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dc.creatorHaslemo, Tore
dc.creatorEliasson, Erik
dc.creatorJukić, Marin
dc.creatorIngelman-Sundberg, Magnus
dc.creatorMolden, Espen
dc.date.accessioned2019-09-02T12:11:47Z
dc.date.available2019-09-02T12:11:47Z
dc.date.issued2019
dc.identifier.issn0306-5251
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/3364
dc.description.abstractAims CYP2D6*9, CYP2D6*10 and CYP2D6*41 are the most frequent reduced-function CYP2D6 alleles in Caucasians. Despite lacking in vivo evidence, they are collectively classified with an enzyme activity score of 0.5. Thus, the aim of this study was to compare the functional impact of CYP2D6*9, CYP2D6*10 and CYP2D6*41 on CYP2D6 metabolism in a large patient population. Methods A total of 1003 patients (mainly Caucasians) with data on CYP2D6 genotype and serum concentrations of venlafaxine and metabolites were included from a therapeutic drug monitoring service in Oslo, Norway. The O-desmethyl-to-N-desmethyl-venlafaxine metabolic ratio (MR) was applied as CYP2D6 biomarker and compared (Mann-Whitney) between carriers of CYP2D6*9-10 (merged) and CYP2D6*41, either combined with CYP2D6*1 or non-coding (null) alleles. MR subgroup estimates were obtained by multiple linear regression for calculations of CYP2D6*9-10 and CYP2D6*41 activity scores. Results MR was significantly lower in carriers of CYP2D6*41 than CYP2D6*9-10 (P lt 0.002). The majority of CYP2D6*41/null carriers (86.7%) had MR in the observed range of CYP2D6null/null carriers compared with the minority of CYP2D6*9-10/null carriers (17.4%). CYP2D6 genotype explained 60.7% of MR variability in the multivariate analysis providing subgroup estimates of 9.54 (95% CI; 7.45-12.20), 3.55 (2.06-6.10), 1.33 (0.87-2.05) and 0.47 (0.35-0.61) in carriers of CYP2D6*1/null (n = 269), CYP2D6*9-10/null (n = 17), CYP2D6*41/null (n = 30) and CYP2D6null/null (n = 95), respectively. Based on these estimates, the calculated activity score of CYP2D6*41 was 0.095 compared to 0.34 for CYP2D6*9-10. Conclusions CYP2D6 metabolism measured as the O/N-desmethylvenlafaxine ratio is significantly lower in Scandinavian carriers of CYP2D6*41 vs. CYP2D6*9-10. Thus, these alleles should be differentiated when classifying CYP2D6 phenotype from genotype.en
dc.publisherWiley, Hoboken
dc.rightsopenAccess
dc.sourceBritish Journal of Clinical Pharmacology
dc.subjectCYP2D6en
dc.subjectCYP2D6*10en
dc.subjectCYP2D6*41en
dc.subjectCYP2D6*9en
dc.subjectgenotypeen
dc.subjectphenotypeen
dc.titleSignificantly lower CYP2D6 metabolism measured as the O/N-desmethylvenlafaxine metabolic ratio in carriers of CYP2D6*41 versus CYP2D6*9 or CYP2D6*10: a study on therapeutic drug monitoring data from 1003 genotyped Scandinavian patientsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЕлиассон, Ерик; Молден, Еспен; Хаслемо, Торе; Јукић, Марин; Ингелман-Сундберг, Магнус;
dc.citation.volume85
dc.citation.issue1
dc.citation.spage194
dc.citation.epage201
dc.citation.other85(1): 194-201
dc.citation.rankM21
dc.identifier.wos000454096200017
dc.identifier.doi10.1111/bcp.13788
dc.identifier.pmid30312494
dc.identifier.scopus2-s2.0-85056270090
dc.identifier.fulltexthttps://farfar.pharmacy.bg.ac.rs//bitstream/id/1925/3362.pdf
dc.type.versionpublishedVersion


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