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Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease
Non-invasive methods, such as neurofeedback training, could support cognitive symptom management in Huntington’s disease by targeting brain regions whose function is impaired. The aim of our single-blind, sham-controlled study was to collect rigorous evidence regarding the feasibility of neurofeedba...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425518/ https://www.ncbi.nlm.nih.gov/pubmed/32954301 http://dx.doi.org/10.1093/braincomms/fcaa049 |
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author | Papoutsi, Marina Magerkurth, Joerg Josephs, Oliver Pépés, Sophia E Ibitoye, Temi Reilmann, Ralf Hunt, Nigel Payne, Edwin Weiskopf, Nikolaus Langbehn, Douglas Rees, Geraint Tabrizi, Sarah J |
author_facet | Papoutsi, Marina Magerkurth, Joerg Josephs, Oliver Pépés, Sophia E Ibitoye, Temi Reilmann, Ralf Hunt, Nigel Payne, Edwin Weiskopf, Nikolaus Langbehn, Douglas Rees, Geraint Tabrizi, Sarah J |
author_sort | Papoutsi, Marina |
collection | PubMed |
description | Non-invasive methods, such as neurofeedback training, could support cognitive symptom management in Huntington’s disease by targeting brain regions whose function is impaired. The aim of our single-blind, sham-controlled study was to collect rigorous evidence regarding the feasibility of neurofeedback training in Huntington’s disease by examining two different methods, activity and connectivity real-time functional MRI neurofeedback training. Thirty-two Huntington’s disease gene-carriers completed 16 runs of neurofeedback training, using an optimized real-time functional MRI protocol. Participants were randomized into four groups, two treatment groups, one receiving neurofeedback derived from the activity of the supplementary motor area, and another receiving neurofeedback based on the correlation of supplementary motor area and left striatum activity (connectivity neurofeedback training), and two sham control groups, matched to each of the treatment groups. We examined differences between the groups during neurofeedback training sessions and after training at follow-up sessions. Transfer of training was measured by measuring the participants’ ability to upregulate neurofeedback training target levels without feedback (near transfer), as well as by examining change in objective, a priori defined, behavioural measures of cognitive and psychomotor function (far transfer) before and at 2 months after training. We found that the treatment group had significantly higher neurofeedback training target levels during the training sessions compared to the control group. However, we did not find robust evidence of better transfer in the treatment group compared to controls, or a difference between the two neurofeedback training methods. We also did not find evidence in support of a relationship between change in cognitive and psychomotor function and learning success. We conclude that although there is evidence that neurofeedback training can be used to guide participants to regulate the activity and connectivity of specific regions in the brain, evidence regarding transfer of learning and clinical benefit was not robust. |
format | Online Article Text |
id | pubmed-7425518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74255182020-09-17 Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease Papoutsi, Marina Magerkurth, Joerg Josephs, Oliver Pépés, Sophia E Ibitoye, Temi Reilmann, Ralf Hunt, Nigel Payne, Edwin Weiskopf, Nikolaus Langbehn, Douglas Rees, Geraint Tabrizi, Sarah J Brain Commun Original Article Non-invasive methods, such as neurofeedback training, could support cognitive symptom management in Huntington’s disease by targeting brain regions whose function is impaired. The aim of our single-blind, sham-controlled study was to collect rigorous evidence regarding the feasibility of neurofeedback training in Huntington’s disease by examining two different methods, activity and connectivity real-time functional MRI neurofeedback training. Thirty-two Huntington’s disease gene-carriers completed 16 runs of neurofeedback training, using an optimized real-time functional MRI protocol. Participants were randomized into four groups, two treatment groups, one receiving neurofeedback derived from the activity of the supplementary motor area, and another receiving neurofeedback based on the correlation of supplementary motor area and left striatum activity (connectivity neurofeedback training), and two sham control groups, matched to each of the treatment groups. We examined differences between the groups during neurofeedback training sessions and after training at follow-up sessions. Transfer of training was measured by measuring the participants’ ability to upregulate neurofeedback training target levels without feedback (near transfer), as well as by examining change in objective, a priori defined, behavioural measures of cognitive and psychomotor function (far transfer) before and at 2 months after training. We found that the treatment group had significantly higher neurofeedback training target levels during the training sessions compared to the control group. However, we did not find robust evidence of better transfer in the treatment group compared to controls, or a difference between the two neurofeedback training methods. We also did not find evidence in support of a relationship between change in cognitive and psychomotor function and learning success. We conclude that although there is evidence that neurofeedback training can be used to guide participants to regulate the activity and connectivity of specific regions in the brain, evidence regarding transfer of learning and clinical benefit was not robust. Oxford University Press 2020-04-23 /pmc/articles/PMC7425518/ /pubmed/32954301 http://dx.doi.org/10.1093/braincomms/fcaa049 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Papoutsi, Marina Magerkurth, Joerg Josephs, Oliver Pépés, Sophia E Ibitoye, Temi Reilmann, Ralf Hunt, Nigel Payne, Edwin Weiskopf, Nikolaus Langbehn, Douglas Rees, Geraint Tabrizi, Sarah J Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title | Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title_full | Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title_fullStr | Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title_full_unstemmed | Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title_short | Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington’s disease |
title_sort | activity or connectivity? a randomized controlled feasibility study evaluating neurofeedback training in huntington’s disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425518/ https://www.ncbi.nlm.nih.gov/pubmed/32954301 http://dx.doi.org/10.1093/braincomms/fcaa049 |
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