The BOLD response in primary motor cortex and supplementary motor area during kinesthetic motor imagery based graded fMRI neurofeedback
There is increasing interest in exploring the use of functional MRI neurofeedback (fMRI-NF) as a therapeutic technique for a range of neurological conditions such as stroke and Parkinson's disease (PD). One main therapeutic potential of fMRI-NF is to enhance volitional control of damaged or dys...
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Published in | NeuroImage (Orlando, Fla.) Vol. 184; pp. 36 - 44 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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01.01.2019
Elsevier Limited Academic Press |
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Abstract | There is increasing interest in exploring the use of functional MRI neurofeedback (fMRI-NF) as a therapeutic technique for a range of neurological conditions such as stroke and Parkinson's disease (PD). One main therapeutic potential of fMRI-NF is to enhance volitional control of damaged or dysfunctional neural nodes and networks via a closed-loop feedback model using mental imagery as the catalyst of self-regulation. The choice of target node/network and direction of regulation (increase or decrease activity) are central design considerations in fMRI-NF studies. Whilst it remains unclear whether the primary motor cortex (M1) can be activated during motor imagery, the supplementary motor area (SMA) has been robustly activated during motor imagery. Such differences in the regulation potential between primary and supplementary motor cortex are important because these areas can be differentially affected by a stroke or PD, and the choice of fMRI-NF target and grade of self-regulation of activity likely have substantial influence on the clinical effects and cost effectiveness of NF-based interventions. In this study we therefore investigated firstly whether healthy subjects would be able to achieve self-regulation of the hand-representation areas of M1 and the SMA using fMRI-NF training. There was a significant decrease in M1 neural activity during fMRI-NF, whereas SMA neural activity was increased, albeit not with the predicated graded effect. This study has important implications for fMRI-NF protocols that employ motor imagery to modulate activity in specific target regions of the brain and to determine how they may be tailored for neurorehabilitation.
•Graded fMRI neurofeedback can separate self-regulation effects from general cognitive ones.•There is a significant negative BOLD response in M1 during kinaesthetic motor imagery.•SMA shows robust positive BOLD responses during kinaesthetic motor imagery.•Participants can target discrete levels of BOLD response in SMA using kinaesthetic motor imagery.•For our paradigm neurofeedback provides only minimal extra control of BOLD signals in SMA. |
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AbstractList | There is increasing interest in exploring the use of functional MRI neurofeedback (fMRI-NF) as a therapeutic technique for a range of neurological conditions such as stroke and Parkinson's disease (PD). One main therapeutic potential of fMRI-NF is to enhance volitional control of damaged or dysfunctional neural nodes and networks via a closed-loop feedback model using mental imagery as the catalyst of self-regulation. The choice of target node/network and direction of regulation (increase or decrease activity) are central design considerations in fMRI-NF studies. Whilst it remains unclear whether the primary motor cortex (M1) can be activated during motor imagery, the supplementary motor area (SMA) has been robustly activated during motor imagery. Such differences in the regulation potential between primary and supplementary motor cortex are important because these areas can be differentially affected by a stroke or PD, and the choice of fMRI-NF target and grade of self-regulation of activity likely have substantial influence on the clinical effects and cost effectiveness of NF-based interventions. In this study we therefore investigated firstly whether healthy subjects would be able to achieve self-regulation of the hand-representation areas of M1 and the SMA using fMRI-NF training. There was a significant decrease in M1 neural activity during fMRI-NF, whereas SMA neural activity was increased, albeit not with the predicated graded effect. This study has important implications for fMRI-NF protocols that employ motor imagery to modulate activity in specific target regions of the brain and to determine how they may be tailored for neurorehabilitation.
•
Graded fMRI neurofeedback can separate self-regulation effects from general cognitive ones.
•
There is a significant negative BOLD response in M1 during kinaesthetic motor imagery.
•
SMA shows robust positive BOLD responses during kinaesthetic motor imagery.
•
Participants can target discrete levels of BOLD response in SMA using kinaesthetic motor imagery.
