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Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression

Major depressive disorder (MDD) is widely hypothesized to result from disordered communication across brain-wide networks. Yet, prior resting-state-functional MRI (rs-fMRI) studies of MDD have studied zero-lag temporal synchrony (functional connectivity) in brain activity absent directional informat...

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Autores principales: Mitra, Anish, Raichle, Marcus E., Geoly, Andrew D., Kratter, Ian H., Williams, Nolan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214160/
https://www.ncbi.nlm.nih.gov/pubmed/37186863
http://dx.doi.org/10.1073/pnas.2218958120
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author Mitra, Anish
Raichle, Marcus E.
Geoly, Andrew D.
Kratter, Ian H.
Williams, Nolan R.
author_facet Mitra, Anish
Raichle, Marcus E.
Geoly, Andrew D.
Kratter, Ian H.
Williams, Nolan R.
author_sort Mitra, Anish
collection PubMed
description Major depressive disorder (MDD) is widely hypothesized to result from disordered communication across brain-wide networks. Yet, prior resting-state-functional MRI (rs-fMRI) studies of MDD have studied zero-lag temporal synchrony (functional connectivity) in brain activity absent directional information. We utilize the recent discovery of stereotyped brain-wide directed signaling patterns in humans to investigate the relationship between directed rs-fMRI activity, MDD, and treatment response to FDA-approved neurostimulation paradigm termed Stanford neuromodulation therapy (SNT). We find that SNT over the left dorsolateral prefrontal cortex (DLPFC) induces directed signaling shifts in the left DLPFC and bilateral anterior cingulate cortex (ACC). Directional signaling shifts in the ACC, but not the DLPFC, predict improvement in depression symptoms, and moreover, pretreatment ACC signaling predicts both depression severity and the likelihood of SNT treatment response. Taken together, our findings suggest that ACC-based directed signaling patterns in rs-fMRI are a potential biomarker of MDD.
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spelling pubmed-102141602023-05-27 Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression Mitra, Anish Raichle, Marcus E. Geoly, Andrew D. Kratter, Ian H. Williams, Nolan R. Proc Natl Acad Sci U S A Biological Sciences Major depressive disorder (MDD) is widely hypothesized to result from disordered communication across brain-wide networks. Yet, prior resting-state-functional MRI (rs-fMRI) studies of MDD have studied zero-lag temporal synchrony (functional connectivity) in brain activity absent directional information. We utilize the recent discovery of stereotyped brain-wide directed signaling patterns in humans to investigate the relationship between directed rs-fMRI activity, MDD, and treatment response to FDA-approved neurostimulation paradigm termed Stanford neuromodulation therapy (SNT). We find that SNT over the left dorsolateral prefrontal cortex (DLPFC) induces directed signaling shifts in the left DLPFC and bilateral anterior cingulate cortex (ACC). Directional signaling shifts in the ACC, but not the DLPFC, predict improvement in depression symptoms, and moreover, pretreatment ACC signaling predicts both depression severity and the likelihood of SNT treatment response. Taken together, our findings suggest that ACC-based directed signaling patterns in rs-fMRI are a potential biomarker of MDD. National Academy of Sciences 2023-05-15 2023-05-23 /pmc/articles/PMC10214160/ /pubmed/37186863 http://dx.doi.org/10.1073/pnas.2218958120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Mitra, Anish
Raichle, Marcus E.
Geoly, Andrew D.
Kratter, Ian H.
Williams, Nolan R.
Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title_full Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title_fullStr Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title_full_unstemmed Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title_short Targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
title_sort targeted neurostimulation reverses a spatiotemporal biomarker of treatment-resistant depression
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214160/
https://www.ncbi.nlm.nih.gov/pubmed/37186863
http://dx.doi.org/10.1073/pnas.2218958120
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