Etiologic Determinants and Characteristics of Diabetes in Haitian Youth (EDDHY Study)

<b>Aims:</b> Published information on youth-onset diabetes in Haiti is scarce, with limited data available on diabetes autoimmunity and genetic susceptibility to the disease. We determined the anthropometric, metabolic, and immunological characteristics and human leukocyte antigen (HLA)-associated risks in patients with youth-onset diabetes. <b>Methods:</b> One hundred and ten subjects with type 1 diabetes (T1D) aged <22 years and diagnosed for < 2 years were evaluated. Demographic and clinical information, as well as biochemical parameters, including blood glucose, hemoglobin A1c, fasting C-peptide (FCP), and T1D-associated autoantibodies, were assessed. DNA from 54 subjects and 66 controls was genotyped for classical HLA loci. <b>Results:</b> Of the 110 patients, 54% were male. Onset age was 13.5 ± 4.2 years (range 2-21), and disease duration was 11.7 ± 8.1 months (range 0-24). Idiopathic T1D was found in 62 (56.4%) patients and was diagnosed at an older age than immune-mediated T1D (14.4 ± 3.5 years vs., 12.3 ± 4.8 years, <i>p</i>=0.01), with a higher BMI z-score in patients aged <14 years than in those aged ≥14 years (-0.29 ± 1.52 vs., -1.15 ± 1.18, <i>p</i>=0.01). No correlation was found between immune-mediated T1D and BMI z-score. Diabetic ketoacidosis was present at diagnosis in 18 (16.4%) patients. Zinc transporter 8 autoantibodies (ZnT8A) were marginally more common in younger patients. Low FCP levels were found in 71 (64.5%) patients. Thyroid peroxidase antibodies (TPO-Ab) and thyroglobulin antibodies (TG-Ab) were positive in 1.1% and 2.2% of the patients, respectively. The alleles <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>03:01</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>09:01</i>, <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>02:01</i>, and <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>02:02</i> showed a significant T1D risk, whereas <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>08:04</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>15:03</i>, and <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>06:02</i> were protective. Three <i>DRB1~DQB1</i> haplotypes were strongly associated with T1D: <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>03:01:01~DQB1⁣</i> <sup><i>∗</i></sup> <i>02:01:01</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>09:01:02~DQB1⁣</i> <sup><i>∗</i></sup> <i>02:02:01</i>, both predisposing, and <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>15:03:01~DQB1⁣</i> <sup><i>∗</i></sup> <i>06:02:01</i>, <i>protective</i>. <b>Conclusions:</b> Idiopathic T1D is common among youth in Haiti. A significant proportion of all patients had preserved C-peptide secretion. Overall, predisposing and protective HLA patterns were identified. Study results highlight the importance of distinguishing T1D endotypes within and between populations.

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Journal
Pediatric Diabetes
Published
2025-01-01
DOI
https://doi.org/10.1155/pedi/9974561
Primary Topic
Diabetes and associated disorders
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article
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article

Etiologic Determinants and Characteristics of Diabetes in Haitian Youth (EDDHY Study)

Steven J. Mack, Philippe Larco, Denira Govender, Nancy Charles Larco et al.
Pediatric Diabetes
Diabetes and associated disorders
article

Etiologic Determinants and Characteristics of Diabetes in Haitian Youth (EDDHY Study)

Steven J. Mack, Philippe Larco, Denira Govender, Nancy Charles Larco, Mark A. Atkinson, Julia von Oettingen, Graham D. Ogle, Eddy Jean-Baptiste, Ning Song, Jos le Noble, Harper R. N. Martin, Erik H. Rozemuller
article en

Abstract

<b>Aims:</b> Published information on youth-onset diabetes in Haiti is scarce, with limited data available on diabetes autoimmunity and genetic susceptibility to the disease. We determined the anthropometric, metabolic, and immunological characteristics and human leukocyte antigen (HLA)-associated risks in patients with youth-onset diabetes. <b>Methods:</b> One hundred and ten subjects with type 1 diabetes (T1D) aged <22 years and diagnosed for < 2 years were evaluated. Demographic and clinical information, as well as biochemical parameters, including blood glucose, hemoglobin A1c, fasting C-peptide (FCP), and T1D-associated autoantibodies, were assessed. DNA from 54 subjects and 66 controls was genotyped for classical HLA loci. <b>Results:</b> Of the 110 patients, 54% were male. Onset age was 13.5 ± 4.2 years (range 2-21), and disease duration was 11.7 ± 8.1 months (range 0-24). Idiopathic T1D was found in 62 (56.4%) patients and was diagnosed at an older age than immune-mediated T1D (14.4 ± 3.5 years vs., 12.3 ± 4.8 years, <i>p</i>=0.01), with a higher BMI z-score in patients aged <14 years than in those aged ≥14 years (-0.29 ± 1.52 vs., -1.15 ± 1.18, <i>p</i>=0.01). No correlation was found between immune-mediated T1D and BMI z-score. Diabetic ketoacidosis was present at diagnosis in 18 (16.4%) patients. Zinc transporter 8 autoantibodies (ZnT8A) were marginally more common in younger patients. Low FCP levels were found in 71 (64.5%) patients. Thyroid peroxidase antibodies (TPO-Ab) and thyroglobulin antibodies (TG-Ab) were positive in 1.1% and 2.2% of the patients, respectively. The alleles <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>03:01</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>09:01</i>, <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>02:01</i>, and <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>02:02</i> showed a significant T1D risk, whereas <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>08:04</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>15:03</i>, and <i>DQB1⁣</i> <sup><i>∗</i></sup> <i>06:02</i> were protective. Three <i>DRB1~DQB1</i> haplotypes were strongly associated with T1D: <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>03:01:01~DQB1⁣</i> <sup><i>∗</i></sup> <i>02:01:01</i>, <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>09:01:02~DQB1⁣</i> <sup><i>∗</i></sup> <i>02:02:01</i>, both predisposing, and <i>DRB1⁣</i> <sup><i>∗</i></sup> <i>15:03:01~DQB1⁣</i> <sup><i>∗</i></sup> <i>06:02:01</i>, <i>protective</i>. <b>Conclusions:</b> Idiopathic T1D is common among youth in Haiti. A significant proportion of all patients had preserved C-peptide secretion. Overall, predisposing and protective HLA patterns were identified. Study results highlight the importance of distinguishing T1D endotypes within and between populations.

Pediatric DiabetesVol. 2025(1)
The University of Sydney (AU), University of California, San Francisco (US), Diabetes Australia (AU), Montreal Children's Hospital (CA), McGill University Health Centre (CA), University of Florida (US), Future Diagnostics (Netherlands) (NL), University of Haiti (HT), Tongji Hospital (CN), Huazhong University of Science and Technology (CN)
National Institutes of Health, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 86%
Diabetes and associated disorders
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