Dopamine supersensitivity psychosis and dopamine partial agonist: A retrospective survey of failure of switching to aripiprazole in schizophrenia
Open accessAbstract
The administration of aripiprazole (ARI), a dopamine partial agonist, could provoke abrupt psychotic worsening in patients with schizophrenia. We explored the relationship between this psychotic worsening and dopamine supersensitivity psychosis (DSP), which is a clinically vulnerable state. We conducted a retrospective investigation for 264 patients whose treatment medication was switched to ARI from other antipsychotics. We divided the patients into the DSP(+) group with a history of DSP episode(s) ( N = 70) and the DSP(–) group without such a history ( N = 194), and then compared the clinical factors relevant to the success or failure of the switch to ARI between them. The results revealed that patients in the DSP(+) group experienced psychotic worsening following the switch to ARI with a significant higher rate compared to the DSP(–) group (23% vs. 8%, P < 0.01). Moreover, the dosages of the drugs before the ARI introduction in the patients experiencing the psychotic worsening in the DSP (-) group were higher than those in other patients of the group. Our findings suggest that patients who receive high dosages of antipsychotic drugs form overt or covert DSP and such state is highly associated with psychotic worsening following ARI treatment.
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Ketamine is used for recreational purposes because it produces mental and behavioral changes such as euphoria, perceptual changes, dissociation, and hallucinations.
“Ketamine is used for recreational purposes because it produces mental and behavioral changes, such as euphoria, perceptual changes, dissociation, and hallucinations [140].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [140]
The Introduction and Results discuss aripiprazole switching and dopamine supersensitivity psychosis in schizophrenia. Searches for ketamine, recreational use, dissociation, and hallucinations found no passage addressing the claim; the cited paper’s copy does not verify it. (LLM, conf=0.77)
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References 24 · Cited by 54
- Authors
- Takase, M., Kanahara, N., Oda, Y., Kimura, H., Watanabe, H., & Iyo, M.
- Affiliations
- Chiba University (JP)
- Corresponding author
- Kanahara, Nobuhisa
- Venue
- Journal of Psychopharmacology
- Publisher
- SAGE Publications
- Published
- 2015-03-03
- Volume
- 29
- Issue
- 4
- Pages
- 383-389
- ISSN
- 0269-8811 (ISSN-L)
- 1461-7285
- PMC
- PMC4363127
- OpenAlex
- W2150602432
- Cited by
- 54
- References
- 24
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 3 · 2023: 4 · 2022: 7 · 2021: 6 · 2020: 4 · 2019: 5 · 2018: 7 · 2017: 9 · 2016: 3 · 2015: 3
- FWCI
- 5.96
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Journal of Psychopharmacology (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- SENSHIN Medical Research Foundation
- Japan Society for the Promotion of Science (25860989)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Keywords
- aripiprazole, schizophrenia, antipsychotic switching, partial dopamine agonist, antipsychotic dosing, treatment failure
- MeSH terms
- Aripiprazole, Adolescent, Adult, Aged, Aged, 80 and over, Dopamine, Dose-Response Relationship, Drug, Female, Humans, Male, Middle Aged, Psychoses, Substance-Induced, Retrospective Studies, Schizophrenia, Antipsychotic Agents, Dopamine Agonists, Drug Partial Agonism, Young Adult
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