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Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms
Adults with a history of depression show distinct patterns of grey matter volume (GMV) in frontal cortical (e.g., prefrontal cortex, orbitofrontal cortex) and limbic (e.g., anterior cingulate, amygdala, hippocampus, dorsal striatum) structures, regions relevant to the processing and regulation of re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479290/ https://www.ncbi.nlm.nih.gov/pubmed/32889399 http://dx.doi.org/10.1016/j.nicl.2020.102395 |
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author | Vandermeer, Matthew R.J. Liu, Pan Mohamed Ali, Ola Daoust, Andrew R. Joanisse, Marc F. Barch, Deanna M. Hayden, Elizabeth P. |
author_facet | Vandermeer, Matthew R.J. Liu, Pan Mohamed Ali, Ola Daoust, Andrew R. Joanisse, Marc F. Barch, Deanna M. Hayden, Elizabeth P. |
author_sort | Vandermeer, Matthew R.J. |
collection | PubMed |
description | Adults with a history of depression show distinct patterns of grey matter volume (GMV) in frontal cortical (e.g., prefrontal cortex, orbitofrontal cortex) and limbic (e.g., anterior cingulate, amygdala, hippocampus, dorsal striatum) structures, regions relevant to the processing and regulation of reward, which is impaired in the context of depression. However, it is unclear whether these GMV associations with depression precede depressive disorder onset or whether GMV is related to early emerging symptoms or familial depression. To address these questions, we used voxel-based morphometry (VBM) to examine GMV in 85 community-dwelling children (M = 11.12 years, SD = 0.63 years) screened for current and lifetime depression. Associations between children’s depressive symptoms (self- and mother-report of children’s symptoms), children’s maternal depression history, and GMV were examined. Although maternal depression history was unrelated to children’s GMV, child GMV in the orbitofrontal cortex (OFC) was negatively related to children’s self-reported depressive symptoms, using both a priori ROI and whole-brain analyses. Moderated regression analyses indicated that girls’ GMV was negatively related to girls’ depressive symptoms (as indexed by both self- and mother-report of girls’ symptoms), whereas boys’ symptoms were positively related to GMV. Our findings suggest that brain morphology in the OFC, a region with functional roles in processes relevant to depressive symptoms (i.e., reward-based learning and reward processing), is associated with early depressive symptoms prior to the development of clinically significant depression. |
format | Online Article Text |
id | pubmed-7479290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74792902020-09-15 Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms Vandermeer, Matthew R.J. Liu, Pan Mohamed Ali, Ola Daoust, Andrew R. Joanisse, Marc F. Barch, Deanna M. Hayden, Elizabeth P. Neuroimage Clin Regular Article Adults with a history of depression show distinct patterns of grey matter volume (GMV) in frontal cortical (e.g., prefrontal cortex, orbitofrontal cortex) and limbic (e.g., anterior cingulate, amygdala, hippocampus, dorsal striatum) structures, regions relevant to the processing and regulation of reward, which is impaired in the context of depression. However, it is unclear whether these GMV associations with depression precede depressive disorder onset or whether GMV is related to early emerging symptoms or familial depression. To address these questions, we used voxel-based morphometry (VBM) to examine GMV in 85 community-dwelling children (M = 11.12 years, SD = 0.63 years) screened for current and lifetime depression. Associations between children’s depressive symptoms (self- and mother-report of children’s symptoms), children’s maternal depression history, and GMV were examined. Although maternal depression history was unrelated to children’s GMV, child GMV in the orbitofrontal cortex (OFC) was negatively related to children’s self-reported depressive symptoms, using both a priori ROI and whole-brain analyses. Moderated regression analyses indicated that girls’ GMV was negatively related to girls’ depressive symptoms (as indexed by both self- and mother-report of girls’ symptoms), whereas boys’ symptoms were positively related to GMV. Our findings suggest that brain morphology in the OFC, a region with functional roles in processes relevant to depressive symptoms (i.e., reward-based learning and reward processing), is associated with early depressive symptoms prior to the development of clinically significant depression. Elsevier 2020-08-25 /pmc/articles/PMC7479290/ /pubmed/32889399 http://dx.doi.org/10.1016/j.nicl.2020.102395 Text en © 2020 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 Vandermeer, Matthew R.J. Liu, Pan Mohamed Ali, Ola Daoust, Andrew R. Joanisse, Marc F. Barch, Deanna M. Hayden, Elizabeth P. Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title | Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title_full | Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title_fullStr | Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title_full_unstemmed | Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title_short | Orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
title_sort | orbitofrontal cortex grey matter volume is related to children’s depressive symptoms |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479290/ https://www.ncbi.nlm.nih.gov/pubmed/32889399 http://dx.doi.org/10.1016/j.nicl.2020.102395 |
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