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ADRB3 Gene Trp64Arg Polymorphism and Essential Hypertension: A Meta-Analysis Including 9555 Subjects

机译:ADRB3基因Trp64Arg多态性与原发性高血压:包括9555名受试者的荟萃分析

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摘要

>Background: Presence of the β3-Adrenergic receptor (ADRB3) gene Trp64Arg (T64A) polymorphism may be associated with an increased susceptibility for essential hypertension (EH). A clear consensus, however, has yet to be reached.>Objective and methods: To further elucidate the relationship between the ADRB3 gene Trp64Arg polymorphism and EH, a meta-analysis of 9,555 subjects aggregated from 16 individual studies was performed. The combined odds ratios (ORs) and their corresponding 95% confidence intervals (CI) were evaluated using either a random or fixed effect model.>Results: We found a marginally significant association between ADRB3 gene Trp64Arg polymorphism and EH in the whole population under the additive genetic model (OR: 1.200, 95% CI: 1.00–1.43, P = 0.049). Association within the Chinese subgroup, however, was significant under allelic (OR: 1.150, 95% CI: 1.002–1.320, P = 0.046), dominant (OR: 1.213, 95% CI: 1.005–1.464, P = 0.044), heterozygous (OR: 1.430, 95% CI:1.040–1.970, P = 0.03), and additive genetic models (OR: 1.280, 95% CI: 1.030–1.580, P = 0.02). A significant association was also found in the Caucasian subgroup under allelic (OR: 1.850, 95% CI: 1. 260–2.720, P = 0.002), dominant (OR: 2.004, 95% CI: 1.316–3.052, P = 0.001), heterozygous (OR: 2.220, 95% CI: 1.450–3.400, P = 0.0002), and additive genetic models (OR: 2.000, 95% CI: 1. 330–3.010, P = 0.0009).>Conclusions: The presence of the ADRB3 gene Trp64Arg polymorphism is positively associated with EH, especially in the Chinese and Caucasian population. The Arg allele carriers of ADRB3 gene Trp64Arg polymorphism may be at an increased risk for developing EH.
机译:>背景:β3-肾上腺素能受体(ADRB3)基因Trp64Arg(T64A)多态性的存在可能与原发性高血压(EH)的易感性增加有关。但是,尚未达成明确的共识。>目的和方法:为进一步阐明ADRB3基因Trp64Arg多态性与EH之间的关系,对16个独立研究汇总的9,555名受试者进行了荟萃分析。执行。使用随机或固定效应模型评估了组合的优势比(OR)及其对应的95%置信区间(CI)。>结果:我们发现ADRB3基因Trp64Arg多态性与EH之间存在显着的显着关联遗传模型(OR:1.200,95%CI:1.00-1.43,P = 0.049)在整个人群中的分布。然而,在亚等位基因(OR:1.150,95%CI:1.002–1.320,P = 0.046),显性(OR:1.213,95%CI:1.005–1.464,P = 0.044),杂合子下,中国亚组之间的关联显着。 (或:1.430,95%CI:1.040-1.970,P = 0.03)和加性遗传模型(或:1.280,95%CI:1.030-1.580,P = 0.02)。在白种人亚组中,等位基因(OR:1.850,95%CI:1. 260–2.720,P = 0.002),显性(OR:2.004,95%CI:1.316–3.052,P = 0.001)之间也存在显着关联。 ,杂合(OR:2.220、95%CI:1.450–3.400,P = 0.0002)和加性遗传模型(OR:2.000,95%CI:1.330–3.010,P = 0.0009)。>结论:< / strong> ADRB3基因Trp64Arg多态性的存在与EH正相关,尤其是在中国人和高加索人中。 ADRB3基因Trp64Arg多态性的Arg等位基因携带者罹患EH的风险可能增加。

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