MEG corticomuscular coherence

[TUTORIAL UNDER DEVELOPMENT: NOT READY FOR PUBLIC USE]

Authors: Raymundo Cassani

Corticomuscular coherence relates to the synchrony between electrophysiological signals (MEG, EEG or ECoG) recorded from the contralateral motor cortex, and EMG signal from a muscle during voluntary movement. This synchrony has its origin mainly in the descending communication in corticospinal pathways between primary motor cortex (M1) and muscles. This tutorial replicates the processing pipeline and analysis presented in the Analysis of corticomuscular coherence FieldTrip tutorial.

Background

Coherence is a classic method to measure the linear relationship between two signals in the frequency domain. Previous studies (Conway et al., 1995, Kilner et al., 2000) have used coherence to study the relationship between MEG signals from M1 and muscles, and they have shown synchronized activity in the 15–30 Hz range during maintained voluntary contractions.

IMAGE OF EXPERIMENT, SIGNALS and COHERENCE

Dataset description

The dataset is comprised of MEG (151-channel CTF MEG system) and bipolar EMG (from left and right extensor carpi radialis longus muscles) recordings from one subject during an experiment in which the subject had to lift her hand and exert a constant force against a lever. The force was monitored by strain gauges on the lever. The subject performed two blocks of 25 trials in which either the left or the right wrist was extended for about 10 seconds. In addition to the MEG and EMG signals, EOG signal was recorded to assist the removal of ocular artifacts. Only data for the left wrist will be analyzed in this tutorial.

Download and installation

• Requirements: You should have already followed all the get-started tutorials and you have a working copy of Brainstorm installed on your computer.

• Download the dataset:

  • Download the SubjectCMC.zip file from FieldTrip FTP server:
    ftp://ftp.fieldtriptoolbox.org/pub/fieldtrip/tutorial/SubjectCMC.zip

  • Unzip it in a folder that is not in any of the Brainstorm folders (program or database folder).

• Brainstorm:

  • Start Brainstorm (Matlab scripts or stand-alone version).

  • Select the menu File > Create new protocol. Name it TutorialCMC and select the options:
    No, use individual anatomy,
    No, use one channel file per acquisition run.

The next sections describe: importing the subject's anatomy, reviewing raw data, managing event markers, pre-processing the EMG and MEG signals, epoching and importing recordings, and computing coherence in the sensor and source level.

Importing anatomy data

• Right-click on the TutorialCMC node then New subject > Subject01.
  Keep the default options you defined for the protocol.

• Switch to the Anatomy view of the protocol.

• Right-click on the Subject01 node then Import MRI:

  • Set the file format: All MRI file (subject space)

  • Select the file: SubjectCMC/SubjectCMC.mri

• Compute MNI normalization, in the MRI viewer click on Click here to compute MNI normalization, use the maff8 method. When the normalization is complete, verify the correct location of the fiducials and click on Save.

Once the MRI has been imported and normalized, we need to segment the head and brain tissues to obtain the surfaces that are needed to generate a realistic head model (or forward model).

• Right-click on the SubjectCMC MRI node, then MRI segmentation > FieldTrip: Tissues, BEM surfaces.

• Select all the tissues (scalp, skull, csf, gray and white).

• Click OK.

• For the option Generate surface meshes select No.

• After the segmentation is complete, a tissues node will be shown in the tree.

• Rick-click on the tissues node and select Generate triangular meshes

• Select the 5 layers to mesh
• Use the default parameters:

  • number of vertices: 10,000

  • erode factor: 0

  • fill holes factor: 2

As output, there is a set of (head and brain) surface files that will be used for the head model computation.

By displaying the surfaces, we can note that the cortex, which is related to the gray matter (shown in red) overlaps heavily with the innerskull surface (shown in gray), so it cannot be used to compute a BEM forward model using OpenMEEG. However, as we are dealing with MEG signals, we can still compute the forward model with the overlapping-spheres method, and obtain similar results. We can also notice that the cortex and white surfaces obtained with the method above do not register accurately the cortical surface, they can be used for volume-based source estimation, which is based on a volume grid of source points; but they may not be used for surface-based source estimation. Better surfaces can be obtained by doing MRI segmentation with CAT12 or FreeSurfer.

