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Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study
Interferon-alpha (IFN-α) is a key mediator of antiviral immune responses used to treat Hepatitis C infection. Though clinically effective, IFN-α rapidly impairs mood, motivation and cognition, effects that can appear indistinguishable from major depression and provide powerful empirical support for...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074446/ https://www.ncbi.nlm.nih.gov/pubmed/26697999 http://dx.doi.org/10.1016/j.bbi.2015.12.011 |
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author | Dipasquale, Ottavia Cooper, Ella A. Tibble, Jeremy Voon, Valerie Baglio, Francesca Baselli, Giuseppe Cercignani, Mara Harrison, Neil A. |
author_facet | Dipasquale, Ottavia Cooper, Ella A. Tibble, Jeremy Voon, Valerie Baglio, Francesca Baselli, Giuseppe Cercignani, Mara Harrison, Neil A. |
author_sort | Dipasquale, Ottavia |
collection | PubMed |
description | Interferon-alpha (IFN-α) is a key mediator of antiviral immune responses used to treat Hepatitis C infection. Though clinically effective, IFN-α rapidly impairs mood, motivation and cognition, effects that can appear indistinguishable from major depression and provide powerful empirical support for the inflammation theory of depression. Though inflammation has been shown to modulate activity within discrete brain regions, how it affects distributed information processing and the architecture of whole brain functional connectivity networks have not previously been investigated. Here we use a graph theoretic analysis of resting state functional magnetic resonance imaging (rfMRI) to investigate acute effects of systemic interferon-alpha (IFN-α) on whole brain functional connectivity architecture and its relationship to IFN-α-induced mood change. Twenty-two patients with Hepatitis-C infection, initiating IFN-α-based therapy were scanned at baseline and 4 h after their first IFN-α dose. The whole brain network was parcellated into 110 cortical and sub-cortical nodes based on the Oxford-Harvard Atlas and effects assessed on higher-level graph metrics, including node degree, betweenness centrality, global and local efficiency. IFN-α was associated with a significant reduction in global network connectivity (node degree) (p = 0.033) and efficiency (p = 0.013), indicating a global reduction of information transfer among the nodes forming the whole brain network. Effects were similar for highly connected (hub) and non-hub nodes, with no effect on betweenness centrality (p > 0.1). At a local level, we identified regions with reduced efficiency of information exchange and a sub-network with decreased functional connectivity after IFN-α. Changes in local and particularly global functional connectivity correlated with associated changes in mood measured on the Profile of Mood States (POMS) questionnaire. IFN-α rapidly induced a profound shift in whole brain network structure, impairing global functional connectivity and the efficiency of parallel information exchange. Correlations with multiple indices of mood change support a role for global changes in brain functional connectivity architecture in coordinated behavioral responses to IFN-α. |
format | Online Article Text |
id | pubmed-5074446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50744462016-11-01 Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study Dipasquale, Ottavia Cooper, Ella A. Tibble, Jeremy Voon, Valerie Baglio, Francesca Baselli, Giuseppe Cercignani, Mara Harrison, Neil A. Brain Behav Immun Article Interferon-alpha (IFN-α) is a key mediator of antiviral immune responses used to treat Hepatitis C infection. Though clinically effective, IFN-α rapidly impairs mood, motivation and cognition, effects that can appear indistinguishable from major depression and provide powerful empirical support for the inflammation theory of depression. Though inflammation has been shown to modulate activity within discrete brain regions, how it affects distributed information processing and the architecture of whole brain functional connectivity networks have not previously been investigated. Here we use a graph theoretic analysis of resting state functional magnetic resonance imaging (rfMRI) to investigate acute effects of systemic interferon-alpha (IFN-α) on whole brain functional connectivity architecture and its relationship to IFN-α-induced mood change. Twenty-two patients with Hepatitis-C infection, initiating IFN-α-based therapy were scanned at baseline and 4 h after their first IFN-α dose. The whole brain network was parcellated into 110 cortical and sub-cortical nodes based on the Oxford-Harvard Atlas and effects assessed on higher-level graph metrics, including node degree, betweenness centrality, global and local efficiency. IFN-α was associated with a significant reduction in global network connectivity (node degree) (p = 0.033) and efficiency (p = 0.013), indicating a global reduction of information transfer among the nodes forming the whole brain network. Effects were similar for highly connected (hub) and non-hub nodes, with no effect on betweenness centrality (p > 0.1). At a local level, we identified regions with reduced efficiency of information exchange and a sub-network with decreased functional connectivity after IFN-α. Changes in local and particularly global functional connectivity correlated with associated changes in mood measured on the Profile of Mood States (POMS) questionnaire. IFN-α rapidly induced a profound shift in whole brain network structure, impairing global functional connectivity and the efficiency of parallel information exchange. Correlations with multiple indices of mood change support a role for global changes in brain functional connectivity architecture in coordinated behavioral responses to IFN-α. Elsevier 2016-11 /pmc/articles/PMC5074446/ /pubmed/26697999 http://dx.doi.org/10.1016/j.bbi.2015.12.011 Text en © 2015 The Authors 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 | Article Dipasquale, Ottavia Cooper, Ella A. Tibble, Jeremy Voon, Valerie Baglio, Francesca Baselli, Giuseppe Cercignani, Mara Harrison, Neil A. Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title | Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title_full | Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title_fullStr | Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title_full_unstemmed | Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title_short | Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study |
title_sort | interferon-α acutely impairs whole-brain functional connectivity network architecture – a preliminary study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074446/ https://www.ncbi.nlm.nih.gov/pubmed/26697999 http://dx.doi.org/10.1016/j.bbi.2015.12.011 |
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