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|Title:||Low prevalence of autoimmune diabetes markers in a mixed ethnic population of Singaporean diabetics|
|Citation:||Todd, A.L., Ng, W.Y., Lui, K.F., Thai, A.C. (2004-01). Low prevalence of autoimmune diabetes markers in a mixed ethnic population of Singaporean diabetics. Internal Medicine Journal 34 (1-2) : 24-30. ScholarBank@NUS Repository. https://doi.org/10.1111/j.1444-0903.2004.00482.x|
|Abstract:||Background: Circulating antibodies to glutamic acid decarboxylase (GADab) and tyrosine phosphatase-like molecule IA-2 (IA-2ab) are major indicators for autoimmune destruction of pancreatic islet cells. They identify a majority of Caucasians with type 1 diabetes and approximately 50% of Asians, providing evidence of an idiopathic aetiology in the latter. The present study investigated these autoantibodies in a mixed ethnic group. Methods: Hospital clinic patients with clinically defined type 1 (n - 93) and type 2 (n = 300) diabetes and representing Singapore's major ethnic groups - Chinese, Indians and Malays - were studied. GADab and IA-2ab frequencies, and association of autoimmunity status with clinical and biochemical profiles were analysed. Results: Radio-immunoprecipitation assays detected either or both antibodies (seropositivity) in 41.9% of subjects with type 1 diabetes. GADab was detected in 36.6% and IA-2ab in 23.7% of type 1 diabetics. Prevalence of IA-2ab showed a reduction in frequency with disease duration (P = 0.026). In clinical type 2 diabetics, seropositivity was 10.0% with higher frequency in Malays (17.5%) than Chinese (9.7%) and Indians (4.5%). Multivariate analysis revealed that low fasting C-peptide was associated with seropositivity (odds ratio (OR) = 0.15; 95% confidence interval (CI) = 0.04-0.58). A significant relationship (OR= 13. 5; 95% CI = 5.0-36.7) between insulin requirement and duration (>5 years) was also revealed. In patients with type 2 diabetes there was a trend of gradual progression to insulin dependency. However, there was considerable variation in body mass index between ethnic subgroups of type 2 diabetics, particularly for Chinese (mean (SD) = 26.0 (4.7)) and Malays (mean (SD) = 29.2 (5.9); P < 0.001). Conclusions: Presence of both antibodies in our mixed ethnic group of type 1 diabetes patients was much lower than in Caucasians. Significant numbers of patients were seronegative for antibodies. Influences due to ethnicity and adiposity would require further investigations.|
|Source Title:||Internal Medicine Journal|
|Appears in Collections:||Staff Publications|
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