 · 2014: 39 · 2013: 46 · 2012: 34
- FWCI
- 27.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- Funders
- Wellcome Trust
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK061722, U01DK062418)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- type 1 diabetes, HLA-DRB1, HLA-DQA1, HLA-DQB1, genetic susceptibility, protective haplotypes, family-based association, high-resolution HLA typing
- MeSH terms
- Child, Child, Preschool, Diabetes Mellitus, Type 1, Family, Female, Genotype, HLA-DQ Antigens, HLA-DR Antigens, Humans, Male, Risk Factors, Age of Onset, Genetic Predisposition to Disease, White People, Asian People, HLA-DRB1 Chains, HLA-DQ alpha-Chains, HLA-DQ beta-Chains
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