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Association of KCNE1 Genetic Polymorphisms with Atrial Fibrillation in a Chinese Han Population

机译:中国汉族人群中KCNE1基因多态性与房颤的关系。

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摘要

Objective: The purpose of this study was to investigate the association of the polymorphisms of the KCNE1 gene with atrial fibrillation (AF) in a Chinese Han population. Methods: Three hundred seven AF patients and 330 age- and sex-matched controls were genotyped using the polymerase chain reaction–restriction fragment length polymorphism method for two single-nucleotide polymorphisms (rs1805127 and rs1892593) of the human KCNE1 gene. Results: The frequencies of the AA, AG, and GG genotypes of rs1805127 were 11.7%, 50.0%, and 43.3%, respectively, in the AF group, whereas the ones in the control group had frequencies of 19.4%, 44.9%, and 35.8%, respectively. There were significant differences in frequencies of these three genotypes (χ2=7.820, p=0.016) and G allele (65.8% vs. 58.2%; χ2=8.266, p=0.005). The frequencies of AA, AG, and GG of rs1892593 were 38.4%, 47.9%, and 13.7% in the AF group, whereas the ones in the control group had frequencies of 37.8%, 48.5%, and 14.0%, respectively. There was no difference in distributions of frequencies of these three genotypes and allele (χ2=0.051, p=0.978; χ2=1.024, p=0.837, respectively) between AF patients and control subjects. We also found that rs1805127 was associated with left atrial diameter and left ventricular end diastolic diameter in AF patients (χ2=24.883, p<0.001; χ2=34.901, p<0.001, respectively). Logistic regression analysis showed that rs1805127 was an independent risk factor of AF in a Chinese Han population (odds ratio [OR]=1.66, 95% confidence interval [CI]: 1.02–2.68 for AG; OR=2.03, 95% CI: 1.24–3.31 for GG). Conclusion: The genetic polymorphism of KCNE1 was associated with increased risk of AF in a Chinese Han population.
机译:目的:本研究的目的是研究中国汉族人群中KCNE1基因多态性与房颤的相关性。方法:采用聚合酶链反应-限制性片段长度多态性方法,对人类KCNE1基因的两个单核苷酸多态性(rs1805127和rs1892593)进行基因分型,对370例AF患者和330名年龄和性别匹配的对照进行基因分型。结果:AF组的rs1805127的AA,AG和GG基因型频率分别为11.7%,50.0%和43.3%,而对照组的频率分别为19.4%,44.9%和43.3%。 35.8%,分别。这三种基因型的频率(χ 2 = 7.820,p = 0.016)和G等位基因(65.8%vs. 58.2%;χ 2 = 8.266, p = 0.005)。 AF组中rs1892593的AA,AG和GG频率分别为38.4%,47.9%和13.7%,而对照组的频率分别为37.8%,48.5%和14.0%。这三种基因型和等位基因的频率分布之间无差异(分别为χ 2 = 0.051,p = 0.978;χ 2 = 1.024,p = 0.837)。 AF患者和对照组。我们还发现rs1805127与AF患者的左心房直径和左心室舒张末期直径有关(χ 2 = 24.883,p <0.001;χ 2 = 34.901,< em> p <0.001)。 Logistic回归分析显示,rs1805127是中国汉族人群房颤的独立危险因素(AG的优势比[OR] = 1.66,95%置信区间[CI]:1.02-2.68; OR = 2.03,95%CI:1.24) –3.31(对于GG)。 结论: KCNE1 的基因多态性与中国汉族人群发生房颤的风险增加有关。

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