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Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?

Use of amphetamine and methamphetamine is widespread in the general population and common among patients with psychiatric disorders. Amphetamines may induce symptoms of psychosis very similar to those of acute schizophrenia spectrum psychosis. This has been an argument for using amphetamine-induced...

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Autores principales: Bramness, Jørgen G, Gundersen, Øystein Hoel, Guterstam, Joar, Rognli, Eline Borger, Konstenius, Maija, Løberg, Else-Marie, Medhus, Sigrid, Tanum, Lars, Franck, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554477/
https://www.ncbi.nlm.nih.gov/pubmed/23216941
http://dx.doi.org/10.1186/1471-244X-12-221
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author Bramness, Jørgen G
Gundersen, Øystein Hoel
Guterstam, Joar
Rognli, Eline Borger
Konstenius, Maija
Løberg, Else-Marie
Medhus, Sigrid
Tanum, Lars
Franck, Johan
author_facet Bramness, Jørgen G
Gundersen, Øystein Hoel
Guterstam, Joar
Rognli, Eline Borger
Konstenius, Maija
Løberg, Else-Marie
Medhus, Sigrid
Tanum, Lars
Franck, Johan
author_sort Bramness, Jørgen G
collection PubMed
description Use of amphetamine and methamphetamine is widespread in the general population and common among patients with psychiatric disorders. Amphetamines may induce symptoms of psychosis very similar to those of acute schizophrenia spectrum psychosis. This has been an argument for using amphetamine-induced psychosis as a model for primary psychotic disorders. To distinguish the two types of psychosis on the basis of acute symptoms is difficult. However, acute psychosis induced by amphetamines seems to have a faster recovery and appears to resolve more completely compared to schizophrenic psychosis. The increased vulnerability for acute amphetamine induced psychosis seen among those with schizophrenia, schizotypal personality and, to a certain degree other psychiatric disorders, is also shared by non-psychiatric individuals who previously have experienced amphetamine-induced psychosis. Schizophrenia spectrum disorder and amphetamine-induced psychosis are further linked together by the finding of several susceptibility genes common to both conditions. These genes probably lower the threshold for becoming psychotic and increase the risk for a poorer clinical course of the disease. The complex relationship between amphetamine use and psychosis has received much attention but is still not adequately explored. Our paper reviews the literature in this field and proposes a stress-vulnerability model for understanding the relationship between amphetamine use and psychosis.
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spelling pubmed-35544772013-01-29 Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable? Bramness, Jørgen G Gundersen, Øystein Hoel Guterstam, Joar Rognli, Eline Borger Konstenius, Maija Løberg, Else-Marie Medhus, Sigrid Tanum, Lars Franck, Johan BMC Psychiatry Debate Use of amphetamine and methamphetamine is widespread in the general population and common among patients with psychiatric disorders. Amphetamines may induce symptoms of psychosis very similar to those of acute schizophrenia spectrum psychosis. This has been an argument for using amphetamine-induced psychosis as a model for primary psychotic disorders. To distinguish the two types of psychosis on the basis of acute symptoms is difficult. However, acute psychosis induced by amphetamines seems to have a faster recovery and appears to resolve more completely compared to schizophrenic psychosis. The increased vulnerability for acute amphetamine induced psychosis seen among those with schizophrenia, schizotypal personality and, to a certain degree other psychiatric disorders, is also shared by non-psychiatric individuals who previously have experienced amphetamine-induced psychosis. Schizophrenia spectrum disorder and amphetamine-induced psychosis are further linked together by the finding of several susceptibility genes common to both conditions. These genes probably lower the threshold for becoming psychotic and increase the risk for a poorer clinical course of the disease. The complex relationship between amphetamine use and psychosis has received much attention but is still not adequately explored. Our paper reviews the literature in this field and proposes a stress-vulnerability model for understanding the relationship between amphetamine use and psychosis. BioMed Central 2012-12-05 /pmc/articles/PMC3554477/ /pubmed/23216941 http://dx.doi.org/10.1186/1471-244X-12-221 Text en Copyright ©2012 Bramness et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Debate
Bramness, Jørgen G
Gundersen, Øystein Hoel
Guterstam, Joar
Rognli, Eline Borger
Konstenius, Maija
Løberg, Else-Marie
Medhus, Sigrid
Tanum, Lars
Franck, Johan
Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title_full Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title_fullStr Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title_full_unstemmed Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title_short Amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
title_sort amphetamine-induced psychosis - a separate diagnostic entity or primary psychosis triggered in the vulnerable?
topic Debate
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554477/
https://www.ncbi.nlm.nih.gov/pubmed/23216941
http://dx.doi.org/10.1186/1471-244X-12-221
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