Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event

Background The role of combined prothrombotic genotypes in cancer-related venous thromboembolism (VTE) is scarcely studied. We aimed to investigate the impact of a 5-single nucleotide polymorphism (SNP) score on the risk of VTE in patients with and without cancer using a population-based case-cohort...

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Bibliographic Details
Published in:Journal of Thrombosis and Haemostasis
Main Authors: Skille, H., Paulsen, B., Hveem, K., Gabrielsen, M.E., Brumpton, B., Hindberg, K., Gran, O.V., Rosendaal, F.R., Braekkan, S.K., Hansen, J.B.
Format: Article in Journal/Newspaper
Language:English
Published: 2020
Subjects:
5-SNP score
cancer
deep vein thrombosis
prothrombotic genotypes
pulmonary embolism
risk
venous thromboembolism
Tromso
Online Access:https://hdl.handle.net/1887/3184679
https://onlinelibrary.wiley.com/doi/10.1111/jth.15011
https://doi.org/10.1111/jth.15011
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Summary:Background The role of combined prothrombotic genotypes in cancer-related venous thromboembolism (VTE) is scarcely studied. We aimed to investigate the impact of a 5-single nucleotide polymorphism (SNP) score on the risk of VTE in patients with and without cancer using a population-based case-cohort. Methods Cases with a first VTE (n = 1493) and a subcohort (n = 13 072) were derived from the Tromso Study (1994-2012) and the Nord-Trondelag Health Study (1995-2008). Five SNPs previously reported as a risk score were genotyped: ABO (rs8176719), F5 (rs6025), F2 (rs1799963), FGG (rs2066865), and F11 (rs2036914). Hazard ratios (HRs) for VTE were estimated according to cancer status and the number of risk alleles in the 5-SNP score (0-1, 2-3, and >= 4 alleles). Results During a median follow-up of 12.3 years, 1496 individuals were diagnosed with cancer, of whom 232 experienced VTE. The VTE risk increased with the number of risk alleles in the 5-SNP score among subjects without and with cancer. In cancer-free subjects, the HR was 2.17 (95% confidence interval [CI] 1.79-2.62) for >= 4 versus 0-1 risk alleles. In cancer patients, the corresponding HR was 1.93 (95% CI 1.28-2.91). The combination of cancer and >= 4 risk alleles yielded a 17-fold (HR 17.1, 95% CI 12.5-23.4) higher risk of VTE compared with cancer-free subjects with 0-1 risk alleles. Conclusion The risk of VTE increases with the number of prothrombotic risk alleles in subjects with and without cancer, and the combination of prothrombotic risk alleles and cancer leads to a highly elevated risk of VTE. Clinical epidemiology

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