Abstract Background Differentiating type 1 diabetes from other subtypes in ethnic groups is challenging. Non-white young adults are assumed to be more likely to develop type 2 diabetes, although the… Click to show full abstract
Abstract Background Differentiating type 1 diabetes from other subtypes in ethnic groups is challenging. Non-white young adults are assumed to be more likely to develop type 2 diabetes, although the characteristics of type 1 diabetes have not been studied in non-white ethnic groups. Data suggest that second generation migrant populations adopt the local risk for type 1 diabetes, but the phenotype in these groups remains unexplored. We aimed to investigate the phenotype of type 1 diabetes in a UK multi-ethnic population. Methods The MY DIABETES study is a multicentre cross-sectional study systematically phenotyping people diagnosed with any type of diabetes under 30 years of age from white or South Asian ancestry. In this preliminary analysis we report the clinical and biochemical characteristics, including islet-cell antibody status (GAD and IA-2), of people with type 1 diabetes (fasting C-peptide Findings Of 427 recruits, 305 (71%) were white and 76 (18%) South Asian. Other ethnic groups included African-Caribbean, middle-eastern, and south east Asian. Criteria for type 1 diabetes were met in 218 white (87%) and 34 South Asian (54%) participants (p vs 16·2), body-mass index (26·0 kg/m 2 vs 26·5), and glycated haemoglobin (62 mmol/mol for both). No difference in the proportion with detectable antibodies was observed (56% [122/217] white vs 56% [19/34] South Asian), when adjusted for duration. Islet-cell antibody status was similar (GAD positive 102 [47%] of 218 white vs 16 [48%] of 34 South Asian; IA-2 positive 21 [9·6%] vs 3 [9·7%]). Second generation South Asian people (UK born) were diagnosed at a younger age than were first generation people (median age 11·4 years [IQR 3·1–24·4] vs 23·3 [15·7–27·1], p=0·039) but had similar durations of disease (median 22·8 years [IQR 10·9–36·8] vs 19·8 [6·6–27·3]), and antibody positivity did not differ between the groups (11/16 [68·0%] vs 7/15 [46·7%]). Interpretation Young onset type 1 diabetes in South Asian and white people in the UK is phenotypically very similar. These data suggest that in young people presenting with diabetes, ethnicity should not have an impact on clinical diagnosis, even in those without detectable antibodies. Migration generation might affect phenotype, and additional investigations are needed to study differences between native and migrant ethnic groups. Work is ongoing to further characterise type 1 diabetes and other subtypes in the MY DIABETES cohort. Funding Diabetes Research and Wellness Foundation.
               
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