Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic risk
被引:57
作者:
Aiach, M
论文数: 0引用数: 0
h-index: 0
机构:
Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, FranceHop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Aiach, M
[1
]
Nicaud, V
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Nicaud, V
Alhenc-Gelas, M
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Alhenc-Gelas, M
Gandrille, S
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Gandrille, S
Arnaud, E
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Arnaud, E
Amiral, J
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Amiral, J
Guize, L
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Guize, L
Fiessinger, JN
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Fiessinger, JN
Emmerich, J
论文数: 0引用数: 0
h-index: 0
机构:Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
Emmerich, J
机构:
[1] Hop Broussais, Hemostase Lab, Unite INSERM 428, Unite INSERM 258, F-75674 Paris 14, France
[2] Hop Broussais, Ctr Claude Bernard Rech Malad Vasc, F-75674 Paris, France
The allele and haplotype frequency of the -1654 C/T and -1641 A/G protein C (PC) gene promoter polymorphisms was determined and analyzed according to circulating PC concentrations in 394 healthy subjects aged 20 to 60 years. The CG haplotype was associated with a lower PC concentration in both homozygous and heterozygous subjects compared with noncarriers. The TA allele had the reverse effect, but only in homozygotes. The distribution of the CG and TA alleles was significantly different in 242 patients, aged 17 to 60 years, with venous thromboembolism. The CG allele increased the risk of thrombosis, with an OR of 1.39 (95% confidence interval (CI), 1.04 to 1.87). The TA allele was protective in subjects aged <45 years, with an OR of 0.68 (95% CI, 0.44 to 1.04). TA was also significantly associated with older age at the first thrombosis. This study confirms the link between the PC gene promoter and circulating PC levels, and suggests a complex effect on the risk of thrombosis.