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Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study

BACKGROUND: Lennox–Gastaut syndrome (LGS) is a severe childhood epileptic syndrome with high pharmacoresistance. The treatment outcomes are still unsatisfied. Our previous study of cathodal transcranial direct current stimulation (tDCS) in children with focal epilepsy showed significant reduction in...

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Autores principales: Auvichayapat, Narong, Sinsupan, Katenipa, Tunkamnerdthai, Orathai, Auvichayapat, Paradee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854865/
https://www.ncbi.nlm.nih.gov/pubmed/27199889
http://dx.doi.org/10.3389/fneur.2016.00066
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author Auvichayapat, Narong
Sinsupan, Katenipa
Tunkamnerdthai, Orathai
Auvichayapat, Paradee
author_facet Auvichayapat, Narong
Sinsupan, Katenipa
Tunkamnerdthai, Orathai
Auvichayapat, Paradee
author_sort Auvichayapat, Narong
collection PubMed
description BACKGROUND: Lennox–Gastaut syndrome (LGS) is a severe childhood epileptic syndrome with high pharmacoresistance. The treatment outcomes are still unsatisfied. Our previous study of cathodal transcranial direct current stimulation (tDCS) in children with focal epilepsy showed significant reduction in epileptiform discharges. We hypothesized that cathodal tDCS when applied over the primary motor cortex (M1) combined with pharmacologic treatment will be more effective for reducing seizure frequency in patients with LGS than pharmacologic treatment alone. MATERIALS AND METHODS: Study participants were randomized to receive either (1) pharmacologic treatment with five consecutive days of 2 mA cathodal tDCS over M1 for 20 min or (2) pharmacologic treatment plus sham tDCS. Measures of seizure frequency and epileptic discharges were performed before treatment and again immediately post-treatment and 1-, 2-, 3-, and 4-week follow-up. RESULT: Twenty-two patients with LGS were enrolled. Participants assigned to the active tDCS condition reported significantly more pre- to post-treatment reductions in seizure frequency and epileptic discharges that were sustained for 3 weeks after treatment. CONCLUSION: Five consecutive days of cathodal tDCS over M1 combined with pharmacologic treatment appears to reduce seizure frequency and epileptic discharges. Further studies of the potential mechanisms of tDCS in the LGS are warranted. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02731300 (https://register.clinicaltrials.gov).
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spelling pubmed-48548652016-05-19 Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study Auvichayapat, Narong Sinsupan, Katenipa Tunkamnerdthai, Orathai Auvichayapat, Paradee Front Neurol Neuroscience BACKGROUND: Lennox–Gastaut syndrome (LGS) is a severe childhood epileptic syndrome with high pharmacoresistance. The treatment outcomes are still unsatisfied. Our previous study of cathodal transcranial direct current stimulation (tDCS) in children with focal epilepsy showed significant reduction in epileptiform discharges. We hypothesized that cathodal tDCS when applied over the primary motor cortex (M1) combined with pharmacologic treatment will be more effective for reducing seizure frequency in patients with LGS than pharmacologic treatment alone. MATERIALS AND METHODS: Study participants were randomized to receive either (1) pharmacologic treatment with five consecutive days of 2 mA cathodal tDCS over M1 for 20 min or (2) pharmacologic treatment plus sham tDCS. Measures of seizure frequency and epileptic discharges were performed before treatment and again immediately post-treatment and 1-, 2-, 3-, and 4-week follow-up. RESULT: Twenty-two patients with LGS were enrolled. Participants assigned to the active tDCS condition reported significantly more pre- to post-treatment reductions in seizure frequency and epileptic discharges that were sustained for 3 weeks after treatment. CONCLUSION: Five consecutive days of cathodal tDCS over M1 combined with pharmacologic treatment appears to reduce seizure frequency and epileptic discharges. Further studies of the potential mechanisms of tDCS in the LGS are warranted. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02731300 (https://register.clinicaltrials.gov). Frontiers Media S.A. 2016-05-04 /pmc/articles/PMC4854865/ /pubmed/27199889 http://dx.doi.org/10.3389/fneur.2016.00066 Text en Copyright © 2016 Auvichayapat, Sinsupan, Tunkamnerdthai and Auvichayapat. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Auvichayapat, Narong
Sinsupan, Katenipa
Tunkamnerdthai, Orathai
Auvichayapat, Paradee
Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title_full Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title_fullStr Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title_full_unstemmed Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title_short Transcranial Direct Current Stimulation for Treatment of Childhood Pharmacoresistant Lennox–Gastaut Syndrome: A Pilot Study
title_sort transcranial direct current stimulation for treatment of childhood pharmacoresistant lennox–gastaut syndrome: a pilot study
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854865/
https://www.ncbi.nlm.nih.gov/pubmed/27199889
http://dx.doi.org/10.3389/fneur.2016.00066
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