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Published on: May 6, 2013
Clinical Features and HLA Genetics Differ in Children at Type 1 Diabetes Onset by Hispanic Ethnicity
Kagan E Karakus1, Theodore Fleury1, Erin E Baschal1
1Barbara Davis Center for Diabetes, University of Colorado, Aurora, CO 80045, USA.
Insights
Hispanic White children with type 1 diabetes are diagnosed younger and have higher rates of diabetic ketoacidosis. They also show a significantly higher prevalence of the specific human leukocyte antigen (HLA) DR4-DQ8 genetic marker.
Area of Science:
- Pediatric Endocrinology
- Immunogenetics
- Diabetes Research
Background:
- Type 1 diabetes (T1D) incidence is rising in children, particularly among Hispanic White (HW) populations.
- Understanding ethnic disparities in T1D presentation is crucial for targeted interventions.
Purpose of the Study:
- To compare clinical, immunologic, and genetic factors in HW and non-Hispanic White (NHW) children at T1D diagnosis.
- To identify potential risk factors and differences in disease presentation between ethnic groups.
Main Methods:
- An observational, single-center study included 1297 children (≤20 years) diagnosed with T1D.
- Patients were categorized by Hispanic ethnicity and tested for islet autoantibodies and human leukocyte antigen (HLA) type.
Main Results:
- HW children were diagnosed at a younger age (10.2 vs 11.1 years) and presented more frequently with diabetic ketoacidosis (62.4% vs 51.9%) compared to NHW children.
- No significant differences were observed in sex, A1c, or autoantibody profiles.
- A higher prevalence of the HLA-DR4-DQ8 haplotype was found in HW children (79.1%) versus NHW children (60.1%).
Conclusions:
- HW children with T1D exhibit a high frequency of the HLA-DR4-DQ8 haplotype.
- This genetic marker can aid in identifying HW children at higher risk for T1D.
- Targeted immune monitoring and early intervention strategies may reduce diabetic ketoacidosis and potentially prevent T1D onset in this population.
Context:
Type 1 diabetes incidence continues to increase in children, especially among Hispanic White (HW) children.
Objective:
We investigated the clinical, immunologic, and genetic characteristics of HW and non-Hispanic White (NHW) children who presented at type 1 diabetes diagnosis.
Methods:
In this single-center, observational study, children who were diagnosed with type 1 diabetes (≤20 years old) and tested for islet autoantibodies within 1 year of diagnosis were included in the study and divided into 2 groups by Hispanic ethnicity.
Results:
Of 1297 children, 398 HW children presented with a younger age at diabetes onset (10.2 ± 3.9 vs 11.1 ± 4.1 years, P < .001) and more diabetic ketoacidosis (62.4% vs 51.9%, P < .001) than NHW children (n = 899). There was no difference in sex, A1c levels, or the number and prevalence of islet autoantibodies between the 2 cohorts. A subset of our cohort was human leukocyte antigen (HLA) typed as specific alleles confer strong genetic risk for type 1 diabetes (eg, HLA-DR4 and DQ8). Among 637 HLA-typed children, HW children had a significantly higher prevalence of the DR4-DQ8 haplotype than NHW children (79.1% vs 60.1%, P < .001), and this frequency was much higher than a reference Hispanic population (OR 6.5, 95% CI 4.6-9.3).
Conclusion:
Hispanic White children developing type 1 diabetes have a high prevalence of HLA DR4-DQ8, which can be utilized to select individuals for immune monitoring with islet autoantibodies to lessen diabetic ketoacidosis and potentially prevent diabetes onset.
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