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beta 1-adrenoceptor gene Arg389Gly polymorphism and essential hypertension risk in general population: a meta-analysis

机译:β1-肾上腺素受体基因Arg389Gly多态性与一般人群的原发性高血压风险:一项荟萃分析

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摘要

The beta 1-adrenoceptor (ADRB1) gene Arg389Gly polymorphism has been extensively studied as a candidate gene in essential hypertension (EH), but no consensus has been reached on the relationship between this polymorphism and EH risk. To systematically explore their possible association, a meta-analysis was conducted. All relevant case-control trials in English-language publications before 1 June 2012 were identified by searching the PubMed and Embase databases. Finally, eight articles met our inclusion criteria, including a total of 5,088 patients with EH and 6,515 controls. No evidence of publication bias was found. Fixed-effects model and random-effects model were applied for dichotomous outcomes to combine results from individual studies. Overall, the Gly allelic frequency of Arg389Gly polymorphism was significantly lower in EH subjects than that in controls (Gly versus Arg: P = 0.04, OR = 0.89, 95 % CI [0.80-1.00], P (heterogeneity) = 0.03, I (2) = 52 %, random-effects model; GlyGly + ArgGly versus ArgArg: P = 0.02, OR = 0.86, 95 % CI [0.76-0.97], P (heterogeneity) = 0.08 and I (2) = 42 %, random-effect model). Subgroup analysis by ethnicity detected this association only in East Asians. In sensitivity analysis, the study by Bengtsson K was recognized as the main cause of heterogeneity, which was the only one study with the diagnostic standard for EH as systolic blood pressure (SBP) a parts per thousand yen160 mmHg or diastolic blood pressure (DBP) a parts per thousand yen90 mmHg. We concluded that the Gly allele of ADRB1 Arg389Gly polymorphism might confer lower risk for EH, especially in East Asians.
机译:β1-肾上腺素能受体(ADRB1)基因Arg389Gly多态性已被广泛研究为原发性高血压(EH)的候选基因,但尚未就该多态性与EH风险之间的关系达成共识。为了系统地探讨它们的可能关联,进行了荟萃分析。通过搜索PubMed和Embase数据库,确定了2012年6月1日之前英语出版物中的所有相关病例对照试验。最后,有八篇文章符合我们的纳入标准,包括总共5,088名EH患者和6,515名对照。没有发现出版偏见的证据。将固定效应模型和随机效应模型用于二分结果,以合并各个研究的结果。总体而言,EH受试者中Arg389Gly多态性的Gly等位基因频率显着低于对照组(Gly与Arg:P = 0.04,OR = 0.89,95%CI [0.80-1.00],P(异质性)= 0.03,I( 2)= 52%,随机效应模型; GlyGly + ArgGly与ArgArg:P = 0.02,OR = 0.86,95%CI [0.76-0.97],P(异质性)= 0.08,I(2)= 42%,随机-效果模型)。按种族进行的亚组分析仅在东亚人中发现了这种关联。在敏感性分析中,Bengtsson K的研究被认为是异质性的主要原因,这是唯一一项以EH诊断标准为收缩压(SBP)千分之一或160 mmHg或舒张压(DBP)的研究。每千日元的零件90 mmHg。我们得出的结论是,ADRB1 Arg389Gly多态性的Gly等位基因可能会降低EH风险,尤其是在东亚地区。

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