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CYP2D6基因的遗传变异与β受体阻滞剂使用者较低的心率和血压相关。

Genetic variation in the CYP2D6 gene is associated with a lower heart rate and blood pressure in beta-blocker users.

作者信息

Bijl M J, Visser L E, van Schaik R H N, Kors J A, Witteman J C M, Hofman A, Vulto A G, van Gelder T, Stricker B H Ch

机构信息

Department of Epidemiology and Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Clin Pharmacol Ther. 2009 Jan;85(1):45-50. doi: 10.1038/clpt.2008.172. Epub 2008 Sep 10.

Abstract

Several beta-blockers are metabolized by the polymorphic enzyme cytochrome P450 2D6 (CYP2D6). CYP2D64 is the main polymorphism leading to decreased enzyme activity. The clinical significance of impaired elimination of beta-blockers is controversial, and most studies suffer from inclusion of small numbers of poor metabolizers (PMs) of CYP2D6. In this study, the association between CYP2D64 and blood pressure or heart rate was examined in 1,533 users of beta-blockers in the Rotterdam Study, a population-based cohort study. In CYP2D6 *4/*4 PMs, the adjusted heart rate in metoprolol users was 8.5 beats/min lower compared with *1/*1 extensive metabolizers (EMs) (P < 0.001), leading to an increased risk of bradycardia in PMs (odds ratio = 3.86; 95% confidence interval 1.68-8.86; P = 0.0014). The diastolic blood pressure in PMs was 5.4 mm Hg lower in users of beta-blockers metabolized by CYP2D6 (P = 0.017) and 4.8 mm Hg lower in metoprolol users (P = 0.045) compared with EMs. PMs are at increased risk of bradycardia.

摘要

几种β受体阻滞剂由多态性酶细胞色素P450 2D6(CYP2D6)代谢。CYP2D64是导致酶活性降低的主要多态性。β受体阻滞剂消除受损的临床意义存在争议,并且大多数研究存在纳入少量CYP2D6慢代谢者(PMs)的问题。在这项研究中,在基于人群的队列研究鹿特丹研究中,对1533名β受体阻滞剂使用者进行了CYP2D64与血压或心率之间关联的研究。在CYP2D6 *4/4 PMs中,美托洛尔使用者的校正心率比1/*1快代谢者(EMs)低8.5次/分钟(P<0.001),导致PMs发生心动过缓的风险增加(比值比=3.86;95%置信区间1.68 - 8.86;P = 0.0014)。与EMs相比,CYP2D6代谢的β受体阻滞剂使用者中PMs的舒张压低5.4 mmHg(P = 0.017),美托洛尔使用者中低4.8 mmHg(P = 0.045)。PMs发生心动过缓的风险增加。

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