Literature DB >> 25187485

Gene variants in CYP2C19 are associated with altered in vivo bupropion pharmacokinetics but not bupropion-assisted smoking cessation outcomes.

Andy Z X Zhu1, Qian Zhou1, Lisa Sanderson Cox1, Jasjit S Ahluwalia1, Neal L Benowitz1, Rachel F Tyndale2.   

Abstract

Bupropion is used clinically to treat depression and to promote smoking cessation. It is metabolized by CYP2B6 to its active metabolite hydroxybupropion, yet alterations in CYP2B6 activity have little impact on bupropion plasma levels. Furthermore, less than 10% of a bupropion dose is excreted as urinary bupropion and its characterized metabolites hydroxybupropion, threohydrobupropion, and erythrohydrobupropion, suggesting that alternative metabolic pathways may exist. In vitro data suggested CYP2C19 could metabolize bupropion. The current study investigated the impact of functional CYP2C19 genetic variants on bupropion pharmacokinetics and treatment outcomes. In 42 healthy volunteers, CYP2C19*2 (a reduced activity allele) was associated with higher bupropion area under the plasma concentration-time curve (AUC), but similar hydroxybupropion AUC. The mean bupropion AUC was 771 versus 670 hours⋅ng/ml in individuals with and without CYP2C19*2, respectively (P = 0.017). CYP2C19*2 was also associated with higher threohydrobupropion and erythrohydrobupropion AUC (P < 0.005). Adjusting for CYP2B6 genotype did not alter these associations, and CYP2C19 variants did not alter the utility of the hydroxybupropion/bupropion ratio as a measure of CYP2B6 activity. Finally, in a clinical trial of 540 smokers, CYP2C19 genotype was not associated with smoking cessation outcomes, supporting the hypothesis that bupropion response is mediated by hydroxybupropion, which is not altered by CYP2C19. In conclusion, our study reports the first in vivo evidence that reduced CYP2C19 activity significantly increases the steady-state exposure to bupropion and its reductive metabolites threohydrobupropion and erythrohydrobupropion. These pharmacokinetic changes were not associated with differences in bupropion's ability to promote smoking cessation in smokers, but may influence the side effects and toxicity associated with bupropion.
Copyright © 2014 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2014        PMID: 25187485      PMCID: PMC4201132          DOI: 10.1124/dmd.114.060285

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  35 in total

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Journal:  Clin Pharmacol Ther       Date:  2005-06       Impact factor: 6.875

2.  A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants.

Authors:  Sarah C Sim; Carl Risinger; Marja-Liisa Dahl; Eleni Aklillu; Magnus Christensen; Leif Bertilsson; Magnus Ingelman-Sundberg
Journal:  Clin Pharmacol Ther       Date:  2006-01       Impact factor: 6.875

3.  Pharmacokinetics of bupropion and its metabolites in cigarette smokers versus nonsmokers.

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6.  A comparison of sustained-release bupropion and placebo for smoking cessation.

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Journal:  J Clin Psychiatry       Date:  1983-05       Impact factor: 4.384

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Authors:  S C Laizure; C L DeVane
Journal:  Ther Drug Monit       Date:  1985       Impact factor: 3.681

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Authors:  S C Laizure; C L DeVane; J T Stewart; C S Dommisse; A A Lai
Journal:  Clin Pharmacol Ther       Date:  1985-11       Impact factor: 6.875

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2.  Pharmacokinetics and Pharmacogenomics of Bupropion in Three Different Formulations with Different Release Kinetics in Healthy Human Volunteers.

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Journal:  AAPS J       Date:  2017-07-06       Impact factor: 4.009

Review 3.  Pharmacogenetic Optimization of Smoking Cessation Treatment.

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4.  zzm321990 zzm321990 Influence of CYP2B6 Pharmacogenetics on Stereoselective Inhibition and Induction of Bupropion Metabolism by Efavirenz in Healthy Volunteers.zzm321990 zzm321990

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5.  Common Polymorphisms of CYP2B6 Influence Stereoselective Bupropion Disposition.

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6.  Pharmacokinetics of Bupropion and Its Pharmacologically Active Metabolites in Pregnancy.

Authors:  Valentina M Fokina; Meixiang Xu; Erik Rytting; Sherif Z Abdel-Rahman; Holly West; Cheryl Oncken; Shannon M Clark; Mahmoud S Ahmed; Gary D V Hankins; Tatiana N Nanovskaya
Journal:  Drug Metab Dispos       Date:  2016-08-15       Impact factor: 3.922

7.  Bupropion therapy during pregnancy: the drug and its major metabolites in umbilical cord plasma and amniotic fluid.

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Review 8.  Pharmacotherapy for smoking cessation: effects by subgroup defined by genetically informed biomarkers.

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Review 9.  Pharmacogenetics factors influencing smoking cessation success; the importance of nicotine metabolism.

Authors:  Yadira X Perez-Paramo; Philip Lazarus
Journal:  Expert Opin Drug Metab Toxicol       Date:  2020-12-29       Impact factor: 4.481

10.  Stereoselective Metabolism of Bupropion to OH-bupropion, Threohydrobupropion, Erythrohydrobupropion, and 4'-OH-bupropion in vitro.

Authors:  Jennifer E Sager; Lauren S L Price; Nina Isoherranen
Journal:  Drug Metab Dispos       Date:  2016-08-05       Impact factor: 3.922

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