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Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation

Research suggests electroconvulsive therapy (ECT) induces an acute neuroinflammatory response and changes in white matter (WM) structural connectivity. However, whether these processes are related, either to each other or to eventual treatment outcomes, has yet to be determined. We examined the rela...

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Autores principales: Andreou, Blake, Reid, Benjamin, Lyall, Amanda E., Cetin-Karayumak, Suheyla, Kubicki, Antoni, Espinoza, Randall, Kruse, Jennifer, Narr, Katherine L., Kubicki, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076613/
https://www.ncbi.nlm.nih.gov/pubmed/35523776
http://dx.doi.org/10.1038/s41398-022-01960-8
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author Andreou, Blake
Reid, Benjamin
Lyall, Amanda E.
Cetin-Karayumak, Suheyla
Kubicki, Antoni
Espinoza, Randall
Kruse, Jennifer
Narr, Katherine L.
Kubicki, Marek
author_facet Andreou, Blake
Reid, Benjamin
Lyall, Amanda E.
Cetin-Karayumak, Suheyla
Kubicki, Antoni
Espinoza, Randall
Kruse, Jennifer
Narr, Katherine L.
Kubicki, Marek
author_sort Andreou, Blake
collection PubMed
description Research suggests electroconvulsive therapy (ECT) induces an acute neuroinflammatory response and changes in white matter (WM) structural connectivity. However, whether these processes are related, either to each other or to eventual treatment outcomes, has yet to be determined. We examined the relationship between levels of peripheral pro-inflammatory cytokines and diffusion imaging-indexed changes in WM microstructure in individuals with treatment-resistant depression (TRD) who underwent ECT. Forty-two patients were assessed at baseline, after their second ECT (T2), and after completion of ECT (T3). A Montgomery Åsberg Depression Rating Scale improvement of >50% post-ECT defined ECT-responders (n = 19) from non-responders (n = 23). Thirty-four controls were also examined. Tissue-specific fractional anisotropy (FAt) was estimated using diffusion imaging data and the Free-Water method in 17 WM tracts. Inflammatory panels were evaluated from peripheral blood. Cytokines were examined to characterize the association between potential ECT-induced changes in an inflammatory state and WM microstructure. Longitudinal trajectories of both measures were also examined separately for ECT-responders and non-responders. Patients exhibited elevated Interleukin-8 (IL-8) levels at baseline compared to controls. In patients, correlations between IL-8 and FAt changes from baseline to T2 were significant in the positive direction in the right superior longitudinal fasciculus (R-SLF) and right cingulum (R-CB) (p(sig) = 0.003). In these tracts, linear mixed-effects models revealed that trajectories of IL-8 and FAt were significantly positively correlated across all time points in responders, but not non-responders (R-CB-p = .001; R-SLF-p = 0.008). Our results suggest that response to ECT in TRD may be mediated by IL-8 and WM microstructure.
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spelling pubmed-90766132022-05-08 Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation Andreou, Blake Reid, Benjamin Lyall, Amanda E. Cetin-Karayumak, Suheyla Kubicki, Antoni Espinoza, Randall Kruse, Jennifer Narr, Katherine L. Kubicki, Marek Transl Psychiatry Article Research suggests electroconvulsive therapy (ECT) induces an acute neuroinflammatory response and changes in white matter (WM) structural connectivity. However, whether these processes are related, either to each other or to eventual treatment outcomes, has yet to be determined. We examined the relationship between levels of peripheral pro-inflammatory cytokines and diffusion imaging-indexed changes in WM microstructure in individuals with treatment-resistant depression (TRD) who underwent ECT. Forty-two patients were assessed at baseline, after their second ECT (T2), and after completion of ECT (T3). A Montgomery Åsberg Depression Rating Scale improvement of >50% post-ECT defined ECT-responders (n = 19) from non-responders (n = 23). Thirty-four controls were also examined. Tissue-specific fractional anisotropy (FAt) was estimated using diffusion imaging data and the Free-Water method in 17 WM tracts. Inflammatory panels were evaluated from peripheral blood. Cytokines were examined to characterize the association between potential ECT-induced changes in an inflammatory state and WM microstructure. Longitudinal trajectories of both measures were also examined separately for ECT-responders and non-responders. Patients exhibited elevated Interleukin-8 (IL-8) levels at baseline compared to controls. In patients, correlations between IL-8 and FAt changes from baseline to T2 were significant in the positive direction in the right superior longitudinal fasciculus (R-SLF) and right cingulum (R-CB) (p(sig) = 0.003). In these tracts, linear mixed-effects models revealed that trajectories of IL-8 and FAt were significantly positively correlated across all time points in responders, but not non-responders (R-CB-p = .001; R-SLF-p = 0.008). Our results suggest that response to ECT in TRD may be mediated by IL-8 and WM microstructure. Nature Publishing Group UK 2022-05-07 /pmc/articles/PMC9076613/ /pubmed/35523776 http://dx.doi.org/10.1038/s41398-022-01960-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Andreou, Blake
Reid, Benjamin
Lyall, Amanda E.
Cetin-Karayumak, Suheyla
Kubicki, Antoni
Espinoza, Randall
Kruse, Jennifer
Narr, Katherine L.
Kubicki, Marek
Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title_full Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title_fullStr Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title_full_unstemmed Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title_short Longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
title_sort longitudinal trajectory of response to electroconvulsive therapy associated with transient immune response & white matter alteration post-stimulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076613/
https://www.ncbi.nlm.nih.gov/pubmed/35523776
http://dx.doi.org/10.1038/s41398-022-01960-8
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