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白细胞介素10基因-592C/A多态性与冠状动脉疾病的关联

[Association of interleukin 10 gene -592C/A polymorphism with coronary artery disease].

作者信息

Jin Hu, Wang Yan, Xu Li-xing

机构信息

Department of Cardiology, The First Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang 325027, P.R. China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Dec;30(6):724-8. doi: 10.3760/cma.j.issn.1003-9406.2013.06.020.

DOI:10.3760/cma.j.issn.1003-9406.2013.06.020
PMID:24327156
Abstract

OBJECTIVE

To assess the association of interleukin 10 (IL10) gene -592C/A polymorphism with morbidity of coronary heart disease in a southern Chinese Han population.

METHODS

Frequencies of various genotypes and alleles for the IL10 -592C/A polymorphism (rs1800872) were determined by the means of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) in 249 patients and 132 unaffected controls.

RESULTS

The frequencies of both IL10 -592C/A site and different alleles have reached statistical significance (P<0.05) after correcting the difference in clinical data by logistic regression analysis. The risk of coronary heart disease in the patients with A gene (AA+CA) was 2.449 times greater than those without (95%CI:1.214-4.940, P=0.012).

CONCLUSION

IL10 gene -592C/A polymorphism is associated with the risk of coronary heart disease. Allele A may be a risk factor for this disease in the studied population.

摘要

目的

评估白细胞介素10(IL10)基因-592C/A多态性与中国南方汉族人群冠心病发病的相关性。

方法

采用基质辅助激光解吸/电离飞行时间质谱法(MALDI-TOF-MS)测定249例患者和132例未受影响对照者中IL10 -592C/A多态性(rs1800872)的各种基因型和等位基因频率。

结果

经逻辑回归分析校正临床数据差异后,IL10 -592C/A位点及不同等位基因频率均具有统计学意义(P<0.05)。携带A基因(AA+CA)的患者患冠心病的风险是未携带者的2.449倍(95%CI:1.214-4.940,P=0.012)。

结论

IL10基因-592C/A多态性与冠心病风险相关。在研究人群中,等位基因A可能是该疾病的一个危险因素。

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