Department of Cardiovascular Surgery, First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Department of Cardiology, First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Kidney Blood Press Res. 2022;47(2):94-102. doi: 10.1159/000519839. Epub 2021 Dec 2.
Klotho (KL) plays pivotal roles in the progression of salt-sensitive hypertension. Salt-sensitive hypertension was associated with KL genotypes. We aimed to explore the association of common genetic variants of KL with individual blood pressure (BP) responses to sodium and potassium through a dietary intervention study as well as long-term BP progression.
We conducted family-based dietary interventions among 344 participants from 126 families in rural villages of northern China in 2004. Subjects sequentially underwent a baseline diet, a low-salt diet (51.3 mmol/day Na), a high-salt diet (307.8 mmol/day Na), and a high-salt + potassium supplementation diet (307.8 mmol/day Na + 60 mmol/day K). After dietary intervention, we followed up with these participants in 2009 and 2012. The associations between 6 single-nucleotide polymorphisms (SNPs) of KL and phenotypes were analyzed through a linear mixed-effects model.
SNPs rs211247 and rs1207568 were positively correlated with the BP response to high-salt diet in the dominant model after adjusting for confounders (β = 1.670 and 2.163, p = 0.032 and 0.005, respectively). BPs rs526906 and rs525014 were in a haplotype block. Block rs526906-rs525014 was positively correlated with diastolic BP response to potassium and potassium sensitivity in the additive model (β = 0.845, p = 0.032). In addition, regression analysis indicated that rs211247 was associated with long-term systolic BP alterations after 8 years of follow-up in the recessive model (β = 20.47, p = 0.032).
Common variants of the KL gene might modify individual BP sensitivity to sodium or potassium and influence the long-term progression of BP, suggesting a potential role in the development of salt-sensitive hypertension. Thus, KL may be a new early intervention target for salt-sensitive hypertension.
Klotho(KL)在盐敏感性高血压的进展中起着关键作用。盐敏感性高血压与 KL 基因型有关。我们旨在通过饮食干预研究以及长期血压进展来探索 KL 的常见遗传变异与个体对钠和钾的血压反应之间的关联。
我们于 2004 年在中国北方农村的 126 个家庭中对 344 名参与者进行了基于家庭的饮食干预。受试者依次接受了基线饮食、低盐饮食(51.3mmol/天 Na)、高盐饮食(307.8mmol/天 Na)和高盐+钾补充饮食(307.8mmol/天 Na+60mmol/天 K)。饮食干预后,我们在 2009 年和 2012 年对这些参与者进行了随访。通过线性混合效应模型分析 KL 的 6 个单核苷酸多态性(SNP)与表型之间的关联。
在调整混杂因素后,SNP rs211247 和 rs1207568 在显性模型中与高盐饮食后的血压反应呈正相关(β=1.670 和 2.163,p=0.032 和 0.005)。SNP rs526906 和 rs525014 位于单倍型块中。块 rs526906-rs525014 在加性模型中与钾的舒张压反应和钾敏感性呈正相关(β=0.845,p=0.032)。此外,回归分析表明,在 8 年的随访中,rs211247 在隐性模型中与收缩压的长期变化有关(β=20.47,p=0.032)。
KL 基因的常见变异可能改变个体对钠或钾的血压敏感性,并影响血压的长期进展,这表明 KL 在盐敏感性高血压的发生中可能起作用。因此,KL 可能成为盐敏感性高血压的新的早期干预靶点。