As the imported anatomy data is normalized in the MNI space, it is possible to apply use MNI parcellation templates to define anatomical regions of the brain of the subject. These anatomical regions can be used to create volume and surface scouts, which are convenient when performing the coherence analysis in the source level. Let's add the AAL3 parcellation to the imported data.

• Right-click on Subject01 then go to the menu Add MNI parcellation > AAL3 . The menu will appear as Download: AAL3 if the atlas is not in your system.

Access the recordings

Link the recordings

• Switch to the Functional data view (X button).

• Right-click on the Subject01 node then Review raw file:

  • Select the file format: MEG/EEG: CTF(*.ds; *.meg4; *.res4)

  • Select the file: SubjectCMC.ds

A new folder and its content are now visible in the database explorer:

• The SubjectCMC folder represents the MEG dataset linked to the database. Note the tag "RAW" in the icon of the folder, this means that the files are considered as raw continuous files.

• The CTF channels (191) node is the channel file and defines the types and names of channels that were recorded, the position of the sensors, the head shape and other various details. This information has been read from the MEG datasets and saved as a new file in the database. The total number of data channels recorded in the file is indicated between parenthesis (191).

• The Link to raw file node is a link to the original file that was selected. All the relevant metadata was read from the MEG dataset and copied inside the link itself (sampling rate, number of samples, event markers and other details about the acquisition session). As it is a link, no MEG recordings were copied to the database. When we open this file, the values are read directly from the original files in the .ds folder. More information.

• 
  

Display MEG helmet and sensors

• Right-click on the CTF channels (191) node, then Display sensors > CTF helmet and Display sensors > MEG to show a surface that represents the inner surface the helmet, and the MEG sensors respectively. Try additional display menus.

• 

Reviewing continuous recordings

• Right-click on the Link to raw file node, then Switch epoched/continuous to convert the file to continuous.

• Right-click on the Link to raw file node, then MEG > Display time series (or double-click on the node). This opens a new time series figure and enable the Time panel and the Record tab in the main Brainstorm window. Controls in this panel and tab are used to explore the time series.

• In addition we can display the EMG signals, right-click on the Link to raw file node, then EMG > Display time series.

• 

Event markers

The colored dots on top of the recordings in the time series figures represent the event markers (or triggers) saved in this dataset. In addition to these events, the start of the either left or right trials is saved in the auxiliary channel named Stim. To add these markers:

• With the time series figure open, in the Record tab go to File > Read events from channel. Now, in the options for the Read from channel process, set Event channels = Stim, select Value, and click Run.

• 

This creates new events shown in the Events section of the tab. We are only interested in the events from U1 to U25 that correspond to the 25 left trials. Thus we will delete the other events, and merge the left trial events.

• Delete all the other events: select the events to delete with Ctrl+click, when done go the menu Events > Delete group and confirm. Alternatively, you can do Ctrl+A to select all the events and then deselect the U1 to U25 events.

• To be in line with the original FieldTrip tutorial, we will reject the trial 7. Select the events U1 to U6 and U8 to U25 events, then go the menu Events > Merge group and enter the label Left.

• 

These events are located at the beginning of the 10 s trials of left wrist movement. In the sections below, we will compute the coherence for 1 s epochs for the first 8 s of the trial, thus we need to create extra events.

• Duplicate 7 times the Left events by selecting Duplicate group in the Events menu. The groups Left_02 to Left_08 will be created.

• For each copy of the Left events, we need to add a time offset of 1 s for Left02, 2 s for Left03, and so on. Select the event group to add the offset, then go to the menu Events > Delete group.

• 

• Finally, merge all the Left* events into Left, and select Save modifications in the File menu in the Record tab.

• 

Pre-process

The CTF MEG recordings in this dataset were not saved with the desired 3rd order compensation. To continue with the pre-processing we need to apply the compensation.

• In the Process1 box: Drag and drop the Link to raw file node.

• Run process Artifacts > Apply SSP & CTF compensation:
  

• 

This process create the SubjectCMC_clean folder that contains a copy of the channel file and the raw recordings file Raw | clean, which is de exact copy of the original data but with the CTF compensation applied.

