Lee Sung-Bum, Park Byoungjin, Hong Kyung-Won, Jung Dong-Hyuk
Severance Check-up, Yonsei University Health System, Yongin-si 16995, Korea.
Department of Medicine, Graduate School, Yonsei University Wonju College of Medicine, Wonju-si 26426, Korea.
J Cardiovasc Dev Dis. 2022 Mar 30;9(4):104. doi: 10.3390/jcdd9040104.
The renin-angiotensin system (RAS) is a crucial regulator of vascular resistance and blood volume in the body. This study aimed to examine the genetic predisposition of the plasma renin concentration influencing future hypertension incidence. Based on the Korean Genome and Epidemiology Cohort dataset, 5211 normotensive individuals at enrollment were observed over 12 years, categorized into the low-renin and high-renin groups. We conducted genome-wide association studies for the total, low-renin, and high-renin groups. Among the significant SNPs, the lead SNPs of each locus were focused on for further interpretation. The effect of genotypes was determined by logistic regression analysis between controls and new-onset hypertension, after adjusting for potential confounding variables. During a mean follow-up period of 7.6 years, 1704 participants (32.7%) developed hypertension. The low-renin group showed more incidence rates of new-onset hypertension (35.3%) than the high-renin group (26.5%). Among 153 SNPs in renin-related gene regions, two SNPs (rs11726091 and rs8137145) showed an association in the high-renin group, four SNPs (rs17038966, rs145286444, rs2118663, and rs12336898) in the low-renin group, and three SNPs (rs1938859, rs7968218, and rs117246401) in the total population. Most significantly, the low-renin SNP rs12336898 in the gene, closely related to vascular wall remodeling, was associated with the development of hypertension (-value = 1.3 × 10). We found the candidate genetic polymorphisms according to blood renin concentration. Our results might be a valuable indicator for hypertension risk prediction and preventive measure, considering renin concentration with genetic susceptibility.
肾素-血管紧张素系统(RAS)是人体血管阻力和血容量的关键调节因子。本研究旨在探讨血浆肾素浓度的遗传易感性对未来高血压发病率的影响。基于韩国基因组与流行病学队列数据集,对入组时5211名血压正常个体进行了12年的观察,并分为低肾素组和高肾素组。我们对总人群、低肾素组和高肾素组进行了全基因组关联研究。在显著的单核苷酸多态性(SNP)中,对每个位点的主要SNP进行进一步解读。在调整潜在混杂变量后,通过逻辑回归分析确定基因型对对照人群和新发高血压患者的影响。在平均7.6年的随访期内,1704名参与者(32.7%)发生了高血压。低肾素组新发高血压的发病率(35.3%)高于高肾素组(26.5%)。在肾素相关基因区域的153个SNP中,两个SNP(rs11726091和rs8137,145)在高肾素组中显示出关联性,四个SNP(rs17038966、rs145286444、rs2118663和rs12336898)在低肾素组中显示出关联性,三个SNP(rs1938859、rs7968218和rs117246401)在总人群中显示出关联性。最显著的是,与血管壁重塑密切相关的基因中的低肾素SNP rs12336898与高血压的发生相关(P值 = 1.3×10)。我们根据血液肾素浓度发现了候选基因多态性。考虑到肾素浓度与遗传易感性,我们的结果可能是高血压风险预测和预防措施的有价值指标。