Evidence map›Paper›PMID 41054698›Full record

ArticleTherapeutic advances in psychopharmacology2025

Impact of

Hasan Çağın Lenk, Line Skute Bråten, Ole A Andreassen, Espen Molden

Abstract read
In one paragraph

Article in Therapeutic advances in psychopharmacology, 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hasan Çağın LenkCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.ORCID https://orcid.org/0000-0003-4724-7396
Line Skute BråtenCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.ORCID https://orcid.org/0000-0001-6887-1986
Ole A AndreassenCentre for Precision Psychiatry, Faculty of Medicine, University of Oslo, Oslo, Norway.
Espen MoldenCenter for Psychopharmacology, Diakonhjemmet Hospital, Forskningsveien 13, PO Box 85 Vinderen, Oslo 0319, Norway.ORCID https://orcid.org/0000-0001-6190-2751

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Clozapine is the most effective drug for schizophrenia and is the only drug indicated for use in patients with treatment resistance. The therapeutic range of clozapine is narrow with extensive interindividual differences in serum levels at similar dosing, mainly due to variability in hepatic metabolism mediated by several cytochrome P450 (CYP) enzymes. Tobacco smoking is the most important environmental factor determining clozapine metabolism, while the effect of pharmacogenetic variability is unclear. Objectives: To investigate the impact of Design: This is a retrospective naturalistic/observational study. Methods: The study population was included from the therapeutic drug monitoring/pharmacogenetics service at the Center for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway, during January 2005-November 2024. We assessed the influence of Results: The study comprised 663 participants (55% smokers). Conclusion: The

Indexed as

personalized treatmentpharmacogeneticspharmacokineticsprecision psychiatrytreatment resistant schizophrenia

Identifiers

PMID41054698
PMCPMC12496473

What OpenQuestion holds

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Registered trials

None linked

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.