School of Life Sciences, Anhui University, Hefei, China.
Institute of Physical Science and Information Technology, Anhui University, Hefei, China.
J Hum Hypertens. 2018 Nov;32(11):781-788. doi: 10.1038/s41371-018-0119-1. Epub 2018 Oct 3.
This study was conducted to explore interactions in the association of the kininogen (KNG1) Ile197Met polymorphism and gender with plasma concentrations of irbesartan in Chinese patients with essential hypertension. A total of 1100 subjects with essential hypertension received a daily oral dose of 150 mg irbesartan for twenty-eight consecutive days. High-performance liquid chromatography-fluorescence (HPLC) was used to detect plasma irbesartan concentrations on day 28. The KNG1 Ile197Met gene polymorphism was determined using high-throughput TaqMan technology. The frequency distribution of KNG1 Ile197Met genotype conformed to the Hardy-Weinberg equilibrium. After 28 days of treatment, patients with the GG genotype had significantly lower irbesartan concentrations (P = 0.033) compared to homozygous TT genotype carriers. After stratifying by gender, male G allele carriers had significantly lower irbesartan concentrations (GG, P = 0.015; TG, P = 0.015, respectively) relative to TT genotype after adjusting for age, region, body mass index (BMI), smoking, and alcohol consumption. However, there was no significant difference in female subjects. A further test for a multiplicative interaction between the KNG1 Ile197Met polymorphism and gender in association with ln-plasma irbesartan concentrations in a multiple linear regression model was also significant (P for interaction = 0.033). This is the first study to suggest that gender may influence the association of the Ile197Met variant of KNG1 with ln-plasma irbesartan concentration. This finding may indicate that the interaction of gender and the KNG1 Ile197Met gene polymorphism can influence plasma trough irbesartan concentrations, which may contribute to a better development of personalized hypertensive treatment in Chinese patients.
这项研究旨在探讨激肽原(KNG1)Ile197Met 多态性与性别与中国原发性高血压患者血浆依那普利浓度的相关性中的相互作用。共有 1100 名原发性高血压患者接受了 28 天的每日口服 150mg 依那普利治疗。在第 28 天,使用高效液相色谱-荧光(HPLC)检测血浆依那普利浓度。使用高通量 TaqMan 技术测定 KNG1 Ile197Met 基因多态性。KNG1 Ile197Met 基因型的频率分布符合 Hardy-Weinberg 平衡。经过 28 天的治疗,GG 基因型患者的依那普利浓度明显降低(P=0.033),与纯合 TT 基因型携带者相比。按性别分层后,调整年龄、地区、体重指数(BMI)、吸烟和饮酒后,男性 G 等位基因携带者的依那普利浓度明显降低(GG,P=0.015;TG,P=0.015)与 TT 基因型相比。然而,女性受试者没有明显差异。在多元线性回归模型中,进一步测试 KNG1 Ile197Met 多态性与性别之间的乘法相互作用与 ln 血浆依那普利浓度的关系也具有显著性(P 交互=0.033)。这是第一项表明性别可能影响 KNG1 Ile197Met 变体与 ln 血浆依那普利浓度相关性的研究。这一发现可能表明,性别和 KNG1 Ile197Met 基因多态性的相互作用可能会影响血浆依那普利谷浓度,这可能有助于更好地开发中国高血压患者的个体化降压治疗。