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Endocrine Abstracts (2015) 39 EP39 | DOI: 10.1530/endoabs.39.EP39

BSPED2015 e-Posters Diabetes (47 abstracts)

Young people with type 1 diabetes of non-white ethnicity and lower socioeconomic status have poorer glycaemic control in England and Wales – a national population-based study

Amal R Khanolkar , Rakesh Amin 1 , David Taylor-Robinson 3 , Russell M Viner 1 , Justin T Warner 4 & Terence Stepenhson 1


1Institute of Child Health, University College London, London, UK; 2Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden; 3Institute of Psychology, Health and Society, University of Liverpool, Liverpool, UK; 4Department of Child Health, University Hospital of Wales, Cardiff, UK.


Introduction: The impact of ethnicity and socioeconomic status (SES) on glycaemic control in children with type 1 diabetes (T1D) is poorly understood in England and Wales.

Methods: We studied 18 478 children and young people with T1D aged <19 years attending diabetes clinics in England and Wales and included in the 2012–2013 National Paediatric Diabetes Audit (NPDA). Self-identified ethnicity was categorized as white, Asian, black, mixed, other and ‘not stated’ (those that chose not to divulge ethnicity). A small area measure of SES was estimated using postcode and the Index of Multiple Deprivation (grouped into quintiles). Multivariable linear regression was used to assess impact of ethnicity and SES on glycaemic control (mean HbA1c levels) accounting for age, gender and diabetes duration. Associations between SES and HbA1c were also tested in models stratified by ethnicity. The impact of insulin pump use on the ethnicity/SES-HbA1c associations was tested in 13 962 children.

Results: All ethnic minorities had higher mean HbA1c compared to white children, with the largest differences observed in black and mixed ethnicity children (7.84 mmol/mol, 95% CI 5.07–10.6 and 6.81 mmol/mol, 4.55–9.08 respectively). Lower SES was associated with higher mean HbA1c with a dose effect. The lowest SES group (quintile 5) had on average 6.78 mmol/mol (5.63–7.95) higher mean HbA1c compared to the highest SES group, adjusted for ethnicity. Estimates for ethnicity were attenuated but remained significant on adjustment for SES. Having a lower SES was associated with higher mean HbA1c irrespective of ethnicity in stratified analyses. However, being in the lowest SES group and of Asian (6.90 mmol/mol, 2.52–11.28), mixed (11.26 mmol/mol, 6.31–16.21) and other (8.85 mmol/mol, −0.05–17.5) ethnicity was associated with higher mean HbA1c compared to being in the corresponding lowest SES group and white ethnicity (6.03 mmol/mol, 4.72–7.34). An interaction test between ethnicity and SES was statistically significant (P=0.005). Less non-white (white 20.3 vs Asian 12.1 vs black 5.5%) and deprived (least deprived 21.1 vs most deprived 13.2%) children were on insulin pump therapy. Both ethnicity and SES remained significant predictors of HbA1c after accounting for insulin pump use.

Conclusion: The effect of ethnicity independent to deprivation on glycaemic control persists after adjustment for pump use, indicating that an alternative approach to intensive insulin therapy for the treatment of glycaemic control is required in these vulnerable children.

Volume 39

43rd Meeting of the British Society for Paediatric Endocrinology and Diabetes

British Society for Paediatric Endocrinology and Diabetes 

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