The Center of Diagnosis, Treatment and Research of Hypertension, Urumqi, Xinjiang, China.
BMC Med Genet. 2010 Aug 13;11:124. doi: 10.1186/1471-2350-11-124.
Hypertension is a complex disease influenced by multiple genetic and environmental factors. The Kazakh ethnic group is characterized by a relatively high prevalence of hypertension. Previous research indicates that the FURIN gene may play a pivotal role in the renin-angiotensin system and maintaining the sodium-electrolyte balance. Because these systems influence blood pressure regulation, we considered FURIN as a candidate gene for hypertension. The purpose of this study was to systematically investigate the association between genetic variations in the FURIN gene and essential hypertension in a Xinjiang Kazakh population.
We sequenced all exons and the promoter regions of the FURIN gene in 94 hypertensive individuals to identify genetic variations associated with the disorder. Genotyping was performed using the TaqMan polymerase chain reaction method for four representative common single nucleotide polymorphisms (SNPs, -7315C > T, 1970C > G, 5604C > G, 6262C > T) in 934 Kazakh Chinese people. One SNP (1970C > G) was replicated in 1,219 Uygur Chinese people.
Nine novel and seven known single nucleotide polymorphisms were identified in the FURIN gene. The results suggest that 1970C > G was associated with a hypertension phenotype in Kazakh Chinese (additive model, P = 0.091; dominant model, P = 0.031, allele model, P = 0.030), and after adjustment with logistic regression analysis, ORs were 1.451 (95%CI 1.106-1.905, P = 0.008) and 1.496 (95% 1.103-2.028, P = 0.01) in additive and dominant models, respectively. In addition, the association between 1970C > G and hypertension was replicated in Uygur subjects (additive model, P = 0.042; dominant model, P = 0.102; allele model, P = 0.027) after adjustment in additive and dominant models, ORs were 1.327 (95% 1.07-1.646), P = 0.01 and 1.307 (95%CI 1.015-1.681, P = 0.038), respectively. G allele carriers exhibited significant lower urinary Na+ excretion rate than non-carriers in the Kazakh Chinese population (152.45 ± 76.04 uM/min vs 173.33 ± 90.02 uM/min, P = 0.007).
Our results suggest that the FURIN gene may be a candidate gene involved in human hypertension, and that the G allele of 1970C > G may be a modest risk factor for hypertension in Xinjiang Kazakh and Uygur populations.
高血压是一种受多种遗传和环境因素影响的复杂疾病。哈萨克族的高血压患病率相对较高。先前的研究表明,FURIN 基因可能在肾素-血管紧张素系统和维持钠电解质平衡中发挥关键作用。由于这些系统影响血压调节,我们认为 FURIN 是高血压的候选基因。本研究旨在系统研究 FURIN 基因的遗传变异与新疆哈萨克族原发性高血压之间的关系。
我们对 94 名高血压患者的 FURIN 基因所有外显子和启动子区域进行测序,以鉴定与该疾病相关的遗传变异。使用 TaqMan 聚合酶链反应方法对 934 名哈萨克族中国人的四个代表性常见单核苷酸多态性(SNP,-7315C>T、1970C>G、5604C>G、6262C>T)进行基因分型。在 1,219 名维吾尔族中国人中复制了一个 SNP(1970C>G)。
在 FURIN 基因中发现了 9 个新的和 7 个已知的单核苷酸多态性。结果表明,1970C>G 与哈萨克族中国人的高血压表型相关(加性模型,P=0.091;显性模型,P=0.031,等位基因模型,P=0.030),并且经过逻辑回归分析校正后,加性和显性模型的 OR 值分别为 1.451(95%CI 1.106-1.905,P=0.008)和 1.496(95%CI 1.103-2.028,P=0.01)。此外,在加性和显性模型中校正后,1970C>G 与维吾尔族人群高血压的关联在维吾尔族人群中得到复制(加性模型,P=0.042;显性模型,P=0.102;等位基因模型,P=0.027),加性模型的 OR 值为 1.327(95%CI 1.07-1.646),P=0.01,显性模型的 OR 值为 1.307(95%CI 1.015-1.681,P=0.038)。携带 G 等位基因的哈萨克族中国人的尿钠排泄率明显低于非携带者(152.45±76.04uM/min 与 173.33±90.02uM/min,P=0.007)。
我们的研究结果表明,FURIN 基因可能是人类高血压的候选基因,1970C>G 的 G 等位基因可能是新疆哈萨克族和维吾尔族人群高血压的适度风险因素。