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Volumn 88, Issue 5, 2010, Pages 643-651

Assessment of activity levels for CYP2D6*1, CYP2D6*2, and CYP2D6*41 genes by population pharmacokinetics of dextromethorphan

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 2D6; DEXTROMETHORPHAN; ANTITUSSIVE AGENT; DEXTRORPHAN;

EID: 77958476379     PISSN: 00099236     EISSN: 15326535     Source Type: Journal    
DOI: 10.1038/clpt.2010.137     Document Type: Article
Times cited : (57)

References (45)
  • 1
    • 0037998731 scopus 로고    scopus 로고
    • Physiologically based modelling of inhibition of metabolism and assessment of the relative potency of drug and metabolite: Dextromethorphan vs dextrorphan using quinidine inhibition
    • Moghadamnia, A.A., Rostami-Hodjegan, A., Abdul-Manap, R., Wright, C.E., Morice, A.H. & Tucker, G.T. Physiologically based modelling of inhibition of metabolism and assessment of the relative potency of drug and metabolite: dextromethorphan vs. dextrorphan using quinidine inhibition. Br. J. Clin. Pharmacol. 56, 57-67 (2003).
    • (2003) Br. J. Clin. Pharmacol. , vol.56 , pp. 57-67
    • Moghadamnia, A.A.1    Rostami-Hodjegan, A.2    Abdul-Manap, R.3    Wright, C.E.4    Morice, A.H.5    Tucker, G.T.6
  • 2
    • 0029853347 scopus 로고    scopus 로고
    • The infuence of CYP2D6 polymorphism and quinidine on the disposition and antitussive efect of dextromethorphan in humans
    • Capon, D.A., Bochner, F., Kerry, N., Mikus, G., Danz, C. & Somogyi, A.A. The infuence of CYP2D6 polymorphism and quinidine on the disposition and antitussive efect of dextromethorphan in humans. Clin. Pharmacol. Ther. 60, 295-307 (1996).
    • (1996) Clin. Pharmacol. Ther. , vol.60 , pp. 295-307
    • Capon, D.A.1    Bochner, F.2    Kerry, N.3    Mikus, G.4    Danz, C.5    Somogyi, A.A.6
  • 3
    • 22344435448 scopus 로고    scopus 로고
    • Dextromethorphan to dextrorphan urinary metabolic ratio does not refect dextromethorphan oral clearance
    • Borges, S., Li, L., Hamman, M.A., Jones, D.R., Hall, S.D. & Gorski, J.C. Dextromethorphan to dextrorphan urinary metabolic ratio does not refect dextromethorphan oral clearance. Drug Metab. Dispos. 33, 1052-1055 (2005).
    • (2005) Drug Metab. Dispos. , vol.33 , pp. 1052-1055
    • Borges, S.1    Li, L.2    Hamman, M.A.3    Jones, D.R.4    Hall, S.D.5    Gorski, J.C.6
  • 4
    • 0027265750 scopus 로고
    • CYP2D6-and CYP3A-dependent metabolism of dextromethorphan in humans
    • Jacqz-Aigrain, E., Funck-Brentano, C. & Cresteil, T. CYP2D6-and CYP3A-dependent metabolism of dextromethorphan in humans. Pharmacogenetics 3, 197-204 (1993).
    • (1993) Pharmacogenetics , vol.3 , pp. 197-204
    • Jacqz-Aigrain, E.1    Funck-Brentano, C.2    Cresteil, T.3
  • 5
    • 0018975120 scopus 로고
    • The urinary excretion of dextromethorphan and three metabolites in dogs and humans
    • Barnhart, J.W. The urinary excretion of dextromethorphan and three metabolites in dogs and humans. Toxicol. Appl. Pharmacol. 55, 43-48 (1980).
    • (1980) Toxicol. Appl. Pharmacol. , vol.55 , pp. 43-48
    • Barnhart, J.W.1
  • 6
    • 0034468888 scopus 로고    scopus 로고
    • In-vivo indices of CYP2D6 activity: Comparison of dextromethorphan metabolic ratios in 4-h urine and 3-h plasma
    • Chládek, J., Zimová, G., Beránek, M. & Martínková, J. In-vivo indices of CYP2D6 activity: comparison of dextromethorphan metabolic ratios in 4-h urine and 3-h plasma. Eur. J. Clin. Pharmacol. 56, 651-657 (2000).
