Successful rechallenge with paliperidone after clozapine treatment for a patient with dopamine supersensitivity psychosis.

Dopamine supersensitivity psychosis clozapine dopamine D2 receptor paliperidone treatment-resistant schizophrenia

Journal

SAGE open medical case reports
ISSN: 2050-313X
Titre abrégé: SAGE Open Med Case Rep
Pays: England
ID NLM: 101638686

Informations de publication

Date de publication:
2020
Historique:
received: 28 06 2019
accepted: 04 05 2020
entrez: 20 6 2020
pubmed: 20 6 2020
medline: 20 6 2020
Statut: epublish

Résumé

We describe the case of a 49-year-old Japanese male patient successfully treated with a paliperidone rechallenge following 2-year treatment with clozapine for treatment-resistant schizophrenia. He had responded well to conventional antipsychotic treatment for the initial psychotic episode but gradually developed dopamine supersensitivity; even treatment with paliperidone and another antipsychotic medication (a total up to 1700 mg in chlorpromazine-equivalent dose) had not improved his psychotic symptoms. Clozapine treatment produced temporary symptomatic relief, but the clozapine dose could not be increased to > 150 mg due to the patient's intolerance. Following low-dose clozapine treatment for 2 years, a rechallenge with paliperidone monotherapy ameliorated his psychotic symptoms. This suggests that clozapine may have the potential to release the dopamine supersensitivity state. Our patient's case indicates that for patients with dopamine supersensitivity psychosis, a rechallenge with a previously ineffective antipsychotic after clozapine treatment may be successful.

Identifiants

pubmed: 32551117
doi: 10.1177/2050313X20929561
pii: 10.1177_2050313X20929561
pmc: PMC7278325
doi:

Types de publication

Case Reports

Langues

eng

Pagination

2050313X20929561

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Declaration of conflicting interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Dr. Oda received grant funding from the SENSHIN Medical Research Foundation. Dr. Sasaki has received speakers’ honoraria from Dai-ichi Sankyo, Eli Lilly, Glaxo Smith Kline, Kyowa, Novartis, Janssen, Otsuka, Shionogi, Shire, Taisho, and Tanabe Mitsubishi, and he has also received research support from Novartis, Otsuka, Shionogi, and Taisho (from April 2014 to March 2019). Dr. Iyo received consultant fees from Eli Lilly, Sumitomo Dainippon, Pfizer, and Abbott and reports honoraria from Janssen, Eli Lilly, Otsuka, Meiji Seika, Astellas, Sumitomo Dainippon, Ono, GlaxoSmithKline, Takeda, Mochida, Kyowa Hakko, MSD, Eisai, Daiichi-Sankyo, Novartis, Teijin, Shionogi, Hisamitsu, and Asahi Kasei. Dr. Kobayashi, Dr. Hayatsu, Dr. Ohki, Dr. Akutsu, Dr. Oiwa, Dr. Komatsu, and Dr. Niitsu have no potential conflicts of interest to report.

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Auteurs

Remiko Kobayashi (R)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yasunori Oda (Y)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Ryunosuke Hayatsu (R)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Nozomi Ohki (N)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Misa Akutsu (M)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Takahiro Oiwa (T)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Hideki Komatsu (H)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Tomihisa Niitsu (T)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Tsuyoshi Sasaki (T)

Department of Child Psychiatry, Chiba University Hospital, Chiba, Japan.

Masaomi Iyo (M)

Department of Psychiatry, Graduate School of Medicine, Chiba University, Chiba, Japan.

Classifications MeSH