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Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)

BACKGROUND: Depressive symptoms are frequent in schizophrenia and associated with a poorer outcome. Currently, the optimal treatment for depressive symptoms in schizophrenia remains undetermined. Amisulpride, aripiprazole, and olanzapine all have antidepressive pharmacodynamic properties, ranging fr...

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Autores principales: Kjelby, Eirik, Gjestad, Rolf, Fathian, Farivar, Sinkeviciute, Igne, Alisauskiene, Renata, Anda, Liss, Løberg, Else-Marie, Reitan, Solveig Klæbo, Joa, Inge, Larsen, Tor Ketil, Rettenbacher, Maria, Berle, Jan Øystein, Fasmer, Ole Bernt, Kroken, Rune Andreas, Johnsen, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155702/
https://www.ncbi.nlm.nih.gov/pubmed/37083542
http://dx.doi.org/10.1097/JCP.0000000000001679
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author Kjelby, Eirik
Gjestad, Rolf
Fathian, Farivar
Sinkeviciute, Igne
Alisauskiene, Renata
Anda, Liss
Løberg, Else-Marie
Reitan, Solveig Klæbo
Joa, Inge
Larsen, Tor Ketil
Rettenbacher, Maria
Berle, Jan Øystein
Fasmer, Ole Bernt
Kroken, Rune Andreas
Johnsen, Erik
author_facet Kjelby, Eirik
Gjestad, Rolf
Fathian, Farivar
Sinkeviciute, Igne
Alisauskiene, Renata
Anda, Liss
Løberg, Else-Marie
Reitan, Solveig Klæbo
Joa, Inge
Larsen, Tor Ketil
Rettenbacher, Maria
Berle, Jan Øystein
Fasmer, Ole Bernt
Kroken, Rune Andreas
Johnsen, Erik
author_sort Kjelby, Eirik
collection PubMed
description BACKGROUND: Depressive symptoms are frequent in schizophrenia and associated with a poorer outcome. Currently, the optimal treatment for depressive symptoms in schizophrenia remains undetermined. Amisulpride, aripiprazole, and olanzapine all have antidepressive pharmacodynamic properties, ranging from serotonergic affinities to limbic dopaminergic selectivity. Consequently, in a 12-month pragmatic, randomized clinical trial, we aimed to investigate differences in antidepressive effectiveness among amisulpride, aripiprazole, and olanzapine as a secondary outcome, measured by change in the Calgary Depression Scale for Schizophrenia sum score in patients within the schizophrenia spectrum. METHODS: Psychotic patients within the schizophrenia spectrum were included, and effectiveness was analyzed with latent growth curve modeling. RESULTS: Of the 144 patients, 51 (35%) were women, the mean age was 31.7 (SD 12.7), and 39% were antipsychotic naive. At inclusion, 68 (47%) participants had a Calgary Depression Scale for Schizophrenia sum score >6, indicating severe depressive symptoms. Across the 12-month follow-up, there was a depressive symptom reduction in all medication groups, but no statistically significant differences between the study drugs. Separate analyses of the subcohort with elevated depressive symptoms at inclusion also failed to find differences in depressive symptom reduction between study drugs. The reduction in depressive symptoms mainly occurred within 6 weeks after randomization. CONCLUSIONS: There was a reduction in depressive symptoms under treatment with amisulpride, aripiprazole, and olanzapine in acutely psychotic patients with schizophrenia spectrum disorder, but no differences between the drugs.
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spelling pubmed-101557022023-05-04 Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro) Kjelby, Eirik Gjestad, Rolf Fathian, Farivar Sinkeviciute, Igne Alisauskiene, Renata Anda, Liss Løberg, Else-Marie Reitan, Solveig Klæbo Joa, Inge Larsen, Tor Ketil Rettenbacher, Maria Berle, Jan Øystein Fasmer, Ole Bernt Kroken, Rune Andreas Johnsen, Erik J Clin Psychopharmacol Original Contributions BACKGROUND: Depressive symptoms are frequent in schizophrenia and associated with a poorer outcome. Currently, the optimal treatment for depressive symptoms in schizophrenia remains undetermined. Amisulpride, aripiprazole, and olanzapine all have antidepressive pharmacodynamic properties, ranging from serotonergic affinities to limbic dopaminergic selectivity. Consequently, in a 12-month pragmatic, randomized clinical trial, we aimed to investigate differences in antidepressive effectiveness among amisulpride, aripiprazole, and olanzapine as a secondary outcome, measured by change in the Calgary Depression Scale for Schizophrenia sum score in patients within the schizophrenia spectrum. METHODS: Psychotic patients within the schizophrenia spectrum were included, and effectiveness was analyzed with latent growth curve modeling. RESULTS: Of the 144 patients, 51 (35%) were women, the mean age was 31.7 (SD 12.7), and 39% were antipsychotic naive. At inclusion, 68 (47%) participants had a Calgary Depression Scale for Schizophrenia sum score >6, indicating severe depressive symptoms. Across the 12-month follow-up, there was a depressive symptom reduction in all medication groups, but no statistically significant differences between the study drugs. Separate analyses of the subcohort with elevated depressive symptoms at inclusion also failed to find differences in depressive symptom reduction between study drugs. The reduction in depressive symptoms mainly occurred within 6 weeks after randomization. CONCLUSIONS: There was a reduction in depressive symptoms under treatment with amisulpride, aripiprazole, and olanzapine in acutely psychotic patients with schizophrenia spectrum disorder, but no differences between the drugs. Lippincott Williams & Wilkins 2023 2023-04-22 /pmc/articles/PMC10155702/ /pubmed/37083542 http://dx.doi.org/10.1097/JCP.0000000000001679 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Contributions
Kjelby, Eirik
Gjestad, Rolf
Fathian, Farivar
Sinkeviciute, Igne
Alisauskiene, Renata
Anda, Liss
Løberg, Else-Marie
Reitan, Solveig Klæbo
Joa, Inge
Larsen, Tor Ketil
Rettenbacher, Maria
Berle, Jan Øystein
Fasmer, Ole Bernt
Kroken, Rune Andreas
Johnsen, Erik
Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title_full Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title_fullStr Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title_full_unstemmed Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title_short Antidepressive Effectiveness of Amisulpride, Aripiprazole, and Olanzapine in Patients With Schizophrenia Spectrum Disorders: A Secondary Outcome Analysis of a Pragmatic, Randomized Trial (BeSt InTro)
title_sort antidepressive effectiveness of amisulpride, aripiprazole, and olanzapine in patients with schizophrenia spectrum disorders: a secondary outcome analysis of a pragmatic, randomized trial (best intro)
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155702/
https://www.ncbi.nlm.nih.gov/pubmed/37083542
http://dx.doi.org/10.1097/JCP.0000000000001679
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