Fibrinogen gamma gene 3’-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population

Summary Genetic determinants of venous thromboembolism (VTE) in the African-American population are poorly characterised. It was recently shown that fibrinogen gamma gene ( FGG ) polymorphisms 10034C>T and 9340T>C influence VTE risk in the Caucasian population. In the African-American populati...

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Veröffentlicht in:Thrombosis and haemostasis 2009-06, Vol.101 (6), p.1078-1084
Hauptverfasser: Willige, Shirley Uitte de, Pyle, Meridith E., Vos, Hans L., de Visser, Marieke C. H., Lally, Cathy, Dowling, Nicole F., Hooper, W. Craig, Bertina, Rogier M., Austin, Harland
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Sprache:eng
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Zusammenfassung:Summary Genetic determinants of venous thromboembolism (VTE) in the African-American population are poorly characterised. It was recently shown that fibrinogen gamma gene ( FGG ) polymorphisms 10034C>T and 9340T>C influence VTE risk in the Caucasian population. In the African-American population these polymorphisms are common, with allele frequencies above 25%. Here we evaluated whether these and other FGG 3’-end polymorphisms were associated with VTE risk in the African-American population and aimed to replicate the association in the Caucasian population. We examined 557 Caucasian patients and 678 Caucasian controls, and 537 African-American patients and 586 African-American controls from the ‘Genetic Attributes and Thrombosis Epidemiology’ (GATE) study. In the African-American population, 10034C>T and 9340T>C marginally influenced VTE-risk, with a 20% increase in risk for 10034TT carriers and a 20% reduction in risk for 9340CC carriers. In the Caucasian population, 10034TT was associated with a 1.7-fold increase in risk, which increased to 2.1-fold for idiopathic VTE patients. 9340CC significantly reduced VTE risk approximately two-fold. In conclusion, both FGG polymorphisms 10034C>T and 9340T>C influence VTE-risk, with the strongest effects observed in the Caucasian population, confirming previous data on these polymorphisms in this population.
ISSN:0340-6245
2567-689X
DOI:10.1160/TH08-12-0813