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Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder

OBJECTIVES: : Bipolar disorder (BD) is a severe, chronic, affective disorder characterized by recurrent switching between mood states, psychomotor and cognitive symptoms, which can linger in euthymic states as residual symptoms. Hippocampal alterations may play a key role in the neural processing of...

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Autores principales: Saccaro, Luigi F, Gaviria, Julian, Ville, Dimitri Van De, Piguet, Camille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275545/
https://www.ncbi.nlm.nih.gov/pubmed/37062926
http://dx.doi.org/10.1002/brb3.3010
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author Saccaro, Luigi F
Gaviria, Julian
Ville, Dimitri Van De
Piguet, Camille
author_facet Saccaro, Luigi F
Gaviria, Julian
Ville, Dimitri Van De
Piguet, Camille
author_sort Saccaro, Luigi F
collection PubMed
description OBJECTIVES: : Bipolar disorder (BD) is a severe, chronic, affective disorder characterized by recurrent switching between mood states, psychomotor and cognitive symptoms, which can linger in euthymic states as residual symptoms. Hippocampal alterations may play a key role in the neural processing of BD symptoms. However, its dynamic functional connectivity (dFC) remains unclear. Therefore, the present study explores hippocampal dFC in relation to BD symptoms. METHODS: : We assessed hippocampus‐based dFC coactivation patterns (CAPs) on resting‐state fMRI data of 25 euthymic BD patients and 25 age‐ and sex‐matched healthy controls (HC). RESULTS: : Bilateral hippocampal dFC with somatomotor networks (SMN) was reduced in BD, compared to HC, while at the same time dFC between the left hippocampus and midcingulo‐insular salience system (SN) was higher in BD. Correlational analysis between CAPs and clinical scores revealed that dFC between the bilateral hippocampus and the default‐like network (DMN) correlated with depression scores in BD. Furthermore, pathological hyperconnectivity between the default mode network (DMN) and SMN and the frontoparietal network (FPN) was modulated by the same depression scores in BD. CONCLUSIONS: : Overall, we observed alterations of large‐scale functional brain networks associated with decreased flexibility in cognitive control, salience detection, and emotion processing in BD. Additionally, the present study provides new insights on the neural architecture underlying a self‐centered perspective on the environment in BD patients. dFC markers may improve detection, treatment, and follow‐up of BD patients and of disabling residual depressive symptoms in particular.
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spelling pubmed-102755452023-06-17 Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder Saccaro, Luigi F Gaviria, Julian Ville, Dimitri Van De Piguet, Camille Brain Behav Original Articles OBJECTIVES: : Bipolar disorder (BD) is a severe, chronic, affective disorder characterized by recurrent switching between mood states, psychomotor and cognitive symptoms, which can linger in euthymic states as residual symptoms. Hippocampal alterations may play a key role in the neural processing of BD symptoms. However, its dynamic functional connectivity (dFC) remains unclear. Therefore, the present study explores hippocampal dFC in relation to BD symptoms. METHODS: : We assessed hippocampus‐based dFC coactivation patterns (CAPs) on resting‐state fMRI data of 25 euthymic BD patients and 25 age‐ and sex‐matched healthy controls (HC). RESULTS: : Bilateral hippocampal dFC with somatomotor networks (SMN) was reduced in BD, compared to HC, while at the same time dFC between the left hippocampus and midcingulo‐insular salience system (SN) was higher in BD. Correlational analysis between CAPs and clinical scores revealed that dFC between the bilateral hippocampus and the default‐like network (DMN) correlated with depression scores in BD. Furthermore, pathological hyperconnectivity between the default mode network (DMN) and SMN and the frontoparietal network (FPN) was modulated by the same depression scores in BD. CONCLUSIONS: : Overall, we observed alterations of large‐scale functional brain networks associated with decreased flexibility in cognitive control, salience detection, and emotion processing in BD. Additionally, the present study provides new insights on the neural architecture underlying a self‐centered perspective on the environment in BD patients. dFC markers may improve detection, treatment, and follow‐up of BD patients and of disabling residual depressive symptoms in particular. John Wiley and Sons Inc. 2023-04-16 /pmc/articles/PMC10275545/ /pubmed/37062926 http://dx.doi.org/10.1002/brb3.3010 Text en © 2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Saccaro, Luigi F
Gaviria, Julian
Ville, Dimitri Van De
Piguet, Camille
Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title_full Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title_fullStr Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title_full_unstemmed Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title_short Dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
title_sort dynamic functional hippocampal markers of residual depressive symptoms in euthymic bipolar disorder
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275545/
https://www.ncbi.nlm.nih.gov/pubmed/37062926
http://dx.doi.org/10.1002/brb3.3010
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