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Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials

PURPOSE: The purpose of this study was to compare the efficacy and safety of brexpiprazole 4 mg/day (B4) and 2 mg/day (B2) for treating acute schizophrenia. PATIENTS AND METHODS: We performed three categorical meta-analyses (B4 vs placebo, B2 vs placebo, and B4 vs B2) of double-blind, randomized pla...

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Autores principales: Kishi, Taro, Oya, Kazuto, Matsui, Yuki, Nomura, Ikuo, Sakuma, Kenji, Okuya, Makoto, Matsuda, Yuki, Fujita, Kiyoshi, Funahashi, Toshihiko, Yoshimura, Reiji, Iwata, Nakao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171755/
https://www.ncbi.nlm.nih.gov/pubmed/30319261
http://dx.doi.org/10.2147/NDT.S176676
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author Kishi, Taro
Oya, Kazuto
Matsui, Yuki
Nomura, Ikuo
Sakuma, Kenji
Okuya, Makoto
Matsuda, Yuki
Fujita, Kiyoshi
Funahashi, Toshihiko
Yoshimura, Reiji
Iwata, Nakao
author_facet Kishi, Taro
Oya, Kazuto
Matsui, Yuki
Nomura, Ikuo
Sakuma, Kenji
Okuya, Makoto
Matsuda, Yuki
Fujita, Kiyoshi
Funahashi, Toshihiko
Yoshimura, Reiji
Iwata, Nakao
author_sort Kishi, Taro
collection PubMed
description PURPOSE: The purpose of this study was to compare the efficacy and safety of brexpiprazole 4 mg/day (B4) and 2 mg/day (B2) for treating acute schizophrenia. PATIENTS AND METHODS: We performed three categorical meta-analyses (B4 vs placebo, B2 vs placebo, and B4 vs B2) of double-blind, randomized placebo-controlled trials (DBRCTs) that reported improvements in the Positive and Negative Syndrome Scale (PANSS) scores, response rate, Clinical Global Impression–Improvement and Severity (CGI-I and CGI-S) scores, discontinuation rate, and incidence of individual adverse events. RESULTS: We identified three DBRCTs with 1,444 patients. Both B4 and B2 were superior to placebo for PANSS total score (B4: standardized mean difference [SMD] =−0.30, 95% CI =−0.43, −0.17; B2: SMD =−0.30, 95% CI =−0.46, −0.13), PANSS negative score, response rate, CGI-S score, and CGI-I score. B2, but not B4, was superior to placebo for the PANSS positive score. However, there was considerable heterogeneity in the meta-analysis for B4’s PANSS positive score, which disappeared after excluding a 2018 Japanese study from the meta-analysis that included more patients on a high-dose antipsychotic prior to their participation. A meta-analysis that excluded the data from the abovementioned patients showed B4 to be superior to the placebo in terms of the PANSS positive score (SMD =−0.22, 95% CI =−0.40, −0.03). B2, but not B4, was associated with a lower incidence of all-cause discontinuation compared with placebo. Both B4 and B2 were superior to placebo for discontinuation due to adverse events and schizophrenia, but both were associated with a higher incidence of weight gain compared with placebo. B4 was also associated with a higher risk of extrapyramidal symptoms than B2. CONCLUSION: Both B4 and B2 benefitted patients with schizophrenia, particularly those who were not previously on high-dose antipsychotics. Both the regimens were well-tolerated, but carried a risk of weight gain and extrapyramidal symptoms, although the latter risk was higher for B4 than B2.
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spelling pubmed-61717552018-10-12 Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials Kishi, Taro Oya, Kazuto Matsui, Yuki Nomura, Ikuo Sakuma, Kenji Okuya, Makoto Matsuda, Yuki Fujita, Kiyoshi Funahashi, Toshihiko Yoshimura, Reiji Iwata, Nakao Neuropsychiatr Dis Treat Original Research PURPOSE: The purpose of this study was to compare the efficacy and safety of brexpiprazole 4 mg/day (B4) and 2 mg/day (B2) for treating acute schizophrenia. PATIENTS AND METHODS: We performed three categorical meta-analyses (B4 vs placebo, B2 vs placebo, and B4 vs B2) of double-blind, randomized placebo-controlled trials (DBRCTs) that reported improvements in the Positive and Negative Syndrome Scale (PANSS) scores, response rate, Clinical Global Impression–Improvement and Severity (CGI-I and CGI-S) scores, discontinuation rate, and incidence of individual adverse events. RESULTS: We identified three DBRCTs with 1,444 patients. Both B4 and B2 were superior to placebo for PANSS total score (B4: standardized mean difference [SMD] =−0.30, 95% CI =−0.43, −0.17; B2: SMD =−0.30, 95% CI =−0.46, −0.13), PANSS negative score, response rate, CGI-S score, and CGI-I score. B2, but not B4, was superior to placebo for the PANSS positive score. However, there was considerable heterogeneity in the meta-analysis for B4’s PANSS positive score, which disappeared after excluding a 2018 Japanese study from the meta-analysis that included more patients on a high-dose antipsychotic prior to their participation. A meta-analysis that excluded the data from the abovementioned patients showed B4 to be superior to the placebo in terms of the PANSS positive score (SMD =−0.22, 95% CI =−0.40, −0.03). B2, but not B4, was associated with a lower incidence of all-cause discontinuation compared with placebo. Both B4 and B2 were superior to placebo for discontinuation due to adverse events and schizophrenia, but both were associated with a higher incidence of weight gain compared with placebo. B4 was also associated with a higher risk of extrapyramidal symptoms than B2. CONCLUSION: Both B4 and B2 benefitted patients with schizophrenia, particularly those who were not previously on high-dose antipsychotics. Both the regimens were well-tolerated, but carried a risk of weight gain and extrapyramidal symptoms, although the latter risk was higher for B4 than B2. Dove Medical Press 2018-10-01 /pmc/articles/PMC6171755/ /pubmed/30319261 http://dx.doi.org/10.2147/NDT.S176676 Text en © 2018 Kishi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Kishi, Taro
Oya, Kazuto
Matsui, Yuki
Nomura, Ikuo
Sakuma, Kenji
Okuya, Makoto
Matsuda, Yuki
Fujita, Kiyoshi
Funahashi, Toshihiko
Yoshimura, Reiji
Iwata, Nakao
Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title_full Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title_fullStr Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title_full_unstemmed Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title_short Comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
title_sort comparison of the efficacy and safety of 4 and 2 mg/day brexpiprazole for acute schizophrenia: a meta-analysis of double-blind, randomized placebo-controlled trials
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171755/
https://www.ncbi.nlm.nih.gov/pubmed/30319261
http://dx.doi.org/10.2147/NDT.S176676
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