Pharmacogenomic markers of metoprolol and α-OH-metoprolol concentrations: a genome-wide association study

Author:

Laverdière Jean123ORCID,Meloche Maxime123ORCID,Provost Sylvie23,Leclair Grégoire1ORCID,Oussaïd Essaïd23,Jutras Martin1,Perreault Louis-Philippe Lemieux23ORCID,Valois Diane23,Mongrain Ian23,Busseuil David23,Rouleau Jean Lucien24,Tardif Jean-Claude234ORCID,Dubé Marie-Pierre234ORCID,Denus Simon de123

Affiliation:

1. Faculty of Pharmacy, Université de Montréal, H3T 1J4, Montreal, Quebec, Canada

2. Montreal Heart Institute, H1T 1C8, Montreal, Quebec, Canada

3. Université de Montreal Beaulieu-Saucier Pharmacogenomics Centre, H1T 1C8, Montreal, Quebec, Canada

4. Faculty of Medicine, Université de Montréal, H3T 1J4, Montreal, Quebec, Canada

Abstract

Aim: Few genome-wide association studies (GWASs) have been conducted to identify predictors of drug concentrations. The authors therefore sought to discover the pharmacogenomic markers involved in metoprolol pharmacokinetics. Patients & methods: The authors performed a GWAS of a cross-sectional study of 993 patients from the Montreal Heart Institute Biobank taking metoprolol. Results: A total of 391 and 444 SNPs reached the significance threshold of 5 × 10-8 for metoprolol and α-OH-metoprolol concentrations, respectively. All were located on chromosome 22 at or near the CYP2D6 gene, encoding CYP450 2D6, metoprolol's main metabolizing enzyme. Conclusion: The results reinforce previous findings of the importance of the CYP2D6 locus for metoprolol concentrations and confirm that large biobanks can be used to identify genetic determinants of drug pharmacokinetics at a GWAS significance level.

Funder

Canadian Institutes of Health Research

Fondation Institut de Cardiologie de Montréal

Université de Montréal Beaulieu-Saucier Chair in Pharmacogenomics

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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