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Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia

BACKGROUND: According to the current schizophrenia treatment guidelines, 3 levels of responsiveness to antipsychotic medication exist: those who respond to first-line antipsychotics, those with treatment-resistant schizophrenia who respond to clozapine, and those with clozapine-resistant or ultra-tr...

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Autores principales: Goldstein, Meghan Elizabeth, Anderson, Valerie Margaret, Pillai, Avinesh, Kydd, Robert R., Russell, Bruce R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438552/
https://www.ncbi.nlm.nih.gov/pubmed/25603859
http://dx.doi.org/10.1093/ijnp/pyu117
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author Goldstein, Meghan Elizabeth
Anderson, Valerie Margaret
Pillai, Avinesh
Kydd, Robert R.
Russell, Bruce R.
author_facet Goldstein, Meghan Elizabeth
Anderson, Valerie Margaret
Pillai, Avinesh
Kydd, Robert R.
Russell, Bruce R.
author_sort Goldstein, Meghan Elizabeth
collection PubMed
description BACKGROUND: According to the current schizophrenia treatment guidelines, 3 levels of responsiveness to antipsychotic medication exist: those who respond to first-line antipsychotics, those with treatment-resistant schizophrenia who respond to clozapine, and those with clozapine-resistant or ultra-treatment resistant schizophrenia. Proton magnetic resonance spectroscopy studies indicate that antipsychotic medication decreases glutamate or total glutamate + glutamine in the brains of patients with schizophrenia and may represent a biomarker of treatment response; however, the 3 levels of treatment responsiveness have not been evaluated. METHODS: Proton magnetic resonance spectroscopy spectra were acquired at 3 Tesla from patients taking a second generation non-clozapine antipsychotic (first-line responders), patients with treatment-resistant schizophrenia taking clozapine, patients with ultra-treatment resistant schizophrenia taking a combination of antipsychotics, and healthy comparison subjects. RESULTS: Group differences in cerebrospinal fluid-corrected total glutamate + glutamine levels scaled to creatine were detected in the dorsolateral prefrontal cortex [df(3,48); F = 3.07, P = .04, partial η(2) = 0.16] and the putamen [df(3,32); F = 2.93, P = .05, partial η(2) = 0.22]. The first-line responder group had higher dorsolateral prefrontal cortex total glutamate + glutamine levels scaled to creatine than those with ultra-treatment resistant schizophrenia [mean difference = 0.25, standard error = 0.09, P = .04, family-wise error-corrected]. Those with treatment-resistant schizophrenia had higher total glutamate + glutamine levels scaled to creatine in the putamen than the first-line responders (mean difference = 0.31, standard error = 0.12, P = .05, family-wise error-corrected) and those with ultra-treatment-resistant schizophrenia (mean difference = 0.39, standard error = 0.12, P = .02, family-wise error-corrected). CONCLUSIONS: Total glutamate + glutamine levels scaled to creatine in the putamen may represent a marker of response to clozapine. Future studies should investigate glutamatergic anomalies prior to clozapine initiation and following successful treatment.
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spelling pubmed-44385522015-09-01 Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia Goldstein, Meghan Elizabeth Anderson, Valerie Margaret Pillai, Avinesh Kydd, Robert R. Russell, Bruce R. Int J Neuropsychopharmacol Research Article BACKGROUND: According to the current schizophrenia treatment guidelines, 3 levels of responsiveness to antipsychotic medication exist: those who respond to first-line antipsychotics, those with treatment-resistant schizophrenia who respond to clozapine, and those with clozapine-resistant or ultra-treatment resistant schizophrenia. Proton magnetic resonance spectroscopy studies indicate that antipsychotic medication decreases glutamate or total glutamate + glutamine in the brains of patients with schizophrenia and may represent a biomarker of treatment response; however, the 3 levels of treatment responsiveness have not been evaluated. METHODS: Proton magnetic resonance spectroscopy spectra were acquired at 3 Tesla from patients taking a second generation non-clozapine antipsychotic (first-line responders), patients with treatment-resistant schizophrenia taking clozapine, patients with ultra-treatment resistant schizophrenia taking a combination of antipsychotics, and healthy comparison subjects. RESULTS: Group differences in cerebrospinal fluid-corrected total glutamate + glutamine levels scaled to creatine were detected in the dorsolateral prefrontal cortex [df(3,48); F = 3.07, P = .04, partial η(2) = 0.16] and the putamen [df(3,32); F = 2.93, P = .05, partial η(2) = 0.22]. The first-line responder group had higher dorsolateral prefrontal cortex total glutamate + glutamine levels scaled to creatine than those with ultra-treatment resistant schizophrenia [mean difference = 0.25, standard error = 0.09, P = .04, family-wise error-corrected]. Those with treatment-resistant schizophrenia had higher total glutamate + glutamine levels scaled to creatine in the putamen than the first-line responders (mean difference = 0.31, standard error = 0.12, P = .05, family-wise error-corrected) and those with ultra-treatment-resistant schizophrenia (mean difference = 0.39, standard error = 0.12, P = .02, family-wise error-corrected). CONCLUSIONS: Total glutamate + glutamine levels scaled to creatine in the putamen may represent a marker of response to clozapine. Future studies should investigate glutamatergic anomalies prior to clozapine initiation and following successful treatment. Oxford University Press 2015-03-10 /pmc/articles/PMC4438552/ /pubmed/25603859 http://dx.doi.org/10.1093/ijnp/pyu117 Text en © The Author 2015. Published by Oxford University Press on behalf of CINP. 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 Research Article
Goldstein, Meghan Elizabeth
Anderson, Valerie Margaret
Pillai, Avinesh
Kydd, Robert R.
Russell, Bruce R.
Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title_full Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title_fullStr Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title_full_unstemmed Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title_short Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
title_sort glutamatergic neurometabolites in clozapine-responsive and -resistant schizophrenia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438552/
https://www.ncbi.nlm.nih.gov/pubmed/25603859
http://dx.doi.org/10.1093/ijnp/pyu117
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