Evidence map›Paper›PMID 41150635›Full record

ArticleSchizophrenia bulletin2026

Trajectories of Clozapine Concentrations in Women Across Menopausal Age.

Franciska de Beer, Iris M H Hamers, Michalina Prycka, Georgios Schoretsanitis, Shiral S Gangadin, Daan J Touw, Iris E C Sommer

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2026. 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

7 authors.

Franciska de BeerCentre for Clinical Neuroscience and Cognition, University Medical Centre Groningen, University of Groningen, 9713 AP Groningen, The Netherlands.
Iris M H HamersCentre for Clinical Neuroscience and Cognition, University Medical Centre Groningen, University of Groningen, 9713 AP Groningen, The Netherlands.ORCID 0009-0007-0296-3969
Michalina PryckaCentre for Clinical Neuroscience and Cognition, University Medical Centre Groningen, University of Groningen, 9713 AP Groningen, The Netherlands.
Georgios SchoretsanitisDepartment of Psychiatry, Psychotherapy and Psychosomatics, Hospital of Psychiatry, University of Zurich, CH 8032 Zurich, Switzerland.ORCID 0000-0002-3851-4117
Shiral S GangadinCentre for Clinical Neuroscience and Cognition, University Medical Centre Groningen, University of Groningen, 9713 AP Groningen, The Netherlands.ORCID 0000-0002-0084-8226
Daan J TouwDepartment of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, 9713 AV Groningen, The Netherlands.
Iris E C SommerCentre for Clinical Neuroscience and Cognition, University Medical Centre Groningen, University of Groningen, 9713 AP Groningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesisDuring menopause, estrogen levels change dramatically, which may decrease clozapine blood concentrations in women via estrogen's inhibitory effect on CYP1A2 activity. This reduction could contribute to increased relapse rates seen in older women with psychotic disorders. STUDY

designClozapine blood concentration data were retrieved from the University Medical Center Groningen, the Netherlands. A total of 982 patients (720 men, 262 women), aged 40-60, with 17 104 measurements, were included for analyses. Latent class growth analysis (LCGA) assessed clozapine trajectories by sex, while linear mixed-effects models (LMEM) assessed sex differences between trajectory classes. STUDY

resultsThe optimal LCGA model (7-quantile splines) identified 3 clusters. Most women (n = 157, 60%) showed a decline in clozapine levels from 520 to 400 μg/L between the ages of 40-60. In contrast, most men (n = 392, 54%) had stable levels (mean 460 μg/L). Two other trajectories appeared in both sexes: a mild increase starting at age 45 (men: n = 272, 38%; women: n = 97, 37%) and a marked increase from 40 to 60 (men: n = 56, ~8%; women: n = 8, ~3%). LMEM showed significantly higher levels in women than men with stable trajectories (estimate = 177.03, t = 2.62, P < .01). A significant age-by-sex interaction (estimate = -0.067, t = -2.63, P < .01) suggested these differences varied over time.

conclusionsSex-specific longitudinal trajectories of clozapine concentrations showed declines in 60% of women aged 40-60, while most men remained stable. As decreasing blood levels could increase relapse vulnerability, monitoring clinical efficacy and side effects is warranted during menopause.

Indexed as

Antipsychotic AgentsClozapineMenopausePsychotic DisordersSchizophreniaAdultAge FactorsFemaleHumansMaleMiddle AgedNetherlandsSex FactorsAntipsychotic AgentsClozapineclozapineclozapine pharmacokineticsCYP1A2menopause

Identifiers

PMID41150635
PMCPMC13005174

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Registered trials

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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.