Liu F, Yang X, Mo X, Huang J, Chen J, Kelly T N, Hixson J E, Rao D C, Gu C C, Shimmin L C, Chen J, Rice T K, Li J, Schwander K, He J, Liu D-P, Gu D
State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center of Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
1] Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, USA [2] Department of Medicine, Tulane University School of Medicine, New Orleans, LA, USA.
J Hum Hypertens. 2015 Apr;29(4):224-8. doi: 10.1038/jhh.2014.78. Epub 2014 Sep 18.
In order to investigate the associations of SCNN1A, SCNN1G and SCNN1B genes with blood pressure (BP) in the Han Chinese population, we included 2880 participants did not use antihypertensive medication in the month prior to the baseline survey in the current analysis. Forty-four tag-single-nucleotide polymorphisms (SNPs) in epithelial sodium channel (ENaC) genes were selected and genotyped, and nine BP measurements were obtained during the 3-day examination. In the single-marker analyses, we identified significant associations of SCNN1A marker rs13306613 with diastolic BP (DBP) and SCNN1B marker rs12447134 with systolic BP (SBP) under codominant model after Bonferroni's correction (P=2.82 × 10(-5) and 4.63 × 10(-4), respectively). In addition, five SNPs in SCNN1G and four SNPs in SCNN1B achieved nominal significance for SBP, DBP or mean arterial pressure (MAP) under the additive model. For example, the minor C allele of rs5735 in SCNN1G gene was associated with decreased SBP, DBP and MAP (P=0.016, 5.41 × 10(-3) and 4.36 × 10(-3), respectively). Gene-based results showed significant associations of SCNN1G and SCNN1B with BP levels. This study suggested that ENaC genes have important roles in BP regulation in the Han Chinese population. Future studies are warranted to replicate these findings, and functional studies are needed to identify true causal variants in ENaC genes.
为了研究汉族人群中SCNN1A、SCNN1G和SCNN1B基因与血压(BP)的关联,我们纳入了2880名在基线调查前一个月未使用抗高血压药物的参与者进行当前分析。选择上皮钠通道(ENaC)基因中的44个标签单核苷酸多态性(SNP)进行基因分型,并在为期3天的检查中获得9次血压测量值。在单标记分析中,经Bonferroni校正后,我们在共显性模型下确定SCNN1A标记rs13306613与舒张压(DBP)以及SCNN1B标记rs12447134与收缩压(SBP)存在显著关联(P值分别为2.82×10⁻⁵和4.63×10⁻⁴)。此外,在加性模型下,SCNN1G中的5个SNP和SCNN1B中的4个SNP在SBP、DBP或平均动脉压(MAP)方面达到名义显著性。例如,SCNN1G基因中rs5735的次要C等位基因与SBP、DBP和MAP降低相关(P值分别为0.016、5.41×10⁻³和4.36×10⁻³)。基于基因的结果显示SCNN1G和SCNN1B与血压水平存在显著关联。本研究表明ENaC基因在汉族人群的血压调节中具有重要作用。未来的研究有必要重复这些发现,并且需要进行功能研究以确定ENaC基因中的真正因果变异。