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New Developments in the Treatment of Schizophrenia: An Expert Roundtable

BACKGROUND: Schizophrenia is a disabling disorder that profoundly affects functioning and quality of life. While available antipsychotics have improved outcomes for patients with schizophrenia, they are relatively ineffective for negative and cognitive symptoms and are associated with a range of tro...

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Autores principales: Kantrowitz, Joshua T, Correll, Christoph U, Jain, Rakesh, Cutler, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229849/
https://www.ncbi.nlm.nih.gov/pubmed/36932673
http://dx.doi.org/10.1093/ijnp/pyad011
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author Kantrowitz, Joshua T
Correll, Christoph U
Jain, Rakesh
Cutler, Andrew J
author_facet Kantrowitz, Joshua T
Correll, Christoph U
Jain, Rakesh
Cutler, Andrew J
author_sort Kantrowitz, Joshua T
collection PubMed
description BACKGROUND: Schizophrenia is a disabling disorder that profoundly affects functioning and quality of life. While available antipsychotics have improved outcomes for patients with schizophrenia, they are relatively ineffective for negative and cognitive symptoms and are associated with a range of troublesome side effects. A significant unmet medical need for more effective and better-tolerated therapies remains. METHODS: A roundtable consisting of 4 experts in the treatment of patients with schizophrenia convened to discuss the current treatment landscape, unmet needs from patient and societal perspectives, and the potential of emerging therapies with novel mechanisms of action (MOAs). RESULTS: Key areas of unmet need include optimal implementation of available treatments, effective treatment of negative and cognitive symptoms, improvements in medication adherence, novel MOAs, avoidance of postsynaptic dopamine blockade–related adverse effects, and individualized approaches to treatment. With the possible exception of clozapine, all currently available antipsychotics primarily act by blocking dopamine D(2) receptors. Agents with novel MOAs are urgently needed to effectively target the full range of symptoms in schizophrenia and facilitate an individualized treatment approach. Discussion focused on promising novel MOAs that have demonstrated potential in phase 2 and 3 trials include muscarinic receptor agonism, trace amine-associated receptor 1 agonism, serotonin receptor antagonism/inverse agonism, and glutamatergic modulation. CONCLUSIONS: Results from early clinical trials of agents with novel MOAs are encouraging, particularly for muscarinic and trace amine-associated receptor 1 agonists. These agents offer renewed hope for meaningful improvement in the management of patients with schizophrenia.
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spelling pubmed-102298492023-06-01 New Developments in the Treatment of Schizophrenia: An Expert Roundtable Kantrowitz, Joshua T Correll, Christoph U Jain, Rakesh Cutler, Andrew J Int J Neuropsychopharmacol Reviews BACKGROUND: Schizophrenia is a disabling disorder that profoundly affects functioning and quality of life. While available antipsychotics have improved outcomes for patients with schizophrenia, they are relatively ineffective for negative and cognitive symptoms and are associated with a range of troublesome side effects. A significant unmet medical need for more effective and better-tolerated therapies remains. METHODS: A roundtable consisting of 4 experts in the treatment of patients with schizophrenia convened to discuss the current treatment landscape, unmet needs from patient and societal perspectives, and the potential of emerging therapies with novel mechanisms of action (MOAs). RESULTS: Key areas of unmet need include optimal implementation of available treatments, effective treatment of negative and cognitive symptoms, improvements in medication adherence, novel MOAs, avoidance of postsynaptic dopamine blockade–related adverse effects, and individualized approaches to treatment. With the possible exception of clozapine, all currently available antipsychotics primarily act by blocking dopamine D(2) receptors. Agents with novel MOAs are urgently needed to effectively target the full range of symptoms in schizophrenia and facilitate an individualized treatment approach. Discussion focused on promising novel MOAs that have demonstrated potential in phase 2 and 3 trials include muscarinic receptor agonism, trace amine-associated receptor 1 agonism, serotonin receptor antagonism/inverse agonism, and glutamatergic modulation. CONCLUSIONS: Results from early clinical trials of agents with novel MOAs are encouraging, particularly for muscarinic and trace amine-associated receptor 1 agonists. These agents offer renewed hope for meaningful improvement in the management of patients with schizophrenia. Oxford University Press 2023-03-18 /pmc/articles/PMC10229849/ /pubmed/36932673 http://dx.doi.org/10.1093/ijnp/pyad011 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of CINP. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Kantrowitz, Joshua T
Correll, Christoph U
Jain, Rakesh
Cutler, Andrew J
New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title_full New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title_fullStr New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title_full_unstemmed New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title_short New Developments in the Treatment of Schizophrenia: An Expert Roundtable
title_sort new developments in the treatment of schizophrenia: an expert roundtable
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229849/
https://www.ncbi.nlm.nih.gov/pubmed/36932673
http://dx.doi.org/10.1093/ijnp/pyad011
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