Trends in high-risk HLA susceptibility genes among Colorado youth with type 1 diabetes
Open accessAbstract
OBJECTIVE—Type 1 diabetes is associated with a wide spectrum of susceptibility and protective genotypes within the HLA class II system. It has been reported that adults diagnosed with youth-onset type 1 diabetes more recently have been found to have fewer classical high-risk HLA class II genotypes than those diagnosed several decades ago. We hypothesized that such temporal trends in the distribution of HLA-DR, DQ genotypes would be evident, and perhaps even stronger, among 5- to 17-year-old Hispanic and non-Hispanic white (NHW) youth diagnosed with type 1 diabetes in Colorado between 1978 and 2004. RESEARCH DESIGN AND METHODS—HLA-DR, DQ was typed using PCR and sequence-specific oligonucleotide hybridization in 100 youth diagnosed during the period of 1978–1988 and 264 diagnosed during 2002–2004. Logistic regression was used to adjust for confounders and assess temporal trends. RESULTS—The frequency of the highest-risk genotype (DRB1*03-DQB1*02/DRB1*04-DQB1*03) was higher (39%) in children diagnosed during the period 1978–1988 than in those diagnosed during 2002–2004 (28%). A similar pattern was observed in NHWs and Hispanics. CONCLUSIONS—We found that high-risk HLA genotypes are becoming less frequent over time in youth with type 1 diabetes of NHW and Hispanic origin. This temporal trend may suggest that increasing environmental exposure is now able to trigger type 1 diabetes in subjects who are less genetically susceptible.
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Reports suggest a recent temporal trend of fewer high-risk HLA genotypes in youth diagnosed with type 1 diabetes, suggesting an increased influence of environmental factors during recent decades.
“A number of reports suggest a recent temporal trend of fewer high-risk HLA genotypes in youth diagnosed with T1D, suggesting an increased influence of environmental factors in the development of T1D during the past few decades19,44,45.”
From Epidemiology of type 1 diabetes (2010) · cites this paper as [44]
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References 22 · Cited by 82
- Authors
- Vehik, K., Hamman, R. F., Lezotte, D., Norris, J. M., Klingensmith, G. J., Rewers, M., & Dabelea, D.
- Affiliations
- University of Colorado Denver (US)
- Corresponding author
- Vehik, Kendra
- Venue
- Diabetes Care
- Publisher
- American Diabetes Association
- Published
- 2008-07-01
- Volume
- 31
- Issue
- 7
- Pages
- 1392-1396
- ISSN
- 0149-5992 (ISSN-L)
- 1935-5548
- PMC
- PMC2453682
- OpenAlex
- W2117948630
- Cited by
- 82
- References
- 22
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 5 · 2023: 3 · 2021: 5 · 2020: 3 · 2019: 2 · 2018: 7 · 2017: 4 · 2016: 1 · 2015: 8 · 2014: 7 · 2013: 4 · 2012: 9
- FWCI
- 4.18
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Diabetes Care (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- Centers for Disease Control and Prevention
- U.S. Public Health Service (432/CCU 800-435-01)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 32493, R01DK032493, R37DK032493)
- National Center for Chronic Disease Prevention and Health Promotion (U01 DP-000247, 00097/DP-05-069)
- 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 › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- type 1 diabetes, youth-onset diabetes, HLA class II, HLA-DR, HLA-DQ, temporal trends, genetic susceptibility, Latino youth, environmental triggers, Colorado
- MeSH terms
- Adolescent, Adult, Histocompatibility Antigens Class II, Child, Child, Preschool, Colorado, Diabetes Mellitus, Type 1, Female, Genetic Carrier Screening, Hispanic or Latino, HLA Antigens, HLA-DQ Antigens, HLA-DR Antigens, Humans, Male, Risk Factors, Polymerase Chain Reaction, Genetic Predisposition to Disease, White People, HLA-DRB1 Chains, HLA-DQ beta-Chains
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