    • (2000) Eur. J. Clin. Pharmacol. , vol.56 , pp. 651-657
    • Chládek, J.1    Zimová, G.2    Beránek, M.3    Martí nková, J.4
  • 7
    • 33947180388 scopus 로고    scopus 로고
    • Evaluation of probe drugs and pharmacokinetic metrics for CYP2D6 phenotyping
    • Frank, D., Jaehde, U. & Fuhr, U. Evaluation of probe drugs and pharmacokinetic metrics for CYP2D6 phenotyping. Eur. J. Clin. Pharmacol. 63, 321-333 (2007).
    • (2007) Eur. J. Clin. Pharmacol. , vol.63 , pp. 321-333
    • Frank, D.1    Jaehde, U.2    Fuhr, U.3
  • 9
    • 0036339071 scopus 로고    scopus 로고
    • Unique CYP2D6 activity distribution and genotype-phenotype discordance in black Americans
    • Gaedigk, A., Bradford, L.D., Marcucci, K.A. & Leeder, J.S. Unique CYP2D6 activity distribution and genotype-phenotype discordance in black Americans. Clin. Pharmacol. Ther. 72, 76-89 (2002).
    • (2002) Clin. Pharmacol. Ther. , vol.72 , pp. 76-89
    • Gaedigk, A.1    Bradford, L.D.2    Marcucci, K.A.3    Leeder, J.S.4
  • 10
    • 73949123393 scopus 로고    scopus 로고
    • Intermediate metabolizer: Increased side efects in psychoactive drug therapy. The key to cost-efectiveness of pretreatment CYP2D6 screening?
    • Laika, B., Leucht, S., Heres, S. & Steimer, W. Intermediate metabolizer: increased side efects in psychoactive drug therapy. The key to cost-efectiveness of pretreatment CYP2D6 screening? Pharmacogenomics J. 9, 395-403 (2009).
    • (2009) Pharmacogenomics J. , vol.9 , pp. 395-403
    • Laika, B.1    Leucht, S.2    Heres, S.3    Steimer, W.4
  • 11
    • 3142519666 scopus 로고    scopus 로고
    • Pharmacogenetics of antidepressants and antipsychotics: The contribution of allelic variations to the phenotype of drug response
    • Kirchheiner, J. et al. Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response. Mol. Psychiatry 9, 442-473 (2004).
    • (2004) Mol. Psychiatry , vol.9 , pp. 442-473
    • Kirchheiner, J.1
  • 12
    • 38349163777 scopus 로고    scopus 로고
    • Efects of the CYP2D6 gene duplication on the pharmacokinetics and pharmacodynamics of tramadol
    • Kirchheiner, J., Keulen, J.T., Bauer, S., Roots, I. & Brockmöller, J. Efects of the CYP2D6 gene duplication on the pharmacokinetics and pharmacodynamics of tramadol. J. Clin. Psychopharmacol. 28, 78-83 (2008).
    • (2008) J. Clin. Psychopharmacol. , vol.28 , pp. 78-83
    • Kirchheiner, J.1    Keulen, J.T.2    Bauer, S.3    Roots, I.4    Brockmöller, J.5
  • 13
    • 34547644659 scopus 로고    scopus 로고
    • Pharmacokinetics of codeine and its metabolite morphine in ultra-rapid metabolizers due to CYP2D6 duplication
    • Kirchheiner, J. et al. Pharmacokinetics of codeine and its metabolite morphine in ultra-rapid metabolizers due to CYP2D6 duplication. Pharmacogenomics J. 7, 257-265 (2007).
    • (2007) Pharmacogenomics J. , vol.7 , pp. 257-265
    • Kirchheiner, J.1
  • 14
    • 0034894010 scopus 로고    scopus 로고
    • CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: A frst step towards subpopulation-specifc dosages
    • Kirchheiner, J. et al. CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: a frst step towards subpopulation-specifc dosages. Acta Psychiatr. Scand. 104, 173-192 (2001).
