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Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review

PURPOSE: Deep brain stimulation (DBS) is a relatively new and still experimental treatment modality for treatment-resistant depression (TRD). There is preliminary evidence that stimulation of brain reward circuit structures or their connecting white matter bundles may exert an antidepressant effect....

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Autores principales: Sobstyl, Michał, Stapińska-Syniec, Angelika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881632/
https://www.ncbi.nlm.nih.gov/pubmed/37082768
http://dx.doi.org/10.5114/ppn.2021.110788
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author Sobstyl, Michał
Stapińska-Syniec, Angelika
author_facet Sobstyl, Michał
Stapińska-Syniec, Angelika
author_sort Sobstyl, Michał
collection PubMed
description PURPOSE: Deep brain stimulation (DBS) is a relatively new and still experimental treatment modality for treatment-resistant depression (TRD). There is preliminary evidence that stimulation of brain reward circuit structures or their connecting white matter bundles may exert an antidepressant effect. The main nucleus of the reward circuit is the nucleus accumbens (NAc), which plays a critical role in reward-seeking behavior, motivation, and addiction. Also, white matter bundles connecting different structures of the reward circuit have been studied clinically as targets for DBS, including the medial forebrain bundle (MFB) – a central component of the mesolimbic dopaminergic reward circuit. This review aims to present the clinical outcomes of MFB DBS for TRD. VIEWS: The scientific literature was reviewed using the following keywords: ‘DBS’, ‘major depressive disorders’, ‘TRD’, and ‘MFB’. The identified studies were assessed on the basis of patient characteristics, clinical outcomes, and adverse events related to DBS. The search revealed five open-label clinical case studies and four case reports reporting the cumulative number of 35 patients treated by MFB DBS for TRD. CONCLUSIONS: The current clinical data of MFB DBS are limited by small sample size and the small number of clinical open-label trials. There is an urgent need for more clinical trials targeting the MFB for TRD. The results obtained in these studies showed a very rapid antidepressant effect observed within one week after the start of stimulation. MFB DBS for TRD should be considered as a last resort treatment due to its invasive character. However, this treatment may be a promising alternative for TRD patients.
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spelling pubmed-98816322023-04-19 Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review Sobstyl, Michał Stapińska-Syniec, Angelika Postep Psychiatr Neurol Review Article / Artykuł Przeglądowy PURPOSE: Deep brain stimulation (DBS) is a relatively new and still experimental treatment modality for treatment-resistant depression (TRD). There is preliminary evidence that stimulation of brain reward circuit structures or their connecting white matter bundles may exert an antidepressant effect. The main nucleus of the reward circuit is the nucleus accumbens (NAc), which plays a critical role in reward-seeking behavior, motivation, and addiction. Also, white matter bundles connecting different structures of the reward circuit have been studied clinically as targets for DBS, including the medial forebrain bundle (MFB) – a central component of the mesolimbic dopaminergic reward circuit. This review aims to present the clinical outcomes of MFB DBS for TRD. VIEWS: The scientific literature was reviewed using the following keywords: ‘DBS’, ‘major depressive disorders’, ‘TRD’, and ‘MFB’. The identified studies were assessed on the basis of patient characteristics, clinical outcomes, and adverse events related to DBS. The search revealed five open-label clinical case studies and four case reports reporting the cumulative number of 35 patients treated by MFB DBS for TRD. CONCLUSIONS: The current clinical data of MFB DBS are limited by small sample size and the small number of clinical open-label trials. There is an urgent need for more clinical trials targeting the MFB for TRD. The results obtained in these studies showed a very rapid antidepressant effect observed within one week after the start of stimulation. MFB DBS for TRD should be considered as a last resort treatment due to its invasive character. However, this treatment may be a promising alternative for TRD patients. Termedia Publishing House 2021-11-26 2021-09 /pmc/articles/PMC9881632/ /pubmed/37082768 http://dx.doi.org/10.5114/ppn.2021.110788 Text en Copyright © 2021 Institute of Psychiatry and Neurology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0). License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review Article / Artykuł Przeglądowy
Sobstyl, Michał
Stapińska-Syniec, Angelika
Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title_full Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title_fullStr Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title_full_unstemmed Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title_short Deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
title_sort deep brain stimulation of the medial forebrain bundle for treatment-resistant depression – a narrative literature review
topic Review Article / Artykuł Przeglądowy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881632/
https://www.ncbi.nlm.nih.gov/pubmed/37082768
http://dx.doi.org/10.5114/ppn.2021.110788
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