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Early prediction of blonanserin response in Japanese patients with schizophrenia

BACKGROUND: Blonanserin is a second-generation antipsychotic used for the treatment of schizophrenia in Japan and Korea. The present study aimed to examine early prediction of blonanserin in patients with schizophrenia. METHODS: An 8-week, prospective, single-arm, flexible-dose clinical trial of blo...

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Autores principales: Kishi, Taro, Matsuda, Yuki, Fujita, Kiyoshi, Iwata, Nakao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181750/
https://www.ncbi.nlm.nih.gov/pubmed/25285009
http://dx.doi.org/10.2147/NDT.S70227
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author Kishi, Taro
Matsuda, Yuki
Fujita, Kiyoshi
Iwata, Nakao
author_facet Kishi, Taro
Matsuda, Yuki
Fujita, Kiyoshi
Iwata, Nakao
author_sort Kishi, Taro
collection PubMed
description BACKGROUND: Blonanserin is a second-generation antipsychotic used for the treatment of schizophrenia in Japan and Korea. The present study aimed to examine early prediction of blonanserin in patients with schizophrenia. METHODS: An 8-week, prospective, single-arm, flexible-dose clinical trial of blonanserin in patients with schizophrenia was conducted under real-world conditions. The inclusion criteria were antipsychotic naïve, and first-episode schizophrenia patients or schizophrenia patients with no consumption of any antipsychotic medication for more than 4 weeks before enrollment in this study. The positive predictive value, negative predictive value, sensitivity, specificity, and predictive power were calculated for the response status at week 4 to predict the subsequent response at week 8. RESULTS: Thirty-seven patients were recruited (56.8% of them had first-episode schizophrenia), and 28 (75.7%) completed the trial. At week 8, blonanserin was associated with a significant improvement in the Positive and Negative Syndrome Scale (PANSS) total score (P<0.0001) and in positive (P<0.0001), negative (P<0.0001), and general subscale scores (P<0.0001). In terms of percentage improvement of PANSS total scores from baseline to week 8, 64.9% of patients showed a ≥20% reduction in the PANSS total score and 48.6% showed a ≥30% reduction. However, 8.1% of patients experienced at least one adverse event. Using the 20% reduction in the PANSS total score at week 4 as a definition of an early response, the negative predictive values for later responses (ie, reductions of ≥30 and ≥40 in the PANSS total scores) were 88.9% and 94.1%, respectively. The specificities were 80.0% and 51.6%, respectively. CONCLUSION: Our results suggest that the blonanserin response at week 4 could predict the later response at week 8.
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spelling pubmed-41817502014-10-03 Early prediction of blonanserin response in Japanese patients with schizophrenia Kishi, Taro Matsuda, Yuki Fujita, Kiyoshi Iwata, Nakao Neuropsychiatr Dis Treat Original Research BACKGROUND: Blonanserin is a second-generation antipsychotic used for the treatment of schizophrenia in Japan and Korea. The present study aimed to examine early prediction of blonanserin in patients with schizophrenia. METHODS: An 8-week, prospective, single-arm, flexible-dose clinical trial of blonanserin in patients with schizophrenia was conducted under real-world conditions. The inclusion criteria were antipsychotic naïve, and first-episode schizophrenia patients or schizophrenia patients with no consumption of any antipsychotic medication for more than 4 weeks before enrollment in this study. The positive predictive value, negative predictive value, sensitivity, specificity, and predictive power were calculated for the response status at week 4 to predict the subsequent response at week 8. RESULTS: Thirty-seven patients were recruited (56.8% of them had first-episode schizophrenia), and 28 (75.7%) completed the trial. At week 8, blonanserin was associated with a significant improvement in the Positive and Negative Syndrome Scale (PANSS) total score (P<0.0001) and in positive (P<0.0001), negative (P<0.0001), and general subscale scores (P<0.0001). In terms of percentage improvement of PANSS total scores from baseline to week 8, 64.9% of patients showed a ≥20% reduction in the PANSS total score and 48.6% showed a ≥30% reduction. However, 8.1% of patients experienced at least one adverse event. Using the 20% reduction in the PANSS total score at week 4 as a definition of an early response, the negative predictive values for later responses (ie, reductions of ≥30 and ≥40 in the PANSS total scores) were 88.9% and 94.1%, respectively. The specificities were 80.0% and 51.6%, respectively. CONCLUSION: Our results suggest that the blonanserin response at week 4 could predict the later response at week 8. Dove Medical Press 2014-09-23 /pmc/articles/PMC4181750/ /pubmed/25285009 http://dx.doi.org/10.2147/NDT.S70227 Text en © 2014 Kishi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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
Matsuda, Yuki
Fujita, Kiyoshi
Iwata, Nakao
Early prediction of blonanserin response in Japanese patients with schizophrenia
title Early prediction of blonanserin response in Japanese patients with schizophrenia
title_full Early prediction of blonanserin response in Japanese patients with schizophrenia
title_fullStr Early prediction of blonanserin response in Japanese patients with schizophrenia
title_full_unstemmed Early prediction of blonanserin response in Japanese patients with schizophrenia
title_short Early prediction of blonanserin response in Japanese patients with schizophrenia
title_sort early prediction of blonanserin response in japanese patients with schizophrenia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181750/
https://www.ncbi.nlm.nih.gov/pubmed/25285009
http://dx.doi.org/10.2147/NDT.S70227
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