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白细胞介素-27基因变异对心房颤动易感性的影响。

Effect of Interleukin-27 Genetic Variants on Atrial Fibrillation Susceptibility.

作者信息

Chen Yu, Zeng Jianhui, Zhang Rui, Zeng Linjun, Li Yajiao, Wei Hong, Yang Qing

机构信息

1 Department of Cardiology, Hospital of The University of Electronic Science and Technology of China and Sichuan Provincial People's Hospital , Chengdu, China .

2 Department of Cardiology, The Affiliated Hospital of North Sichuan Medical College , Nanchong, China .

出版信息

Genet Test Mol Biomarkers. 2017 Feb;21(2):97-101. doi: 10.1089/gtmb.2016.0219. Epub 2017 Jan 5.

Abstract

AIM

Atrial fibrillation (AF) is the most common cardiac arrhythmia. No data are available on the association between the polymorphisms of interleukin-27 (IL-27) and AF in the Chinese Han population. This study was performed to determine if polymorphisms within the IL-27 gene are involved in the AF susceptibility.

METHODS

Two hundred seventy AF patients and 303 healthy individuals were examined for two IL-27 gene polymorphisms (rs153109 and rs17855750) by polymerase chain reaction-restriction fragment length polymorphism methodology.

RESULTS

An association between the IL-27 single nucleotide polymorphism (SNP) rs153109 and AF was found in Chinese Han population. The G allele and GG genotype of rs153109 were associated with increased AF risk (odds ratio [OR]: 1.35, 95% confidence intervals [CI] = 1.06-1.71, p = 0.02 and OR: 1.66, 95% CI = 1.03-2.65, p = 0.03 in the recessive genetic model, respectively). The significance of the association between the GG genotype and AF risk did not survive a Bonferroni's correction. Similarly, no significant differences in the allele and genotype frequencies of the rs17855750 SNP was observed between the AF patients and controls.

CONCLUSIONS

Our findings indicated that the IL-27 genetic polymorphisms may be associated with susceptibility of AF in Chinese Han population.

摘要

目的

心房颤动(AF)是最常见的心律失常。在中国汉族人群中,关于白细胞介素-27(IL-27)基因多态性与AF之间的关联尚无数据。本研究旨在确定IL-27基因内的多态性是否与AF易感性有关。

方法

采用聚合酶链反应-限制性片段长度多态性方法,对270例AF患者和303名健康个体进行了两种IL-27基因多态性(rs153109和rs17855750)检测。

结果

在中国汉族人群中发现IL-27单核苷酸多态性(SNP)rs153109与AF之间存在关联。rs153109的G等位基因和GG基因型与AF风险增加相关(隐性遗传模型中,比值比[OR]:1.35,95%置信区间[CI]=1.06-1.71,p=0.02;OR:1.66,95%CI=1.03-2.65,p=0.03)。GG基因型与AF风险之间关联的显著性在Bonferroni校正后不复存在。同样,在AF患者和对照组之间,未观察到rs17855750 SNP的等位基因和基因型频率有显著差异。

结论

我们的研究结果表明,IL-27基因多态性可能与中国汉族人群AF易感性有关。

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