Power line artifacts

Let's start with locating the spectral components and impact of the power line noise in the MEG and EMG signals.

• In the Process1 box: Drag and drop the Raw | clean node.

• Run process Frequency > Power spectrum density (Welch):
  

  • Time window: 0 - 330 s

  • Window length=10 s

  • Overlap=50%

  • Sensor types=`MEG, EMG

• 

• Double-click on the new PSD file to display it.
  

• 

• The PSD shows two groups of sensors, EMG on top and MEG in the bottom. Also, there are peaks at 50Hz and its harmonics. We will use notch filters to remove the power line component and its first two components from the signals.

• Run the process Pre-processing > Notch filter with:
  

  • Sensor types = MEG, EMG

  • Frequencies to remove (Hz) = 50, 100, 150

• 

A new raw folder named SubjectCMC_clean_notch will appear in the database explorer. Compute the PSD for the filtered signals to verify effect of the notch filters. Remember to compute for the Time window from 0 to 330 s.

Pre-process EMG

Two of the typical pre-processing steps for EMG consist in high-pass filtering and rectifying.

• In the Process1 box: drag and drop the Raw | notch(50Hz 100Hz 150Hz) recordings node.

• Add the process Pre-process > Band-pass filter

  • Sensor types = EMG

  • Lower cutoff frequency = 10 Hz

  • Upper cutoff frequency = 0 Hz

• Add the process Pre-process > Absolute values

  • Sensor types = EMG

• Run the pipeline

• 

Once the pipeline ends, the new folders SubjectCMC_clean_notch_high and SubjectCMC_clean_notch_high_abs are added to the database explorer. To avoid any confusion later, we can delete folders that will not be needed.

• Delete the conditions SubjectCMC_clean_notch and SubjectCMC_clean_notch_high. Select both folders containing and press Delete (or right-click File > Delete).

Pre-process MEG

After applying the notch filter to the MEG signals, we still need to remove other type of artifacts, we will perform:

1. Detection and removal of artifacts with SSP

2. Detection of segments with other artifacts

Detection and removal of artifacts with SSP

In the case of stereotypical artifacts, as it is the case of the eye blinks and heartbeats, it is possible to identify their characteristic spatial distribtuion, and then remove it from MEG signals with methods such as Signal-Space Projection (SSP). For more details, consult the tutorials on detection and removal of artifacts with SSP. The dataset of this tutorial contains an EOG channel but not ECG signal, thus will perform only removal of eye blinks.

• Display the MEG and EOG time series. Right-click on the pre-processed (for EMG) continuous file Raw | clean | notch(... (in the SubjectCMC_clean_notch_high_abs folder) then MEG > Display time series and EOG > Display time series.

• In the Events section of the Record tab, select Artifacts > Detect eye blinks, and use the parameters:

  • Channel name= EOG

  • Time window = 0 - 330 s

  • Event name = blink

• 

• As result, there will be 3 blink event groups. Review the traces of EOG channels and the blink events to be sure the detected events make sense. Note that the blink group contains the real blinks, and blink2 and blink3 contain mostly saccades.

• 

• To remove blink artifacts with SSP go to Artifacts > SSP: Eyeblinks, and use the parameters:

  • Event name=blink

  • Sensors=MEG

  • Check Compute using existing SSP/ICA projectors

• 

• Display the time series and topographies for the first two components. Only the first one is clearly related to blink artifacts. Select only component #1 for removal.

• 

• Follow the same procedure for the other blink events (blink2 and blink3). Note that none of first two components for the remaining blink events is clearly related to a ocular artifacts. This figure shows the first two components for the blink2 group.

• 

• In this case, it is safer to unselect the blink2 and blink3 groups, rather than removing spatial components that we are not sure to identify.

• 

• Close all the figures

Detection of segments with other artifacts

Here we will used automatic detection of artifacts. It aims to identify typical artifacts such as the ones related to eye movements, subject movement and muscle contractions.

• Display the MEG and EOG time series. In the Record tab, select Artifacts > Detect other artifacts, use the following parameters:

  • Time window = 0 - 330 s

  • Sensor types=MEG

  • Sensitivity=3

  • Check both frequency bands 1-7 Hz and 40-240 Hz

• 

While this process can help identify segments with artifacts in the signals, it is still advised to review the selected segments. After a quick browse, it can be noticed that the selected segments indeed correspond to irregularities in the MEG signal. Then, we will label these events are bad.

