Thromb Haemost 2000; 84(02): 244-249
DOI: 10.1055/s-0037-1614003
Review Article
Schattauer GmbH

A New T-287C Polymorphism in the 5’ Regulatory Region of the Tissue Factor Pathway Inhibitor Gene

Association Study of the T-287C and C-399T Polymorphisms with Coronary Artery Disease and Plasma TFPI Levels
Didier Moatti
1   From INSERM U479, Paris, France
,
Bassam Haidar
1   From INSERM U479, Paris, France
,
Frédéric Fumeron
2   Service de Nutrition Humaine, CHU Xavier Bichat, Paris, France
,
Laurent Gauci
3   Service de Cardiologie, Paris, France
,
Olivier Boudvillain
3   Service de Cardiologie, Paris, France
,
Patrick Seknadji
3   Service de Cardiologie, Paris, France
,
Véronique Ollivier
1   From INSERM U479, Paris, France
,
Marie Claude Aumont
3   Service de Cardiologie, Paris, France
,
Dominique de Prost
1   From INSERM U479, Paris, France
*   Service d’Hématologie, Hopital Louis Mourier, AP-HP, Paris, France
› Author Affiliations
This study was supported by a grant from AP-HP (CRC 95135). We thank C. Lacombe and L. Sustendal for their excellent technical assistance; and Drs. A. M. Becker, S. Menasie, and R. Babou (E.T.S. de l’AP-HP, Site Transfusionnel, Hôpital Bichat-Claude Bernard) for collecting blood samples from the control subjects.
Further Information

Publication History

Received 17 December 1999

Accepted after resubmission 21 February 2000

Publication Date:
14 December 2017 (online)

Summary

Tissue factor pathway inhibitor (TFPI) is an important regulator of the extrinsic blood coagulation pathway. We screened the untranslated 5’ region of the TFPI gene for polymorphisms and investigated their possible involvement in arterial thrombosis. The allele frequencies of a new polymorphism, located 287 base pairs upstream of the transcription start site (T-287C), and that of the previously described C-399T polymorphism, were similar in cases and controls. In controls, the -287C allele was associated with significantly higher levels of total TFPI antigen, arguing for an effect of this polymorphism on TFPI gene expression. In controls, the C-399T polymorphism did not alter TFPI levels. In the cases, however, decreased total and post-heparin free TFPI levels and increased F1+2 levels were significantly associated with the -399T allele. These findings suggest that the T-287C and C-399T polymorphisms are not associated with an increased risk of coronary heart disease, a result which should be confirmed by a larger study. However, their influence on outcome, or a link with subtypes of acute coronary syndromes, cannot be excluded.

 
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