Evidence map›Paper›PMID 40781498›Full record

ArticleEuropean journal of clinical pharmacology2025

Impact of CYP2D6 genotype on fluoxetine exposure and treatment switch in adults and children/adolescents.

Karoline Linnea Nordby, Pari Faraj, Espen Molden, Kristine Hole

Abstract read
In one paragraph

Article in European journal of clinical pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Pharmacogenomics ofPharmaceutics · 2025
    Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Karoline Linnea NordbyCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Pari FarajCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Espen MoldenCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0001-6190-2751
Kristine HoleCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway. oldriver@oslomet.no.ORCID http://orcid.org/0000-0001-7300-5329

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe relevance of CYP2D6 activity on serum levels and clinical response of fluoxetine remains unclear. The present study aim was to evaluate the impact of CYP2D6 genotype on i) fluoxetine and norfluoxetine exposure, and ii) treatment switch from fluoxetine to alternative antidepressants in adults and children/adolescents.

methodsPatients were included retrospectively from a therapeutic drug monitoring service. Patients were subgrouped by age, i.e. < 18 yrs (young) and ≥ 18 yrs (adult), and divided into CYP2D6 genotype-predicted phenotype subgroups of poor metabolizers (PMs), intermediate metabolizers (IMs), normal metabolizers (NMs) and ultrarapid metabolizers (UMs).

resultsAmong 1027 adult patients, the metabolic ratio was lowest in PMs and highest in UMs (p ≤ 0.04), but there was no difference in active moiety (fluoxetine + norfluoxetine) across CYP2D6 phenotype groups (p ≥ 0.1). Similar trends were observed in 196 young patients, both for metabolic ratio and active moiety. In adult patients, switching from fluoxetine to an alternative antidepressant had odds ratio of 2.9 in UMs (p = 0.004) and 2.3 in PMs (p = 0.007) compared with NMs. The number of switches per genotype group was too low for meaningful comparisons in young patients.

conclusionThe fluoxetine and norfluoxetine active moiety was unaffected by CYP2D6 genotype in adults and children/adolescents. Still, adult CYP2D6 PMs and UMs switched antidepressant treatment two to three times more often than NMs, indicating that relative levels of fluoxetine and norfluoxetine may affect treatment outcome rather than active moiety in relation to CYP2D6 phenotype.

Indexed as

Antidepressive Agents, Second-GenerationCytochrome P-450 CYP2D6FluoxetineSelective Serotonin Reuptake InhibitorsAdolescentAdultAgedChildDrug MonitoringFemaleGenotypeHumansMaleMiddle AgedPhenotypeRetrospective StudiesAntidepressive Agents, Second-GenerationCytochrome P-450 CYP2D6FluoxetinenorfluoxetineSelective Serotonin Reuptake InhibitorsCYP2D6FluoxetineGenotypePharmacogeneticsTherapeutic drug monitoring

Identifiers

PMID40781498
PMCPMC12511196

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.