1. Frequency of factor II G20210A, factor V Leiden, MTHFR C677T and PAI-1 5G/4G polymorphism in patients with venous thromboembolism: Croatian case control study
- Author
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Alfirević, Zrinka, Šimundić, Ana-Maria, Nikolac, Nora, Sobočan, Nikola, Alfirević, Igor, Štefanović, Mario, Vučićević, Željko, Topić, and Elizabeta.
- Subjects
Croatian ,medicine.medical_specialty ,biology ,business.industry ,Biochemistry (medical) ,Clinical Biochemistry ,Case-control study ,Thrombophilia ,medicine.disease ,Gastroenterology ,language.human_language ,coagulation disorders ,polymorphism ,FV Leiden ,PAI-1 ,MTHFR ,chemistry.chemical_compound ,chemistry ,Polymorphism (computer science) ,Methylenetetrahydrofolate reductase ,Plasminogen activator inhibitor-1 ,Internal medicine ,medicine ,biology.protein ,language ,Factor V Leiden ,business ,Coagulation Disorder - Abstract
Introduction: Venous thromboembolic disease is one of the leading causes of morbidity and mortality in the developed world. Identification of hereditary factors of thrombophilia is contributing to a better understanding of the etiology and prevention of the disease. The aim of this study was to assess the prevalence of factor II G20210A, factor V Leiden, MTHFR C677T and PAI-1 5G/4G polymorphisms in healthy Croatian subjects and in patients with thromboembolism. Materials and methods: This prospective study included 106 healthy subjects and 100 thromboembolic patients who were consecutively admitted to the Intensive Care Unit, University Hospital "Sestre milosrdnice". Results: Heterozygotes for Factor V Leiden polymorphism were more frequent in the group of patients with the thromboembolic disease (16%) than in the control healthy subjects (2.9%), with OR 6.413 (1.807 - 22.758 ; P = 0.004). Allele and genotype frequencies of other studied polymorphisms did not differ between cases and controls. Conclusion: This study confirmed the association of factor V Leiden polymorphism with the development of the thromboembolic disease in Croatian population.
- Published
- 2010
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