Evidence map›Paper›PMID 39680690›Full record

ArticleSchizophrenia bulletin2026

Relationship Between Clozapine-Induced Inflammation and Eosinophilia: A Retrospective Cohort Study.

Yuki Kikuchi, Yuji Otsuka, Fumiaki Ito, Yuji Yada, Hiroaki Tanifuji, Hiroshi Komatsu, Hiroaki Tomita

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 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Yuki KikuchiDepartment of Psychiatry, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, 980-8574, Japan.ORCID 0000-0002-1184-8918
Yuji OtsukaDepartment of Psychiatry, Asahi General Hospital, Asahi, 289-2511, Japan.
Fumiaki ItoNational Hospital Organization Hanamaki Hospital, Hanamaki, 025-0033, Japan.
Yuji YadaDepartment of Psychiatry, Okayama Psychiatric Medical Center, Okayama, 700-0915, Japan.
Hiroaki TanifujiDepartment of Pharmacy, Kodama Hospital, Ishinomaki, Miyagi, 986-0873, Japan.
Hiroshi KomatsuDepartment of Psychiatry, Tohoku University Hospital, Sendai, Miyagi, 980-8574, Japan.
Hiroaki TomitaDepartment of Psychiatry, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, 980-8574, Japan.ORCID 0000-0003-2628-880X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesisEosinophilia has not been highlighted in clozapine-induced adverse inflammatory events, as it is often asymptomatic and self-limiting, while drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome occurs rarely. This study aimed to reveal the temporal relationships between eosinophilia and other inflammatory events during clozapine initiation. STUDY

designThe temporal relationships between eosinophilia and other inflammatory events were evaluated among 241 patients with schizophrenia treated with clozapine for the first time at 7 hospitals. Risk factors for eosinophilia were investigated among preceding inflammatory events and other clinical characteristics. Furthermore, patients with eosinophilia were stratified by the severity of adverse inflammatory events and their clinical characteristics were compared. STUDY

resultsOf the 54 patients who experienced inflammatory adverse events, 27 (50%) developed eosinophilia. In all but 1 patient, clinical symptoms of inflammatory adverse events preceded eosinophilia. In contrast, of the 187 patients without inflammatory events, 21 (11%) developed eosinophilia. Multivariate analysis revealed that more severe preceding inflammatory adverse events were associated with a greater risk of eosinophilia. The median time to the first detection of eosinophilia and peak eosinophil count occurred significantly earlier in patients with severe adverse events than in asymptomatic patients.

conclusionsIn most cases, eosinophilia developed after the onset of inflammatory symptoms. Preceding inflammation was associated with the development of clozapine-induced eosinophilia. Eosinophilia may not be suitable as an early detection marker of severe inflammatory adverse effects. These findings enhanced our understanding of the involvement of eosinophilia in clozapine-induced inflammatory events.

Indexed as

Antipsychotic AgentsClozapineEosinophiliaInflammationSchizophreniaAdultFemaleHumansMaleMiddle AgedRetrospective StudiesAntipsychotic AgentsClozapineC-reactive proteinDRESSfevermyocarditispneumonia

Identifiers

PMID39680690
PMCPMC12809819

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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.