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Grünbacher, G; Weger, W; Marx-Neuhold, E; Pilger, E; Köppel, H; Wascher, T; März, W; Renner, W.
The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.
Thromb Res. 2007; 121(1): 33-36.
Doi: 10.1016/j.thromres.2007.03.007
Web of Science
PubMed
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FullText_MUG
- Führende Autor*innen der Med Uni Graz
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Grünbacher Gerda
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Renner Wilfried
- Co-Autor*innen der Med Uni Graz
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Köppel Herwig
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März Winfried
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Pilger Ernst
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Wascher Thomas
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Weger Wolfgang
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- Abstract:
- INTRODUCTION: Thrombin-induced conversion of fibrinogen to fibrin plays an essential role in hemostasis and results in the stabilization of thrombi. Elevated plasma fibrinogen levels have been associated with both increased plasma viscosity and platelet aggregability. Recently, a haplotype-tagging single nucleotide polymorphism characterized by a C to T substitution at nucleotide 10034 of the fibrinogen gamma gene (FGG 10034C>T, rs2066865), has been proposed as a novel risk factor for deep venous thrombosis (DVT). Aim of the present study was to provide further data on the role of the FGG 10034C>T polymorphism for DVT. MATERIALS AND METHODS: FGG genotypes were determined by 5'-exonuclease assay (TaqMan) in 358 patients with documented DVT and a total of 783 control subjects. RESULTS: In a multivariate analysis adjusting for age, sex, presence of factor V Leiden and carriage of prothrombin 20210A, homozygosity for the FGG 10034 TT genotype yielded an odds ratio of 2.01 (95% CI 1.23-3.31; p=0.006) for DVT. CONCLUSIONS: Our data confirm the primary finding that the FGG 10034C>T polymorphism is associated with DVT risk.
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Adult -
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Aged -
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Austria - epidemiology
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Case-Control Studies - epidemiology
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DNA Mutational Analysis - epidemiology
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Female - epidemiology
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Fibrinogen - genetics
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Genetic Predisposition to Disease - genetics
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Genotype - genetics
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Humans - genetics
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Male - genetics
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Middle Aged - genetics
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Multivariate Analysis - genetics
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Odds Ratio - genetics
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Polymorphism, Single Nucleotide - genetics
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Risk Factors - genetics
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Venous Thrombosis - genetics
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fibrinogen
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polymorphism
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thrombosis
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risk factor