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Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity
BACKGROUND: To determine whether depressive symptoms in traumatic brain injury (TBI) patients were associated with altered resting-state functional connectivity (rs-fc) or voxel-based morphology in brain regions involved in emotional regulation and associated with depression. METHODS: In the present...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123829/ https://www.ncbi.nlm.nih.gov/pubmed/37310305 http://dx.doi.org/10.1017/S0033291721004724 |
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author | Luo, Lizhu Langley, Christelle Moreno-Lopez, Laura Kendrick, Keith Menon, David K. Stamatakis, Emmanuel A. Sahakian, Barbara J. |
author_facet | Luo, Lizhu Langley, Christelle Moreno-Lopez, Laura Kendrick, Keith Menon, David K. Stamatakis, Emmanuel A. Sahakian, Barbara J. |
author_sort | Luo, Lizhu |
collection | PubMed |
description | BACKGROUND: To determine whether depressive symptoms in traumatic brain injury (TBI) patients were associated with altered resting-state functional connectivity (rs-fc) or voxel-based morphology in brain regions involved in emotional regulation and associated with depression. METHODS: In the present study, we examined 79 patients (57 males; age range = 17–70 years, M ± s.d. = 38 ± 16.13; BDI-II, M ± s.d. = 9.84 ± 8.67) with TBI. We used structural MRI and resting-state fMRI to examine whether there was a relationship between depression, as measured with the Beck Depression Inventory (BDI-II), and the voxel-based morphology or functional connectivity in regions previously identified as involved in emotional regulation in patients following TBI. Patients were at least 4 months post-TBI (M ± s.d. = 15.13 ± 11.67 months) and the severity of the injury included mild to severe cases [Glasgow Coma Scale (GCS), M ± s.d. = 6.87 ± 3.31]. RESULTS: Our results showed that BDI-II scores were unrelated to voxel-based morphology in the examined regions. We found a positive association between depression scores and rs-fc between limbic regions and cognitive control regions. Conversely, there was a negative association between depression scores and rs-fc between limbic and frontal regions involved in emotion regulation. CONCLUSION: These findings lead to a better understanding of the exact mechanisms that contribute to depression following TBI and better inform treatment decisions. |
format | Online Article Text |
id | pubmed-10123829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101238292023-04-25 Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity Luo, Lizhu Langley, Christelle Moreno-Lopez, Laura Kendrick, Keith Menon, David K. Stamatakis, Emmanuel A. Sahakian, Barbara J. Psychol Med Original Article BACKGROUND: To determine whether depressive symptoms in traumatic brain injury (TBI) patients were associated with altered resting-state functional connectivity (rs-fc) or voxel-based morphology in brain regions involved in emotional regulation and associated with depression. METHODS: In the present study, we examined 79 patients (57 males; age range = 17–70 years, M ± s.d. = 38 ± 16.13; BDI-II, M ± s.d. = 9.84 ± 8.67) with TBI. We used structural MRI and resting-state fMRI to examine whether there was a relationship between depression, as measured with the Beck Depression Inventory (BDI-II), and the voxel-based morphology or functional connectivity in regions previously identified as involved in emotional regulation in patients following TBI. Patients were at least 4 months post-TBI (M ± s.d. = 15.13 ± 11.67 months) and the severity of the injury included mild to severe cases [Glasgow Coma Scale (GCS), M ± s.d. = 6.87 ± 3.31]. RESULTS: Our results showed that BDI-II scores were unrelated to voxel-based morphology in the examined regions. We found a positive association between depression scores and rs-fc between limbic regions and cognitive control regions. Conversely, there was a negative association between depression scores and rs-fc between limbic and frontal regions involved in emotion regulation. CONCLUSION: These findings lead to a better understanding of the exact mechanisms that contribute to depression following TBI and better inform treatment decisions. Cambridge University Press 2023-04 2021-12-20 /pmc/articles/PMC10123829/ /pubmed/37310305 http://dx.doi.org/10.1017/S0033291721004724 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited. |
spellingShingle | Original Article Luo, Lizhu Langley, Christelle Moreno-Lopez, Laura Kendrick, Keith Menon, David K. Stamatakis, Emmanuel A. Sahakian, Barbara J. Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title | Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title_full | Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title_fullStr | Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title_full_unstemmed | Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title_short | Depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
title_sort | depressive symptoms following traumatic brain injury are associated with resting-state functional connectivity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123829/ https://www.ncbi.nlm.nih.gov/pubmed/37310305 http://dx.doi.org/10.1017/S0033291721004724 |
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