    • (2001) Acta Psychiatr. Scand. , vol.104 , pp. 173-192
    • Kirchheiner, J.1
  • 15
    • 0022338958 scopus 로고
    • Polymorphic dextromethorphan metabolism: Co-segregation of oxidative O-demethylation with debrisoquin hydroxylation
    • Schmid, B., Bircher, J., Preisig, R. & Küpfer, A. Polymorphic dextromethorphan metabolism: co-segregation of oxidative O-demethylation with debrisoquin hydroxylation. Clin. Pharmacol. Ther. 38, 618-624 (1985).
    • (1985) Clin. Pharmacol. Ther. , vol.38 , pp. 618-624
    • Schmid, B.1    Bircher, J.2    Preisig, R.3    Küpfer, A.4
  • 16
    • 0028018821 scopus 로고
    • The infuence of environmental and genetic factors on CYP2D6, CYP1A2 and UDP-glucuronosyltransferases in man using sparteine, cafeine, and paracetamol as probes
    • Bock, K.W. et al. The infuence of environmental and genetic factors on CYP2D6, CYP1A2 and UDP-glucuronosyltransferases in man using sparteine, cafeine, and paracetamol as probes. Pharmacogenetics 4, 209-218 (1994).
    • (1994) Pharmacogenetics , vol.4 , pp. 209-218
    • Bock, K.W.1
  • 17
    • 0031038038 scopus 로고    scopus 로고
    • Cytochrome P450 2D6 variants in a Caucasian population: Allele frequencies and phenotypic consequences
    • Sachse, C., Brockmöller, J., Bauer, S. & Roots, I. Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. Am. J. Hum. Genet. 60, 284-295 (1997).
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 284-295
    • Sachse, C.1    Brockmöller, J.2    Bauer, S.3    Roots, I.4
  • 18
    • 4344613464 scopus 로고    scopus 로고
    • Allele-specifc change of concentration and functional gene dose for the prediction of steady-state serum concentrations of amitriptyline and nortriptyline in CYP2C19 and CYP2D6 extensive and intermediate metabolizers
    • Steimer, W. et al. Allele-specifc change of concentration and functional gene dose for the prediction of steady-state serum concentrations of amitriptyline and nortriptyline in CYP2C19 and CYP2D6 extensive and intermediate metabolizers. Clin. Chem. 50, 1623-1633 (2004).
    • (2004) Clin. Chem. , vol.50 , pp. 1623-1633
    • Steimer, W.1
  • 19
    • 0030909597 scopus 로고    scopus 로고
    • A model with separate hepato-portal compartment ("frst-pass" model): Ftting to plasma concentration-time profles in humans
    • Piotrovskij, V. & Van Peer, A. A model with separate hepato-portal compartment ("frst-pass" model): ftting to plasma concentration-time profles in humans. Pharm. Res. 14, 230-237 (1997).
    • (1997) Pharm. Res. , vol.14 , pp. 230-237
    • Piotrovskij, V.1    Van Peer, A.2
  • 22
    • 33947314331 scopus 로고    scopus 로고
    • Large scale docking of amines with CYP2D6 and scoring for druglike properties-towards defning the scope of the chemical defense against foreign amines in humans
    • Costache, A.D., Trawick, D., Bohl, D. & Sem, D.S. Amine DB: large scale docking of amines with CYP2D6 and scoring for druglike properties-towards defning the scope of the chemical defense against foreign amines in humans. Xenobiotica. 37, 221-245 (2007).
    • (2007) Xenobiotica. , vol.37 , pp. 221-245
    • Costache, A.D.1    Trawick, D.2    Bohl, D.3    Sem Amine S D, D.B.4
  • 23
    • 0026542989 scopus 로고
    • Substrate recognition sites in cytochrome P450 family 2 (CYP2) proteins inferred from comparative analyses of amino acid and coding nucleotide sequences
    • Gotoh, O. Substrate recognition sites in cytochrome P450 family 2 (CYP2) proteins inferred from comparative analyses of amino acid and coding nucleotide sequences. J. Biol. Chem. 267, 83-90 (1992).
