Er Leay-Kiaw, Teng Ming-Sheng, Wu Semon, Hsu Lung-An, Tzeng I-Shiang, Cheng Ching-Feng, Chang Hsin-I, Chou Hsin-Hua, Ko Yu-Lin
Division of Endocrinology and Metabolism, Department of Internal Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei, Taiwan.
Department of Research, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei, Taiwan.
Tzu Chi Med J. 2018 Jan-Mar;30(1):29-36. doi: 10.4103/tcmj.tcmj_187_17.
Both acid-sensing ion channel acid-sensing ion channel 3 (ASIC3) and transient receptor potential vanilloid 1 (TRPV1) have been proposed to be involved in the pathophysiology of hypertension. Common colocalization of ASIC3 and TRPV1 channels in the same sensory neuron has been reported. We aimed to study the combined and gene polymorphisms in the risk of hypertension.
To test the statistical association between genetic polymorphisms of the and genes and blood pressure (BP) variations in Taiwanese, 551 unrelated individuals (286 men and 265 women) having routine health examinations were recruited. The participants had no history of cardiovascular disease or use of medication for hypertension.
Six and four gene polymorphisms were genotyped, and only the rs2288646 polymorphism was associated with variations in BP in the participants. In subgroup analysis, we found participants carrying the combined rs2288646 or and rs8065080 genotypes (combined genotypes) had significantly higher systolic, mean and diastolic BP compared with the other subgroups ( = 0.009, 0.003, and 0.006, respectively, after Bonferroni correction). Interaction analysis also revealed significant gene-gene interaction in the systolic, mean, and diastolic BP in the and genotypes (interaction = 0.006, 0.002, and 0.002, respectively). A trend of increasing frequencies of the combined genotype was observed in normotensive, prehypertensive, and hypertensive subgroups ( for trend = 0.001), as well as in those with higher systolic and diastolic BPs ( for trend = 9.13 × 10 and for trend = 5.5 × 10, respectively).
Our data show a combined effect of and gene polymorphisms in BP variations in Taiwanese. These results suggest that the interaction between and is involved in BP regulation.
酸敏感离子通道3(ASIC3)和瞬时受体电位香草酸受体1(TRPV1)均被认为参与了高血压的病理生理过程。已有报道称ASIC3和TRPV1通道在同一感觉神经元中共同定位。我们旨在研究ASIC3和TRPV1基因多态性与高血压风险的关系。
为检测ASIC3和TRPV1基因多态性与台湾人群血压(BP)变化之间的统计学关联,招募了551名进行常规健康检查的无亲属关系个体(286名男性和265名女性)。参与者无心血管疾病史或未使用过抗高血压药物。
对6个ASIC3和4个TRPV1基因多态性进行了基因分型,只有ASIC3基因的rs2288646多态性与参与者的血压变化相关。在亚组分析中,我们发现携带ASIC3基因rs2288646和/或TRPV1基因rs8065080联合基因型(联合基因型)的参与者与其他亚组相比,收缩压、平均血压和舒张压显著更高(经Bonferroni校正后,P值分别为0.009、0.003和0.006)。交互作用分析还显示,在收缩压、平均血压和舒张压方面,ASIC3和TRPV1基因型之间存在显著的基因-基因交互作用(交互作用P值分别为0.006、0.002和0.002)。在正常血压、高血压前期和高血压亚组中,以及收缩压和舒张压较高的人群中,均观察到联合基因型频率增加的趋势(趋势P值分别为0.001、9.13×10⁻⁴和5.5×10⁻⁴)。
我们的数据显示了ASIC3和TRPV1基因多态性对台湾人群血压变化的联合作用。这些结果表明,ASIC3和TRPV1之间的相互作用参与了血压调节。