Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
06 03 2019
Historique:
received: 07 08 2018
accepted: 06 02 2019
entrez: 8 3 2019
pubmed: 8 3 2019
medline: 2 10 2020
Statut: epublish

Résumé

Factor V serves an important role in the regulation of blood coagulation. The rs6025 (R534Q) and rs4524 (K858R) polymorphisms in the F5 gene, are known to influence the risk of venous thrombosis. While the rare Q534 (factor V Leiden) allele is associated with an increased risk of venous thrombosis, the minor R858 allele is associated with a lower risk of disease. However, no study has deeply examined the cumulative impact of these two variations on venous thrombosis risk. We study the association of these polymorphisms with the risk of venous thrombosis in 4 French case-control populations comprising 3719 patients and 4086 controls. We demonstrate that the Q534 allele has a dominant effect over R858. Besides, we show that in individuals not carrying the Q534 allele, the protective effect of the R858 allele acts in a dominant mode. Thrombin generation-based normalized activated protein C sensitivity ratio was lower in the 858R/R homozygotes than in the 858K/K homozygotes (1.92 ± 1.61 vs 2.81 ± 1.57, p = 0.025). We demonstrate that the R858 allele of the F5 rs4524 variant protects from venous thrombosis only in non-carriers of the Q534 allele of the F5 rs6025. Its protective effect is mediated by reduced factor VIII levels and reduced activated protein C resistance.

Identifiants

pubmed: 30842582
doi: 10.1038/s41598-019-40172-x
pii: 10.1038/s41598-019-40172-x
pmc: PMC6403374
doi:

Substances chimiques

Protein C 0
factor V Leiden 0
Factor V 9001-24-5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3750

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Auteurs

M Ibrahim-Kosta (M)

Laboratory of Haematology, La Timone Hospital, Marseille, France.
C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.

P Suchon (P)

Laboratory of Haematology, La Timone Hospital, Marseille, France.
C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.

F Couturaud (F)

University Brest, France, Department of Chest Diseases and Internal Medicine, Hôpital de la Cavale Blanche, Brest, France.

D Smadja (D)

Service d'hématologie biologique, AP-HP, Hôpital Européen Georges Pompidou, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, France, Inserm, UMR-S1140, Paris, France.

R Olaso (R)

Centre National de Recherche en Génomique Humaine, Direction de la Recherche Fondamentale, CEA, Evry, France.

M Germain (M)

INSERM UMR_S 1219, Bordeaux Population Health Research Center, University of Bordeaux, Bordeaux, France.

N Saut (N)

Laboratory of Haematology, La Timone Hospital, Marseille, France.
C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.
CRB Assistance Publique - Hôpitaux de Marseille, HemoVasc (CRB AP-HM HemoVasc), Marseille, France.

L Goumidi (L)

C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.

C Derbois (C)

Centre National de Recherche en Génomique Humaine, Direction de la Recherche Fondamentale, CEA, Evry, France.

F Thibord (F)

INSERM UMR_S 1219, Bordeaux Population Health Research Center, University of Bordeaux, Bordeaux, France.
Sorbonne-Université, Pierre Louis Doctoral School of Public Health, Paris, France.

S Debette (S)

INSERM UMR_S 1219, Bordeaux Population Health Research Center, University of Bordeaux, Bordeaux, France.
Department of Neurology, Bordeaux University Hospital, Bordeaux, France.

P Amouyel (P)

Univ. Lille, INSERM, Centre Hosp. Univ Lille, Institut Pasteur de Lille, LabEx DISTALZ-UMR1167 - RID-AGE - Risk factors and molecular determinants of aging-related diseases, Epidemiology and Public Health Department, F-Lille, France.

J F Deleuze (JF)

Centre National de Recherche en Génomique Humaine, Direction de la Recherche Fondamentale, CEA, Evry, France.
CEPH, Fondation Jean Dausset, Paris, France.

P van Doorn (P)

Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.

E Castoldi (E)

Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.

E Patin (E)

Human Evolutionary Genetics Unit, Department of Genomes & Genetics, Institut Pasteur, Paris, France.
CNRS, UMR2000, Paris, France.
Center of Bioinformatics, Biostatistics and Integrative Biology, Institut Pasteur, Paris, France.

M C Alessi (MC)

Laboratory of Haematology, La Timone Hospital, Marseille, France.
C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.

D A Trégouët (DA)

INSERM UMR_S 1219, Bordeaux Population Health Research Center, University of Bordeaux, Bordeaux, France.

P E Morange (PE)

Laboratory of Haematology, La Timone Hospital, Marseille, France. pierre.morange@ap-hm.fr.
C2VN, Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France. pierre.morange@ap-hm.fr.
CRB Assistance Publique - Hôpitaux de Marseille, HemoVasc (CRB AP-HM HemoVasc), Marseille, France. pierre.morange@ap-hm.fr.

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