    • (1992) J. Biol. Chem. , vol.267 , pp. 83-90
    • Gotoh, O.1
  • 24
    • 0036897469 scopus 로고    scopus 로고
    • Expression purifcation, biochemical characterization, and comparative function of human cytochrome P450 2D6.1, 2D6.2, 2D6.10, and 2D6.17 allelic isoforms
    • Yu, A., Kneller, B.M., Rettie, A.E. & Haining, R.L. Expression, purifcation, biochemical characterization, and comparative function of human cytochrome P450 2D6.1, 2D6.2, 2D6.10, and 2D6.17 allelic isoforms. J. Pharmacol. Exp. Ther. 303, 1291-1300 (2002).
    • (2002) J. Pharmacol. Exp. Ther. , vol.303 , pp. 1291-1300
    • Yu, A.1    Kneller, B.M.2    Rettie, A.E.3    Haining, R.L.4
  • 25
    • 61449111025 scopus 로고    scopus 로고
    • Pinoline may be used as a probe for CYP2D6 activity
    • Jiang, X.L., Shen, H.W. & Yu, A.M. Pinoline may be used as a probe for CYP2D6 activity. Drug Metab. Dispos. 37, 443-446 (2009).
    • (2009) Drug Metab. Dispos. , vol.37 , pp. 443-446
    • Jiang, X.L.1    Shen, H.W.2    Yu, A.M.3
  • 26
    • 4644295005 scopus 로고    scopus 로고
    • Efect of genetic polymorphism on the metabolism of endogenous neuroactive substances, progesterone and p-tyramine, catalyzed by CYP2D6
    • Niwa, T. et al. Efect of genetic polymorphism on the metabolism of endogenous neuroactive substances, progesterone and p-tyramine, catalyzed by CYP2D6. Brain Res. Mol. Brain Res. 129, 117-123 (2004).
    • (2004) Brain Res. Mol. Brain Res. , vol.129 , pp. 117-123
    • Niwa, T.1
  • 27
    • 0036828964 scopus 로고    scopus 로고
    • The molecular and enzyme kinetic basis for the diminished activity of the cytochrome P450 2D6.17 (CYP2D6.17) variant. Potential implications for CYP2D6 phenotyping studies and the clinical use of CYP2D6 substrate drugs in some African populations
    • Bapiro, T.E., Hasler, J.A., Ridderström, M. & Masimirembwa, C.M. The molecular and enzyme kinetic basis for the diminished activity of the cytochrome P450 2D6.17 (CYP2D6.17) variant. Potential implications for CYP2D6 phenotyping studies and the clinical use of CYP2D6 substrate drugs in some African populations. Biochem. Pharmacol. 64, 1387-1398 (2002).
    • (2002) Biochem. Pharmacol. , vol.64 , pp. 1387-1398
    • Bapiro, T.E.1    Hasler, J.A.2    Ridderström, M.3    Masimirembwa, C.M.4
  • 28
    • 0036233696 scopus 로고    scopus 로고
    • Characterization of cytochrome P450 2D6.1 (CYP2D6.1), CYP2D6.2, and CYP2D6.17 activities toward model CYP2D6 substrates dextromethorphan, bufuralol, and debrisoquine
    • Marcucci, K.A., Pearce, R.E., Crespi, C., Steimel, D.T., Leeder, J.S. & Gaedigk, A. Characterization of cytochrome P450 2D6.1 (CYP2D6.1), CYP2D6.2, and CYP2D6.17 activities toward model CYP2D6 substrates dextromethorphan, bufuralol, and debrisoquine. Drug Metab. Dispos. 30, 595-601 (2002).
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 595-601
    • Marcucci, K.A.1    Pearce, R.E.2    Crespi, C.3    Steimel, D.T.4    Leeder, J.S.5    Gaedigk, A.6
  • 29
    • 65549132771 scopus 로고    scopus 로고
    • Methodological uncertainty in quantitative prediction of human hepatic clearance from in vitro experimental systems
    • Hallifax, D. & Houston, J.B. Methodological uncertainty in quantitative prediction of human hepatic clearance from in vitro experimental systems. Curr. Drug Metab. 10, 307-321 (2009).
