The Low Prevalence of Immunogenetic Markers in Korean Adult-Onset IDDM Patients

Author:

Park Yongsoo1,Lee Hongkyu2,Koh Chang-Soon2,Min Hunki2,Rowley Merrill3,Mackay Ian R3,Zimmet Paul4,McCarthy Bridget5,McCanlies Erin5,Dorman Janice5,Trucco Massimo6

Affiliation:

1. Department of Internal Medicine, Hanyang University College of Medicine, and Biomedical Research Center, Korea Institute of Science and Technology, Seoul National University College of Medicine Seoul, Korea

2. Department of Internal Medicine, Seoul National University College of Medicine Seoul, Korea

3. Centre for Molecular Biology and Medicine, Monash University Melbourne, Australia

4. International Diabetes Institute Melbourne, Australia

5. Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh Pittsburgh, Pennsylvania

6. Department of Pediatrics, School of Medicine and Children's Hospital of Pittsburgh Pittsburgh, Pennsylvania

Abstract

OBJECTIVE IDDM is an autoimmune disease that occurs among genetically susceptible individuals. In Asian populations, it is not uncommon for adult patients with NIDDM to eventually lose β-cell function and develop IDDM. These individuals may be characterized by autoantibodies to GAD and high-risk HLA-DQ alleles, which are unlikely to be prevalent among patients with true NIDDM or in the general population. The objective of the present study was to evaluate and compare the prevalence of these immunogenetic markers in NIDDM patients and healthy nondiabetic individuals from Korea. RESEARCH DESIGN AND METHODS The prevalences of anti-GAD antibodies and HLA-DQA1 and DQB1 alleles among 121 patients with newly diagnosed NIDDM identified from a population-based study in Yonchon, Korea, and 100 matched healthy control subjects were evaluated and compared. RESULTS The overall prevalence of anti-GAD antibodies was 1.7% (2 of 121) in patients with previously undiagnosed NIDDM, whereas 1 of 100 control subjects had a positive test for antibodies. Among those who tested positive, titers of antibodies to GAD were not high. No statistically significant differences in the distributions of either mean levels of anti-GAD antibodies or DQA1 and DQB1 alleles were found comparing NIDDM patients with control subjects. Interestingly, the frequency of DQB1*non-Asp-57 and DQA1*Arg-52 alleles in the Korean adult control population was similar to that in the U.S. white population (DQB1*non-Asp-57: 0.431 vs. 0.475; DQA1*Arg-52: 0.492 vs. 0.463). CONCLUSIONS The low prevalence of anti-GAD antibodies and HLA-DQA1 and DQB1 susceptibility alleles among recent-onset NIDDM patients, which was similar to observations in control subjects, suggests that diabetes in Korean adults is unlikely to have an autoimmune component to its pathogenesis.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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