Combining EEG and fMRI to investigate the post-movement beta rebound

The relationship between synchronous neuronal activity as measured with EEG and the blood oxygenation level dependent (BOLD) signal as measured during fMRI is not clear. This work investigates the relationship by combining EEG and fMRI measures of the strong increase in beta frequency power following movement, the so-called post-movement beta rebound (PMBR). The time course of the PMBR, as measured by EEG, was included as a regressor in the fMRI analysis, allowing identification of a region of associated BOLD signal increase in the sensorimotor cortex, with the most significant region in the post-central sulcus. The increase in the BOLD signal suggests that the number of active neurons and/or their synaptic rate is increased during the PMBR. The duration of the BOLD response curve in the PMBR region is significantly longer than in the activated motor region, and is well fitted by a model including both motor and PMBR regressors. An intersubject correlation between the BOLD signal amplitude associated with the PMBR regressor and the PMBR strength as measured with EEG provides further evidence that this region is a source of the PMBR. There is a strong intra-subject correlation between the BOLD signal amplitude in the sensorimotor cortex during movement and the PMBR strength as measured by EEG, suggesting either that the motor activity itself, or somatosensory inputs associated with the motor activity, influence the PMBR. This work provides further evidence for a BOLD signal change associated with changes in neuronal synchrony, so opening up the possibility of studying other event-related oscillatory changes using fMRI.

[1]  G Pfurtscheller,et al.  Event-related beta synchronization after wrist, finger and thumb movement. , 1998, Electroencephalography and clinical neurophysiology.

[2]  Mark S. Cohen,et al.  Simultaneous EEG and fMRI of the alpha rhythm , 2002, Neuroreport.

[3]  C. Mathiesen,et al.  Modification of activity‐dependent increases of cerebral blood flow by excitatory synaptic activity and spikes in rat cerebellar cortex , 1998, The Journal of physiology.

[4]  Hellmuth Obrig,et al.  Correlates of alpha rhythm in functional magnetic resonance imaging and near infrared spectroscopy , 2003, NeuroImage.

[5]  Adrian L. Williams,et al.  Task-Related Changes in Cortical Synchronization Are Spatially Coincident with the Hemodynamic Response , 2002, NeuroImage.

[6]  P. Derambure,et al.  Does post-movement beta synchronization reflect an idling motor cortex? , 2001, Neuroreport.

[7]  H. Alkadhi,et al.  Localization of the motor hand area to a knob on the precentral gyrus. A new landmark. , 1997, Brain : a journal of neurology.

[8]  Louis Lemieux,et al.  Identification of EEG Events in the MR Scanner: The Problem of Pulse Artifact and a Method for Its Subtraction , 1998, NeuroImage.

[9]  F. L. D. Silva,et al.  Event-related EEG/MEG synchronization and desynchronization: basic principles , 1999, Clinical Neurophysiology.

[10]  Mark Hallett,et al.  Time course of corticospinal excitability in reaction time and self‐paced movements , 1998, Annals of neurology.

[11]  Andreas Kleinschmidt,et al.  EEG-correlated fMRI of human alpha activity , 2003, NeuroImage.

[12]  Robert Turner,et al.  A Method for Removing Imaging Artifact from Continuous EEG Recorded during Functional MRI , 2000, NeuroImage.

[13]  G. Pfurtscheller,et al.  Event-related dynamics of cortical rhythms: frequency-specific features and functional correlates. , 2001, International journal of psychophysiology : official journal of the International Organization of Psychophysiology.

[14]  G. Pfurtscheller,et al.  The effects of external load on movement-related changes of the sensorimotor EEG rhythms. , 1997, Electroencephalography and clinical neurophysiology.

[15]  Daniel Gounot,et al.  The BOLD response and the gamma oscillations respond differently than evoked potentials: an interleaved EEG-fMRI study , 2003, BMC Neuroscience.

[16]  P. Derambure,et al.  Basic mechanisms of central rhythms reactivity to preparation and execution of a voluntary movement: a stereoelectroencephalographic study , 2003, Clinical Neurophysiology.

[17]  Karl J. Friston,et al.  Relating Macroscopic Measures of Brain Activity to Fast, Dynamic Neuronal Interactions , 2000, Neural Computation.

[18]  G. Glover Deconvolution of Impulse Response in Event-Related BOLD fMRI1 , 1999, NeuroImage.

[19]  D. Attwell,et al.  The neural basis of functional brain imaging signals , 2002, Trends in Neurosciences.

[20]  A. Kleinschmidt,et al.  Electroencephalographic signatures of attentional and cognitive default modes in spontaneous brain activity fluctuations at rest , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[21]  J. Rajapakse,et al.  Human Brain Mapping 6:283–300(1998) � Modeling Hemodynamic Response for Analysis of Functional MRI Time-Series , 2022 .

[22]  R. Hari,et al.  Functional Segregation of Movement-Related Rhythmic Activity in the Human Brain , 1995, NeuroImage.

[23]  Christian Kaufmann,et al.  Functional MRI during sleep: BOLD signal decreases and their electrophysiological correlates , 2004, The European journal of neuroscience.

[24]  J. Mugler,et al.  Three‐dimensional magnetization‐prepared rapid gradient‐echo imaging (3D MP RAGE) , 1990, Magnetic resonance in medicine.

[25]  Mikko Pohja,et al.  On the human sensorimotor-cortex beta rhythm: Sources and modeling , 2005, NeuroImage.

[26]  Karl J. Friston,et al.  The Relationship Between Synchronization Among Neuronal Populations and Their Mean Activity Levels , 1999, Neural Computation.

[27]  W.J.R. Dunseath,et al.  fMRI of the Responses to Vibratory Stimulation of Digit Tips , 2000, NeuroImage.

[28]  David C. Alsop,et al.  The Sensory Somatotopic Map of the Human Hand Demonstrated at 4 Tesla , 1999, NeuroImage.

[29]  Kyung K Peck,et al.  Comparison of hemodynamic response nonlinearity across primary cortical areas , 2004, NeuroImage.

[30]  J. Artieda,et al.  Beta electroencephalograph changes during passive movements: sensory afferences contribute to beta event-related desynchronization in humans , 2002, Neuroscience Letters.

[31]  D. G. Albrecht,et al.  Spikes versus BOLD: what does neuroimaging tell us about neuronal activity? , 2000, Nature Neuroscience.

[32]  G. Pfurtscheller,et al.  Functional imaging of postmovement beta event-related synchronization. , 1999, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

[33]  P. Mitra,et al.  Analysis of dynamic brain imaging data. , 1998, Biophysical journal.

[34]  R. Lesser,et al.  Functional mapping of human sensorimotor cortex with electrocorticographic spectral analysis. I. Alpha and beta event-related desynchronization. , 1998, Brain : a journal of neurology.

[35]  M. Hallett,et al.  The relative metabolic demand of inhibition and excitation , 2000, Nature.

[36]  N. Logothetis,et al.  Neurophysiological investigation of the basis of the fMRI signal , 2001, Nature.

[37]  H. Shibasaki,et al.  Movement-related change of electrocorticographic activity in human supplementary motor area proper. , 2000, Brain : a journal of neurology.

[38]  G. Pfurtscheller,et al.  Post-movement beta synchronization. A correlate of an idling motor area? , 1996, Electroencephalography and clinical neurophysiology.