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Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study
BACKGROUND: Cancer and factor V Leiden mutation are both risk factors for venous thromboembolism (VTE). Cancer critically increases the thrombotic risk whereas Factor V Leiden is the most common pro-thrombotic mutation. The impact of the factor V Leiden on the risk of VTE in cancer patients remains...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959061/ https://www.ncbi.nlm.nih.gov/pubmed/29775482 http://dx.doi.org/10.1371/journal.pone.0194973 |
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author | Heraudeau, Adeline Delluc, Aurélien Le Henaff, Mickaël Lacut, Karine Leroyer, Christophe Desrues, Benoit Couturaud, Francis Tromeur, Cécile |
author_facet | Heraudeau, Adeline Delluc, Aurélien Le Henaff, Mickaël Lacut, Karine Leroyer, Christophe Desrues, Benoit Couturaud, Francis Tromeur, Cécile |
author_sort | Heraudeau, Adeline |
collection | PubMed |
description | BACKGROUND: Cancer and factor V Leiden mutation are both risk factors for venous thromboembolism (VTE). Cancer critically increases the thrombotic risk whereas Factor V Leiden is the most common pro-thrombotic mutation. The impact of the factor V Leiden on the risk of VTE in cancer patients remains uncertain. OBJECTIVE: To assess the impact of factor V Leiden mutation in cancer-associated thrombosis. METHODS: The EDITH hospital-based case-control study enrolled 182 patients with cancer and VTE as well as 182 control patients with cancer, matched for gender, age and cancer location, between 2000 and 2012, in the University Hospital of Brest. All cases and controls were genotyped for the factor V Leiden mutation and interviewed with a standardized questionnaire. RESULTS: Twenty one of 182 (11.5%) patients with cancer-associated thrombosis carried the factor V Leiden mutation and 4 of 182 (2.2%) controls with cancer but no venous thrombosis. In multivariate analysis including cancer stage and family history of VTE, cancer patients with factor V Leiden mutation had a seven-fold increased risk of venous thromboembolism (adjusted odds ratio [OR], 7.04; 95% CI, 2.01–24.63). CONCLUSION: The pro-thrombotic Factor V Leiden mutation was found to be an independent additional risk factor for venous thromboembolism in cancer patients and might therefore be considered in the individual thrombotic risk assessment. |
format | Online Article Text |
id | pubmed-5959061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59590612018-05-31 Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study Heraudeau, Adeline Delluc, Aurélien Le Henaff, Mickaël Lacut, Karine Leroyer, Christophe Desrues, Benoit Couturaud, Francis Tromeur, Cécile PLoS One Research Article BACKGROUND: Cancer and factor V Leiden mutation are both risk factors for venous thromboembolism (VTE). Cancer critically increases the thrombotic risk whereas Factor V Leiden is the most common pro-thrombotic mutation. The impact of the factor V Leiden on the risk of VTE in cancer patients remains uncertain. OBJECTIVE: To assess the impact of factor V Leiden mutation in cancer-associated thrombosis. METHODS: The EDITH hospital-based case-control study enrolled 182 patients with cancer and VTE as well as 182 control patients with cancer, matched for gender, age and cancer location, between 2000 and 2012, in the University Hospital of Brest. All cases and controls were genotyped for the factor V Leiden mutation and interviewed with a standardized questionnaire. RESULTS: Twenty one of 182 (11.5%) patients with cancer-associated thrombosis carried the factor V Leiden mutation and 4 of 182 (2.2%) controls with cancer but no venous thrombosis. In multivariate analysis including cancer stage and family history of VTE, cancer patients with factor V Leiden mutation had a seven-fold increased risk of venous thromboembolism (adjusted odds ratio [OR], 7.04; 95% CI, 2.01–24.63). CONCLUSION: The pro-thrombotic Factor V Leiden mutation was found to be an independent additional risk factor for venous thromboembolism in cancer patients and might therefore be considered in the individual thrombotic risk assessment. Public Library of Science 2018-05-18 /pmc/articles/PMC5959061/ /pubmed/29775482 http://dx.doi.org/10.1371/journal.pone.0194973 Text en © 2018 Heraudeau et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Heraudeau, Adeline Delluc, Aurélien Le Henaff, Mickaël Lacut, Karine Leroyer, Christophe Desrues, Benoit Couturaud, Francis Tromeur, Cécile Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title | Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title_full | Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title_fullStr | Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title_full_unstemmed | Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title_short | Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study |
title_sort | risk of venous thromboembolism in association with factor v leiden in cancer patients – the edith case-control study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959061/ https://www.ncbi.nlm.nih.gov/pubmed/29775482 http://dx.doi.org/10.1371/journal.pone.0194973 |
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