Factor V Leiden, prothrombin 20210A and the risk of venous thrombosis among cancer patients

Summary Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT in cancer patients is not established. We genotyped 101 cancer patients with VT and 101 cancer patients without VT for these polymorphisms. Fi...

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Published inBritish journal of haematology Vol. 128; no. 3; pp. 386 - 388
Main Authors Kennedy, Margaret, Andreescu, Astrid C. M., Greenblatt, Marc S., Jiang, Hongyu, Thomas, Christian A., Chassereau, Laurie, Wong, Cheung, Durda, Peter, Cushman, Mary
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.02.2005
Blackwell
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Abstract Summary Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT in cancer patients is not established. We genotyped 101 cancer patients with VT and 101 cancer patients without VT for these polymorphisms. Five cases and three controls were heterozygous for FVL, yielding an odds ratio of 1·7 (95% confidence interval (CI) 0·3–10·7). Five cases and no controls were heterozygous for prothrombin 20210A, for an odds ratio of 6·7 (95% CI 0·9–infinity). Prothrombin 20210A may be associated with VT risk among cancer patients.
AbstractList Summary Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT in cancer patients is not established. We genotyped 101 cancer patients with VT and 101 cancer patients without VT for these polymorphisms. Five cases and three controls were heterozygous for FVL, yielding an odds ratio of 1·7 (95% confidence interval (CI) 0·3–10·7). Five cases and no controls were heterozygous for prothrombin 20210A, for an odds ratio of 6·7 (95% CI 0·9–infinity). Prothrombin 20210A may be associated with VT risk among cancer patients.
Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT in cancer patients is not established. We genotyped 101 cancer patients with VT and 101 cancer patients without VT for these polymorphisms. Five cases and three controls were heterozygous for FVL, yielding an odds ratio of 1.7 (95% confidence interval (CI) 0.3-10.7). Five cases and no controls were heterozygous for prothrombin 20210A, for an odds ratio of 6.7 (95% CI 0.9-infinity). Prothrombin 20210A may be associated with VT risk among cancer patients.
Author Chassereau, Laurie
Durda, Peter
Kennedy, Margaret
Thomas, Christian A.
Greenblatt, Marc S.
Andreescu, Astrid C. M.
Jiang, Hongyu
Wong, Cheung
Cushman, Mary
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  surname: Thomas
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Issue 3
Keywords Human
Factor V Leiden
Hematology
Vein thrombosis
Cardiovascular disease
Malignant tumor
Epidemiology
Venous disease
Vascular disease
Thrombophilia
prothrombin 20210A
Risk factor
Prothrombin
Venous thrombosis
cancer
Language English
License CC BY 4.0
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Snippet Summary Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT...
Cancer patients have an increased risk of venous thrombosis (VT). The association of factor V Leiden (FVL) and the prothrombin 20210A variant with VT in cancer...
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SubjectTerms Aged
Biological and medical sciences
Blood and lymphatic vessels
cancer
Cardiology. Vascular system
Case-Control Studies
Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
Factor V - genetics
factor V Leiden
Female
Genetic Predisposition to Disease
Hematologic and hematopoietic diseases
Hematology
Humans
Male
Medical sciences
Middle Aged
Neoplasms - complications
Neoplasms - genetics
Polymorphism, Genetic
Prothrombin - genetics
prothrombin 20210A
risk factor
Risk Factors
venous thrombosis
Venous Thrombosis - etiology
Venous Thrombosis - genetics
Title Factor V Leiden, prothrombin 20210A and the risk of venous thrombosis among cancer patients
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1365-2141.2004.05327.x
https://www.ncbi.nlm.nih.gov/pubmed/15667542
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