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Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder
BACKGROUND: Differences in the thalamocortical system have been shown in patients with major depressive disorder (MDD). Given prior evidence of phenotypic heterogeneity by the age of onset in MDD, we examined whether differences in thalamocortical connectivity could identify biological subtypes of M...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306066/ https://www.ncbi.nlm.nih.gov/pubmed/30613149 http://dx.doi.org/10.2147/NDT.S184425 |
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author | Brown, Elliot C Clark, Darren L Hassel, Stefanie MacQueen, Glenda Ramasubbu, Rajamannar |
author_facet | Brown, Elliot C Clark, Darren L Hassel, Stefanie MacQueen, Glenda Ramasubbu, Rajamannar |
author_sort | Brown, Elliot C |
collection | PubMed |
description | BACKGROUND: Differences in the thalamocortical system have been shown in patients with major depressive disorder (MDD). Given prior evidence of phenotypic heterogeneity by the age of onset in MDD, we examined whether differences in thalamocortical connectivity could identify biological subtypes of MDD defined by the age of illness onset. METHODS: A total of 94 subjects including 20 early-onset (EO) MDD (onset, 18 years), 34 adult-onset (AO) MDD, and 40 healthy controls (HCs) underwent resting-state functional MRI. Blood-oxygen-level-dependent time courses were extracted from six cortical regions of interest (ROIs) consisting of frontal, temporal, parietal, and occipital lobes and precentral and postcentral gyri. Each ROI’s time course was then correlated with each voxel in thalamus, while covarying out signal from every other ROI. RESULTS: The analysis of variance results showed significant main effects of group in frontal and temporal connectivity with thalamus. Group contrasts showed a right fronto-thalamic hypo-connectivity only in AO-MDD, but not in EO-MDD, when compared to HCs. However, direct comparison between EO-MDD and AO-MDD showed no differences. Furthermore, there was a right temporal–thalamic hyperconnectivity in both EO-MDD and AO-MDD patients relative to HCs. These results were not accounted for by sex, age, or illness burden. CONCLUSION: The age of illness onset may be a source of heterogeneity in fronto-thalamic intrinsic connectivity in MDD. |
format | Online Article Text |
id | pubmed-6306066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63060662019-01-04 Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder Brown, Elliot C Clark, Darren L Hassel, Stefanie MacQueen, Glenda Ramasubbu, Rajamannar Neuropsychiatr Dis Treat Original Research BACKGROUND: Differences in the thalamocortical system have been shown in patients with major depressive disorder (MDD). Given prior evidence of phenotypic heterogeneity by the age of onset in MDD, we examined whether differences in thalamocortical connectivity could identify biological subtypes of MDD defined by the age of illness onset. METHODS: A total of 94 subjects including 20 early-onset (EO) MDD (onset, 18 years), 34 adult-onset (AO) MDD, and 40 healthy controls (HCs) underwent resting-state functional MRI. Blood-oxygen-level-dependent time courses were extracted from six cortical regions of interest (ROIs) consisting of frontal, temporal, parietal, and occipital lobes and precentral and postcentral gyri. Each ROI’s time course was then correlated with each voxel in thalamus, while covarying out signal from every other ROI. RESULTS: The analysis of variance results showed significant main effects of group in frontal and temporal connectivity with thalamus. Group contrasts showed a right fronto-thalamic hypo-connectivity only in AO-MDD, but not in EO-MDD, when compared to HCs. However, direct comparison between EO-MDD and AO-MDD showed no differences. Furthermore, there was a right temporal–thalamic hyperconnectivity in both EO-MDD and AO-MDD patients relative to HCs. These results were not accounted for by sex, age, or illness burden. CONCLUSION: The age of illness onset may be a source of heterogeneity in fronto-thalamic intrinsic connectivity in MDD. Dove Medical Press 2018-12-21 /pmc/articles/PMC6306066/ /pubmed/30613149 http://dx.doi.org/10.2147/NDT.S184425 Text en © 2019 Brown et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Brown, Elliot C Clark, Darren L Hassel, Stefanie MacQueen, Glenda Ramasubbu, Rajamannar Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title | Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title_full | Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title_fullStr | Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title_full_unstemmed | Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title_short | Intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
title_sort | intrinsic thalamocortical connectivity varies in the age of onset subtypes in major depressive disorder |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306066/ https://www.ncbi.nlm.nih.gov/pubmed/30613149 http://dx.doi.org/10.2147/NDT.S184425 |
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