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Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals
Activity changes within the anterior cingulate cortex (ACC) are implicated in the antidepressant effects of ketamine, but the ACC is cytoarchitectonically and functionally heterogeneous and ketamine’s effects may be subregion specific. In the context of a double-blind randomized placebo-controlled c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692230/ https://www.ncbi.nlm.nih.gov/pubmed/38040678 http://dx.doi.org/10.1038/s41398-023-02674-1 |
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author | Alexander, Laith Hawkins, Peter C. T. Evans, Jennifer W. Mehta, Mitul A. Zarate, Carlos A. |
author_facet | Alexander, Laith Hawkins, Peter C. T. Evans, Jennifer W. Mehta, Mitul A. Zarate, Carlos A. |
author_sort | Alexander, Laith |
collection | PubMed |
description | Activity changes within the anterior cingulate cortex (ACC) are implicated in the antidepressant effects of ketamine, but the ACC is cytoarchitectonically and functionally heterogeneous and ketamine’s effects may be subregion specific. In the context of a double-blind randomized placebo-controlled crossover trial investigating the clinical and resting-state fMRI effects of intravenous ketamine vs. placebo in patients with treatment resistant depression (TRD) vs. healthy volunteers (HV), we used seed-based resting-state functional connectivity (rsFC) analyses to determine differential changes in subgenual ACC (sgACC), perigenual ACC (pgACC) and dorsal ACC (dACC) rsFC two days post-infusion. Across cingulate subregions, ketamine differentially modulated rsFC to the right insula and anterior ventromedial prefrontal cortex, compared to placebo, in TRD vs. HV; changes to pgACC-insula connectivity correlated with improvements in depression scores. Post-hoc analysis of each cingulate subregion separately revealed differential modulation of sgACC-hippocampal, sgACC-vmPFC, pgACC-posterior cingulate, and dACC-supramarginal gyrus connectivity. By comparing rsFC changes following ketamine vs. placebo in the TRD group alone, we found that sgACC rsFC was most substantially modulated by ketamine vs. placebo. Changes to sgACC-pgACC, sgACC-ventral striatal, and sgACC-dACC connectivity correlated with improvements in anhedonia symptoms. This preliminary evidence suggests that accurate segmentation of the ACC is needed to understand the precise effects of ketamine’s antidepressant and anti-anhedonic action. |
format | Online Article Text |
id | pubmed-10692230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106922302023-12-03 Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals Alexander, Laith Hawkins, Peter C. T. Evans, Jennifer W. Mehta, Mitul A. Zarate, Carlos A. Transl Psychiatry Article Activity changes within the anterior cingulate cortex (ACC) are implicated in the antidepressant effects of ketamine, but the ACC is cytoarchitectonically and functionally heterogeneous and ketamine’s effects may be subregion specific. In the context of a double-blind randomized placebo-controlled crossover trial investigating the clinical and resting-state fMRI effects of intravenous ketamine vs. placebo in patients with treatment resistant depression (TRD) vs. healthy volunteers (HV), we used seed-based resting-state functional connectivity (rsFC) analyses to determine differential changes in subgenual ACC (sgACC), perigenual ACC (pgACC) and dorsal ACC (dACC) rsFC two days post-infusion. Across cingulate subregions, ketamine differentially modulated rsFC to the right insula and anterior ventromedial prefrontal cortex, compared to placebo, in TRD vs. HV; changes to pgACC-insula connectivity correlated with improvements in depression scores. Post-hoc analysis of each cingulate subregion separately revealed differential modulation of sgACC-hippocampal, sgACC-vmPFC, pgACC-posterior cingulate, and dACC-supramarginal gyrus connectivity. By comparing rsFC changes following ketamine vs. placebo in the TRD group alone, we found that sgACC rsFC was most substantially modulated by ketamine vs. placebo. Changes to sgACC-pgACC, sgACC-ventral striatal, and sgACC-dACC connectivity correlated with improvements in anhedonia symptoms. This preliminary evidence suggests that accurate segmentation of the ACC is needed to understand the precise effects of ketamine’s antidepressant and anti-anhedonic action. Nature Publishing Group UK 2023-12-01 /pmc/articles/PMC10692230/ /pubmed/38040678 http://dx.doi.org/10.1038/s41398-023-02674-1 Text en © The Author(s) 2023 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 Alexander, Laith Hawkins, Peter C. T. Evans, Jennifer W. Mehta, Mitul A. Zarate, Carlos A. Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title | Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title_full | Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title_fullStr | Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title_full_unstemmed | Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title_short | Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
title_sort | preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692230/ https://www.ncbi.nlm.nih.gov/pubmed/38040678 http://dx.doi.org/10.1038/s41398-023-02674-1 |
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