首页> 外文期刊>Pharmacogenetics and genomics >Association between beta-1 and beta-2 adrenergic receptor gene polymorphisms and the response to beta-blockade in patients with stable congestive heart failure.
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Association between beta-1 and beta-2 adrenergic receptor gene polymorphisms and the response to beta-blockade in patients with stable congestive heart failure.

机译:稳定充血性心力衰竭患者中β-1和β-2肾上腺素能受体基因多态性与对β受体阻滞反应的关联。

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Previous studies have clearly demonstrated the beneficial effect of beta-blockers in patients with stable congestive heart failure (CHF). beta-blockers improve left ventricular ejection fraction (LVEF) and reduce cardiac mortality. However, there is an interindividual variability in the response to these agents. Two studies have suggested a possible impact of some functional betaAR gene polymorphisms on the effects of beta-blockade. The objective of the study is to analyse the association between genetic variations in the beta1 or the beta2 adrenoreceptor (AR) gene and the effects of beta-blockade in patients with stable CHF. We studied 199 consecutive patients with stable CHF not treated with beta-blockers. Before introduction of beta-blockers and 3 months after the maximal tolerated dose was reached, patients underwent an echocardiography and a radionuclide angiography. The beta1ARGly389Arg, beta1ARSer49Gly, beta2ARGly16Arg, beta2ARGln27Glu and beta2ARThr164Ile polymorphisms were determined: beta-blockade resulted in a significant decrease in heart rate, a significant increase in LVEF (from 30+/-10% to 40+/-13%, P<0.0001). There was no association between the five polymorphisms and heart rate or LVEF, either before or after beta-blockade. Heart rate and LVEF responses to beta-blockade were not associated with the beta1AR or the beta2AR polymorphisms. betaAR polymorphisms did not explain the interindividual variability in the response to beta-blockers.
机译:先前的研究清楚地证明了β受体阻滞剂对稳定充血性心力衰竭(CHF)患者的有益作用。 β受体阻滞剂可改善左心室射血分数(LVEF)并降低心脏死亡率。但是,对这些药物的反应存在个体差异。两项研究表明,某些功能betaAR基因多态性可能会对β受体阻滞作用产生影响。这项研究的目的是分析β1或β2肾上腺素能受体(AR)基因的遗传变异与稳定CHF患者的β受体阻滞作用之间的关系。我们研究了199例连续稳定的CHF患者,未接受β受体阻滞剂治疗。在引入β受体阻滞剂之前和达到最大耐受剂量后3个月,患者接受了超声心动图和放射性核素血管造影。确定了beta1ARGly389Arg,beta1ARSer49Gly,beta2ARGly16Arg,beta2ARGln27Glu和beta2ARThr164Ile多态性:beta阻滞导致心率显着下降,LVEF显着增加(从30 +/- 10%降至40 +/- 13%,P <0.0001 )。在β受体阻滞剂之前或之后,这五个多态性与心率或LVEF之间没有关联。心率和LVEF对β-受体阻滞的反应与beta1AR或beta2AR多态性无关。 betaAR多态性不能解释对β受体阻滞剂的个体差异。

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