首页> 外文期刊>American Journal of Translational Research >Polymorphism rs2200733 at chromosome 4q25 is associated with atrial fibrillation recurrence after radiofrequency catheter ablation in the Chinese Han population
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Polymorphism rs2200733 at chromosome 4q25 is associated with atrial fibrillation recurrence after radiofrequency catheter ablation in the Chinese Han population

机译:染色体4q25的rs2200733基因多态性与中国汉族人群射频导管消融后房颤复发有关

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To test polymorphisms rs2200733 (chromosome 4q25) and rs2106261 (ZFHX3) were associated with AF recurrence after catheter ablation in a Chinese Han cohort. A total of 235 AF patients who underwent catheter ablation were recruited consecutively. Two polymorphisms were amplified by polymerase chain reaction and genotyped using high resolution melting analysis. Primary endpoints for AF recurrence were defined as the time to the first recurrence of atrial tachycardia/flutter/fibrillation (AT/AF). AT/AF recurrence was observed in 76 patients (35%). Allelic analysis demonstrated that rs2200733 was strongly associated with AF recurrence after ablation (P = 0.011) and the minor allele T increased the risk for recurrence (OR = 1.715). Diameters of the right atrium as well as the left and right superior pulmonary veins (PVs) were associated with rs2200733 in different genetic models (P = 0.040, 0.047 and 0.028, respectively). No significant association was detected between rs2106261 and AT/AF recurrence after ablation or atrial/PV diameters in any models. On multivariate Cox regression analysis, only rs2200733 was an independent factor of AF recurrence after ablation (HR = 0.532, P = 0.022). In Chinese Han population, rs2200733 but not rs2106261 is associated with AT/AF recurrence after ablation. The patients with genotype TT have larger size of right atrium and superior PVs than those of CC genotype. The findings suggest that rs2200733 may play a key role in regulating proper development and differentiation of atria/PVs.
机译:为了测试多态性,将rs2200733(染色体4q25)和rs2106261(ZFHX3)与中国汉族人群导管消融后的AF复发相关联。连续招募了235例接受导管消融的房颤患者。通过聚合酶链反应扩增两个多态性,并使用高分辨率熔解分析进行基因分型。 AF复发的主要终点定义为心房心动过速/颤动/原纤维形成(AT / AF)首次复发的时间。在76名患者(35%)中观察到AT / AF复发。等位基因分析表明,rs2200733与消融后房颤复发密切相关(P = 0.011),次要等位基因T增加了复发风险(OR = 1.715)。在不同的遗传模型中,右心房的直径以及左右肺上静脉(PVs)与rs2200733相关(分别为P = 0.040、0.047和0.028)。在任何模型中,在消融或房/ PV直径后,rs2106261与AT / AF复发之间均未检测到显着相关性。在多因素Cox回归分析中,只有rs2200733是消融后房颤复发的独立因素(HR = 0.532,P = 0.022)。在中国汉族人群中,rs2200733而非rs2106261与消融后AT / AF复发相关。 TT基因型患者的右心房面积较大,PV较CC基因型患者高。这些发现表明,rs2200733可能在调节心房/ PV的正常发育和分化中起关键作用。

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