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White matter alterations in the internal capsule and psychomotor impairment in melancholic depression

Emerging evidence suggests that structural brain abnormalities may play a role in the pathophysiology of melancholic depression. We set out to test whether diffusion-derived estimates of white matter structure were disrupted in melancholia in regions underpinning psychomotor function. We hypothesize...

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Autores principales: Hyett, Matthew P., Perry, Alistair, Breakspear, Michael, Wen, Wei, Parker, Gordon B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908181/
https://www.ncbi.nlm.nih.gov/pubmed/29672517
http://dx.doi.org/10.1371/journal.pone.0195672
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author Hyett, Matthew P.
Perry, Alistair
Breakspear, Michael
Wen, Wei
Parker, Gordon B.
author_facet Hyett, Matthew P.
Perry, Alistair
Breakspear, Michael
Wen, Wei
Parker, Gordon B.
author_sort Hyett, Matthew P.
collection PubMed
description Emerging evidence suggests that structural brain abnormalities may play a role in the pathophysiology of melancholic depression. We set out to test whether diffusion-derived estimates of white matter structure were disrupted in melancholia in regions underpinning psychomotor function. We hypothesized that those with melancholia (and evidencing impaired psychomotor function) would show disrupted white matter organization in internal capsule subdivisions. Diffusion magnetic resonance imaging (dMRI) data were acquired from 22 melancholic depressed, 23 non-melancholic depressed, and 29 healthy control participants. Voxel-wise fractional anisotropy (FA), radial diffusivity (RD), and axial diffusivity (AD) values were derived for anterior, posterior, and retrolenticular limbs of the internal capsule and compared between groups. Neuropsychological (reaction time) and psychomotor functioning were assessed and correlated against FA. Fractional anisotropy was distinctly increased, whilst RD was decreased, in the right anterior internal capsule in those with melancholia, compared to controls. The right anterior limb of the internal capsule correlated with clinical ratings of psychomotor disturbance, and reduced psychomotor speed was associated with increased FA values in the right retrolenticular limb in those with melancholia. Our findings highlight a distinct disturbance in the local white matter arrangement in specific regions of the internal capsule in melancholia, which in turn is associated with psychomotor dysfunction. This study clarifies the contribution of structural brain integrity to the phenomenology of melancholia, and may assist future efforts seeking to integrate neurobiological markers into depression subtyping.
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spelling pubmed-59081812018-05-06 White matter alterations in the internal capsule and psychomotor impairment in melancholic depression Hyett, Matthew P. Perry, Alistair Breakspear, Michael Wen, Wei Parker, Gordon B. PLoS One Research Article Emerging evidence suggests that structural brain abnormalities may play a role in the pathophysiology of melancholic depression. We set out to test whether diffusion-derived estimates of white matter structure were disrupted in melancholia in regions underpinning psychomotor function. We hypothesized that those with melancholia (and evidencing impaired psychomotor function) would show disrupted white matter organization in internal capsule subdivisions. Diffusion magnetic resonance imaging (dMRI) data were acquired from 22 melancholic depressed, 23 non-melancholic depressed, and 29 healthy control participants. Voxel-wise fractional anisotropy (FA), radial diffusivity (RD), and axial diffusivity (AD) values were derived for anterior, posterior, and retrolenticular limbs of the internal capsule and compared between groups. Neuropsychological (reaction time) and psychomotor functioning were assessed and correlated against FA. Fractional anisotropy was distinctly increased, whilst RD was decreased, in the right anterior internal capsule in those with melancholia, compared to controls. The right anterior limb of the internal capsule correlated with clinical ratings of psychomotor disturbance, and reduced psychomotor speed was associated with increased FA values in the right retrolenticular limb in those with melancholia. Our findings highlight a distinct disturbance in the local white matter arrangement in specific regions of the internal capsule in melancholia, which in turn is associated with psychomotor dysfunction. This study clarifies the contribution of structural brain integrity to the phenomenology of melancholia, and may assist future efforts seeking to integrate neurobiological markers into depression subtyping. Public Library of Science 2018-04-19 /pmc/articles/PMC5908181/ /pubmed/29672517 http://dx.doi.org/10.1371/journal.pone.0195672 Text en © 2018 Hyett et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hyett, Matthew P.
Perry, Alistair
Breakspear, Michael
Wen, Wei
Parker, Gordon B.
White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title_full White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title_fullStr White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title_full_unstemmed White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title_short White matter alterations in the internal capsule and psychomotor impairment in melancholic depression
title_sort white matter alterations in the internal capsule and psychomotor impairment in melancholic depression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908181/
https://www.ncbi.nlm.nih.gov/pubmed/29672517
http://dx.doi.org/10.1371/journal.pone.0195672
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