•
For our paradigm neurofeedback provides only minimal extra control of BOLD signals in SMA. There is increasing interest in exploring the use of functional MRI neurofeedback (fMRI-NF) as a therapeutic technique for a range of neurological conditions such as stroke and Parkinson's disease (PD). One main therapeutic potential of fMRI-NF is to enhance volitional control of damaged or dysfunctional neural nodes and networks via a closed-loop feedback model using mental imagery as the catalyst of self-regulation. The choice of target node/network and direction of regulation (increase or decrease activity) are central design considerations in fMRI-NF studies. Whilst it remains unclear whether the primary motor cortex (M1) can be activated during motor imagery, the supplementary motor area (SMA) has been robustly activated during motor imagery. Such differences in the regulation potential between primary and supplementary motor cortex are important because these areas can be differentially affected by a stroke or PD, and the choice of fMRI-NF target and grade of self-regulation of activity likely have substantial influence on the clinical effects and cost effectiveness of NF-based interventions. In this study we therefore investigated firstly whether healthy subjects would be able to achieve self-regulation of the hand-representation areas of M1 and the SMA using fMRI-NF training. There was a significant decrease in M1 neural activity during fMRI-NF, whereas SMA neural activity was increased, albeit not with the predicated graded effect. This study has important implications for fMRI-NF protocols that employ motor imagery to modulate activity in specific target regions of the brain and to determine how they may be tailored for neurorehabilitation. •Graded fMRI neurofeedback can separate self-regulation effects from general cognitive ones.•There is a significant negative BOLD response in M1 during kinaesthetic motor imagery.•SMA shows robust positive BOLD responses during kinaesthetic motor imagery.•Participants can target discrete levels of BOLD response in SMA using kinaesthetic motor imagery.•For our paradigm neurofeedback provides only minimal extra control of BOLD signals in SMA. There is increasing interest in exploring the use of functional MRI neurofeedback (fMRI-NF) as a therapeutic technique for a range of neurological conditions such as stroke and Parkinson's disease (PD). One main therapeutic potential of fMRI-NF is to enhance volitional control of damaged or dysfunctional neural nodes and networks via a closed-loop feedback model using mental imagery as the catalyst of self-regulation. The choice of target node/network and direction of regulation (increase or decrease activity) are central design considerations in fMRI-NF studies. Whilst it remains unclear whether the primary motor cortex (M1) can be activated during motor imagery, the supplementary motor area (SMA) has been robustly activated during motor imagery. Such differences in the regulation potential between primary and supplementary motor cortex are important because these areas can be differentially affected by a stroke or PD, and the choice of fMRI-NF target and grade of self-regulation of activity likely have substantial influence on the clinical effects and cost effectiveness of NF-based interventions. In this study we therefore investigated firstly whether healthy subjects would be able to achieve self-regulation of the hand-representation areas of M1 and the SMA using fMRI-NF training. There was a significant decrease in M1 neural activity during fMRI-NF, whereas SMA neural activity was increased, albeit not with the predicated graded effect. This study has important implications for fMRI-NF protocols that employ motor imagery to modulate activity in specific target regions of the brain and to determine how they may be tailored for neurorehabilitation. |
Author | Turner, Duncan L. Mehler, David M.A. Linden, David E.J. Whittaker, Joseph R. Williams, Angharad N. Lührs, Michael Wise, Richard G. Krause, Florian |
AuthorAffiliation | f Neurorehabilitation Unit, School of Health, Sport and Bioscience, University of East London, London, E15 4LZ, United Kingdom c Donders Institute for Brain, Cognition and Behaviour Radboud University Medical Center, 6500 HB, Nijmegen, The Netherlands b Cardiff University Brain Research Imaging Centre, School of Psychology, Cardiff University, Cardiff, CF24 4HQ, United Kingdom e Brain Innovation B.V, Oxfordlaan 55, 6229 EV, Maastricht, The Netherlands a MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, United Kingdom h School of Physics and Astronomy, Cardiff University, Cardiff, CF24 3AA, United Kingdom g School of Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Universiteitssingel 40, 6229 ER, Maastricht, The Netherlands d Faculty of Psychology and Neuroscience, Maastricht University, Universiteitssingel 40, 6229 |
AuthorAffiliation_xml | – name: g School of Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Universiteitssingel 40, 6229 ER, Maastricht, The Netherlands – name: b Cardiff University Brain Research Imaging Centre, School of Psychology, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – name: f Neurorehabilitation Unit, School of Health, Sport and Bioscience, University of East London, London, E15 4LZ, United Kingdom – name: c Donders Institute for Brain, Cognition and Behaviour Radboud University Medical Center, 6500 HB, Nijmegen, The Netherlands – name: a MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – name: d Faculty of Psychology and Neuroscience, Maastricht University, Universiteitssingel 40, 6229 ER, Maastricht, The Netherlands – name: e Brain Innovation B.V, Oxfordlaan 55, 6229 EV, Maastricht, The Netherlands – name: h School of Physics and Astronomy, Cardiff University, Cardiff, CF24 3AA, United Kingdom |
Author_xml | – sequence: 1 givenname: David M.A. surname: Mehler fullname: Mehler, David M.A. organization: MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – sequence: 2 givenname: Angharad N. surname: Williams fullname: Williams, Angharad N. organization: Cardiff University Brain Research Imaging Centre, School of Psychology, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – sequence: 3 givenname: Florian surname: Krause fullname: Krause, Florian organization: Donders Institute for Brain, Cognition and Behaviour Radboud University Medical Center, 6500 HB, Nijmegen, The Netherlands – sequence: 4 givenname: Michael surname: Lührs fullname: Lührs, Michael organization: Faculty of Psychology and Neuroscience, Maastricht University, Universiteitssingel 40, 6229 ER, Maastricht, The Netherlands – sequence: 5 givenname: Richard G. surname: Wise fullname: Wise, Richard G. organization: Cardiff University Brain Research Imaging Centre, School of Psychology, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – sequence: 6 givenname: Duncan L. surname: Turner fullname: Turner, Duncan L. organization: Neurorehabilitation Unit, School of Health, Sport and Bioscience, University of East London, London, E15 4LZ, United Kingdom – sequence: 7 givenname: David E.J. surname: Linden fullname: Linden, David E.J. organization: MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, United Kingdom – sequence: 8 givenname: Joseph R. surname: Whittaker fullname: Whittaker, Joseph R. email: whittakerj3@cardiff.ac.uk organization: Cardiff University Brain Research Imaging Centre, School of Psychology, Cardiff University, Cardiff, CF24 4HQ, United Kingdom |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30205210$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Adult Biofeedback Brain Mapping Brain research Cortex (motor) Electroencephalography Emulation Feedback Female Functional magnetic resonance imaging Humans Imagination Kinesthesis Magnetic Resonance Imaging Male Mental task performance Motor Cortex - physiology Movement disorders Neurodegenerative diseases Neurofeedback Neurology Parkinson's disease Rehabilitation Self-Control Stroke Studies Success Supplementary motor area Young Adult |
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Title | The BOLD response in primary motor cortex and supplementary motor area during kinesthetic motor imagery based graded fMRI neurofeedback |
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