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Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease  期刊论文  

  • 编号:
    500e17de-37b2-4aa6-9c33-71e8e8d727ba
  • 作者:
    Li, Yafei#[1]Xie, Zhiyong#[1]Chen, Lei[2];Yan, Jianjun[1];Ma, Yao[1];Wang, Liansheng*[1]Chen, Zhong*[3]
  • 语种:
    英文
  • 期刊:
    BMC CARDIOVASCULAR DISORDERS ISSN:1471-2261 2017 年 17 卷 ; FEB 10
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  • 摘要:

    Background: Early B-cell factor 1 (EBF1) is a transcription factor expressed primarily during early B cell development. Previous studies have shown EBF1 regulates blood glucose and lipid metabolism in mice with diabetes and central adiposity. Recently, a genetic variation (rs36071027) located in an EBF1 gene intron was associated with carotid artery intima-media thickness. However, whether this polymorphism is actually linked with coronary artery disease (CAD) and its severity remains unclear. Methods: This study includes 293 CAD cases and 262 controls without CAD. All participants were devided into two groups based on their coronary angiography results. A polymerase chain reaction-ligase detection reaction was used to identify genotypes at rs36071027, and CAD patients were further divided into subgroups with one-, two-, or three-vessel stenosis reflective of CAD severity. Results: The frequency of the rs36071027 TT genotype was significantly higher in CAD cases versus controls (4.8% vs. 1.5%, 95% CI: 1.13-10.81 P = 0.029). Subjects with a variant genotype T allele had an increased risk of CAD compared to C allele carriers (additive model: 95% CI: 1.13-2.23, P = 0.008). After adjustment for cardiovascular risk factors, analysis of the additive and dominant models involving rs36071027 also revealed that T allele carriers had a significantly higher risk for CAD than C allele carriers (additive model: OR 1.56, 95% CI 1.10-2.22, P = 0.013; dominant model: OR 1.60, 95% CI 1.07-2.41, P = 0.023). Furthermore, both diabetes and the CT + TT rs36071027 genotype were significantly associated with three-vessel stenosis. Conclusion: Our results in a Chinese population suggest that the TT genotype and T alleles in rs36071027 in the EBF1 gene are associated with an increased risk of CAD and its severity.

  • 推荐引用方式
    GB/T 7714:
    Li Yafei,Xie Zhiyong,Chen Lei, et al. Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease [J].BMC CARDIOVASCULAR DISORDERS,2017,17.
  • APA:
    Li Yafei,Xie Zhiyong,Chen Lei,Yan Jianjun,&Chen Zhong.(2017).Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease .BMC CARDIOVASCULAR DISORDERS,17.
  • MLA:
    Li Yafei, et al. "Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease" .BMC CARDIOVASCULAR DISORDERS 17(2017).
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