Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2000;20:585-592

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Arnaud, E.
Right arrow Articles by Aiach, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arnaud, E.
Right arrow Articles by Aiach, M.
Related Collections
Right arrow Coagulation and fibronolysis
Right arrow Genetics of cardiovascular disease
Right arrow Platelets
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2000;20:585.)
© 2000 American Heart Association, Inc.


Thrombosis

Protective Effect of a Thrombin Receptor (Protease-Activated Receptor 1) Gene Polymorphism Toward Venous Thromboembolism

Emmanuel Arnaud; Viviane Nicaud; Odette Poirier; Francine Rendu; Martine Alhenc-Gelas; Jean-Noël Fiessinger; Joseph Emmerich; Martine Aiach

From the Laboratoire d’Hémostase and Service des Maladies Vasculaires (E.A., M.A.-G., J.-N.F., J.E., M.A.), Hôpital Broussais-AP-HP; Unité INSERM 428 (E.A., F.R., M.A.-G., J.-N.F., J.E., M.A.), Faculté de Pharmacie, Université René Descartes; and Unité INSERM 525 (V.N., O.P.), Paris, France.

Correspondence to Dr Emmanuel Arnaud, Laboratoire d’Hémostase, Hôpital Broussais, 96, rue Didot, F-75674 Paris Cedex 14, France. E-mail emmanuel.arnaud{at}brs.ap-hop-paris.fr

Abstract—The human protease-activated receptor 1 (PAR-1) is activated by thrombin at the surface of platelets and endothelial cells, 2 cells that are implicated in hemostasis and thrombosis. We studied the PAR-1 gene in a large case-control study from the Paris Thrombosis Study (PATHROS), and the possible implication of polymorphisms in venous thromboembolism was evaluated. Two polymorphisms were found in the 5' regulatory region. The first is a C to T transition that is 1426 nucleotides upstream from the translation start site (-1426 C/T), and the second is a 13-bp insertion repeating the preceding -506 5'-CGGCCGCGGGAAG-3' sequence (-506 I/D, where I indicates insertion and D indicates deletion), a putative cis-acting element of the Ets family. The third polymorphism is an A to T transversion in the intervening sequence (IVS) that is 14 nucleotides upstream from the exon 2 start site (IVS-14 A/T). The distribution of the 3 polymorphisms was otherwise similar in the 250 cases and the 1214 controls. A noteworthy sex heterogeneity led us to analyze men and women separately with regard to the -506 I/D polymorphism. We found that allele I was less frequent in male cases than in male controls (0.154 versus 0.247, P<0.01), with an odds ratio at 0.52 (95% CI 0.32 to 0.82, P<0.01). Furthermore, a reduction of prothrombin fragment 1+2 levels was observed in homozygous carriers of allele -506 I (P=0.04). Altogether, these data suggested a protective effect in men of -506 I/D polymorphism for venous thromboembolism.


Key Words: human thrombin receptor • gene polymorphism • venous thromboembolism




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
B. Gigante, A. Bellis, R. Visconti, M. Marino, C. Morisco, V. Trimarco, G. Galasso, F. Piscione, N. De Luca, J. A. Prince, et al.
Retrospective Analysis of Coagulation Factor II Receptor (F2R) Sequence Variation and Coronary Heart Disease in Hypertensive Patients
Arterioscler. Thromb. Vasc. Biol., May 1, 2007; 27(5): 1213 - 1219.
[Abstract] [Full Text] [PDF]


Home page
ThoraxHome page
Spoken sessions
Thorax, December 1, 2005; 60(suppl_2): ii4 - ii52.
[Full Text] [PDF]


Home page
Endocr. Rev.Home page
M. Steinhoff, J. Buddenkotte, V. Shpacovitch, A. Rattenholl, C. Moormann, N. Vergnolle, T. A. Luger, and M. D. Hollenberg
Proteinase-Activated Receptors: Transducers of Proteinase-Mediated Signaling in Inflammation and Immune Response
Endocr. Rev., February 1, 2005; 26(1): 1 - 43.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
B. Saposnik, J.-L. Reny, P. Gaussem, J. Emmerich, M. Aiach, and S. Gandrille
A haplotype of the EPCR gene is associated with increased plasma levels of sEPCR and is a candidate risk factor for thrombosis
Blood, February 15, 2004; 103(4): 1311 - 1318.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
P. Fontana, P. Gaussem, M. Aiach, J.-N. Fiessinger, J. Emmerich, and J.-L. Reny
P2Y12 H2 Haplotype Is Associated With Peripheral Arterial Disease: A Case-Control Study
Circulation, December 16, 2003; 108(24): 2971 - 2973.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
A. Dupont, P. Fontana, C. Bachelot-Loza, J.-L. Reny, I. Bieche, F. Desvard, M. Aiach, and P. Gaussem
An intronic polymorphism in the PAR-1 gene is associated with platelet receptor density and the response to SFLLRN
Blood, March 1, 2003; 101(5): 1833 - 1840.
[Abstract] [Full Text] [PDF]