experimentyijun/pdfs/hbm09poster.pdf · 2009. 6. 15. · introduction the role of the posterior...

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0 0.1 0.2 0.3 0.4 0.5 6 4 2 0 2 4 Time (s) Potential (uV) 0 0.1 0.2 0.3 0.4 0.5 6 4 2 0 2 4 Time (s) Potential (uV) 0 0.1 0.2 0.3 0.4 0.5 4 3 2 1 0 1 2 3 4 Time (s) Potential (uV) 0 0.1 0.2 0.3 0.4 0.5 6 4 2 0 2 4 Time (s) Potential (uV) 0 100 200 300 400 500 600 4 2 0 2 Latency (ms) Potential ( µV) 220 302 + 0 100 200 300 400 500 600 4 2 0 2 Latency (ms) Potential ( µV) 220 302 + 0 100 200 300 400 500 600 4 2 0 2 4 Latency (ms) Potential ( µV) 220 302 + Right Decoding Intended Movement from Human EEG in the Posterior Parietal Cortex Yijun Wang, Scott Makeig Swartz Center for Computational Neuroscience, Institute for Neural Computation, University of California San Diego, CA 92093, USA Effectors: (1) Hand (2) Eye (3)Eye&Hand Directions: (1) Left (2) Center (3) Right Response 500ms 1000ms 700ms + Hand / Eye/ H+E Left / Center/ Right + Experiment Results Summary References (2) Clustering parietal components (1) Independent Component Analysis (ICA) Introduction The role of the posterior parietal cortex (PPC) in sensorimotor transformations has been explored by neuronal recording in monkey studies (Quiroga et al., 2006; Calton et al., 2002). Direction and effector information for an intended movement can be predicted using firing rates of neurons in specific PPC subareas: the lateral intraparietal area (LIP) for saccades and the parietal reach region (PRR) for reaches. In humans, functional magnetic resonance imaging (fMRI) studies on the PPC have identified regions corresponding to the monkey LIP and PRR areas (Sereno et al., 2001; Connolly et al., 2003). In the present study, we asked whether it is possible to decode intended movement using human EEG recorded in the PPC. To this end, we recorded multi-channel EEGs with a delayed saccade-or-reach task and proposed an approach based on single-trial EEG classification. [1] Calton, J. L., Dickinson, A. R., & Snyder, L. H. (2002), ‘Non-spatial, motor-specific activation in posterior parietal cortex’, Nature Neuroscience, vol. 5, no. 6, pp.580-588. [2] Connolly, J. D., Andersen, R. A., & Goodale, M. A. (2003), ‘FMRI evidence for a ‘parietal reach region’ in the human brain’, Experimental Brain Research, vol. 153, pp. 140-145. [3] Delorme, A., & Makeig, S. (2004), ‘EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis’, Journal of Neuroscience Methods, vol. 134, pp. 9-21. [4] Quiroga, R. Q., Snyder, L. H., Bastista, A. P., & Andersen, R. A. (2006), ‘Movement intention is better predicted than attention in the posterior parietal cortex’, The Journal of Neuroscience, vol. 26, no. 13, pp. 3615-3620. [5] Sereno, M. I., Pitzalis, S., & Martinez, A. (2001), ‘Mapping of contralateral space in retinotopic coordinates by a parietal cortical area in humans’, Science, vol. 294, pp. 1350-1354. Human Brain Mapping 2009, San Francisco, USA (3) Direction decoding Left Center (4) Effector decoding Left Parietal IC Right Parietal IC As shown in the ERP envelops of the lateralized parietal ICs, effector- specific information involved distinct changes in ERP amplitude and latency (reach vs. saccade), while movement direction information was reflected by hemispheric asymmetry. For 4-class classification, we obtained an average accuracy of 49.8% (44.8%-55.0% across all subjects; chance level, 25%). Considered separately, direction classification accuracy was 80.3%, effector classification 69.1%. Binary condition classification was performed for all 6 pairwise condition combinations for each subject; the most distinguishable pair (mean, 84.9%; range, 80.0%-90.5%) differed across subjects. Method We recorded 128-channel EEG from four healthy subjects. The task comprised nine conditions differing by movement type (saccade, reach to touch without eye movement, and visually guided reach to touch) and movement direction (left, center, and right). Each task was indicated to the subject by an effector cue, followed by a direction cue and then an action (go) cue. EEG data between the direction and action cues were extracted for further analysis. Independent component analysis (ICA) was applied to decompose the scalp EEG into functionally specific component processes using the EEGLAB toolbox (Delorme and Makeig, 2004). Parietal ICs were selected and then back projected onto the scalp. Normalized single-trial amplitudes of these ICs were concatenated and input into a support vector machine (SVM) classifier. Cross validation was run to estimate classification performance. For simplicity, we included four tasks: saccade left, saccade right, reach left, and reach right. Time-frequency parameters and classification performance (left vs. right) Two lateralized temporal-parietal and one medial parietal components were identified in each subject’s decomposition based on their spatial distributions and prominent contributions to the average event-related potential (ERP) waveforms. Equivalent dipole localization fitting two symmetric bilateral model dipoles to each IC scalp map indicated that these lateralized IC processes originated from the bilateral PPC (Brodmann Area 39/40). 1. The PPC (BA 7,39,40) plays an important role in intended movement planning. 2. Two lateral tempo-parietal components (BA 39,40) and a medial parietal component (BA 7), which contribute most to scalp ERPs, can be easily identified after ICA. 3. Direction and effector information during intended movement planning can be decoded using features derived from two lateral tempo-parietal (BA 39,40) ICs. Conclusion: Here we have shown that brain activity in the PPC is modulated by movement planning. We obtained classification accuracy well above chance level for direction and effector estimation. Based on these findings, we find that intended movements can be predicted using EEG recordings, providing a new basis for design of a noninvasive brain- machine interface (BMI). Motor planning Independent component analysis (ICA) has been widely used in EEG analysis. It can decompose the overlapping source activities constituting the scalp EEG into functionally specific component processes. Here, we used ICA as an unsupervised spatial filtering technique to extract parietal EEG independent component (IC) activities that excluded noise from eye and muscle components as well as brain activities from other functional processes (e.g., in motor, visual, and frontal areas). For each subject, all trials were band-pass filtered (1-30 Hz), concatenated, and then decomposed using the extended infomax ICA algorithm. 80.25±2.22 Mean 81.9±0.81 0-35 210-510 S4 77.2±0.86 0-20 180-450 S3 81.9±0.94 0-25 150-480 S2 79.9±0.45 0-25 180-500 S1 Accuracy (%) Frequency Window (Hz) Time Window (ms) Subject Binary classification of “leftversus “righttrials was performed using standard machine learning techniques. Because this study focused on EEG modulation in the parietal cortex, only the parietal IC components were used for feature extraction. After low-pass filtering, normalized amplitudes in the selected time window, normalized at each time point to have a range of [-1 1] across trials, were employed as features. Feature vectors from both parietal components were concatenated and then input to a support vector machine (SVM) classifier using an RBF kernel. Reach Left Reach Right Saccade Left Saccade Right gil/ic2 michael/ic3 yijun/ic17 zeynep/ic3 left parietal 3 (4 Ss, 4 ICs) gil/ic8 michael/ic1 yijun/ic23 zeynep/ic2 right parietal 2 (4 Ss, 4 ICs) gil/ic11 michael/ic9 yijun/ic5 zeynep/ic4 medial parietal 4 (4 Ss, 4 ICs) BA 7 BA 39 BA 40 0 100 200 300 400 500 5 0 5 Latency (ms) Potential ( µV) 190 240 320 500 + 0 0.1 0.2 0.3 0.4 0.5 10 8 6 4 2 0 2 4 6 ppaf 60.63% Time (s) Potential (uV) Largest ERP components of pointing epochs + ICA Fixate Effector Cue Delay Period Direction cue Delay Period Go Cue Saccade or Reach

