How Can Drug Metabolism and Transporter Genetics Inform Psychotropic Prescribing?

被引:21
|
作者
Henriques, Beatriz Carvalho [1 ]
Yang, Esther H. [1 ,2 ]
Lapetina, Diego [1 ,2 ]
Carr, Michael S. [1 ]
Yavorskyy, Vasyl [1 ]
Hague, Joshua [1 ,2 ]
Aitchison, Katherine J. [1 ,2 ,3 ]
机构
[1] Univ Alberta, Dept Psychiat, Edmonton, AB, Canada
[2] Univ Alberta, Dept Med Genet, Edmonton, AB, Canada
[3] Univ Alberta, Neurosci & Mental Hlth Inst, Edmonton, AB, Canada
关键词
pharmacogenomics (PGx); drug metabolism; drug transporters; cytochrome P450 enzymes; psychotropic drugs; PHARMACOGENETICS IMPLEMENTATION CONSORTIUM; SEROTONIN REUPTAKE INHIBITORS; CATECHOL-O-METHYLTRANSFERASE; FLAVIN-CONTAINING MONOOXYGENASES; HUMAN CYTOCHROME-P450 ENZYMES; MAJOR DEPRESSIVE DISORDER; HUMAN LIVER-MICROSOMES; PREGNANE-X RECEPTOR; UDP-GLUCURONOSYLTRANSFERASE POLYMORPHISMS; ABSOLUTE PROTEIN QUANTIFICATION;
D O I
10.3389/fgene.2020.491895
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Many genetic variants in drug metabolizing enzymes and transporters have been shown to be relevant for treating psychiatric disorders. Associations are strong enough to feature on drug labels and for prescribing guidelines based on such data. A range of commercial tests are available; however, there is variability in included genetic variants, methodology, and interpretation. We herein provide relevant background for understanding clinical associations with specific variants, other factors that are relevant to consider when interpreting such data (such as age, gender, drug-drug interactions), and summarize the data relevant to clinical utility of pharmacogenetic testing in psychiatry and the available prescribing guidelines. We also highlight areas for future research focus in this field.
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页数:39
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