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首页> 外文期刊>Nutrients >Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults
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Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults

机译:单核苷酸多态性与尿钠,钾和钠钾比对韩国成年人高血压风险的相互作用

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Hypertension is a complex disease explained with diverse factors including environmental factors and genetic factors. The objectives of this study were to determine the interaction effects between gene variants and 24 h estimated urinary sodium and potassium excretion and sodium-potassium excretion ratios on the risk of hypertension. A total of 8839 participants were included in the genome-wide association study (GWAS) to find genetic factors associated with hypertension. Tanaka and Kawasaki formulas were applied to estimate 24 h urinary sodium and potassium excretion. A total of 4414 participants were included in interaction analyses to identify the interaction effects of gene variants according to 24 h estimated urinary factors on the risk of hypertension. CSK rs1378942 and CSK-MIR4513 rs3784789 were significantly modified by urinary sodium-potassium excretion ratio. In addition, MKLN rs1643270 with urinary potassium excretion, LOC101929750 rs7554672 with urinary sodium and potassium excretion, and TENM4 rs10466739 with urinary sodium-potassium excretion ratio showed significant interaction effects. The present study results indicated that the mutant alleles of CSK rs1378942 and CSK-MIR4513 rs3784789 had the strongest protective effects against hypertension in the middle group of 24 h estimated urinary sodium-potassium excretion ratio. Further studies are needed to replicate these analyses in other populations.
机译:高血压是一种复杂的疾病,其解释因素包括环境因素和遗传因素。这项研究的目的是确定基因变异与24 h估计的尿钠钾排泄率和钠钾排泄率之间的相互作用对高血压风险的影响。全基因组关联研究(GWAS)中共有8839名参与者,以寻找与高血压相关的遗传因素。田中和川崎公式应用于估计24小时尿钠和钾的排泄。共有4414名参与者参与了相互作用分析,以根据估计的24 h泌尿因子对高血压风险的影响,确定基因变异的相互作用。 CSK rs1378942和CSK-MIR4513 rs3784789被尿钠钾排泄率显着修饰。此外,尿钾排泄的MKLN rs1643270,尿钠和钾排泄的LOC101929750 rs7554672和尿钠钾排泄比的TENM4 rs10466739表现出显着的相互作用。本研究结果表明,CSK rs1378942和CSK-MIR4513 rs3784789突变等位基因在估计的24 h尿钠钾排泄率中间组中对高血压的保护作用最强。需要进一步的研究以在其他人群中复制这些分析。

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