Cargando…

A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism

BACKGROUND: Activated protein C resistance (APCR) due to factor V Leiden (FVL) mutation (R506Q) is a major risk factor in patients with venous thromboembolism (VTE). The present study investigated the clinical manifestations and the risk of venous thromboembolism regarding multiple clinical, laborat...

Descripción completa

Detalles Bibliográficos
Autores principales: Takhviji, Vahideh, Zibara, Kazem, Maleki, Asma, Azizi, Ebrahim, Hommayoun, Sanaz, Tabatabaei, Mohammadreza, Ahmadi, Seyed Esmaeil, Soleymani, Maral, Ghalesardi, Omid Kiani, Farokhian, Mina, Davari, Afshin, Paridar, Pouria, Kalantari, Anahita, Khosravi, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527672/
https://www.ncbi.nlm.nih.gov/pubmed/34666770
http://dx.doi.org/10.1186/s12959-021-00328-0
_version_ 1784586116194631680
author Takhviji, Vahideh
Zibara, Kazem
Maleki, Asma
Azizi, Ebrahim
Hommayoun, Sanaz
Tabatabaei, Mohammadreza
Ahmadi, Seyed Esmaeil
Soleymani, Maral
Ghalesardi, Omid Kiani
Farokhian, Mina
Davari, Afshin
Paridar, Pouria
Kalantari, Anahita
Khosravi, Abbas
author_facet Takhviji, Vahideh
Zibara, Kazem
Maleki, Asma
Azizi, Ebrahim
Hommayoun, Sanaz
Tabatabaei, Mohammadreza
Ahmadi, Seyed Esmaeil
Soleymani, Maral
Ghalesardi, Omid Kiani
Farokhian, Mina
Davari, Afshin
Paridar, Pouria
Kalantari, Anahita
Khosravi, Abbas
author_sort Takhviji, Vahideh
collection PubMed
description BACKGROUND: Activated protein C resistance (APCR) due to factor V Leiden (FVL) mutation (R506Q) is a major risk factor in patients with venous thromboembolism (VTE). The present study investigated the clinical manifestations and the risk of venous thromboembolism regarding multiple clinical, laboratory, and demographic properties in FVL patients. MATERIAL AND METHODS: A retrospective cross-sectional analysis was conducted on a total of 288 FVL patients with VTE according to APCR. In addition, 288 VET control samples, without FVL mutation, were also randomly selected. Demographic information, clinical manifestations, family and treatment history were recorded, and specific tests including t-test, chi-square and uni- and multi-variable regression tests applied. RESULTS: APCR was found to be 2.3 times significantly more likely in men (OR: 2.1, p < 0.05) than women. The risk of deep vein thrombosis (DVT) and pulmonary embolism (PE) in APCR patients was 4.5 and 3.2 times more than the control group, respectively (p < 0.05). However, APCR could not be an independent risk factor for arterial thrombosis (AT) and pregnancy complications. Moreover, patients were evaluated for thrombophilia panel tests and showed significantly lower protein C and S than the control group and patients without DVT (p < 0.0001). CONCLUSION: FVL mutation and APCR abnormality are noticeable risk factors for VTE. Screening strategies for FVL mutation in patients undergoing surgery, oral contraceptive medication, and pregnancy cannot be recommended, but a phenotypic test for activated protein C resistance should be endorsed in patients with VTE.
format Online
Article
Text
id pubmed-8527672
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85276722021-10-25 A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism Takhviji, Vahideh Zibara, Kazem Maleki, Asma Azizi, Ebrahim Hommayoun, Sanaz Tabatabaei, Mohammadreza Ahmadi, Seyed Esmaeil Soleymani, Maral Ghalesardi, Omid Kiani Farokhian, Mina Davari, Afshin Paridar, Pouria Kalantari, Anahita Khosravi, Abbas Thromb J Research BACKGROUND: Activated protein C resistance (APCR) due to factor V Leiden (FVL) mutation (R506Q) is a major risk factor in patients with venous thromboembolism (VTE). The present study investigated the clinical manifestations and the risk of venous thromboembolism regarding multiple clinical, laboratory, and demographic properties in FVL patients. MATERIAL AND METHODS: A retrospective cross-sectional analysis was conducted on a total of 288 FVL patients with VTE according to APCR. In addition, 288 VET control samples, without FVL mutation, were also randomly selected. Demographic information, clinical manifestations, family and treatment history were recorded, and specific tests including t-test, chi-square and uni- and multi-variable regression tests applied. RESULTS: APCR was found to be 2.3 times significantly more likely in men (OR: 2.1, p < 0.05) than women. The risk of deep vein thrombosis (DVT) and pulmonary embolism (PE) in APCR patients was 4.5 and 3.2 times more than the control group, respectively (p < 0.05). However, APCR could not be an independent risk factor for arterial thrombosis (AT) and pregnancy complications. Moreover, patients were evaluated for thrombophilia panel tests and showed significantly lower protein C and S than the control group and patients without DVT (p < 0.0001). CONCLUSION: FVL mutation and APCR abnormality are noticeable risk factors for VTE. Screening strategies for FVL mutation in patients undergoing surgery, oral contraceptive medication, and pregnancy cannot be recommended, but a phenotypic test for activated protein C resistance should be endorsed in patients with VTE. BioMed Central 2021-10-19 /pmc/articles/PMC8527672/ /pubmed/34666770 http://dx.doi.org/10.1186/s12959-021-00328-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Takhviji, Vahideh
Zibara, Kazem
Maleki, Asma
Azizi, Ebrahim
Hommayoun, Sanaz
Tabatabaei, Mohammadreza
Ahmadi, Seyed Esmaeil
Soleymani, Maral
Ghalesardi, Omid Kiani
Farokhian, Mina
Davari, Afshin
Paridar, Pouria
Kalantari, Anahita
Khosravi, Abbas
A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title_full A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title_fullStr A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title_full_unstemmed A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title_short A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
title_sort case-control study on factor v leiden: an independent, gender-dependent risk factor for venous thromboembolism
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527672/
https://www.ncbi.nlm.nih.gov/pubmed/34666770
http://dx.doi.org/10.1186/s12959-021-00328-0
work_keys_str_mv AT takhvijivahideh acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT zibarakazem acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT malekiasma acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT aziziebrahim acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT hommayounsanaz acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT tabatabaeimohammadreza acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT ahmadiseyedesmaeil acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT soleymanimaral acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT ghalesardiomidkiani acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT farokhianmina acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT davariafshin acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT paridarpouria acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT kalantarianahita acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT khosraviabbas acasecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT takhvijivahideh casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT zibarakazem casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT malekiasma casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT aziziebrahim casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT hommayounsanaz casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT tabatabaeimohammadreza casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT ahmadiseyedesmaeil casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT soleymanimaral casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT ghalesardiomidkiani casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT farokhianmina casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT davariafshin casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT paridarpouria casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT kalantarianahita casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism
AT khosraviabbas casecontrolstudyonfactorvleidenanindependentgenderdependentriskfactorforvenousthromboembolism