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The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia

BACKGROUND: Current treatments for schizophrenia act directly on dopamine (DA) receptors but are ineffective for many patients, highlighting the need to develop new treatment approaches. Striatal DA dysfunction, indexed using [(18)F]-FDOPA imaging, is linked to the pathoetiology of schizophrenia. We...

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Autores principales: Angelescu, Ilinca, Kaar, Stephen J, Marques, Tiago Reis, Borgan, Faith, Veronesse, Mattia, Sharman, Alice, Sajjala, Anil, Deakin, Bill, Hutchison, John, Large, Charles, Howes, Oliver D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554157/
https://www.ncbi.nlm.nih.gov/pubmed/36164687
http://dx.doi.org/10.1177/02698811221122031
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author Angelescu, Ilinca
Kaar, Stephen J
Marques, Tiago Reis
Borgan, Faith
Veronesse, Mattia
Sharman, Alice
Sajjala, Anil
Deakin, Bill
Hutchison, John
Large, Charles
Howes, Oliver D
author_facet Angelescu, Ilinca
Kaar, Stephen J
Marques, Tiago Reis
Borgan, Faith
Veronesse, Mattia
Sharman, Alice
Sajjala, Anil
Deakin, Bill
Hutchison, John
Large, Charles
Howes, Oliver D
author_sort Angelescu, Ilinca
collection PubMed
description BACKGROUND: Current treatments for schizophrenia act directly on dopamine (DA) receptors but are ineffective for many patients, highlighting the need to develop new treatment approaches. Striatal DA dysfunction, indexed using [(18)F]-FDOPA imaging, is linked to the pathoetiology of schizophrenia. We evaluated the effect of a novel drug, AUT00206, a Kv3.1/3.2 potassium channel modulator, on dopaminergic function in schizophrenia and its relationship with symptom change. Additionally, we investigated the test–retest reliability of [(18)F]-FDOPA PET in schizophrenia to determine its potential as a biomarker for drug discovery. METHODS: Twenty patients with schizophrenia received symptom measures and [(18)F]-FDOPA PET scans, before and after being randomised to AUT00206 or placebo groups for up to 28 days treatment. RESULTS: AUT00206 had no significant effect on DA synthesis capacity. However, there was a correlation between reduction in striatal dopamine synthesis capacity (indexed as Ki(cer)) and reduction in symptoms, in the AUT00206 group (r = 0.58, p = 0.03). This was not observed in the placebo group (r = −0.15, p = 0.75), although the placebo group may have been underpowered to detect an effect. The intraclass correlation coefficients of [(18)F]-FDOPA indices in the placebo group ranged from 0.83 to 0.93 across striatal regions. CONCLUSIONS: The relationship between reduction in DA synthesis capacity and improvement in symptoms in the AUT00206 group provides evidence for a pharmacodynamic effect of the Kv3 channel modulator. The lack of a significant overall reduction in DA synthesis capacity in the AUT00206 group could be due to variability and the low number of subjects in this study. These findings support further investigation of Kv3 channel modulators for schizophrenia treatment. [(18)F]-FDOPA PET imaging showed very good test–retest reliability in patients with schizophrenia.
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spelling pubmed-95541572022-10-13 The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia Angelescu, Ilinca Kaar, Stephen J Marques, Tiago Reis Borgan, Faith Veronesse, Mattia Sharman, Alice Sajjala, Anil Deakin, Bill Hutchison, John Large, Charles Howes, Oliver D J Psychopharmacol Original Papers BACKGROUND: Current treatments for schizophrenia act directly on dopamine (DA) receptors but are ineffective for many patients, highlighting the need to develop new treatment approaches. Striatal DA dysfunction, indexed using [(18)F]-FDOPA imaging, is linked to the pathoetiology of schizophrenia. We evaluated the effect of a novel drug, AUT00206, a Kv3.1/3.2 potassium channel modulator, on dopaminergic function in schizophrenia and its relationship with symptom change. Additionally, we investigated the test–retest reliability of [(18)F]-FDOPA PET in schizophrenia to determine its potential as a biomarker for drug discovery. METHODS: Twenty patients with schizophrenia received symptom measures and [(18)F]-FDOPA PET scans, before and after being randomised to AUT00206 or placebo groups for up to 28 days treatment. RESULTS: AUT00206 had no significant effect on DA synthesis capacity. However, there was a correlation between reduction in striatal dopamine synthesis capacity (indexed as Ki(cer)) and reduction in symptoms, in the AUT00206 group (r = 0.58, p = 0.03). This was not observed in the placebo group (r = −0.15, p = 0.75), although the placebo group may have been underpowered to detect an effect. The intraclass correlation coefficients of [(18)F]-FDOPA indices in the placebo group ranged from 0.83 to 0.93 across striatal regions. CONCLUSIONS: The relationship between reduction in DA synthesis capacity and improvement in symptoms in the AUT00206 group provides evidence for a pharmacodynamic effect of the Kv3 channel modulator. The lack of a significant overall reduction in DA synthesis capacity in the AUT00206 group could be due to variability and the low number of subjects in this study. These findings support further investigation of Kv3 channel modulators for schizophrenia treatment. [(18)F]-FDOPA PET imaging showed very good test–retest reliability in patients with schizophrenia. SAGE Publications 2022-09-26 2022-09 /pmc/articles/PMC9554157/ /pubmed/36164687 http://dx.doi.org/10.1177/02698811221122031 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Papers
Angelescu, Ilinca
Kaar, Stephen J
Marques, Tiago Reis
Borgan, Faith
Veronesse, Mattia
Sharman, Alice
Sajjala, Anil
Deakin, Bill
Hutchison, John
Large, Charles
Howes, Oliver D
The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title_full The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title_fullStr The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title_full_unstemmed The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title_short The effect of AUT00206, a Kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)F]-FDOPA imaging in schizophrenia
title_sort effect of aut00206, a kv3 potassium channel modulator, on dopamine synthesis capacity and the reliability of [(18)f]-fdopa imaging in schizophrenia
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554157/
https://www.ncbi.nlm.nih.gov/pubmed/36164687
http://dx.doi.org/10.1177/02698811221122031
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