    • (2009) Curr. Drug Metab. , vol.10 , pp. 307-321
    • Hallifax, D.1    Houston, J.B.2
  • 30
    • 0032922093 scopus 로고    scopus 로고
    • CYP2D6 polymorphism in a Gabonese population: Contribution of the CYP2D6*2 and CYP2D6*17 alleles to the high prevalence of the intermediate metabolic phenotype
    • Panserat, S., Sica, L., Gérard, N., Mathieu, H., Jacqz-Aigrain, E. & Krishnamoorthy, R. CYP2D6 polymorphism in a Gabonese population: contribution of the CYP2D6*2 and CYP2D6*17 alleles to the high prevalence of the intermediate metabolic phenotype. Br. J. Clin. Pharmacol. 47, 121-124 (1999).
    • (1999) Br. J. Clin. Pharmacol. , vol.47 , pp. 121-124
    • Panserat, S.1    Sica, L.2    Gérard, N.3    Mathieu, H.4    Jacqz-Aigrain, E.5    Krishnamoorthy, R.6
  • 31
    • 33749005081 scopus 로고    scopus 로고
    • Impaired expression of CYP2D6 in intermediate metabolizers carrying the *41 allele caused by the intronic SNP 2988GA: Evidence for modulation of splicing events
    • Toscano, C. et al. Impaired expression of CYP2D6 in intermediate metabolizers carrying the *41 allele caused by the intronic SNP 2988GA: evidence for modulation of splicing events. Pharmacogenet. Genomics 16, 755-766 (2006).
    • (2006) Pharmacogenet. Genomics , vol.16 , pp. 755-766
    • Toscano, C.1
  • 32
    • 3543014421 scopus 로고    scopus 로고
    • A novel intronic mutation, 2988GA, with high predictivity for impaired function of cytochrome P450 2D6 in white subjects
    • Raimundo, S. et al. A novel intronic mutation, 2988GA, with high predictivity for impaired function of cytochrome P450 2D6 in white subjects. Clin. Pharmacol. Ther. 76, 128-138 (2004).
    • (2004) Clin. Pharmacol. Ther. , vol.76 , pp. 128-138
    • Raimundo, S.1
  • 33
    • 61549083067 scopus 로고    scopus 로고
    • Prediction of the efects of genetic polymorphism on the pharmacokinetics of CYP2C9 substrates from in vitro data
    • Kusama, M., Maeda, K., Chiba, K., Aoyama, A. & Sugiyama, Y. Prediction of the efects of genetic polymorphism on the pharmacokinetics of CYP2C9 substrates from in vitro data. Pharm. Res. 26, 822-835 (2009).
    • (2009) Pharm. Res. , vol.26 , pp. 822-835
    • Kusama, M.1    Maeda, K.2    Chiba, K.3    Aoyama, A.4    Sugiyama, Y.5
  • 34
    • 34547165040 scopus 로고    scopus 로고
    • Comparative metabolic capabilities and inhibitory profles of CYP2D6.1, CYP2D6.10, and CYP2D6.17
    • Shen, H. et al. Comparative metabolic capabilities and inhibitory profles of CYP2D6.1, CYP2D6.10, and CYP2D6.17. Drug Metab. Dispos. 35, 1292-1300 (2007).
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 1292-1300
    • Shen, H.1
  • 35
    • 12344305178 scopus 로고    scopus 로고
    • Intravenous dextromethorphan to human volunteers: Relationship between pharmacokinetics and anti-hyperalgesic efect
    • Duedahl, T.H., Dirks, J., Petersen, K.B., Romsing, J., Larsen, N.E. & Dahl, J.B. Intravenous dextromethorphan to human volunteers: relationship between pharmacokinetics and anti-hyperalgesic efect. Pain 113, 360-368 (2005).
