Genetic analysis of kallikrein‐kinin system in the Korean hypertensives

B. Kang, J. Bae, Kang Oh Lee
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引用次数: 1

Abstract

The kallikrein‐kinin system affects regulation of blood pressure, and genes encoding for the components of this system have been considered as good candidates for hypertension. To evaluate the relationship between genetic polymorphisms of candidate genes involved in this system and hypertension, we performed case‐control studies using genetic markers in Korean normotensives and hypertensives, respectively. By association study, there was a marginal association with hypertension in AA genotype distribution of A1789G polymorphism in the hKLK1 gene (P=0.0754). Thus, this genetic polymorphism may weakly contribute to the susceptibility to hypertension in Koreans. We also observed that significant linkage disequilibrium exists among three polymorphic sites in the hKLK1 gene studied, suggesting that the three genetic polymorphisms can be useful as genetic markers in clinical association studies. Further studies using larger sample sizes and more genetic markers will be needed to clarify genetic influence of kallikrein‐kinin system for hypertension.
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韩国高血压患者钾likrein - kinin系统的遗传分析
钾likrein - kinin系统影响血压调节,编码该系统成分的基因被认为是高血压的良好候选者。为了评估参与该系统的候选基因的遗传多态性与高血压之间的关系,我们分别在韩国血压正常者和高血压患者中使用遗传标记进行了病例对照研究。关联研究发现,hKLK1基因A1789G多态性AA基因型分布与高血压存在边际相关性(P=0.0754)。因此,这种遗传多态性可能对韩国人的高血压易感性有微弱的影响。我们还观察到,在研究的hKLK1基因的三个多态性位点之间存在显著的连锁不平衡,这表明这三个遗传多态性可以作为临床关联研究的遗传标记。进一步的研究需要使用更大的样本量和更多的遗传标记来阐明钾likrein‐kinin系统对高血压的遗传影响。
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