Effects of transcranial direct current stimulation and transcranial random noise stimulation on working memory and task-related EEG in major depressive disorder.


Journal

Brain and cognition
ISSN: 1090-2147
Titre abrégé: Brain Cogn
Pays: United States
ID NLM: 8218014

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 19 06 2023
revised: 25 09 2023
accepted: 31 10 2023
medline: 11 12 2023
pubmed: 14 11 2023
entrez: 14 11 2023
Statut: ppublish

Résumé

To compare effects of transcranial direct current stimulation (tDCS) and transcranial random noise stimulation with a direct-current offset (tRNS + DC-offset) on working memory (WM) performance and task-related electroencephalography (EEG) in individuals with Major Depressive Disorder (MDD). Using a sham-controlled, parallel-groups design, 49 participants with MDD received either anodal tDCS (N = 16), high-frequency tRNS + DC-offset (N = 16), or sham stimulation (N = 17) to the left dorsolateral prefrontal cortex (DLPFC) for 20-minutes. The Sternberg WM task was completed with concurrent EEG recording before and at 5- and 25-minutes post-stimulation. Event-related synchronisation/desynchronisation (ERS/ERD) was calculated for theta, upper alpha, and gamma oscillations during WM encoding and maintenance. tDCS significantly increased parieto-occipital upper alpha ERS/ERD during WM maintenance, observed on EEG recorded 5- and 25-minutes post-stimulation. tRNS + DC-offset did not significantly alter WM-related oscillatory activity when compared to sham stimulation. Neither tDCS nor tRNS + DC-offset improved WM performance to a significantly greater degree than sham stimulation. Although tDCS induced persistent effects on WM-related oscillatory activity, neither tDCS nor tRNS + DC-offset enhanced WM performance in MDD. This reflects the first sham-controlled comparison of tDCS and tRNS + DC-offset in MDD. These findings directly contrast with evidence of tRNS-induced enhancements in WM in healthy individuals.

Identifiants

pubmed: 37963422
pii: S0278-2626(23)00164-1
doi: 10.1016/j.bandc.2023.106105
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106105

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: In the last three years PBF has received equipment for research from Neurosoft, Nexstim and Brainsway Ltd. PBF has served on scientific advisory boards for Magstim and LivaNova and acted as a founder and board member for TMS Clinics Australia and Resonance Therapeutics. All other authors have no conflicts to report.

Auteurs

O W Murphy (OW)

Central Clinical School, Monash University, Clayton, VIC, Australia; Bionics Institute, East Melbourne, VIC, Australia. Electronic address: omurphy@bionicsinstitute.org.

K E Hoy (KE)

Central Clinical School, Monash University, Clayton, VIC, Australia; Bionics Institute, East Melbourne, VIC, Australia.

D Wong (D)

School of Psychology and Public Health, La Trobe University, Bundoora, VIC, Australia.

N W Bailey (NW)

Central Clinical School, Monash University, Clayton, VIC, Australia; Monarch Research Institute Monarch Mental Health Group, Sydney, NSW, Australia; School of Medicine and Psychology, Australian National University, Canberra, ACT, Australia.

P B Fitzgerald (PB)

Monarch Research Institute Monarch Mental Health Group, Sydney, NSW, Australia; School of Medicine and Psychology, Australian National University, Canberra, ACT, Australia.

R A Segrave (RA)

BrainPark, Turner Institute for Brain and Mental Health, Monash University, Clayton, VIC, Australia.

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