• Select the 1-7Hz and 40-240Hz event groups and use the menu Events > Mark group as bad. Alternatively, you can rename the events and add the tag bad_ in their name, it would have the same effect.

• 

• Close all the figures, and save the modifications.

Importing the recordings

At this point we have finished with the pre-processing of our EMG and MEG recordings. Many operations operations can only be applied to short segments of recordings that have been imported in the database. We refer to these as epochs or trials. Thus, the next step is to import the data taking into account the Left events.

• Right-click on the filtered continuous file Raw | clean | notch(... (in the SubjectCMC_clean_notch_high_abs condition), then Import in database.

• 

• Set the following parameters:

  • Time window = 0 - 330 s

  • Check Use events and highlight the Left(x192) event group

  • Epoch time = 0 - 1000 ms

  • Check Apply SSP/ICA projectors

  • Check Remove DC offset and select All recordings

• 

The new folder SubjectCMC_clean_notch_high_abs appears for Subject01. It contains a copy of the channel file in the continuous file, and the Left trial group. By expanding the trial group, we can notice that there are trials marked with an interrogation sign in a red circle (ICON). These bad trials are the ones that were overlapped with the bad segments identified in the previous section. All the bad trials are automatically ignored in the Process1 and Process2 tabs.

Coherence (sensor level)

Once we have imported the trials, we will compute the magnitude square coherence (MSC) between the left EMG signal and the signals from each of the MEG sensors.

• In the Process1 box, drag and drop the Left (192 files) trial group. Note that the number between square brackets is [185], as the 7 bad trials are ignored.

• 

• To compute the coherence between EMG and MEG signals. Run the process Connectivity > Coherence 1xN [2021] with the following parameters:

  • Time window = 0 - 1000 ms or check All file

  • Source channel = EMGlft

  • Do not check Include bad channels nor Remove evoke response

  • Magnitude squared coherence

  • Window length for PSD estimation = 0.5 s

  • Overlap for PSD estimation = 50%

  • Highest frequency of interest = 80 Hz

  • Average cross-spectra of input files (one output file)

  • More details on the Coherence process can be found in the ?connectivity tutorial.

• 

• Double-click on the resulting node mscohere(0.6Hz,555win): EMGlft to display the MSC spectra. Click on the maximum peak in the 15 to 20 Hz range, and press Enter to plot it in a new figure. This spectrum corresponds to channel MRC21, and has its peak at 17.58 Hz. You can also use the frequency slider (below the Time panel) to explore the spectral representations.

* Right-click on the spectrum and select 2D Sensor cap for a spatial visualization of the coherence results, alternatively, the short cut Ctrl-T can be used. Once the 2D Sensor cap is show, the sensor locations can be displayed with right-click then Channels > Display sensors or the shortcut Ctrl-E.

The results above are based in the identification of single peak, as alternative we can average the MSC in a given frequency band (15 - 20 Hz), and observe its topographical distribution.

• In the Process1 box, drag-and-drop the mscohere(0.6Hz,555win): EMGlft node, and add the process Frequency > Group in time or frequency bands with the parameters:

  • Select Group by frequency

  • Type cmc_band / 15, 20 / mean in the text box.

• 

The resulting file mscohere(0.6Hz,555win): EMGlft | tfbands has only one MSC value for each sensor (the average in the 15-20 Hz band). Thus, it is more useful to display the result in a spatial representation. Brainstorm provides 3 spatial representations: 2D Sensor cap, 2D Sensor cap and 2D Disk, which are accessible with right-click on the MSC node. Sensor MRC21 is selected as reference.

In agreement with the literature, we observe higher MSC values between the EMG signal and the MEG signal for MEG sensors over the contralateral primary motor cortex in the beta band range. In the next sections we will perform source estimation and compute coherence in the source level.

Source analysis

Before estimating the brain source, we need to compute the head model and the noise covariance.

Head model

The head model describes how neural electric currents produce magnetic fields and differences in electrical potentials at external sensors, given the different head tissues. This model is independent of sensor recordings. See the head model tutorial for more details.