    • (2005) Pain , vol.113 , pp. 360-368
    • Duedahl, T.H.1    Dirks, J.2    Petersen, K.B.3    Romsing, J.4    Larsen, N.E.5    Dahl, J.B.6
  • 37
    • 0028870990 scopus 로고
    • Safety tolerability, and pharmacokinetics of the N-methyl-D-aspartate antagonist dextrorphan in patients with acute stroke
    • Albers, G.W., Atkinson, R.P., Kelley, R.E. & Rosenbaum, D.M. Safety, tolerability, and pharmacokinetics of the N-methyl-D-aspartate antagonist dextrorphan in patients with acute stroke. Dextrorphan Study Group. Stroke. 26, 254-258 (1995).
    • (1995) Dextrorphan Study Group. Stroke. , vol.26 , pp. 254-258
    • Albers, G.W.1    Atkinson, R.P.2    Kelley, R.E.3    Rosenbaum, D.M.4
  • 38
    • 0031740452 scopus 로고    scopus 로고
    • Bioavailability of dextromethorphan (as dextrorphan) from sustained release formulations in the presence of guaifenesin in human volunteers
    • Demirbas, S., Reyderman, L. & Stavchansky, S. Bioavailability of dextromethorphan (as dextrorphan) from sustained release formulations in the presence of guaifenesin in human volunteers. Biopharm. Drug Dispos. 19, 541-545 (1998).
    • (1998) Biopharm. Drug Dispos. , vol.19 , pp. 541-545
    • Demirbas, S.1    Reyderman, L.2    Stavchansky, S.3
  • 39
    • 0033933541 scopus 로고    scopus 로고
    • Efect of gender, sex hormones, time variables and physiological urinary pH on apparent CYP2D6 activity as assessed by metabolic ratios of marker substrates
    • Labbé, L. et al. Efect of gender, sex hormones, time variables and physiological urinary pH on apparent CYP2D6 activity as assessed by metabolic ratios of marker substrates. Pharmacogenetics 10, 425-438 (2000).
    • (2000) Pharmacogenetics , vol.10 , pp. 425-438
    • Labbé, L.1
  • 40
    • 77957264624 scopus 로고    scopus 로고
    • Pharmacogenetic-based clinical scores: A useful, simple tool to predict tamoxifen-based CYP2D6 phenotype? J
    • Fuhr, U. Pharmacogenetic-based clinical scores: a useful, simple tool to predict tamoxifen-based CYP2D6 phenotype? J. Clin. Pharmacol. 50, 370-372 (2010).
    • (2010) Clin. Pharmacol. , vol.50 , pp. 370-372
    • Fuhr, U.1
  • 41
    • 40049101739 scopus 로고    scopus 로고
    • Assessment of urinary mephenytoin metrics to phenotype for CYP2C19 and CYP2B6 activity
    • Klaassen, T. et al. Assessment of urinary mephenytoin metrics to phenotype for CYP2C19 and CYP2B6 activity. Eur. J. Clin. Pharmacol. 64, 387-398 (2008).
    • (2008) Eur. J. Clin. Pharmacol. , vol.64 , pp. 387-398
    • Klaassen, T.1
  • 43
    • 45549095805 scopus 로고    scopus 로고
    • Efect of an antiretroviral regimen containing ritonavir boosted lopinavir on intestinal and hepatic CYP3A. CYP2D6 and P-glycoprotein in HIV-infected patients
    • Wyen, C. et al. Efect of an antiretroviral regimen containing ritonavir boosted lopinavir on intestinal and hepatic CYP3A, CYP2D6 and P-glycoprotein in HIV-infected patients. Clin. Pharmacol. Ther. 84, 75-82 (2008).
    • (2008) Clin. Pharmacol. Ther. , vol.84 , pp. 75-82
    • Wyen, C.1
  • 44
    • 33846643134 scopus 로고    scopus 로고
    • Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: Characterization of gene duplication events
    • Gaedigk, A. et al. Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: characterization of gene duplication events. Clin. Pharmacol. Ther. 81, 242-251 (2007).
    • (2007) Clin. Pharmacol. Ther. , vol.81 , pp. 242-251
    • Gaedigk, A.1


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