State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Ruijin Second Road 197, Shanghai 200025, China.
Clin Chim Acta. 2010 Oct 9;411(19-20):1491-5. doi: 10.1016/j.cca.2010.06.004. Epub 2010 Jun 10.
Confirmation of genome wide association (GWA) results in independent samples has recently become new research tendency.
We focused on 8 positive top polymorphisms identified in the to-date largest hypertension GWA study and determined whether these polymorphisms were associated with hypertension among Han Chinese. Genotyping was performed among 548 patients diagnosed with essential hypertension and 560 age- and gender-matched controls using ligase detection reactions method. Statistical analyses were conducted using Logistic regression and genotype risk score.
Except for a rare polymorphism (rs653178), no deviation from Hardy-Weinberg equilibrium was observed for genotype distributions of others. There was significant differences in the genotype/allele distribution (P=0.006/P=0.002) of rs16998073 in FGF5 (fibroblast growth factor 5) upstream and the allele distribution (P=0.037) of rs16948048 in ZNF652 (zinc finger protein 652) upstream between hypertensive patients and controls. Strong significance was also noted under assumption of different genetic models for the two coalescent polymorphisms, even after controlling covariates of interest. For example, rs16998073 had a 72% increased risk for hypertension under the co-dominant model (95% confidence interval: 1.20-2.45; P=0.003). However, construction of genetic risk scores on common polymorphisms did not reveal any significance with both hypertension and blood pressure, suggesting that contribution of these polymorphisms to hypertension moderate or small in magnitude.
Our results implicate variation in FGF5 and ZNF652 gene upstream regions with altered susceptibility to hypertension in Han Chinese.
最近,在独立样本中确认全基因组关联(GWA)结果已成为新的研究趋势。
我们专注于迄今为止最大的高血压 GWA 研究中确定的 8 个阳性顶级多态性,并确定这些多态性是否与汉族人群中的高血压有关。使用连接酶检测反应方法,在 548 名确诊为原发性高血压的患者和 560 名年龄和性别匹配的对照中进行基因分型。使用 Logistic 回归和基因型风险评分进行统计分析。
除了罕见的多态性(rs653178)外,其他多态性的基因型分布均未偏离 Hardy-Weinberg 平衡。FGF5(成纤维细胞生长因子 5)上游的 rs16998073 和 ZNF652(锌指蛋白 652)上游的 rs16948048 基因型/等位基因分布(P=0.006/P=0.002)和等位基因分布(P=0.037)在高血压患者和对照组之间存在显著差异。在假设两种合并多态性具有不同遗传模型的情况下,即使控制了感兴趣的协变量,也观察到了强烈的显著性。例如,rs16998073 在共显性模型下使高血压的风险增加了 72%(95%置信区间:1.20-2.45;P=0.003)。然而,常见多态性的遗传风险评分构建并未显示出与高血压和血压相关的任何意义,表明这些多态性对高血压的贡献适中或较小。
我们的结果表明,FGF5 和 ZNF652 基因上游区域的变异与汉族人群中高血压的易感性改变有关。