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White matter microstructural perturbations after total sleep deprivation in depression

BACKGROUND: Total sleep deprivation (TSD) transiently reverses depressive symptoms in a majority of patients with depression. How TSD modulates diffusion tensor imaging (DTI) measures of white matter (WM) microstructure, which may be linked with TSD’s rapid antidepressant effects, remains uncharacte...

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Autores principales: Taraku, Brandon, Zavaliangos-Petropulu, Artemis, Loureiro, Joana R., Al-Sharif, Noor B., Kubicki, Antoni, Joshi, Shantanu H., Woods, Roger P., Espinoza, Randall, Narr, Katherine L., Sahib, Ashish K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345348/
https://www.ncbi.nlm.nih.gov/pubmed/37457774
http://dx.doi.org/10.3389/fpsyt.2023.1195763
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author Taraku, Brandon
Zavaliangos-Petropulu, Artemis
Loureiro, Joana R.
Al-Sharif, Noor B.
Kubicki, Antoni
Joshi, Shantanu H.
Woods, Roger P.
Espinoza, Randall
Narr, Katherine L.
Sahib, Ashish K.
author_facet Taraku, Brandon
Zavaliangos-Petropulu, Artemis
Loureiro, Joana R.
Al-Sharif, Noor B.
Kubicki, Antoni
Joshi, Shantanu H.
Woods, Roger P.
Espinoza, Randall
Narr, Katherine L.
Sahib, Ashish K.
author_sort Taraku, Brandon
collection PubMed
description BACKGROUND: Total sleep deprivation (TSD) transiently reverses depressive symptoms in a majority of patients with depression. How TSD modulates diffusion tensor imaging (DTI) measures of white matter (WM) microstructure, which may be linked with TSD’s rapid antidepressant effects, remains uncharacterized. METHODS: Patients with depression (N = 48, mean age = 33, 26 women) completed diffusion-weighted imaging and Hamilton Depression Rating (HDRS) and rumination scales before and after >24 h of TSD. Healthy controls (HC) (N = 53, 23 women) completed the same assessments at baseline, and after receiving TSD in a subset of HCs (N = 15). Tract based spatial statistics (TBSS) investigated voxelwise changes in fractional anisotropy (FA) across major WM pathways pre-to-post TSD in patients and HCs and between patients and HCs at baseline. Post hoc analyses tested for TSD effects for other diffusion metrics, and the relationships between change in diffusion measures with change in mood and rumination symptoms. RESULTS: Significant improvements in mood and rumination occurred in patients with depression (both p < 0.001), but not in HCs following TSD. Patients showed significant (p < 0.05, corrected) decreases in FA values in multiple WM tracts, including the body of the corpus callosum and anterior corona radiata post-TSD. Significant voxel-level changes in FA were not observed in HCs who received TSD (p > 0.05). However, differential effects of TSD between HCs and patients were found in the superior corona radiata, frontal WM and the posterior thalamic radiation (p < 0.05, corrected). A significant (p < 0.05) association between change in FA and axial diffusivity within the right superior corona radiata and improvement in rumination was found post-TSD in patients. CONCLUSION: Total sleep deprivation leads to rapid microstructural changes in WM pathways in patients with depression that are distinct from WM changes associated with TSD observed in HCs. WM tracts including the superior corona radiata and posterior thalamic radiation could be potential biomarkers of the rapid therapeutic effects of TSD. Changes in superior corona radiata FA, in particular, may relate to improvements in maladaptive rumination.
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spelling pubmed-103453482023-07-15 White matter microstructural perturbations after total sleep deprivation in depression Taraku, Brandon Zavaliangos-Petropulu, Artemis Loureiro, Joana R. Al-Sharif, Noor B. Kubicki, Antoni Joshi, Shantanu H. Woods, Roger P. Espinoza, Randall Narr, Katherine L. Sahib, Ashish K. Front Psychiatry Psychiatry BACKGROUND: Total sleep deprivation (TSD) transiently reverses depressive symptoms in a majority of patients with depression. How TSD modulates diffusion tensor imaging (DTI) measures of white matter (WM) microstructure, which may be linked with TSD’s rapid antidepressant effects, remains uncharacterized. METHODS: Patients with depression (N = 48, mean age = 33, 26 women) completed diffusion-weighted imaging and Hamilton Depression Rating (HDRS) and rumination scales before and after >24 h of TSD. Healthy controls (HC) (N = 53, 23 women) completed the same assessments at baseline, and after receiving TSD in a subset of HCs (N = 15). Tract based spatial statistics (TBSS) investigated voxelwise changes in fractional anisotropy (FA) across major WM pathways pre-to-post TSD in patients and HCs and between patients and HCs at baseline. Post hoc analyses tested for TSD effects for other diffusion metrics, and the relationships between change in diffusion measures with change in mood and rumination symptoms. RESULTS: Significant improvements in mood and rumination occurred in patients with depression (both p < 0.001), but not in HCs following TSD. Patients showed significant (p < 0.05, corrected) decreases in FA values in multiple WM tracts, including the body of the corpus callosum and anterior corona radiata post-TSD. Significant voxel-level changes in FA were not observed in HCs who received TSD (p > 0.05). However, differential effects of TSD between HCs and patients were found in the superior corona radiata, frontal WM and the posterior thalamic radiation (p < 0.05, corrected). A significant (p < 0.05) association between change in FA and axial diffusivity within the right superior corona radiata and improvement in rumination was found post-TSD in patients. CONCLUSION: Total sleep deprivation leads to rapid microstructural changes in WM pathways in patients with depression that are distinct from WM changes associated with TSD observed in HCs. WM tracts including the superior corona radiata and posterior thalamic radiation could be potential biomarkers of the rapid therapeutic effects of TSD. Changes in superior corona radiata FA, in particular, may relate to improvements in maladaptive rumination. Frontiers Media S.A. 2023-06-28 /pmc/articles/PMC10345348/ /pubmed/37457774 http://dx.doi.org/10.3389/fpsyt.2023.1195763 Text en Copyright © 2023 Taraku, Zavaliangos-Petropulu, Loureiro, Al-Sharif, Kubicki, Joshi, Woods, Espinoza, Narr and Sahib. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Taraku, Brandon
Zavaliangos-Petropulu, Artemis
Loureiro, Joana R.
Al-Sharif, Noor B.
Kubicki, Antoni
Joshi, Shantanu H.
Woods, Roger P.
Espinoza, Randall
Narr, Katherine L.
Sahib, Ashish K.
White matter microstructural perturbations after total sleep deprivation in depression
title White matter microstructural perturbations after total sleep deprivation in depression
title_full White matter microstructural perturbations after total sleep deprivation in depression
title_fullStr White matter microstructural perturbations after total sleep deprivation in depression
title_full_unstemmed White matter microstructural perturbations after total sleep deprivation in depression
title_short White matter microstructural perturbations after total sleep deprivation in depression
title_sort white matter microstructural perturbations after total sleep deprivation in depression
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345348/
https://www.ncbi.nlm.nih.gov/pubmed/37457774
http://dx.doi.org/10.3389/fpsyt.2023.1195763
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