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Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication

In schizophrenia, alterations of proinflammatory cytokine levels have been reported and related to the disease and psychopathology. However, only limited conclusions can be drawn in view of confounding factors such as infection, age, sex, smoking, and antipsychotic medication. Chronic schizophrenic...

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Autores principales: Schmitt, Andrea, Bertsch, Thomas, Tost, Heike, Bergmann, Andrea, Henning, Uwe, Klimke, Ansgar, Falkai, Peter
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2413198/
https://www.ncbi.nlm.nih.gov/pubmed/18568063
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author Schmitt, Andrea
Bertsch, Thomas
Tost, Heike
Bergmann, Andrea
Henning, Uwe
Klimke, Ansgar
Falkai, Peter
author_facet Schmitt, Andrea
Bertsch, Thomas
Tost, Heike
Bergmann, Andrea
Henning, Uwe
Klimke, Ansgar
Falkai, Peter
author_sort Schmitt, Andrea
collection PubMed
description In schizophrenia, alterations of proinflammatory cytokine levels have been reported and related to the disease and psychopathology. However, only limited conclusions can be drawn in view of confounding factors such as infection, age, sex, smoking, and antipsychotic medication. Chronic schizophrenic patients with a long-term disease process and medication period have not been investigated so far. We have measured serum levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)α in 41 elderly, chronic schizophrenic patients and 23 age- and sex-matched controls using enzyme-linked immunosorbent assay (ELISA). We assessed detailed psychopathology and neuropsychological performance and determined serum levels of haloperidol, clozapine, and the two main clozapine metabolites, desmethylclozapine and clozapine metabolite N-oxide, by high-pressure liquid chromatography (HPLC). IL-1β and IL-6 levels were increased in treatment-resistant schizophrenic patients compared with healthy controls, whereas TNFα showed no difference. We did not find statistically significant differences of cytokine levels between medication groups and there was no correlation with serum levels of antipsychotics or psychopathological rating scores. Elevations of IL-1β and IL-6 in elderly chronic schizophrenic patients may be related to an active disease process lasting until old age. Despite missing correlations, long-term treatment effects in treatment-resistant patients may have affected TNFα, leading to control levels. Post-mortem and animal studies should clarify the presence of altered immune function in the brain as well as the effect of cytokine levels in relation to neurodevelopmental disturbances and schizophrenia-associated behavior.
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spelling pubmed-24131982008-06-20 Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication Schmitt, Andrea Bertsch, Thomas Tost, Heike Bergmann, Andrea Henning, Uwe Klimke, Ansgar Falkai, Peter Neuropsychiatr Dis Treat Original Research In schizophrenia, alterations of proinflammatory cytokine levels have been reported and related to the disease and psychopathology. However, only limited conclusions can be drawn in view of confounding factors such as infection, age, sex, smoking, and antipsychotic medication. Chronic schizophrenic patients with a long-term disease process and medication period have not been investigated so far. We have measured serum levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)α in 41 elderly, chronic schizophrenic patients and 23 age- and sex-matched controls using enzyme-linked immunosorbent assay (ELISA). We assessed detailed psychopathology and neuropsychological performance and determined serum levels of haloperidol, clozapine, and the two main clozapine metabolites, desmethylclozapine and clozapine metabolite N-oxide, by high-pressure liquid chromatography (HPLC). IL-1β and IL-6 levels were increased in treatment-resistant schizophrenic patients compared with healthy controls, whereas TNFα showed no difference. We did not find statistically significant differences of cytokine levels between medication groups and there was no correlation with serum levels of antipsychotics or psychopathological rating scores. Elevations of IL-1β and IL-6 in elderly chronic schizophrenic patients may be related to an active disease process lasting until old age. Despite missing correlations, long-term treatment effects in treatment-resistant patients may have affected TNFα, leading to control levels. Post-mortem and animal studies should clarify the presence of altered immune function in the brain as well as the effect of cytokine levels in relation to neurodevelopmental disturbances and schizophrenia-associated behavior. Dove Medical Press 2005-06 /pmc/articles/PMC2413198/ /pubmed/18568063 Text en © 2005 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Schmitt, Andrea
Bertsch, Thomas
Tost, Heike
Bergmann, Andrea
Henning, Uwe
Klimke, Ansgar
Falkai, Peter
Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title_full Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title_fullStr Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title_full_unstemmed Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title_short Increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
title_sort increased serum interleukin-1β and interleukin-6 in elderly, chronic schizophrenic patients on stable antipsychotic medication
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2413198/
https://www.ncbi.nlm.nih.gov/pubmed/18568063
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