| Title | Association study to evaluate TFPI gene in CAD in Han Chinese |
| Authors | Zhao, Ying Yu, Yanbo Shi, Maowei Yang, Xi Li, Xueqi Jiang, Feng Chen, Yundai Tian, Xiaoli |
| Affiliation | Jinan Mil Gen Hosp, Dept Geriatr, Jinan 250031, Shandong, Peoples R China. Shandong Univ, Qilu Hosp, Dept Gastroenterol, Jinan 250012, Shandong, Peoples R China. Peking Univ, Inst Mol Med, Dept Human Populat Genet, Beijing 100871, Peoples R China. Harbin Med Univ, Affiliated Hosp 4, Dept Cardiol, Harbin 150001, Heilongjiang, Peoples R China. Chinese Peoples Liberat Army Gen Hosp, Dept Cardiol, Beijing 100853, Peoples R China. Peking Univ, Inst Mol Med, Dept Human Populat Genet, Beijing 100871, Peoples R China. Chen, YD (reprint author), Chinese Peoples Liberat Army Gen Hosp, Dept Cardiol, Beijing 100853, Peoples R China. |
| Keywords | Tissue factor pathway inhibitor Coronary artery disease Single nucleotide polymorphism Han Chinese FACTOR PATHWAY INHIBITOR FACTOR PROCOAGULANT ACTIVITY CARDIOVASCULAR RISK-FACTORS INCREASED TISSUE FACTOR DIABETES-MELLITUS COAGULATION INHIBITOR ARTERIAL THROMBOSIS PLASMA-LEVELS MURINE MODEL ATHEROSCLEROSIS |
| Issue Date | 2017 |
| Publisher | BMC CARDIOVASCULAR DISORDERS |
| Citation | BMC CARDIOVASCULAR DISORDERS.2017,17. |
| Abstract | Background: Tissue factor pathway inhibitor (TFPI) is the main physiological inhibitor of TF-induced blood coagulation process, and may play essential roles in the pathogenesis of major adverse cardiac events. This study was designed to determine whether the variation of TFPI was related with coronary artery disease (CAD) in the Han Chinese populations. Methods: A total of 1271 patients with coronary atherosclerosis and 1287 normal individuals from northern China were enrolled in the present study. Four tagging single-nucleotide polymorphisms (SNPs) (rs7586970, rs6434222, rs10153820 and rs8176528) from TFPI were selected and genotyped by direct sequencing. And the genotypes of the above SNPs were determined in all these participants. Results: In the populations from Beijing and Harbin, no significant case-control differences in the frequencies of TFPI polymorphism (rs10153820 and rs8176528) were observed between CAD patients and controls. Meanwhile, two SNPs of TFPI (rs7586970 and rs6434222) were found to be associated with CAD in both groups. In stratified analyses based on gender, smoking, hypertension, diabetes mellitus and hyperlipidemia, we further determined that the investigated genetic variations of the TFPI genes seemed to be related with diabetes mellitus in CAD patients. Conclusions: Genetic variations of the TFPI genes seem to be related with CAD, which likely cooperate with metabolic risk factor (diabetes mellitus) and play critical roles in the pathogenesis of coronary artery disease. |
| URI | http://hdl.handle.net/20.500.11897/472112 |
| ISSN | 1471-2261 |
| DOI | 10.1186/s12872-017-0626-y |
| Indexed | SCI(E) |
| Appears in Collections: | 分子医学研究所 |
