Volumetric changes in the Basal Ganglia after antipsychotic monotherapy: a systematic review

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Standard

Volumetric changes in the Basal Ganglia after antipsychotic monotherapy : a systematic review. / Ebdrup, B H; Nørbak, H; Borgwardt, S; Glenthøj, B.

I: Current Medicinal Chemistry, Bind 20, Nr. 3, 2013, s. 438-47.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ebdrup, BH, Nørbak, H, Borgwardt, S & Glenthøj, B 2013, 'Volumetric changes in the Basal Ganglia after antipsychotic monotherapy: a systematic review', Current Medicinal Chemistry, bind 20, nr. 3, s. 438-47. https://doi.org/10.2174/0929867311320030015

APA

Ebdrup, B. H., Nørbak, H., Borgwardt, S., & Glenthøj, B. (2013). Volumetric changes in the Basal Ganglia after antipsychotic monotherapy: a systematic review. Current Medicinal Chemistry, 20(3), 438-47. https://doi.org/10.2174/0929867311320030015

Vancouver

Ebdrup BH, Nørbak H, Borgwardt S, Glenthøj B. Volumetric changes in the Basal Ganglia after antipsychotic monotherapy: a systematic review. Current Medicinal Chemistry. 2013;20(3):438-47. https://doi.org/10.2174/0929867311320030015

Author

Ebdrup, B H ; Nørbak, H ; Borgwardt, S ; Glenthøj, B. / Volumetric changes in the Basal Ganglia after antipsychotic monotherapy : a systematic review. I: Current Medicinal Chemistry. 2013 ; Bind 20, Nr. 3. s. 438-47.

Bibtex

@article{27ff61bb5a8943a986f60b100a32ed28,
title = "Volumetric changes in the Basal Ganglia after antipsychotic monotherapy: a systematic review",
abstract = "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.",
author = "Ebdrup, {B H} and H N{\o}rbak and S Borgwardt and B Glenth{\o}j",
year = "2013",
doi = "10.2174/0929867311320030015",
language = "English",
volume = "20",
pages = "438--47",
journal = "Current Medicinal Chemistry",
issn = "0929-8673",
publisher = "Bentham Science Publishers",
number = "3",

}

RIS

TY - JOUR

T1 - Volumetric changes in the Basal Ganglia after antipsychotic monotherapy

T2 - a systematic review

AU - Ebdrup, B H

AU - Nørbak, H

AU - Borgwardt, S

AU - Glenthøj, B

PY - 2013

Y1 - 2013

N2 - 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.

AB - 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.

U2 - 10.2174/0929867311320030015

DO - 10.2174/0929867311320030015

M3 - Journal article

VL - 20

SP - 438

EP - 447

JO - Current Medicinal Chemistry

JF - Current Medicinal Chemistry

SN - 0929-8673

IS - 3

ER -

ID: 48454517