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The Role of the Kallikrein-Kinin System Genes in the Salt Sensitivity of Blood Pressure

机译:激肽释放酶-激肽系统基因在血压盐敏感性中的作用

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摘要

The current study comprehensively examined the association between common genetic variants of the kallikrein-kinin system (KKS) and blood pressure salt sensitivity. A 7-day low-sodium followed by a 7-day high-sodium dietary intervention was conducted among 1,906 Han Chinese participants recruited from 2003 to 2005. Blood pressure was measured by using a random-zero sphygmomanometer through the study. A total of 205 single nucleotide polymorphisms (SNPs) covering 11 genes of the KKS were selected for the analyses. Genetic variants of the bradykinin receptor B2 gene (BDKRB2) and the endothelin converting enzyme 1 gene (ECE1) showed significant associations with the salt-sensitivity phenotypes even after adjustment for multiple testing. Compared with the major G allele, the BDKRB2 rs11847625 minor C allele was significantly associated with increased systolic blood pressure responses to low-sodium intervention (P = 0.0001). Furthermore, a haplotype containing allele C was associated with an increased systolic blood pressure response to high-sodium intervention (P = 0.0009). Seven highly correlated ECE1 SNPs were shown to increase the diastolic blood pressure response to low-sodium intervention (P values ranged from 0.0003 to 0.002), with 2 haplotypes containing these 7 SNPs also associated with this same phenotype (P values ranged from 0.0004 to 0.002). In summary, genetic variants of the genes involved in the regulation of KKS may contribute to the salt sensitivity of blood pressure.
机译:本研究全面检查了激肽释放酶激肽系统(KKS)的常见遗传变异与血压盐敏感性之间的关联。在2003年至2005年招募的1906名汉族汉族人群中,进行了7天低钠饮食,然后是7天高钠饮食干预。通过该研究,使用随机零血压计测量了血压。总共205个覆盖KKS的11个基因的单核苷酸多态性(SNP)被选择进行分析。缓激肽受体B2基因(BDKRB2)和内皮素转化酶1基因(ECE1)的遗传变异即使在经过多重测试调整后仍显示与盐敏感性表型显着相关。与主要的G等位基因相比,BDKRB2 rs11847625轻微的C等位基因与对低钠干预的收缩压升高反应显着相关(P = 0.0001)。此外,含有等位基因C的单倍型与高钠干预引起的收缩压升高相关(P = 0.0009)。研究表明,七个高度相关的ECE1 SNP可增加对低钠干预的舒张压反应(P值范围为0.0003至0.002),其中两个包含这7个SNP的单倍型也与此表型相关(P值范围为0.0004至0.002) )。总之,参与KKS调控的基因的遗传变异可能有助于血压的盐敏感性。

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