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Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments

This paper examines the role of selective serotonin reuptake inhibitors (SSRIs) in the treatment of hepatitis-C virus (HCV) patients who have developed interferon-α induced depression. A 2-year data analysis of HCV psychiatric liaison clinic has been undertaken. The diagnosis, treatment, and progres...

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Detalles Bibliográficos
Autores principales: Gupta, Ramesh K, Kumar, Rajeev, Bassett, Mark
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671809/
https://www.ncbi.nlm.nih.gov/pubmed/19412482
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author Gupta, Ramesh K
Kumar, Rajeev
Bassett, Mark
author_facet Gupta, Ramesh K
Kumar, Rajeev
Bassett, Mark
author_sort Gupta, Ramesh K
collection PubMed
description This paper examines the role of selective serotonin reuptake inhibitors (SSRIs) in the treatment of hepatitis-C virus (HCV) patients who have developed interferon-α induced depression. A 2-year data analysis of HCV psychiatric liaison clinic has been undertaken. The diagnosis, treatment, and progress of those patients who were treated with interferon-α (INF-α) are reported. 53 of the 78 patients enrolled at the HCV Clinic and treated with INF-α were referred for psychiatric consultation. Six patients developed major depressive illness following INF therapy. They were all treated with SSRIs and they made full recovery. This is a significant observation and is concordant with other studies. Its biochemical ramifications are presented. It is concluded that INF-induced depression is fully reversible. A hypothesis is proposed that SSRIs modulate the neuro-protective neurotoxic ratio by possibly inhibiting the indole-2,3-dioxygenase induction of the kynurenine pathway.
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spelling pubmed-26718092009-04-30 Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments Gupta, Ramesh K Kumar, Rajeev Bassett, Mark Neuropsychiatr Dis Treat Original Research This paper examines the role of selective serotonin reuptake inhibitors (SSRIs) in the treatment of hepatitis-C virus (HCV) patients who have developed interferon-α induced depression. A 2-year data analysis of HCV psychiatric liaison clinic has been undertaken. The diagnosis, treatment, and progress of those patients who were treated with interferon-α (INF-α) are reported. 53 of the 78 patients enrolled at the HCV Clinic and treated with INF-α were referred for psychiatric consultation. Six patients developed major depressive illness following INF therapy. They were all treated with SSRIs and they made full recovery. This is a significant observation and is concordant with other studies. Its biochemical ramifications are presented. It is concluded that INF-induced depression is fully reversible. A hypothesis is proposed that SSRIs modulate the neuro-protective neurotoxic ratio by possibly inhibiting the indole-2,3-dioxygenase induction of the kynurenine pathway. Dove Medical Press 2006-09 /pmc/articles/PMC2671809/ /pubmed/19412482 Text en © 2006 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Gupta, Ramesh K
Kumar, Rajeev
Bassett, Mark
Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title_full Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title_fullStr Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title_full_unstemmed Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title_short Interferon-induced depressive illness in hep C patients responds to SSRI antidepressant treatments
title_sort interferon-induced depressive illness in hep c patients responds to ssri antidepressant treatments
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671809/
https://www.ncbi.nlm.nih.gov/pubmed/19412482
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