Department of Geriatrics, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
PLoS One. 2012;7(1):e30214. doi: 10.1371/journal.pone.0030214. Epub 2012 Jan 17.
The α-adducin Gly460Trp (G460W) gene polymorphism may be associated with susceptibility to essential hypertension (EH), but this relationship remains controversial. In an attempt to resolve this issue, we conducted a meta-analysis.
Twenty-three separated studies involving 5939 EH patients and 5021 controls were retrieved and analyzed. Four ethnicities were included: Han, Kazakh, Mongolian, and She. Eighteen studies with 5087 EH patients and 4183 controls were included in the Han subgroup. Three studies with 636 EH patients and 462 controls were included in the Kazakh subgroup. The Mongolian subgroup was represented by only one study with 100 EH patients and 50 controls; similarly, only one study with 116 EH patients and 326 controls was available for the She subgroup. The pooled and ethnic group odds ratios (ORs) along with the corresponding 95% confidence intervals (95% CI) were assessed using a random effects model.
There was a significant association between the α-adducin G460W gene polymorphism and EH in the pooled Chinese population under both an allelic genetic model (OR: 1.12, 95% CI: 1.04-1.20, P = 0.002) and a recessive genetic model (OR: 1.40, 95% CI: 1.16-1.70, P = 0.0005). In contrast, no significant association between the α-adducin G460W gene polymorphism and EH was observed in the dominant genetic model (OR: 0.88, 95% CI: 0.72-1.09, P = 0.24). In stratified analysis by ethnicity, significantly increased risk was detected in the Han subgroup under an allelic genetic model (OR: 1.13, 95% CI: 1.04-1.23, P = 0.003) and a recessive genetic model (OR: 1.43, 95% CI: 1.17-1.75, P = 0.0006).
In a Chinese population of mixed ethnicity, the α-adducin G460W gene polymorphism was linked to EH susceptibility, most strongly in Han Chinese.
α-内收蛋白 Gly460Trp(G460W)基因多态性可能与原发性高血压(EH)的易感性有关,但这种关系仍存在争议。为了解决这个问题,我们进行了荟萃分析。
检索并分析了 23 项涉及 5939 例 EH 患者和 5021 例对照的独立研究。包括四个民族:汉族、哈萨克族、蒙古族和畲族。汉族亚组包括 18 项研究,共 5087 例 EH 患者和 4183 例对照。哈萨克亚组包括 3 项研究,共 636 例 EH 患者和 462 例对照。蒙古族亚组仅由一项研究,共 100 例 EH 患者和 50 例对照组成;同样,畲族亚组也仅由一项研究,共 116 例 EH 患者和 326 例对照组成。采用随机效应模型评估合并和各民族的比值比(OR)及其相应的 95%置信区间(95%CI)。
在合并的中国人群中,α-内收蛋白 G460W 基因多态性与 EH 之间存在显著关联,在等位基因遗传模型下(OR:1.12,95%CI:1.04-1.20,P=0.002)和隐性遗传模型下(OR:1.40,95%CI:1.16-1.70,P=0.0005)均如此。相反,在显性遗传模型下(OR:0.88,95%CI:0.72-1.09,P=0.24),α-内收蛋白 G460W 基因多态性与 EH 之间无显著关联。按种族进行分层分析,汉族亚组在等位基因遗传模型下(OR:1.13,95%CI:1.04-1.23,P=0.003)和隐性遗传模型下(OR:1.43,95%CI:1.17-1.75,P=0.0006)风险显著增加。
在中国混合人群中,α-内收蛋白 G460W 基因多态性与 EH 易感性相关,在汉族人群中相关性最强。