Cargando…

T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY

BACKGROUND: There is a pressing need for new classes of treatment for psychosis. A key therapeutic target for novel compounds is the NMDA receptor, which may be modulated by nitric oxide donors such as sodium nitroprusside (SNP). Recent early phase studies of SNP in patients with psychosis have had...

Descripción completa

Detalles Bibliográficos
Autores principales: Merritt, Kate, Catalan, Ana, Cowley, Samuel, Demjaha, Arsime, Taylor, Matthew, McGuire, Philip, Cooper, Ruth, Morrison, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234164/
http://dx.doi.org/10.1093/schbul/sbaa029.600
_version_ 1783535701780856832
author Merritt, Kate
Catalan, Ana
Cowley, Samuel
Demjaha, Arsime
Taylor, Matthew
McGuire, Philip
Cooper, Ruth
Morrison, Paul
author_facet Merritt, Kate
Catalan, Ana
Cowley, Samuel
Demjaha, Arsime
Taylor, Matthew
McGuire, Philip
Cooper, Ruth
Morrison, Paul
author_sort Merritt, Kate
collection PubMed
description BACKGROUND: There is a pressing need for new classes of treatment for psychosis. A key therapeutic target for novel compounds is the NMDA receptor, which may be modulated by nitric oxide donors such as sodium nitroprusside (SNP). Recent early phase studies of SNP in patients with psychosis have had mixed results, and the drug has to be administered intravenously. GTN is a well-established cardiovascular medicine that is also a nitric oxide donor, and can be given orally. We explored the safety and effectiveness of GTN in unmedicated patients with a first episode of psychosis. METHODS: A single-centre, randomized, double-blind, placebo-controlled trial was conducted from December 2016 to April 2019 (ClinicalTrials.gov identifier: NCT02906553). Patients with a first episode of psychosis were recruited from the South London and Maudsley NHS Trust, London, UK. Nineteen patients were randomised to receive 3 x sprays of GTN or placebo for 3 consecutive days, and re-assessed on Day 7. Thirteen participants were included in the final analyses. At each assessment point, symptom levels were measured using the Positive and Negative Syndrome Scale (PANSS), and cognitive performance was evaluated using the Jumping to Conclusions (JTC) and the Hopkins Verbal Learning (HVLT) tasks. RESULTS: Compared to placebo, GTN was well tolerated, but it was not associated with significant effects on either psychotic symptoms or cognition. Bayesian statistics indicated with moderate confidence that GTN does not have a therapeutic effect. DISCUSSION: This study indicates that nitric oxide donors are not therapeutically beneficial in psychosis. It also highlights the difficulties in recruiting unmedicated patients with psychosis. Future clinical trials would benefit from frameworks built into clinical services, to signpost patients not responding to medication and those discontinuing medication to clinical trials of alternatives.
format Online
Article
Text
id pubmed-7234164
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72341642020-05-23 T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY Merritt, Kate Catalan, Ana Cowley, Samuel Demjaha, Arsime Taylor, Matthew McGuire, Philip Cooper, Ruth Morrison, Paul Schizophr Bull Poster Session III BACKGROUND: There is a pressing need for new classes of treatment for psychosis. A key therapeutic target for novel compounds is the NMDA receptor, which may be modulated by nitric oxide donors such as sodium nitroprusside (SNP). Recent early phase studies of SNP in patients with psychosis have had mixed results, and the drug has to be administered intravenously. GTN is a well-established cardiovascular medicine that is also a nitric oxide donor, and can be given orally. We explored the safety and effectiveness of GTN in unmedicated patients with a first episode of psychosis. METHODS: A single-centre, randomized, double-blind, placebo-controlled trial was conducted from December 2016 to April 2019 (ClinicalTrials.gov identifier: NCT02906553). Patients with a first episode of psychosis were recruited from the South London and Maudsley NHS Trust, London, UK. Nineteen patients were randomised to receive 3 x sprays of GTN or placebo for 3 consecutive days, and re-assessed on Day 7. Thirteen participants were included in the final analyses. At each assessment point, symptom levels were measured using the Positive and Negative Syndrome Scale (PANSS), and cognitive performance was evaluated using the Jumping to Conclusions (JTC) and the Hopkins Verbal Learning (HVLT) tasks. RESULTS: Compared to placebo, GTN was well tolerated, but it was not associated with significant effects on either psychotic symptoms or cognition. Bayesian statistics indicated with moderate confidence that GTN does not have a therapeutic effect. DISCUSSION: This study indicates that nitric oxide donors are not therapeutically beneficial in psychosis. It also highlights the difficulties in recruiting unmedicated patients with psychosis. Future clinical trials would benefit from frameworks built into clinical services, to signpost patients not responding to medication and those discontinuing medication to clinical trials of alternatives. Oxford University Press 2020-05 2020-05-18 /pmc/articles/PMC7234164/ http://dx.doi.org/10.1093/schbul/sbaa029.600 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Session III
Merritt, Kate
Catalan, Ana
Cowley, Samuel
Demjaha, Arsime
Taylor, Matthew
McGuire, Philip
Cooper, Ruth
Morrison, Paul
T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title_full T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title_fullStr T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title_full_unstemmed T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title_short T40. GLYCERYL TRINITRATE IN FIRST EPISODE PSYCHOSIS UNMEDICATED WITH ANTIPSYCHOTICS: A RANDOMISED CONTROLLED FEASIBILITY STUDY
title_sort t40. glyceryl trinitrate in first episode psychosis unmedicated with antipsychotics: a randomised controlled feasibility study
topic Poster Session III
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234164/
http://dx.doi.org/10.1093/schbul/sbaa029.600
work_keys_str_mv AT merrittkate t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT catalanana t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT cowleysamuel t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT demjahaarsime t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT taylormatthew t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT mcguirephilip t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT cooperruth t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy
AT morrisonpaul t40glyceryltrinitrateinfirstepisodepsychosisunmedicatedwithantipsychoticsarandomisedcontrolledfeasibilitystudy