Investigating Endothelial Activation and Oxidative Stress in relation to Glycaemic Control in a Multiethnic Population

Author:

Brady E. M.1,Webb D. R.2,Morris D. H.2,Khunti K.3,Talbot D. S. C.4,Sattar N.5,Davies M. J.2

Affiliation:

1. Department of Diabetes Research, University Hospitals of Leicester, NHS Trust, Leicester LE5 4PW, UK

2. Department of Cardiovascular Sciences, University of Leicester, Leicester LE3 9QP, UK

3. Department of Health Sciences, University of Leicester, Leicester LE1 6TP, UK

4. Unilever Discover, Colworth Science Park, Sharnbrook MK44 ILQ, UK

5. BHF Institute for Cardiovascular and Medical Sciences, University of Glasgow, Glasgow G12 8QQ, UK

Abstract

Aim. An exploration of ethnic differences in measures of oxidative stress and endothelial activation in relation to known cardiovascular risk factors within South Asians (SA) and White Europeans (WE) residing in the UK.Methods. 202 participants within a UK multiethnic population provided biomedical and anthropometric data. Human urinary 2,3-dinor-8-iso-prostaglandin-F1αand plasma ICAM-1 were quantified as measures of oxidative stress and endothelial activation, respectively.Results. 2,3-Dinor-8-iso-prostaglandin-F1αlevels were significantly higher in the SA group compared to WE group (10.36 (95% CI: 9.09, 11.79) versus 8.46 (7.71, 9.29),P=0.021) after adjustment for age, gender, smoking status, body weight, HbA1c, and medication. Oxidative stress was positively associated with HbA1c (β=1.08, 95% CI:1.02, 1.14,P=0.009), fasting=1.06, 95% CI: 1.02, 1.10,P=0.002), and 2 hr glucose (β=1.02, 95% CI: 1.00, 1.04,P=0.052). In each adjusted model, SA continued to have elevated levels of oxidative stress compared to WE. ICAM-1 levels were significantly higher in the composite IGR group compared to the normoglycaemic group (P<0.001). No ethnic differences in ICAM-1 were observed.Conclusion. These results suggest that SA are more susceptible to the detrimental effects of hyperglycaemia-induced oxidative stress at lower blood glucose thresholds than WE. Further research into the potential mechanisms involved is warranted.

Funder

Biotechnology and Biological Sciences Research Council

Publisher

Hindawi Limited

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

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