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Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review

INTRODUCTION: Exposure to antipsychotic medication has been extensively associated with structural brain changes in the basal ganglia (BG). Traditionally antipsychotics have been divided into first and second generation antipsychotics (FGAs and SGAs) however, the validity of this classification has...

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Autores principales: Ebdrup, B.H, Nørbak, H, Borgwardt, S, Glenthøj, B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715891/
https://www.ncbi.nlm.nih.gov/pubmed/23157636
http://dx.doi.org/10.2174/0929867311320030015
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author Ebdrup, B.H
Nørbak, H
Borgwardt, S
Glenthøj, B
author_facet Ebdrup, B.H
Nørbak, H
Borgwardt, S
Glenthøj, B
author_sort Ebdrup, B.H
collection PubMed
description INTRODUCTION: Exposure to antipsychotic medication has been extensively associated with structural brain changes in the basal ganglia (BG). Traditionally antipsychotics have been divided into first and second generation antipsychotics (FGAs and SGAs) however, the validity of this classification has become increasingly controversial. To address if specific antipsychotics induce differential effects on BG volumes or whether volumetric effects are explained by FGA or SGA classification, we reviewed longitudinal structural magnetic resonance imaging (MRI) studies investigating effects of antipsychotic monotherapy. MATERIAL AND METHODS: We systematically searched PubMed for longitudinal MRI studies of patients with schizophrenia or non-affective psychosis who had undergone a period of antipsychotic monotherapy. We used specific, predefined search terms and extracted studies were hand searched for additional studies. RESULTS: We identified 13 studies published in the period from 1996 to 2011. Overall six compounds (two classified as FGAs and four as SGAs) have been investigated: haloperidol, zuclophentixol, risperidone, olanzapine, clozapine, and quetiapine. The follow-up period ranged from 3-24 months. Unexpectedly, no studies found that specific FGAs induce significant BG volume increases. Conversely, both volumetric increases and decreases in the BG have been associated with SGA monotherapy. DISCUSSION: Induction of striatal volume increases is not a specific feature of FGAs. Except for clozapine treatment in chronic patients, volume reductions are not restricted to specific SGAs. The current review adds brain structural support to the notion that antipsychotics should no longer be classified as either FGAs or SGAs. Future clinical MRI studies should strive to elucidate effects of specific antipsychotic drugs.
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spelling pubmed-37158912013-07-22 Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review Ebdrup, B.H Nørbak, H Borgwardt, S Glenthøj, B Curr Med Chem Article INTRODUCTION: Exposure to antipsychotic medication has been extensively associated with structural brain changes in the basal ganglia (BG). Traditionally antipsychotics have been divided into first and second generation antipsychotics (FGAs and SGAs) however, the validity of this classification has become increasingly controversial. To address if specific antipsychotics induce differential effects on BG volumes or whether volumetric effects are explained by FGA or SGA classification, we reviewed longitudinal structural magnetic resonance imaging (MRI) studies investigating effects of antipsychotic monotherapy. MATERIAL AND METHODS: We systematically searched PubMed for longitudinal MRI studies of patients with schizophrenia or non-affective psychosis who had undergone a period of antipsychotic monotherapy. We used specific, predefined search terms and extracted studies were hand searched for additional studies. RESULTS: We identified 13 studies published in the period from 1996 to 2011. Overall six compounds (two classified as FGAs and four as SGAs) have been investigated: haloperidol, zuclophentixol, risperidone, olanzapine, clozapine, and quetiapine. The follow-up period ranged from 3-24 months. Unexpectedly, no studies found that specific FGAs induce significant BG volume increases. Conversely, both volumetric increases and decreases in the BG have been associated with SGA monotherapy. DISCUSSION: Induction of striatal volume increases is not a specific feature of FGAs. Except for clozapine treatment in chronic patients, volume reductions are not restricted to specific SGAs. The current review adds brain structural support to the notion that antipsychotics should no longer be classified as either FGAs or SGAs. Future clinical MRI studies should strive to elucidate effects of specific antipsychotic drugs. Bentham Science Publishers 2013-01 2013-01 /pmc/articles/PMC3715891/ /pubmed/23157636 http://dx.doi.org/10.2174/0929867311320030015 Text en © 2013 Bentham Science Publishers http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Ebdrup, B.H
Nørbak, H
Borgwardt, S
Glenthøj, B
Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title_full Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title_fullStr Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title_full_unstemmed Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title_short Volumetric Changes in the Basal Ganglia After Antipsychotic Monotherapy: A Systematic Review
title_sort volumetric changes in the basal ganglia after antipsychotic monotherapy: a systematic review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715891/
https://www.ncbi.nlm.nih.gov/pubmed/23157636
http://dx.doi.org/10.2174/0929867311320030015
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