The Distribution of Autoantibodies by Age Group in Children with Type 1 Diabetes versus Type 2 Diabetes in Southern Vietnam

Author:

Huynh Quynh Thi Vu12,Trinh Minh Thi Tuyet3,Doan Khang Kim4,Ho Ban Tran56,Shen Szu-Chuan7,Trinh Tung Huu6ORCID,Vo Thanh Hoa8,Le Nguyen Quoc Khanh91011ORCID,Nguyen Ngan Thi Kim7

Affiliation:

1. Department of Pediatrics, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 700000, Vietnam

2. Department of Nephrology and Endocrinology, Children’s Hospital 2, Ho Chi Minh City 700000, Vietnam

3. Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 700000, Vietnam

4. Le Van Thinh Hospital, Ho Chi Minh City 700000, Vietnam

5. Department of Pediatric Surgery, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 700000, Vietnam

6. Children’s Hospital 2, Ho Chi Minh City 700000, Vietnam

7. Programs of Nutrition Science, School of Life Science, National Taiwan Normal University, Taipei 11677, Taiwan

8. Department of Science, Pharmaceutical and Molecular Biotechnology Research Center, South East Technological University, X91 K0EK Waterford, Ireland

9. Professional Master Program in Artificial Intelligence in Medicine, College of Medicine, Taipei Medical University, Taipei 106, Taiwan

10. Research Center for Artificial Intelligence in Medicine, Taipei Medical University, Taipei 106, Taiwan

11. Translational Imaging Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan

Abstract

Asian children are increasingly being diagnosed with type 1 diabetes (T1D) or type 2 diabetes (T2D), and the presence of coexisting islet autoimmune antibodies complicate diagnosis. Here, we aimed to determine the prevalence of islet cell autoantibodies (ICAs) and glutamic acid decarboxylase 65 autoantibodies (GADAs) in children with T1D versus T2D living in Vietnam. This cross-sectional study included 145 pediatric patients aged 10.3 ± 3.6 years, with 53.1% and 46.9% having T1D and T2D, respectively. ICAs were reported in only 3.9% of pediatric T1Ds, which was not significantly different from the 1.5% of those with T2D. Older children with T1D were positive for either ICAs, or ICAs and GADAs (5–9 and 10–15 years), whereas only a small proportion of children aged 0–4 years were positive for GADAs (18%). Notably, 27.9% of children with T2D aged 10–15 were positive for GADAs, and all were classified as overweight (n = 9) or obese (n = 10). GADAs were more commonly observed in T1D patients younger than four years than ICAs, which were more prevalent in older children (5–15 years). Even though few children with T2D carried ICAs and GADAs, finding a better biomarker or an appropriate time to confirm diabetes type may require further investigation.

Publisher

MDPI AG

Subject

General Medicine

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