Eddy Jean-Baptiste, Philippe Larco, Julia E Von Oettingen, Janelle A Noble, Steven J Mack, Ningyi Song, Harper R N Martin, Erik Rozemuller, Mark A Atkinson, Denira Govender, Nancy Charles Larco, Graham D Ogle
{"title":"Etiologic Determinants and Characteristics of Diabetes in Haitian Youth (EDDHY Study).","authors":"Eddy Jean-Baptiste, Philippe Larco, Julia E Von Oettingen, Janelle A Noble, Steven J Mack, Ningyi Song, Harper R N Martin, Erik Rozemuller, Mark A Atkinson, Denira Govender, Nancy Charles Larco, Graham D Ogle","doi":"10.1155/pedi/9974561","DOIUrl":null,"url":null,"abstract":"<p><p><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.</p>","PeriodicalId":19797,"journal":{"name":"Pediatric Diabetes","volume":"2025 ","pages":"9974561"},"PeriodicalIF":3.9000,"publicationDate":"2025-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12127126/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Diabetes","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/pedi/9974561","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Aims: 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. Methods: 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. Results: 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, p=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, p=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 DRB1∗03:01, DRB1∗09:01, DQB1∗02:01, and DQB1∗02:02 showed a significant T1D risk, whereas DRB1∗08:04, DRB1∗15:03, and DQB1∗06:02 were protective. Three DRB1~DQB1 haplotypes were strongly associated with T1D: DRB1∗03:01:01~DQB1∗02:01:01, DRB1∗09:01:02~DQB1∗02:02:01, both predisposing, and DRB1∗15:03:01~DQB1∗06:02:01, protective. Conclusions: 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.
期刊介绍:
Pediatric Diabetes is a bi-monthly journal devoted to disseminating new knowledge relating to the epidemiology, etiology, pathogenesis, management, complications and prevention of diabetes in childhood and adolescence. The aim of the journal is to become the leading vehicle for international dissemination of research and practice relating to diabetes in youth. Papers are considered for publication based on the rigor of scientific approach, novelty, and importance for understanding mechanisms involved in the epidemiology and etiology of this disease, especially its molecular, biochemical and physiological aspects. Work relating to the clinical presentation, course, management and outcome of diabetes, including its physical and emotional sequelae, is considered. In vitro studies using animal or human tissues, whole animal and clinical studies in humans are also considered. The journal reviews full-length papers, preliminary communications with important new information, clinical reports, and reviews of major topics. Invited editorials, commentaries, and perspectives are a regular feature. The editors, based in the USA, Europe, and Australasia, maintain regular communications to assure rapid turnaround time of submitted manuscripts.