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Brain signatures of chronic gut inflammation
Gut inflammation is thought to modify brain activity and behaviour via modulation of the gut-brain axis. However, how relapsing and remitting exposure to peripheral inflammation over the natural history of inflammatory bowel disease (IBD) contributes to altered brain dynamics is poorly understood. H...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661239/ https://www.ncbi.nlm.nih.gov/pubmed/38025434 http://dx.doi.org/10.3389/fpsyt.2023.1250268 |
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author | Hall, Caitlin V. Radford-Smith, Graham Savage, Emma Robinson, Conor Cocchi, Luca Moran, Rosalyn J. |
author_facet | Hall, Caitlin V. Radford-Smith, Graham Savage, Emma Robinson, Conor Cocchi, Luca Moran, Rosalyn J. |
author_sort | Hall, Caitlin V. |
collection | PubMed |
description | Gut inflammation is thought to modify brain activity and behaviour via modulation of the gut-brain axis. However, how relapsing and remitting exposure to peripheral inflammation over the natural history of inflammatory bowel disease (IBD) contributes to altered brain dynamics is poorly understood. Here, we used electroencephalography (EEG) to characterise changes in spontaneous spatiotemporal brain states in Crohn’s Disease (CD) (n = 40) and Ulcerative Colitis (UC) (n = 30), compared to healthy individuals (n = 28). We first provide evidence of a significantly perturbed and heterogeneous microbial profile in CD, consistent with previous work showing enduring and long-standing dysbiosis in clinical remission. Results from our brain state assessment show that CD and UC exhibit alterations in the temporal properties of states implicating default-mode network, parietal, and visual regions, reflecting a shift in the predominance from externally to internally-oriented attentional modes. We investigated these dynamics at a finer sub-network resolution, showing a CD-specific and highly selective enhancement of connectivity between the insula and medial prefrontal cortex (mPFC), regions implicated in cognitive-interoceptive appraisal mechanisms. Alongside overall higher anxiety scores in CD, we also provide preliminary support to suggest that the strength of chronic interoceptive hyper-signalling in the brain co-occurs with disease duration. Together, our results demonstrate that a long-standing diagnosis of CD is, in itself, a key factor in determining the risk of developing altered brain network signatures. |
format | Online Article Text |
id | pubmed-10661239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106612392023-11-07 Brain signatures of chronic gut inflammation Hall, Caitlin V. Radford-Smith, Graham Savage, Emma Robinson, Conor Cocchi, Luca Moran, Rosalyn J. Front Psychiatry Psychiatry Gut inflammation is thought to modify brain activity and behaviour via modulation of the gut-brain axis. However, how relapsing and remitting exposure to peripheral inflammation over the natural history of inflammatory bowel disease (IBD) contributes to altered brain dynamics is poorly understood. Here, we used electroencephalography (EEG) to characterise changes in spontaneous spatiotemporal brain states in Crohn’s Disease (CD) (n = 40) and Ulcerative Colitis (UC) (n = 30), compared to healthy individuals (n = 28). We first provide evidence of a significantly perturbed and heterogeneous microbial profile in CD, consistent with previous work showing enduring and long-standing dysbiosis in clinical remission. Results from our brain state assessment show that CD and UC exhibit alterations in the temporal properties of states implicating default-mode network, parietal, and visual regions, reflecting a shift in the predominance from externally to internally-oriented attentional modes. We investigated these dynamics at a finer sub-network resolution, showing a CD-specific and highly selective enhancement of connectivity between the insula and medial prefrontal cortex (mPFC), regions implicated in cognitive-interoceptive appraisal mechanisms. Alongside overall higher anxiety scores in CD, we also provide preliminary support to suggest that the strength of chronic interoceptive hyper-signalling in the brain co-occurs with disease duration. Together, our results demonstrate that a long-standing diagnosis of CD is, in itself, a key factor in determining the risk of developing altered brain network signatures. Frontiers Media S.A. 2023-11-07 /pmc/articles/PMC10661239/ /pubmed/38025434 http://dx.doi.org/10.3389/fpsyt.2023.1250268 Text en Copyright © 2023 Hall, Radford-Smith, Savage, Robinson, Cocchi and Moran. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Hall, Caitlin V. Radford-Smith, Graham Savage, Emma Robinson, Conor Cocchi, Luca Moran, Rosalyn J. Brain signatures of chronic gut inflammation |
title | Brain signatures of chronic gut inflammation |
title_full | Brain signatures of chronic gut inflammation |
title_fullStr | Brain signatures of chronic gut inflammation |
title_full_unstemmed | Brain signatures of chronic gut inflammation |
title_short | Brain signatures of chronic gut inflammation |
title_sort | brain signatures of chronic gut inflammation |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661239/ https://www.ncbi.nlm.nih.gov/pubmed/38025434 http://dx.doi.org/10.3389/fpsyt.2023.1250268 |
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