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Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial

Transcranial direct current stimulation (tDCS) has been proposed as a potential intervention for subjective tinnitus, but supporting evidence remains limited. We aimed to investigate the effect of anodal high-definition tDCS of the left temporal area and right dorsolateral prefrontal cortex on tinni...

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Autores principales: Cardon, Emilie, Jacquemin, Laure, Vermeersch, Hanne, Joossen, Iris, Moyaert, Julie, Mertens, Griet, Vanderveken, Olivier M, Lammers, Marc J W, Van de Heyning, Paul, Van Rompaey, Vincent, Gilles, Annick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762937/
https://www.ncbi.nlm.nih.gov/pubmed/36450310
http://dx.doi.org/10.1093/brain/awac263
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author Cardon, Emilie
Jacquemin, Laure
Vermeersch, Hanne
Joossen, Iris
Moyaert, Julie
Mertens, Griet
Vanderveken, Olivier M
Lammers, Marc J W
Van de Heyning, Paul
Van Rompaey, Vincent
Gilles, Annick
author_facet Cardon, Emilie
Jacquemin, Laure
Vermeersch, Hanne
Joossen, Iris
Moyaert, Julie
Mertens, Griet
Vanderveken, Olivier M
Lammers, Marc J W
Van de Heyning, Paul
Van Rompaey, Vincent
Gilles, Annick
author_sort Cardon, Emilie
collection PubMed
description Transcranial direct current stimulation (tDCS) has been proposed as a potential intervention for subjective tinnitus, but supporting evidence remains limited. We aimed to investigate the effect of anodal high-definition tDCS of the left temporal area and right dorsolateral prefrontal cortex on tinnitus severity. This double-blind randomized controlled trial included 77 patients (age range 18–79, 43 male) with chronic subjective tinnitus as their primary complaint. Thirty-eight subjects received six consecutive sessions of dual-site sequential high-definition-tDCS with electrodes positioned over the left temporal area and right dorsolateral prefrontal cortex. Both areas were stimulated for 15 min per session, with total stimulation time amounting to 30 min. Thirty-nine subjects received sham stimulation. The primary outcome measure was the change in tinnitus severity, as evaluated by the Tinnitus Functional Index, from baseline to a follow-up visit at 8 ± 2 weeks after treatment completion. Secondary outcomes included changes in perceived tinnitus loudness, as measured with a visual analogue scale and a tinnitus matching procedure, as well as scores on the Hospital Anxiety and Depression Scale, and the Hyperacusis Questionnaire. No differences in Tinnitus Functional Index change scores were identified between the active treatment and sham control groups (linear regression: P = 0.86). The Tinnitus Functional Index scores decreased significantly over time in both groups (P = 0.0012), indicating the presence of a considerable placebo effect. These change scores were significantly influenced by sex (linear regression: P = 0.037) and baseline symptoms of anxiety (linear regression: P = 0.049) in both groups. In general, Tinnitus Functional Index scores decreased more profoundly in males and in subjects with a higher degree of anxiety at baseline. None of the included secondary measures differed significantly between experimental arms. Our results suggest that dual-site sequential high-definition-tDCS of the left temporal area and right dorsolateral prefrontal cortex does not alleviate tinnitus severity. Interestingly, in our study population, fluctuations in tinnitus severity were influenced by gender and concurrent mental condition. It is therefore important to take these factors into account when conducting or planning randomized controlled trials in tinnitus populations.
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spelling pubmed-97629372022-12-20 Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial Cardon, Emilie Jacquemin, Laure Vermeersch, Hanne Joossen, Iris Moyaert, Julie Mertens, Griet Vanderveken, Olivier M Lammers, Marc J W Van de Heyning, Paul Van Rompaey, Vincent Gilles, Annick Brain Clinical Trial Transcranial direct current stimulation (tDCS) has been proposed as a potential intervention for subjective tinnitus, but supporting evidence remains limited. We aimed to investigate the effect of anodal high-definition tDCS of the left temporal area and right dorsolateral prefrontal cortex on tinnitus severity. This double-blind randomized controlled trial included 77 patients (age range 18–79, 43 male) with chronic subjective tinnitus as their primary complaint. Thirty-eight subjects received six consecutive sessions of dual-site sequential high-definition-tDCS with electrodes positioned over the left temporal area and right dorsolateral prefrontal cortex. Both areas were stimulated for 15 min per session, with total stimulation time amounting to 30 min. Thirty-nine subjects received sham stimulation. The primary outcome measure was the change in tinnitus severity, as evaluated by the Tinnitus Functional Index, from baseline to a follow-up visit at 8 ± 2 weeks after treatment completion. Secondary outcomes included changes in perceived tinnitus loudness, as measured with a visual analogue scale and a tinnitus matching procedure, as well as scores on the Hospital Anxiety and Depression Scale, and the Hyperacusis Questionnaire. No differences in Tinnitus Functional Index change scores were identified between the active treatment and sham control groups (linear regression: P = 0.86). The Tinnitus Functional Index scores decreased significantly over time in both groups (P = 0.0012), indicating the presence of a considerable placebo effect. These change scores were significantly influenced by sex (linear regression: P = 0.037) and baseline symptoms of anxiety (linear regression: P = 0.049) in both groups. In general, Tinnitus Functional Index scores decreased more profoundly in males and in subjects with a higher degree of anxiety at baseline. None of the included secondary measures differed significantly between experimental arms. Our results suggest that dual-site sequential high-definition-tDCS of the left temporal area and right dorsolateral prefrontal cortex does not alleviate tinnitus severity. Interestingly, in our study population, fluctuations in tinnitus severity were influenced by gender and concurrent mental condition. It is therefore important to take these factors into account when conducting or planning randomized controlled trials in tinnitus populations. Oxford University Press 2022-12-01 /pmc/articles/PMC9762937/ /pubmed/36450310 http://dx.doi.org/10.1093/brain/awac263 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Trial
Cardon, Emilie
Jacquemin, Laure
Vermeersch, Hanne
Joossen, Iris
Moyaert, Julie
Mertens, Griet
Vanderveken, Olivier M
Lammers, Marc J W
Van de Heyning, Paul
Van Rompaey, Vincent
Gilles, Annick
Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title_full Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title_fullStr Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title_full_unstemmed Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title_short Dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
title_sort dual-site transcranial direct current stimulation to treat tinnitus: a randomized controlled trial
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762937/
https://www.ncbi.nlm.nih.gov/pubmed/36450310
http://dx.doi.org/10.1093/brain/awac263
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