Evidence map›Paper›PMID 37732835›Full record

ArticlePharmacology research & perspectives2023

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

Sabrina Robert, Marc-Olivier Pilon, Essaïd Oussaïd, Maxime Meloche, Grégoire Leclair, Martin Jutras, Marie-Josée Gaulin, Ian Mongrain, David Busseuil, Jean-Claude Tardif and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. CYP2D6 Metabolizer Status and Mortality in Metoprolol Users.Clinical and translational science · 2026
    Article
  2. Article
  3. Safety and efficacy of amiodarone and dronedarone for early rhythm control in EAST-AFNET 4.Clinical research in cardiology : official journal of the German Cardiac Society · 2025
    Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Sabrina RobertFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Marc-Olivier PilonFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.ORCID 0000-0003-2718-6151
Essaïd OussaïdMontreal Heart Institute, Montreal, Quebec, Canada.
Maxime MelocheFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Grégoire LeclairFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Martin JutrasFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Marie-Josée GaulinMontreal Heart Institute, Montreal, Quebec, Canada.
Ian MongrainMontreal Heart Institute, Montreal, Quebec, Canada.
David BusseuilMontreal Heart Institute, Montreal, Quebec, Canada.
Jean-Claude TardifMontreal Heart Institute, Montreal, Quebec, Canada.
Marie-Pierre DubéMontreal Heart Institute, Montreal, Quebec, Canada.
Simon de DenusFaculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Montreal Heart Institute · CAUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AmiodaroneAdultBradycardiaCross-Sectional StudiesCytochrome P-450 CYP2D6Heart RateHumansMetoprololAmiodaroneCytochrome P-450 CYP2D6Metoprololamiodaronecytochrome P-450 CYP2D6drug interactionsmetoprololpharmacogeneticspharmacokinetics

Identifiers

PMID37732835
PMCPMC10512912
OpenAlexW4386910959

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.