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DOI: 10.1055/s-0044-1779558
CYP2D6 genotypes and phenotypes, plasma levels and treatment failure with risperidone or aripiprazole: results from a one-year longitudinal study
Risperidone and aripiprazole are metabolized by the cytochrome P450 2D6 (CYP2D6). Individuals can be categorized as ultrarapid, normal, intermediate, or poor metabolizers (UM, NM, IM and PM, respectively). Greater odds of switching from risperidone (but not from aripiprazole) were previously reported among PM and UM. Importantly, the duration of treatment up to switching was unknown.
Treatment duration up to switching was analyzed for risperidone (N=515) and for aripiprazole (N=467). CYP2D6 *3, *4, *5, *6, *9, *10, *41 and *XN alleles were analyzed. Phenoconversion due to co-medication with CYP2D6 strong inhibitors was also considered.
CYP2D6 genotypes and phenotypes significantly influenced plasma levels of aripiprazole plus dehydroaripiprazole, and of risperidone plus 9-OH-risperidone. Considering PM and (IM+NM+UM), 70% and 42% of switching probability from risperidone was found, respectively (p=0.026). The risk of switching increased over time for PM (interaction term:1.01; p=0.011), becoming significant after three months (HR:1.79; p=0.028). Similar results were obtained when considering phenoconversion, although phenoconverted PM risk of switch was constant over time. The incidence of discontinuation from aripiprazole was increased at 3 months (OR:2.57; CI:1.15-5.58) in UM or PM when compared to NM or IM.
Over one year, CYP2D6 PM presented an increasing risk to switch from risperidone over time, the risk becoming significant after three months. PMs or UMs are associated with increased discontinuation rates after 3 months aripiprazole treatment. This supports preemptive genotyping for CYP2D6 prior to using risperidone and aripiprazole with phenoconversion also being taken into account.
Publication History
Article published online:
12 March 2024
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