Thrombosis Journal | |
Gender differences of polymorphisms in the TF and TFPI genes, as related to phenotypes in patients with coronary heart disease and type-2 diabetes | |
Original Clinical Investigation | |
Alf Åge Pettersen1  Thomas Weiss1  Trine B Opstad1  Ingebjørg Seljeflot2  Harald Arnesen3  | |
[1] Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ulleval, Oslo, Norway;Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ulleval, Oslo, Norway;Center for Clinical Research, Oslo University Hospital Ulleval, Oslo, Norway;Faculty of Medicine, University of Oslo, Norway;Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ulleval, Oslo, Norway;Faculty of Medicine, University of Oslo, Norway; | |
关键词: Coronary Heart Disease; Tissue Factor; Tissue Factor Pathway Inhibitor; Coronary Heart Disease Patient; Stable Coronary Heart Disease; | |
DOI : 10.1186/1477-9560-8-7 | |
received in 2009-11-09, accepted in 2010-05-05, 发布年份 2010 | |
来源: Springer | |
【 摘 要 】
BackgroundTissue factor (TF) and its inhibitor tissue factor pathway inhibitor (TFPI) are the main regulators of the initiation of the coagulation process, important in atherothrombosis. In this study we have investigated the frequency of six known TF and TFPI single nucleotide polymorphisms (SNPs) in CHD patients as compared to healthy individuals. These genotypes and the phenotypes (TF, TFPI free and total antigen) were evaluated with special reference to gender and diabetes in the CHD population.MethodsPatients with angiographically verified CHD (n = 1001; 22% women, 20% diabetics), and 204 healthy controls (28% women), were included. The investigated SNPs were: TF -1812C/T and TF -603A/G in the 5'upstream region, TF 5466A/G in intron 2, TFPI -399C/T and TFPI -287T/C in the 5'upstream region and the TFPI -33T/C in intron 7.ResultsNo significant differences in frequencies between the CHD population and the controls of any polymorphisms were observed. In the CHD population, the TF 5466 A/G SNP were significantly more frequent in women as compared to men (p < 0.001). The TF-1812C/T and the TF-603A/G SNPs were significantly more frequent in women without type-2 diabetes compared to those with diabetes (p < 0.018, both), and the heterozygous genotypes were associated with significantly lower TF plasma levels compared to the homozygous genotypes (p < 0.02, both).The TFPI-399C/T and the TFPI-33T/C SNPs were associated with lower and higher TFPI total antigen levels, respectively (p < 0.001, both).ConclusionGenetic variations in the TF and TFPI genes seem to be associated with gender and type-2 diabetes, partly affecting their respective phenotypes.
【 授权许可】
CC BY
© Opstad et al; licensee BioMed Central Ltd. 2010
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
RO202311109151445ZK.pdf | 903KB | download |
【 参考文献 】
- [1]
- [2]
- [3]
- [4]
- [5]
- [6]
- [7]
- [8]
- [9]
- [10]
- [11]
- [12]
- [13]
- [14]
- [15]
- [16]
- [17]
- [18]
- [19]
- [20]
- [21]
- [22]
- [23]
- [24]
- [25]
- [26]
- [27]
- [28]
- [29]
- [30]