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Thrombosis |
2 Subunit Gene With Human Platelets
2ß1 Receptor Density
From the Departments of Hematology (N.A., P.D., M.-C.G.), Anesthesiology (C.B., I.P.), and Biochemistry (B.G.), the Clinical Investigation Center (V.H.), Biostatistics (P.V.), Hopital Bichat, Assistance Publique-Hopitaux de Paris, and INSERM U698 (N.A., C.B., M.-C.G., J.B.), Hopital Bichat, University Paris, France.
Correspondence to Dr N. Ajzenberg, Service dHématologie et Immunologie, Hôpital Bichat, 46 rue Henri Huchard, 75018, Paris, France. E-mail nadine.ajzenberg{at}bch.ap-hop-paris.fr
Objective Platelet adhesion to the subendothelial tissue via the collagen receptor
2ß1 is a crucial event in vascular biology. Although evidence has been provided that the number of platelets
2ß1 copies is genetically determined, the molecular change primary responsible has not been yet elucidated. The aim of our present study was to investigate the effect of combined polymorphisms within both regulatory (52C/T and 92C/G) and coding regions (807C/T and 1648A/G) of the
2 subunit gene on human platelets
2ß1 receptor density and/or susceptibility to coronary artery disease (CAD).
Methods and Results Among 254 cardiac surgery patients, no evidence was found for an association between the
2 subunit gene polymorphisms and CAD. In contrast, in a subgroup of 113 patients, we observed a significant association between all polymorphisms except 52C/T and
2ß1 receptor level. Furthermore, when 3 groups of patients were defined according to the tertiles of platelets
2ß1 copies, the 92C/807T haplotype was more frequent in the group of patients with high
2ß1 receptor level.
Conclusion These results suggest that an individual effect of each polymorphism located either in the coding or promoter sequence of the
2 gene may act in combination to modulate variations in platelets
2ß1 receptor density.
An important combined effect of the 92C and 807T polymorphisms of the
2 gene in increasing the expression of human platelet
2ß1 receptors has been observed, suggesting that this haplotype could modulate variations in
2ß1 receptor density.
Key Words: 92C/G 807C/T polymorphism
2ß1 density
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