Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset.


Journal

Case reports in psychiatry
ISSN: 2090-682X
Titre abrégé: Case Rep Psychiatry
Pays: United States
ID NLM: 101583308

Informations de publication

Date de publication:
2023
Historique:
received: 18 10 2022
revised: 23 12 2022
accepted: 11 02 2023
entrez: 9 3 2023
pubmed: 10 3 2023
medline: 10 3 2023
Statut: epublish

Résumé

Borna disease virus 1 (BoDV-1) was proven to cause fatal encephalitis in humans in 2018. However, the effects of persistent infections remain unclear. Here, we present the case of a 50-year-old woman with a 30-year history of severe schizophrenia, who was exposed to fleas from stray cats prior to disease onset, suggesting the possibility of zoonosis including BoDV-1 infection. The patient had experienced significant social impairment, thought deterioration, delusions, and hallucinations for more than 20 years. A radioligand assay was used to test the patient for IgG and IgM antibodies against BoDV-1 nucleoprotein (N) and phosphoprotein (P). Based on the protocol for hepatitis C, we treated the patient with 400 mg/day ribavirin, which was later increased to 600 mg/day. The serological examination revealed anti-BoDV-1 N IgG. Although only subtle changes were observed over the 24 weeks of treatment, the family noticed that the patient's Cotard delusions had disappeared 7 months after completing the treatment, accompanied by some improvements in the relationship with the family. Though definite proof was not obtained, this presumed suppression of BoDV-1 by ribavirin leading to improvements in Cotard syndrome-like symptoms suggests that intractable schizophrenia might be one of the BoDV-1 infection phenotypes. Further studies are needed to clarify the effect of persistent BoDV-1 infections in humans.

Identifiants

pubmed: 36891160
doi: 10.1155/2023/4899364
pmc: PMC9988380
doi:

Types de publication

Case Reports

Langues

eng

Pagination

4899364

Informations de copyright

Copyright © 2023 Hidenori Matsunaga et al.

Déclaration de conflit d'intérêts

The authors declare that there are no conflicts of interest regarding the publication of this article.

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Auteurs

Hidenori Matsunaga (H)

Department of Psychiatry, Osaka General Medical Center, Osaka, Japan.
Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Akio Fukumori (A)

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Pharmacotherapeutics II, Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Department of Mental Health Promotion, Osaka University Graduate School of Medicine, Toyonaka, Osaka, Japan.

Kohji Mori (K)

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Takashi Morihara (T)

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Psychiatry, Toyonaka Municipal Hospital, Osaka, Japan.

Shunsuke Sato (S)

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Kyoko Kitauchi (K)

Department of Psychiatry, Osaka General Medical Center, Osaka, Japan.

Kanta Yanagida (K)

Department of Pharmacotherapeutics II, Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
Department of Mental Health Promotion, Osaka University Graduate School of Medicine, Toyonaka, Osaka, Japan.

Kazumi Taguchi (K)

Department of Pharmacotherapeutics II, Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.

Tomoyuki Honda (T)

Department of Virology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.

Keizo Tomonaga (K)

Laboratory of RNA Viruses, Department of Virus Research, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.

Classifications MeSH