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Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset
OBJECTIVE: 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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988380/ https://www.ncbi.nlm.nih.gov/pubmed/36891160 http://dx.doi.org/10.1155/2023/4899364 |
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author | Matsunaga, Hidenori Fukumori, Akio Mori, Kohji Morihara, Takashi Sato, Shunsuke Kitauchi, Kyoko Yanagida, Kanta Taguchi, Kazumi Honda, Tomoyuki Tomonaga, Keizo |
author_facet | Matsunaga, Hidenori Fukumori, Akio Mori, Kohji Morihara, Takashi Sato, Shunsuke Kitauchi, Kyoko Yanagida, Kanta Taguchi, Kazumi Honda, Tomoyuki Tomonaga, Keizo |
author_sort | Matsunaga, Hidenori |
collection | PubMed |
description | OBJECTIVE: 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. METHOD: 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. RESULTS: 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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-9988380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-99883802023-03-07 Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset Matsunaga, Hidenori Fukumori, Akio Mori, Kohji Morihara, Takashi Sato, Shunsuke Kitauchi, Kyoko Yanagida, Kanta Taguchi, Kazumi Honda, Tomoyuki Tomonaga, Keizo Case Rep Psychiatry Case Report OBJECTIVE: 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. METHOD: 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. RESULTS: 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. CONCLUSION: 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. Hindawi 2023-02-27 /pmc/articles/PMC9988380/ /pubmed/36891160 http://dx.doi.org/10.1155/2023/4899364 Text en Copyright © 2023 Hidenori Matsunaga et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Matsunaga, Hidenori Fukumori, Akio Mori, Kohji Morihara, Takashi Sato, Shunsuke Kitauchi, Kyoko Yanagida, Kanta Taguchi, Kazumi Honda, Tomoyuki Tomonaga, Keizo Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title | Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title_full | Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title_fullStr | Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title_full_unstemmed | Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title_short | Ribavirin Treatment for Severe Schizophrenia with Anti-Borna Disease Virus 1 Antibodies 30 Years after Onset |
title_sort | ribavirin treatment for severe schizophrenia with anti-borna disease virus 1 antibodies 30 years after onset |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988380/ https://www.ncbi.nlm.nih.gov/pubmed/36891160 http://dx.doi.org/10.1155/2023/4899364 |
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