• In the SubjectCMC_clean_notch_high_abs, right-click the CTF channels (191) node and select Compute head model. Keep the default options:

  • Source space = Cortex

  • Forward model = Overlapping spheres.

As result will have the Overlapping spheres head model in the database explorer.

Noise covariance

For MEG it is recommended to derive the noise covariance from empty room recordings. However, as we do not have those recordings in the dataset, we can compute the noise covariance from the MEG signals before the trials. See the noise covariance tutorial for more details.

• In the raw SubjectCMC_clean_notch_high_abs, right click the Raw | clean | notch(... node and select Noise covariance > Compute from recordings. As parameters select a Baseline from 18 - 30 s, and the Block by block option.

• 

• Lastly, we need to copy the Noise covariance node to the SubjectCMC_clean_notch_high_abs folder with the head model. This can be done with the shortcuts Ctrl-C and Ctrl-V.

Source estimation

With the help of the head model and the noise covariance, we can solve the inverse problem by computing an inverse kernel that will estimate the brain activity that gives origin to the observed recordings in the sensors. See the source estimation tutorial for more details.

• To compute the inversion kernel, right click in the Overlapping spheres head model and select Compute sources [2018]. With the parameters: Minimum norm imaging, dSPM and Constrained.

• 

The inversion kernel dSPM-unscaled: MEG(Constr) 2018 was created, and note that the each recordings node has an associated source link.

Coherence (source level)

From the earlier section importing anatomy data, we can observe that the cortex surface has 10,000 vertices, thus as many sources were estimated. AS it can be seen, it is not practical to compute coherence between the left EMG signal and each source. A way to address this issue is with the use of regions of interest or Scouts.

• Double-click the source link for any of the trials to visualize the source space. This will enable the tab Scout in the main Brainstorm window.

• 

• In the Scout tab select the menu Atlas > Surface clustering > Homogeneous parcellation (deterministic), and set the Number of scouts to 80.

• 

It is important to note that the coherence will be performed between a sensor signal (EMG) and source signals in the scouts.

• Change to the Process2 tab, and drag-and-drop the Left (192 files) trial group into the Files A and into the Files B boxes. And select Process recordings for Files A, and Process sources for Files B.

• 

• Run the process Connectivity > Coherence AxB [2021] with the following parameters:

  • All file, Source channel (A) = EMGlft, check Use scouts (B)

  • Select Surface clustering: 80 in the drop-down list, and select all the scouts (shortcut Ctrl-A).

  • Scout function = Mean, and When to apply = Before. Do not Remove evoked responses from each trial.

  • Magnitude squared coherence, Window length = 0.5 s, Overlap = 50%, Highest frequency = 80 Hz, and Average cross-spectra.

• 

Results with FieldTrip MRI segmentation

• Double-click on the resulting node mscohere(0.6Hz,555win): Left (#1) to display the coherence spectra. Also open the result node as image with Display image in its context menu.

• To verify the location of the scouts on the cortex surface, double-click the source link for any of the trials. In the Surface tab, set the Amplitude threshold to 100% to hide all the cortical activations. Laslty, in the Scouts tab, select the Show only the selected scouts and the Show/hide the scout labels. Note that the plots are linked by the scout selected in the image representation of the coherence results.

• 

Results with FieldTrip MRI segmentation

Script

Additional documentation

Articles

• Conway BA, Halliday DM, Farmer SF, Shahani U, Maas P, Weir AI, et al.
  Synchronization between motor cortex and spinal motoneuronal pool during the performance of a maintained motor task in man.
  The Journal of Physiology. 1995 Dec 15;489(3):917–24.

• Kilner JM, Baker SN, Salenius S, Hari R, Lemon RN.
  Human Cortical Muscle Coherence Is Directly Related to Specific Motor Parameters.
  J Neurosci. 2000 Dec 1;20(23):8838–45.

• Liu J, Sheng Y, Liu H.
  https://doi.org/10.3389/fnhum.2019.00100Corticomuscular%20Coherence%20and%20Its%20Applications:%20A%20Review. Front Hum Neurosci. 2019 Mar 20;13:100.

Tutorials

• Tutorial: Volume source estimation

• Tutorial: Functional connectivity

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