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Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia

PURPOSE/BACKGROUND: In addition to clozapine, other atypical antipsychotic drugs pharmacologically similar to clozapine, for example, olanzapine, risperidone, and melperone, are also effective in a similar proportion of treatment-resistant schizophrenia (TRS) patients, ~40%. The major goal of this s...

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Autores principales: Meltzer, Herbert Y., Share, Daniel B., Jayathilake, Karu, Salomon, Ronald M., Lee, Myung A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188269/
https://www.ncbi.nlm.nih.gov/pubmed/32332459
http://dx.doi.org/10.1097/JCP.0000000000001205
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author Meltzer, Herbert Y.
Share, Daniel B.
Jayathilake, Karu
Salomon, Ronald M.
Lee, Myung A.
author_facet Meltzer, Herbert Y.
Share, Daniel B.
Jayathilake, Karu
Salomon, Ronald M.
Lee, Myung A.
author_sort Meltzer, Herbert Y.
collection PubMed
description PURPOSE/BACKGROUND: In addition to clozapine, other atypical antipsychotic drugs pharmacologically similar to clozapine, for example, olanzapine, risperidone, and melperone, are also effective in a similar proportion of treatment-resistant schizophrenia (TRS) patients, ~40%. The major goal of this study was to compare 2 doses of lurasidone, another atypical antipsychotic drug, and time to improvement in psychopathology and cognition during a 6-month trial in TRS patients. METHODS/PROCEDURES: The diagnosis of TRS was based on clinical history and lack of improvement in psychopathology during a 6-week open trial of lurasidone 80 mg/d (phase 1). This was followed by a randomized, double-blind, 24-week trial of lurasidone, comparing 80- and 240-mg/d doses (phase 2). FINDINGS/RESULTS: Significant non–dose-related improvement in the Positive and Negative Syndrome Scale—Total and subscales and in 2 of 7 cognitive domains, speed of processing and executive function, were noted. Twenty-eight (41.8%) of 67 patients in the combined sample improved ≥20% in the Positive and Negative Syndrome Scale—Total. Of the 28 responders, 19 (67.9%) first reached ≥20% improvement between weeks 6 and 24 during phase 2, including some who had previously failed to respond to clozapine. IMPLICATIONS/CONCLUSIONS: Improvement with lurasidone is comparable with those previously reported for clozapine, melperone, olanzapine, and risperidone in TRS patients. In addition, this study demonstrated that 80 mg/d lurasidone, an effective and tolerable dose for non-TRS patients, was also effective in TRS patients but required longer duration of treatment. Direct comparison of lurasidone with clozapine in TRS patients is indicated.
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spelling pubmed-71882692020-05-04 Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia Meltzer, Herbert Y. Share, Daniel B. Jayathilake, Karu Salomon, Ronald M. Lee, Myung A. J Clin Psychopharmacol Original Contributions PURPOSE/BACKGROUND: In addition to clozapine, other atypical antipsychotic drugs pharmacologically similar to clozapine, for example, olanzapine, risperidone, and melperone, are also effective in a similar proportion of treatment-resistant schizophrenia (TRS) patients, ~40%. The major goal of this study was to compare 2 doses of lurasidone, another atypical antipsychotic drug, and time to improvement in psychopathology and cognition during a 6-month trial in TRS patients. METHODS/PROCEDURES: The diagnosis of TRS was based on clinical history and lack of improvement in psychopathology during a 6-week open trial of lurasidone 80 mg/d (phase 1). This was followed by a randomized, double-blind, 24-week trial of lurasidone, comparing 80- and 240-mg/d doses (phase 2). FINDINGS/RESULTS: Significant non–dose-related improvement in the Positive and Negative Syndrome Scale—Total and subscales and in 2 of 7 cognitive domains, speed of processing and executive function, were noted. Twenty-eight (41.8%) of 67 patients in the combined sample improved ≥20% in the Positive and Negative Syndrome Scale—Total. Of the 28 responders, 19 (67.9%) first reached ≥20% improvement between weeks 6 and 24 during phase 2, including some who had previously failed to respond to clozapine. IMPLICATIONS/CONCLUSIONS: Improvement with lurasidone is comparable with those previously reported for clozapine, melperone, olanzapine, and risperidone in TRS patients. In addition, this study demonstrated that 80 mg/d lurasidone, an effective and tolerable dose for non-TRS patients, was also effective in TRS patients but required longer duration of treatment. Direct comparison of lurasidone with clozapine in TRS patients is indicated. Lippincott Williams & Wilkins 2020 2020-04-27 /pmc/articles/PMC7188269/ /pubmed/32332459 http://dx.doi.org/10.1097/JCP.0000000000001205 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. 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) (http://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
Meltzer, Herbert Y.
Share, Daniel B.
Jayathilake, Karu
Salomon, Ronald M.
Lee, Myung A.
Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title_full Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title_fullStr Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title_full_unstemmed Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title_short Lurasidone Improves Psychopathology and Cognition in Treatment-Resistant Schizophrenia
title_sort lurasidone improves psychopathology and cognition in treatment-resistant schizophrenia
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188269/
https://www.ncbi.nlm.nih.gov/pubmed/32332459
http://dx.doi.org/10.1097/JCP.0000000000001205
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