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Diabetes Care Publish Ahead of Print published online ahead of print January 30, 2008
DOI: 10.2337/dc07-1569

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Original Research

Tissue plasminogen activator, von Willebrand factor and risk of type 2 diabetes in older men

S Goya Wannamethee, PhD1, Naveed Sattar, MD2, Ann Rumley, PhD2, Peter H Whincup, FRCP3, Lucy Lennon, MSc1 and Gordon DO Lowe, DSc2

1Department of Primary Care and Population Sciences, Royal Free and University College Medical School, London NW3 2PF, UK
2Division of Cardiovascular and Medical Sciences, University of Glasgow, Royal Infirmary, Glasgow G31 2ER, UK
3Department of Community Health Sciences, St George's, University of London SW17 ORE, UK

goya{at}pcps.ucl.ac.uk

ABSTRACT

Abstract: Objective: To assess the relationship between putative markers of endothelial dysfunction (tissue plasminogen activator antigen, t-PA; and von Willebrand factor antigen, vWF) and development of type 2 diabetes; and the role of inflammation, adipokines, hepatic function and insulin resistance in modifying these relationships.

Research Design and Methods: Prospective study of 3562 non-diabetic men aged 60–79 followed up for an average 7 years during which there were 162 incident type 2 diabetes.

Results: Elevated t-PA (top third) was associated with a near three-fold increase in risk of diabetes compared to those in the bottom third after adjustment for lifestyle factors and waist circumference (relative risk, RR 2.98; 95%CI, 1.79–5.00; p<0.0001 for trend); weaker but significant (marginal) associations were seen with vWF (RR 1.24; 95%CI, 0.83-1.85; p=0.05 for trend). Both biomarkers of endothelial dysfunction correlated significantly with markers of inflammation (interleukin-6 (IL-6), C-reactive protein (CRP)), hepatic function (gamma-glutamyl transferase (GGT)), and insulin resistance; with t-PA showing stronger associations with adiposity, hepatic function and insulin resistance than vWF. T-PA was also significantly and inversely associated with adiponectin. Adjustment for IL-6, adiponectin and GGT attenuated the association of incident diabetes with vWF (RR 1.06; 95%CI, 0.71–1.60) but the relationship seen with t-PA remained significant [adjusted RR 2.19; 95%CI, 1.29–3.70). Subsequent adjustment for insulin attenuated the association further but t-PA was still associated with a significant increase in risk (adjusted RR 1.66; 95% CI 0.96–2.85); p=0.02 for trend).

Conclusion: T-PA antigen, but not vWF antigen, is independently associated with risk of type 2 diabetes.


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