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Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up
BACKGROUND: Cariprazine, a novel antipsychotic drug that is a partial agonist with preferential binding to the D3 receptor, has demonstrated efficacy in clinical trials across all symptom domains, including negative symptoms, which can occur early in the course of psychotic illness. However, evidenc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323827/ https://www.ncbi.nlm.nih.gov/pubmed/37426095 http://dx.doi.org/10.3389/fpsyt.2023.1183912 |
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author | Pappa, Sofia Kalniunas, Arturas Maret, Jose |
author_facet | Pappa, Sofia Kalniunas, Arturas Maret, Jose |
author_sort | Pappa, Sofia |
collection | PubMed |
description | BACKGROUND: Cariprazine, a novel antipsychotic drug that is a partial agonist with preferential binding to the D3 receptor, has demonstrated efficacy in clinical trials across all symptom domains, including negative symptoms, which can occur early in the course of psychotic illness. However, evidence, to date regarding its effects in early psychosis patients with primary negative symptoms has been limited. OBJECTIVES: To evaluate the efficacy of cariprazine for negative symptoms in early psychosis patients. METHODS: Demographic and clinical information of the study population were collected from the electronic records and PANSS scale administered at baseline, 3 and 6 months. Tolerability and discontinuation reasons, where applicable, were also recorded. RESULTS: Ten patients with early psychosis (four men and six women, mean age – 25.5 years) with prominent or predominant negative symptoms were treated with cariprazine (range 1.5 – 3 mg). Three patients discontinued cariprazine within the first 3 months due to patient choice, lack of response and non-compliance, respectively. In the remaining patients, there was a significant reduction in the mean negative PANSS score from baseline to 6 months (from 26.3 to 10.6), mean total PANSS score (from 81.4 to 43.3) and in the mean positive PANSS score (from 14.4 to 9.9) which correspond to a 53.1, 41.5, and 28.5% mean score reduction. CONCLUSION: This pilot study suggests that cariprazine is a safe and effective treatment in early psychosis, particularly for the alleviation of negative symptoms which remains an area of unmet treatment need. |
format | Online Article Text |
id | pubmed-10323827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103238272023-07-07 Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up Pappa, Sofia Kalniunas, Arturas Maret, Jose Front Psychiatry Psychiatry BACKGROUND: Cariprazine, a novel antipsychotic drug that is a partial agonist with preferential binding to the D3 receptor, has demonstrated efficacy in clinical trials across all symptom domains, including negative symptoms, which can occur early in the course of psychotic illness. However, evidence, to date regarding its effects in early psychosis patients with primary negative symptoms has been limited. OBJECTIVES: To evaluate the efficacy of cariprazine for negative symptoms in early psychosis patients. METHODS: Demographic and clinical information of the study population were collected from the electronic records and PANSS scale administered at baseline, 3 and 6 months. Tolerability and discontinuation reasons, where applicable, were also recorded. RESULTS: Ten patients with early psychosis (four men and six women, mean age – 25.5 years) with prominent or predominant negative symptoms were treated with cariprazine (range 1.5 – 3 mg). Three patients discontinued cariprazine within the first 3 months due to patient choice, lack of response and non-compliance, respectively. In the remaining patients, there was a significant reduction in the mean negative PANSS score from baseline to 6 months (from 26.3 to 10.6), mean total PANSS score (from 81.4 to 43.3) and in the mean positive PANSS score (from 14.4 to 9.9) which correspond to a 53.1, 41.5, and 28.5% mean score reduction. CONCLUSION: This pilot study suggests that cariprazine is a safe and effective treatment in early psychosis, particularly for the alleviation of negative symptoms which remains an area of unmet treatment need. Frontiers Media S.A. 2023-06-22 /pmc/articles/PMC10323827/ /pubmed/37426095 http://dx.doi.org/10.3389/fpsyt.2023.1183912 Text en Copyright © 2023 Pappa, Kalniunas and Maret. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Pappa, Sofia Kalniunas, Arturas Maret, Jose Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title | Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title_full | Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title_fullStr | Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title_full_unstemmed | Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title_short | Cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
title_sort | cariprazine for negative symptoms in early psychosis: a pilot study with a 6-month follow-up |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323827/ https://www.ncbi.nlm.nih.gov/pubmed/37426095 http://dx.doi.org/10.3389/fpsyt.2023.1183912 |
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