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激肽释放酶-激肽系统基因在血压盐敏感性中的作用:GenSalt 研究。

The role of the kallikrein-kinin system genes in the salt sensitivity of blood pressure: the GenSalt Study.

机构信息

Department of Evidence Based Medicine, Fuwai Hospital and National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, 167 Beilishi Road, Beijing 100037, China.

出版信息

Am J Epidemiol. 2012 Oct 1;176 Suppl 7(Suppl 7):S72-80. doi: 10.1093/aje/kws277.

Abstract

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.

摘要

本研究全面考察了激肽释放酶-激肽系统(KKS)常见遗传变异与血压盐敏感性之间的关系。2003 年至 2005 年期间,从汉族人群中招募了 1906 名参与者,进行了为期 7 天的低钠饮食和 7 天的高钠饮食干预。通过研究期间使用随机零汞柱血压计测量血压。选择了 11 个 KKS 基因中的 205 个单核苷酸多态性(SNP)进行分析。缓激肽受体 B2 基因(BDKRB2)和内皮素转换酶 1 基因(ECE1)的遗传变异与盐敏感性表型显著相关,即使在进行多次检验校正后也是如此。与主要 G 等位基因相比,BDKRB2 rs11847625 次要 C 等位基因与低钠干预下收缩压反应增加显著相关(P=0.0001)。此外,含有 C 等位基因的单倍型与高钠干预下收缩压反应增加相关(P=0.0009)。7 个高度相关的 ECE1 SNP 显示,它们使舒张压对低钠干预的反应增加(P 值范围为 0.0003 至 0.002),含有这 7 个 SNP 的 2 个单倍型也与这种表型相关(P 值范围为 0.0004 至 0.002)。总之,参与 KKS 调节的基因的遗传变异可能导致血压的盐敏感性。

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