CYP2D6和ADRB1基因多态性与高血压患者抗高血压β受体阻滞剂的选择。

IF 1.3
American journal of cardiovascular disease Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Keping Chen, Ying Li, Chuankun Yang, Peng Xiao, Guochun Li, Yurong Xu
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引用次数: 0

摘要

背景:遗传因素导致个体对抗高血压药物反应的变异性。我们试图研究CYP2D6和ADRB1基因多态性的等位基因和基因型频率,并探讨它们在影响抗高血压β受体阻滞剂选择方面的潜在影响。方法:研究人群选自中大医院的汉族患者,包括2419名汉族高血压患者和151名血压正常的对照者。上述每个参与者都接受了静脉血液采样。然后,采用基因芯片平台对CYP2D6和ADRB1基因多态性进行评估。对每个基因的等位基因和基因型频率以及组合基因型进行分析。结果:通过基因芯片分析,CYP2D6野生型纯合子*1/*1的频率为9.71%,而杂合子*1/*10或突变纯合子*10/*10的频率分别为59.16%和31.13%。同样,我们观察到,ADRB1的GG野生型纯合子的基因型频率为10.29%,而GC杂合子或CC突变纯合子的频率分别为44.98%或44.73%。值得注意的是,组合基因型*1/*10+CC(25.88%)和*1/*10+CG(27.78%)的频率最高。重要的是,在高血压患者和血压正常的对照组之间,或在所有不同级别的高血压之间,CYP2D6和ADRB1多态性的分布没有显著差异。结论:这些发现为了解汉族高血压患者的CYP2D6和ADRB1多态性提供了依据,与其他汉族高血压患者相比,这些多态性具有显著差异。这些结果为未来研究β受体阻滞剂对汉族高血压患者的降压作用提供了有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CYP2D6 and ADRB1 genetic polymorphisms and the selection of antihypertensive beta-receptor blockers for hypertensive patients.

Background: Genetic factors contribute to the variability in individual response to antihypertensive medications. We sought to investigate the frequencies of allele and genotype for CYP2D6 and ADRB1 genetic polymorphisms and explore their potential impact in influencing the selection of antihypertensive beta-receptor blockers.

Methods: The study population was selected from the Han Chinese patients in Zhongda Hospital, which contained 2419 Han Chinese hypertensive individuals and 151 normotensive controls. Each of the above participants underwent venous blood sampling. Then, the gene chip platform was adopted to evaluate the CYP2D6 and ADRB1 genetic polymorphisms. The allele as well as genotype frequencies for each gene, along with the combined genotypes, were subjected to analysis.

Results: The frequency of *1/*1 wild-type homozygous for CYP2D6 was 9.71%, while the frequency of *1/*10 heterozygous or *10/*10 mutant homozygous was 59.16% or 31.13%, respectively, as established by gene chip analysis. Similarly, we observed that the genotype frequencies of GG wild-type homozygous for ADRB1 was 10.29%, while that of GC heterozygous, or CC mutant homozygous was 44.98%, or 44.73%, respectively. Notably, combined genotypes *1/*10 + CC (25.88%) and *1/*10 + CG (27.78%) had the highest frequencies. Importantly, no substantial differences in the distributions of CYP2D6 and ADRB1 polymorphism were noted between hypertensive patients and normotensive controls, or among all different grades of hypertension.

Conclusion: These findings provide insights into the CYP2D6 and ADRB1 polymorphisms in hypertensive patients from Han Chinese, which show significant differences compared to other geographic groups of Han Chinese hypertensive patients. These results offer valuable information for future prospective clinical studies on the antihypertensive effects of beta-receptor blockers in Han Chinese hypertensive patients.

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来源期刊
American journal of cardiovascular disease
American journal of cardiovascular disease CARDIAC & CARDIOVASCULAR SYSTEMS-
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