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[中国新疆维吾尔族人群CYP1A1基因多态性与冠状动脉疾病的关联]

[Association between CYP1A1 genetic polymorphisms and coronary artery disease in Uygur population in Xinjiang, China].

作者信息

Zou Jinguo, Ma Yitong, Xie Xiang, Yang Yining, Liu Fen

机构信息

Department of Cardiology; Xinjiang Key Laboratory of Cardiovascular Disease Research, First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, China.

Department of Cardiology; Xinjiang Key Laboratory of Cardiovascular Disease Research, First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, China; Email:

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 2015 Apr;36(4):393-8.

PMID:25975557
Abstract

OBJECTIVE

To assess the association between human CYP1A1 gene polymorphisms and coronary artery disease (CAD) among the Uygur population of China.

METHODS

Genotypes of CYP1A1 single nucleotide polymorphisms (SNPs: rs4886605, rs12441817, rs4646422 and rs1048943) were detected by real-time PCR in 293 CAD patients and 408 controls.

RESULTS

Among the Uygur group, distribution of genotypes and allele of rs4886605 were both significantly different between CAD and the controls (all P < 0.05). The dominant model (CC vs. CT+TT) of rs4886605 was significantly lower among CAD patients than in controls. Significant differences were retained after the adjustment was made in all the participants (OR = 0.368, 95% CI: 0.185-0.530, P = 0.018) and in men (OR = 0.350, 95% CI: 0.235-0.568, P = 0.015). Distributions of genotypes and allele of rs12441817 were both significantly different between CAD and the controls (all P < 0.05). The dominant model (TT vs. CT+CC) of rs12441817 was significantly lower among patients CAD than in controls. Significant difference were retained after the adjustment was made, in total participants (OR = 0.253, 95% CI: 0.231-0.546, P = 0.016) and in men (OR = 0.241, 95% CI: 0.132-0.478, P = 0.002).

CONCLUSION

Both rs4886605 and rs12441817 SNPs of the CYP1A1 gene were associated with CAD in the Uygur population of China.

摘要

目的

评估中国维吾尔族人群中人类细胞色素P450 1A1(CYP1A1)基因多态性与冠状动脉疾病(CAD)之间的关联。

方法

采用实时荧光定量聚合酶链反应(PCR)检测293例CAD患者和408例对照者CYP1A1单核苷酸多态性(SNPs:rs4886605、rs12441817、rs4646422和rs1048943)的基因型。

结果

在维吾尔族人群中,CAD患者与对照者之间rs4886605的基因型和等位基因分布均存在显著差异(均P<0.05)。rs4886605的显性模型(CC与CT+TT)在CAD患者中显著低于对照者。在所有参与者(比值比[OR]=0.368,95%可信区间[CI]:0.185-0.530,P=0.018)和男性(OR=0.350,95%CI:0.235-0.568,P=0.015)中进行校正后,差异仍然显著。CAD患者与对照者之间rs12441817的基因型和等位基因分布均存在显著差异(均P<0.05)。rs12441817的显性模型(TT与CT+CC)在CAD患者中显著低于对照者。在所有参与者(OR=0.253,95%CI:0.231-0.546,P=0.016)和男性(OR=0.241,95%CI:0.132-0.478,P=0.002)中进行校正后,差异仍然显著。

结论

在中国维吾尔族人群中,CYP1A1基因的rs4886605和rs12441817这两个SNPs均与CAD相关。

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