Evidence map›Paper›PMID 39834274›Full record

ArticlePsychiatry and clinical neurosciences2025

Second-generation antipsychotic-induced dystonia: Analysis using the Japanese Adverse Drug Event Report (JADER) database.

Takumi Ebina, Kunihiro Iwamoto, Masahiko Ando, Masashi Ikeda

Abstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Beyond pain relief: the thrombosis threat of celecoxib.Therapeutic advances in drug safety · 2025
    Article
  5. 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.

Takumi EbinaDepartment of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0009-0001-3132-8936
Kunihiro IwamotoDepartment of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0003-3868-3372
Masahiko AndoDepartment of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
Masashi IkedaDepartment of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Funding

Japan Agency for Medical Research and Development JP24dk0307123Japan Society for the Promotion of Science JP21K07518
6 · The paper itself

Abstract

aimThis study aimed to explore the comparative risks for dystonia among different second-generation antipsychotics (SGAs), the influence of sex, and the relationship between the time-to-onset of dystonia and its outcomes.

methodsWe analyzed data from the Japanese Adverse Drug Event Report database from April 2004 to November 2023. Cases involving oral SGAs, excluding clozapine, were extracted. We used the odds ratios to assess the reporting proportions among SGAs and sex, analyzed the median time-to-onset and interquartile ranges (IQRs), and conducted a receiver operating characteristic (ROC) curve analysis to investigate the time-to-onset of dystonia and its relationship to outcomes.

resultsWe extracted 9837 cases involving oral SGAs. Lurasidone was associated with a significantly higher proportion of dystonia reports than risperidone, aripiprazole, quetiapine, and olanzapine. The reporting proportion of dystonia associated with aripiprazole was lower than that of paliperidone and risperidone, but higher than that of quetiapine and olanzapine. Female sex was significantly associated with a higher reporting proportion of dystonia compared with males. Among the 148 cases of oral SGA-induced dystonia, the median time-to-onset was 125 days (IQR, 19.75-453.25 days). Divided into the three outcome groups (recovered, improved, and unrecovered/residual), those with better outcomes had a shorter time-to-onset than those with poorer outcomes. ROC curve analysis suggested a threshold of 91.5 days for discriminating outcomes, with a sensitivity of 71.7% and specificity of 69.9%.

conclusionsThe risks of dystonia may vary among SGAs and between sexes. SGA-induced dystonia often manifests in the tardive form.

Indexed as

Adverse Drug Reaction Reporting SystemsAntipsychotic AgentsDystoniaAdultAgedAripiprazoleDatabases, FactualEast Asian PeopleFemaleHumansJapanLurasidone HydrochlorideMaleMiddle AgedOlanzapineQuetiapine FumarateAntipsychotic AgentsAripiprazoleLurasidone HydrochlorideOlanzapineQuetiapine FumarateRisperidoneadverse drug reaction reporting systemsantipsychotic agentsdrug‐related side effects and adverse reactionsdystoniasex characteristics

Identifiers

PMID39834274
PMCPMC11874247

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.