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Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition.

Publication ,  Journal Article
Wang, P-F; Sharma, A; Montana, M; Neiner, A; Juriga, L; Reddy, KN; Tallchief, D; Blood, J; Kharasch, ED
Published in: Br J Clin Pharmacol
November 2022

AIMS: Methadone metabolism and clearance are determined principally by polymorphic cytochrome P4502B6 (CYP2B6). Some CYP2B6 allelic variants affect methadone metabolism in vitro and disposition in vivo. We assessed methadone metabolism by CYP2B6 minor variants in vitro. We also assessed the influence of CYP2B6 variants, and P450 oxidoreductase (POR) and CYP2C19 variants, on methadone clearance in surgical patients in vivo. METHODS: CYP2B6 and P450 oxidoreductase variants were coexpressed with cytochrome b5 . The metabolism of methadone racemate and enantiomers was measured at therapeutic concentrations and intrinsic clearances were determined. Adolescents receiving methadone for surgery were genotyped for CYP2B6, CYP2C19 and POR, and methadone clearance and metabolite formation clearance were determined. RESULTS: In vitro, CYP2B6.4 was more active than wild-type CYP2B6.1. CYPs 2B6.5, 2B6.6, 2B6.7, 2B6.9, 2B6.17, 2B6.19 and 2B6.26 were less active. CYPs 2B6.16 and 2B6.18 were inactive. CYP2B6.1 expressed with POR variants POR.28, POR.5 and P228L had lower rates of methadone metabolism than wild-type reductase. In vivo, methadone clinical clearance decreased linearly with the number of CYP2B6 slow metabolizer alleles, but was not different in CYP2C19 slow or rapid metabolizer phenotypes, or in carriers of the POR*28 allele. CONCLUSIONS: Several CYP2B6 and POR variants were slow metabolizers of methadone in vitro. Polymorphisms in CYP2B6, but not CYP2C19 or P450 reductase, affected methadone clearance in vivo. CYP2B6 polymorphisms 516G>T and 983T>C code for canonical loss of function variants and should be assessed when considering genetic influences on clinical methadone disposition. These complementary translational in vitro and in vivo results inform on pharmacogenetic variability affecting methadone disposition in patients.

Duke Scholars

Published In

Br J Clin Pharmacol

DOI

EISSN

1365-2125

Publication Date

November 2022

Volume

88

Issue

11

Start / End Page

4881 / 4893

Location

England

Related Subject Headings

  • Pharmacology & Pharmacy
  • Pharmacogenetics
  • Methadone
  • Cytochromes b
  • Cytochrome P-450 Enzyme System
  • Cytochrome P-450 CYP2B6
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
 

Citation

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Wang, P.-F., Sharma, A., Montana, M., Neiner, A., Juriga, L., Reddy, K. N., … Kharasch, E. D. (2022). Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition. Br J Clin Pharmacol, 88(11), 4881–4893. https://doi.org/10.1111/bcp.15393
Wang, Pan-Fen, Anshuman Sharma, Michael Montana, Alicia Neiner, Lindsay Juriga, Kavya Narayana Reddy, Dani Tallchief, Jane Blood, and Evan D. Kharasch. “Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition.Br J Clin Pharmacol 88, no. 11 (November 2022): 4881–93. https://doi.org/10.1111/bcp.15393.
Wang P-F, Sharma A, Montana M, Neiner A, Juriga L, Reddy KN, et al. Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition. Br J Clin Pharmacol. 2022 Nov;88(11):4881–93.
Wang, Pan-Fen, et al. “Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition.Br J Clin Pharmacol, vol. 88, no. 11, Nov. 2022, pp. 4881–93. Pubmed, doi:10.1111/bcp.15393.
Wang P-F, Sharma A, Montana M, Neiner A, Juriga L, Reddy KN, Tallchief D, Blood J, Kharasch ED. Methadone pharmacogenetics in vitro and in vivo: Metabolism by CYP2B6 polymorphic variants and genetic variability in paediatric disposition. Br J Clin Pharmacol. 2022 Nov;88(11):4881–4893.
Journal cover image

Published In

Br J Clin Pharmacol

DOI

EISSN

1365-2125

Publication Date

November 2022

Volume

88

Issue

11

Start / End Page

4881 / 4893

Location

England

Related Subject Headings

  • Pharmacology & Pharmacy
  • Pharmacogenetics
  • Methadone
  • Cytochromes b
  • Cytochrome P-450 Enzyme System
  • Cytochrome P-450 CYP2B6
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences