Impact of amiodarone use on metoprolol concentrations, α-OH-metoprolol concentrations, metoprolol dosing and heart rate: A cross-sectional study.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sabrina Robert, Marc-Olivier Pilon, Essaïd Oussaïd, Maxime Meloche, Grégoire Leclair, Martin Jutras, Marie-Josée Gaulin, Ian Mongrain, David Busseuil, Jean-Claude Tardif, Marie-Pierre Dubé, Simon de Denus
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Abstract

Small studies suggest that amiodarone is a weak inhibitor of cytochrome P450 (CYP) 2D6. Inhibition of CYP2D6 leads to increases in concentrations of drugs metabolized by the enzyme, such as metoprolol. Considering that both metoprolol and amiodarone have β-adrenergic blocking properties and that the modest interaction between the two drugs would result in increased metoprolol concentrations, this could lead to a higher risk of bradycardia and atrioventricular block. The primary objective of this study was to evaluate whether metoprolol plasma concentrations collected at random timepoints from patients enrolled in the Montreal Heart Institute Hospital Cohort could be useful in identifying the modest pharmacokinetic interaction between amiodarone and metoprolol. We performed an analysis of a cross-sectional study, conducted as part of the Montreal Heart Institute Hospital Cohort. All participants were self-described "White" adults with metoprolol being a part of their daily pharmacotherapy regimen. Of the 999 patients being treated with metoprolol, 36 were also taking amiodarone. Amiodarone use was associated with higher metoprolol concentrations following adjustment for different covariates (p = .0132). Consistently, the association between amiodarone use and lower heart rate was apparent and significant after adjustment for all covariates under study (p = .0001). Our results highlight that single randomly collected blood samples can be leveraged to detect modest pharmacokinetic interactions.

胺碘酮的使用对美托洛尔浓度、α-OH美托洛尔的浓度、美托洛尔剂量和心率的影响:一项横断面研究。
小型研究表明胺碘酮是细胞色素P450(CYP)2D6的弱抑制剂。CYP2D6的抑制导致酶代谢的药物浓度增加,如美托洛尔。考虑到美托洛尔和胺碘酮都具有β-肾上腺素能阻断特性,并且两种药物之间的适度相互作用会导致美托洛尔浓度增加,这可能会导致更高的心动过缓和房室传导阻滞风险。本研究的主要目的是评估在蒙特利尔心脏研究所医院队列中随机收集的患者的美托洛尔血浆浓度是否有助于确定胺碘酮和美托洛尔之间的适度药代动力学相互作用。我们对一项横断面研究进行了分析,该研究是蒙特利尔心脏研究所医院队列的一部分。所有参与者都是自称“白人”的成年人,美托洛尔是他们日常药物治疗方案的一部分。在接受美托洛尔治疗的999名患者中,36人同时服用胺碘酮。调整不同协变量后,胺碘酮的使用与较高的美托洛尔浓度有关(p = .0132)。一致地,胺碘酮的使用与较低的心率之间的相关性在调整了所有研究的协变量后是明显和显著的(p = .0001)。我们的研究结果强调,可以利用随机采集的单个血液样本来检测适度的药代动力学相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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