Clinical features, biochemistry, and HLA‐DRB1 status in youth‐onset type 1 diabetes in Sudan
Open accessAbstract
Objective To further understand clinical and biochemical features, and HLA-DRB1 genotypes, in new cases of diabetes in Sudanese children and adolescents. Research Design and Methods Demographic characteristics, clinical information, and biochemical parameters (blood glucose, HbA1c, C-peptide, autoantibodies against glutamic acid decarboxylase 65 [GADA] and insulinoma-associated protein-2 [IA-2A], and HLA-DRB1) were assessed in 99 individuals <18 years, recently (<18 months) clinically diagnosed with T1D. HLA-DRB1 genotypes for 56 of these Arab individuals with T1D were compared to a mixed control group of 198 healthy Arab (75%) and African (25%) individuals without T1D. Results Mean ± SD age at diagnosis was 10.1 ± 4.3 years (range 0.7–17.6 years) with mode at 9–12 years. A female preponderance was observed. Fifty-two individuals (55.3%) presented in diabetic ketoacidosis (DKA). Mean ± SD serum fasting C-peptide values were 0.22 ± 0.25 nmol/L (0.66±0.74 ng/ml). 31.3% were autoantibody negative, 53.4% were GADA positive, 27.2% were IA-2A positive, with 12.1% positive for both autoantibodies. Association analysis compared to 198 controls of similar ethnic origin revealed strong locus association with HLA-DRB1 (p < 2.4 × 10–14). Five HLA-DRB1 alleles exhibited significant T1D association: three alleles (DRB1*03:01, DRB1*04:02, and DRB1*04:05) were positively associated, while three (DRB1*10:01, DRB1*15:02, and DRB1*15:03) were protective. DRB1*03:01 had the strongest association (odds ratio = 5.04, p = 1.7 × 10–10). Conclusions Young Sudanese individuals with T1D generally have similar characteristics to reported European-origin T1D populations. However, they have higher rates of DKA and slightly lower autoantibody rates than reported European-origin populations, and a particularly strong association with HLA-DRB1*03:01.
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C-peptide measurements and other advanced diagnostics and phenotyping are being implemented in youth in less advantaged regions who have been newly diagnosed with diabetes mellitus.
“However, this picture is changing with C-peptide measurements and other advanced diagnostics and phenotyping being implemented in youth in less advantaged regions who have been newly diagnosed with diabetes mellitus93–98.”
From The epidemiology of type 1 diabetes mellitus in older adults (2025) · cites this paper as [94]
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HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk
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., et al. (2008) · Diabetes · doi:10.2337/db07-1331 · Cited by 790 · cited 8× · see citing works
“In comparison to European-origin populations, the rate of DKA at onset was high, autoantibody-negative forms (based on testing for two autoantibodies) were more common, IA-2 autoantibody rates were markedly low, and there was a particularly strong association with HLA-DRB1*03:01.”
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Haller, M. J., Bell, K. J., Besser, R. E. J., Casteels, K., Couper, J. J., Craig, M. E., Elding Larsson, H., Jacobsen, L., Lange, K., Oron, T., et al. (2024) · Hormone Research in Paediatrics · doi:10.1159/000543035 · Cited by 151 · see citing works
The epidemiology of type 1 diabetes mellitus in older adults
Tomic, D., Harding, J. L., Jenkins, A. J., Shaw, J. E., & Magliano, D. J. (2025) · Nature Reviews Endocrinology · doi:10.1038/s41574-024-01046-z · Cited by 58 · see citing works
- Authors
- Ibrahim, T. A. M., Govender, D., Abdullah, M. A., Noble, J. A., Hussien, M. O., Lane, J. A., Mack, S. J., Martin, G. G. N., Atkinson, M. A., Wasserfall, C. H., & Ogle, G. D.
- Affiliations
- Sudanese Children's Diabetes Association Khartoum Sudan
- The University of Sydney (AU)
- University of Khartoum (SD)
- University of California, San Francisco (US)
- Ministry of Higher Education And Scientific Research (SD)
- Children's Hospital Oakland Research Institute Oakland California USA
- University of Florida Health (US)
- Corresponding author
- Ogle, Graham David
- ORCID
- Venue
- Pediatric Diabetes
- Publisher
- Wiley
- Published
- 2021-04-20
- Volume
- 22
- Issue
- 5
- Pages
- 749-757
- ISSN
- 1399-543X (ISSN-L)
- 1399-5448
- PMC
- PMC8274711
- OpenAlex
- W3139790247
- Cited by
- 16
- References
- 2
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 7 · 2023: 5 · 2022: 2
- FWCI
- 1.98
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Pediatric Diabetes (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Leona M. and Harry B. Helmsley Charitable Trust (2019PG‐T1D023)
- National Institutes of Health (R01AI28775)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- type 1 diabetes, youth-onset diabetes, HLA-DRB1, genetic association, GADA, IA-2A, C-peptide, diabetic ketoacidosis, HLA-DRB1*0301, autoantibodies, age at diagnosis, HbA1c, Arabs, genetic susceptibility
- MeSH terms
- Adolescent, Autoantibodies, C-Peptide, Child, Child, Preschool, Diabetes Mellitus, Type 1, Female, Genotype, Glutamate Decarboxylase, Humans, Infant, Male, Sudan, Biomarkers, Case-Control Studies, Diabetic Ketoacidosis, Age of Onset, Genetic Predisposition to Disease, HLA-DRB1 Chains
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