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Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial
Theta-burst stimulation (TBS) represents a brain stimulation technique effective for treatment-resistant depression (TRD) as underlined by meta-analyses. While the methodology undergoes constant refinement, bilateral stimulation of the dorsolateral prefrontal cortex (DLPFC) appears promising to rest...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892572/ https://www.ncbi.nlm.nih.gov/pubmed/36725835 http://dx.doi.org/10.1038/s41398-023-02319-3 |
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author | Murgaš, Matej Unterholzner, Jakob Stöhrmann, Peter Philippe, Cécile Godbersen, Godber M. Nics, Lukas Reed, Murray B. Vraka, Chrysoula Vanicek, Thomas Wadsak, Wolfgang Kranz, Georg S. Hahn, Andreas Mitterhauser, Markus Hacker, Marcus Kasper, Siegfried Lanzenberger, Rupert Baldinger-Melich, Pia |
author_facet | Murgaš, Matej Unterholzner, Jakob Stöhrmann, Peter Philippe, Cécile Godbersen, Godber M. Nics, Lukas Reed, Murray B. Vraka, Chrysoula Vanicek, Thomas Wadsak, Wolfgang Kranz, Georg S. Hahn, Andreas Mitterhauser, Markus Hacker, Marcus Kasper, Siegfried Lanzenberger, Rupert Baldinger-Melich, Pia |
author_sort | Murgaš, Matej |
collection | PubMed |
description | Theta-burst stimulation (TBS) represents a brain stimulation technique effective for treatment-resistant depression (TRD) as underlined by meta-analyses. While the methodology undergoes constant refinement, bilateral stimulation of the dorsolateral prefrontal cortex (DLPFC) appears promising to restore left DLPFC hypoactivity and right hyperactivity found in depression. The post-synaptic inhibitory serotonin-1A (5-HT(1A)) receptor, also occurring in the DLPFC, might be involved in this mechanism of action. To test this hypothesis, we performed PET-imaging using the tracer [carbonyl-(11)C]WAY-100635 including arterial blood sampling before and after a three-week treatment with TBS in 11 TRD patients compared to sham stimulation (n = 8 and n = 3, respectively). Treatment groups were randomly assigned, and TBS protocol consisted of excitatory intermittent TBS to the left and inhibitory continuous TBS to the right DLPFC. A linear mixed model including group, hemisphere, time, and Hamilton Rating Scale for Depression (HAMD) score revealed a 3-way interaction effect of group, time, and HAMD on specific distribution volume (V(S)) of 5-HT(1A) receptor. While post-hoc comparisons showed no significant changes of 5-HT(1A) receptor V(S) in either group, higher 5-HT(1A) receptor V(S) after treatment correlated with greater difference in HAMD (r = −0.62). The results of this proof-of-concept trial hint towards potential effects of TBS on the distribution of the 5-HT(1A) receptor. Due to the small sample size, all results must, however, be regarded with caution. |
format | Online Article Text |
id | pubmed-9892572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98925722023-02-03 Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial Murgaš, Matej Unterholzner, Jakob Stöhrmann, Peter Philippe, Cécile Godbersen, Godber M. Nics, Lukas Reed, Murray B. Vraka, Chrysoula Vanicek, Thomas Wadsak, Wolfgang Kranz, Georg S. Hahn, Andreas Mitterhauser, Markus Hacker, Marcus Kasper, Siegfried Lanzenberger, Rupert Baldinger-Melich, Pia Transl Psychiatry Article Theta-burst stimulation (TBS) represents a brain stimulation technique effective for treatment-resistant depression (TRD) as underlined by meta-analyses. While the methodology undergoes constant refinement, bilateral stimulation of the dorsolateral prefrontal cortex (DLPFC) appears promising to restore left DLPFC hypoactivity and right hyperactivity found in depression. The post-synaptic inhibitory serotonin-1A (5-HT(1A)) receptor, also occurring in the DLPFC, might be involved in this mechanism of action. To test this hypothesis, we performed PET-imaging using the tracer [carbonyl-(11)C]WAY-100635 including arterial blood sampling before and after a three-week treatment with TBS in 11 TRD patients compared to sham stimulation (n = 8 and n = 3, respectively). Treatment groups were randomly assigned, and TBS protocol consisted of excitatory intermittent TBS to the left and inhibitory continuous TBS to the right DLPFC. A linear mixed model including group, hemisphere, time, and Hamilton Rating Scale for Depression (HAMD) score revealed a 3-way interaction effect of group, time, and HAMD on specific distribution volume (V(S)) of 5-HT(1A) receptor. While post-hoc comparisons showed no significant changes of 5-HT(1A) receptor V(S) in either group, higher 5-HT(1A) receptor V(S) after treatment correlated with greater difference in HAMD (r = −0.62). The results of this proof-of-concept trial hint towards potential effects of TBS on the distribution of the 5-HT(1A) receptor. Due to the small sample size, all results must, however, be regarded with caution. Nature Publishing Group UK 2023-02-01 /pmc/articles/PMC9892572/ /pubmed/36725835 http://dx.doi.org/10.1038/s41398-023-02319-3 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 Murgaš, Matej Unterholzner, Jakob Stöhrmann, Peter Philippe, Cécile Godbersen, Godber M. Nics, Lukas Reed, Murray B. Vraka, Chrysoula Vanicek, Thomas Wadsak, Wolfgang Kranz, Georg S. Hahn, Andreas Mitterhauser, Markus Hacker, Marcus Kasper, Siegfried Lanzenberger, Rupert Baldinger-Melich, Pia Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title | Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title_full | Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title_fullStr | Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title_full_unstemmed | Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title_short | Effects of bilateral sequential theta-burst stimulation on 5-HT(1A) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
title_sort | effects of bilateral sequential theta-burst stimulation on 5-ht(1a) receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892572/ https://www.ncbi.nlm.nih.gov/pubmed/36725835 http://dx.doi.org/10.1038/s41398-023-02319-3 |
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