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Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience
Treatment with interferon (IFN) has been associated with depressive side effects. Previous neuroimaging studies have provided information about changes in brain activation patterns in patients under treatment with IFN-alpha, but the effect of other IFNs, or the role of the underlying disease, has ye...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861625/ https://www.ncbi.nlm.nih.gov/pubmed/31734534 http://dx.doi.org/10.1016/j.nicl.2019.102020 |
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author | Coch, Christoph Viviani, Roberto Breitfeld, Jörg Münzer, Katrin Dassler-Plencker, Juliane Holdenrieder, Stefan Coenen, Martin Steffens, Michael Müller, Marcus Hartmann, Gunther Stingl, Julia |
author_facet | Coch, Christoph Viviani, Roberto Breitfeld, Jörg Münzer, Katrin Dassler-Plencker, Juliane Holdenrieder, Stefan Coenen, Martin Steffens, Michael Müller, Marcus Hartmann, Gunther Stingl, Julia |
author_sort | Coch, Christoph |
collection | PubMed |
description | Treatment with interferon (IFN) has been associated with depressive side effects. Previous neuroimaging studies have provided information about changes in brain activation patterns in patients under treatment with IFN-alpha, but the effect of other IFNs, or the role of the underlying disease, has yet to be clarified. In the present fMRI study, we looked at brain changes after 8 days of IFN-beta treatment in N = =17 healthy volunteers, thus avoiding the possible confound of the effects of underlying pathology in studies of IFN-treated patients with neurological or other medical disorders. We followed a symptom dimensional approach by simultaneously investigating two distinct symptom domains of depressiveness: negative affect (amygdala) and appetitive motivation (ventral striatum). In these early phases of IFN treatment we detected a selective change in neural substrates of appetitive motivation, consistent with the predominant symptomatic change recorded in psychopathology ratings. In contrast, the fMRI phenotype of negative affect, which is known to characterize disorders of affect involving anxiety and depressiveness as well as individual vulnerability to depression, was unchanged after treatment. These findings suggest that IFN may induce an affective syndrome through a mechanism involving down-regulation of appetitive motivation. |
format | Online Article Text |
id | pubmed-6861625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68616252019-11-22 Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience Coch, Christoph Viviani, Roberto Breitfeld, Jörg Münzer, Katrin Dassler-Plencker, Juliane Holdenrieder, Stefan Coenen, Martin Steffens, Michael Müller, Marcus Hartmann, Gunther Stingl, Julia Neuroimage Clin Regular Article Treatment with interferon (IFN) has been associated with depressive side effects. Previous neuroimaging studies have provided information about changes in brain activation patterns in patients under treatment with IFN-alpha, but the effect of other IFNs, or the role of the underlying disease, has yet to be clarified. In the present fMRI study, we looked at brain changes after 8 days of IFN-beta treatment in N = =17 healthy volunteers, thus avoiding the possible confound of the effects of underlying pathology in studies of IFN-treated patients with neurological or other medical disorders. We followed a symptom dimensional approach by simultaneously investigating two distinct symptom domains of depressiveness: negative affect (amygdala) and appetitive motivation (ventral striatum). In these early phases of IFN treatment we detected a selective change in neural substrates of appetitive motivation, consistent with the predominant symptomatic change recorded in psychopathology ratings. In contrast, the fMRI phenotype of negative affect, which is known to characterize disorders of affect involving anxiety and depressiveness as well as individual vulnerability to depression, was unchanged after treatment. These findings suggest that IFN may induce an affective syndrome through a mechanism involving down-regulation of appetitive motivation. Elsevier 2019-11-14 /pmc/articles/PMC6861625/ /pubmed/31734534 http://dx.doi.org/10.1016/j.nicl.2019.102020 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article Coch, Christoph Viviani, Roberto Breitfeld, Jörg Münzer, Katrin Dassler-Plencker, Juliane Holdenrieder, Stefan Coenen, Martin Steffens, Michael Müller, Marcus Hartmann, Gunther Stingl, Julia Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title | Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title_full | Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title_fullStr | Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title_full_unstemmed | Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title_short | Interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
title_sort | interferon-beta-induced changes in neuroimaging phenotypes of appetitive motivation and reactivity to emotional salience |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861625/ https://www.ncbi.nlm.nih.gov/pubmed/31734534 http://dx.doi.org/10.1016/j.nicl.2019.102020 |
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