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

• Main Authors: Sabrina Robert (Author), Marc‐Olivier Pilon (Author), Essaïd Oussaïd (Author), Maxime Meloche (Author), Grégoire Leclair (Author), Martin Jutras (Author), Marie‐Josée Gaulin (Author), Ian Mongrain (Author), David Busseuil (Author), Jean‐Claude Tardif (Author), Marie‐Pierre Dubé (Author), Simon deDenus (Author)
• Formato: Livro
• Publicado em: Wiley, 2023-10-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.
• Notes: 2052-1707; 10.1002/prp2.1137
• Keywords: amiodarone; cytochrome P‐450 CYP2D6; drug interactions; metoprolol; pharmacogenetics; pharmacokinetics; Therapeutics. Pharmacology; RM1-950
• Source: Pharmacology Research & Perspectives, Vol 11, Iss 5, Pp n/a-n/a (2023)

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.