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Page 1: Experimentyijun/pdfs/HBM09Poster.pdf · 2009. 6. 15. · Introduction The role of the posterior parietal cortex (PPC) in sensorimotor transformations has been explored by neuronal

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Decoding Intended Movement from Human EEG in the Posterior Parietal CortexYijun Wang, Scott Makeig

Swartz Center for Computational Neuroscience, Institute for Neural Computation, University of California San Diego, CA 92093, USA

Effectors: (1) Hand (2) Eye (3)Eye&Hand Directions: (1) Left (2) Center (3) Right

Response500ms 1000ms 700ms+

Hand / Eye/ H+E Left / Center/ Right+

Experiment

Results

Summary References

(2) Clustering parietal components(1) Independent Component Analysis (ICA)

IntroductionThe role of the posterior parietal cortex (PPC) in sensorimotor transformations has been explored by neuronal recording in monkey studies (Quiroga et al., 2006; Calton et al., 2002). Direction and effector information for an intended movement can be predicted using firing rates of neurons in specific PPC subareas: the lateral intraparietal area (LIP) for saccades and the parietal reach region (PRR) for reaches. In humans, functional magnetic resonance imaging (fMRI) studies on the PPC have identified regions corresponding to the monkey LIP and PRR areas (Sereno et al., 2001; Connolly et al., 2003). In the present study, we asked whether it is possible to decode intended movement using human EEG recorded in the PPC. To this end, we recorded multi-channel EEGs with a delayed saccade-or-reach task and proposed an approach based on single-trial EEG classification.

[1] Calton, J. L., Dickinson, A. R., & Snyder, L. H. (2002), ‘Non-spatial, motor-specific activation in posterior parietal cortex’, Nature Neuroscience, vol. 5, no. 6, pp.580-588.[2] Connolly, J. D., Andersen, R. A., & Goodale, M. A. (2003), ‘FMRI evidence for a ‘parietal reach region’ in the human brain’, Experimental Brain Research, vol. 153, pp. 140-145.[3] Delorme, A., & Makeig, S. (2004), ‘EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis’, Journal of Neuroscience Methods, vol. 134, pp. 9-21.[4] Quiroga, R. Q., Snyder, L. H., Bastista, A. P., & Andersen, R. A. (2006), ‘Movement intention is better predicted than attention in the posterior parietal cortex’, The Journal of Neuroscience, vol. 26, no. 13, pp. 3615-3620.[5] Sereno, M. I., Pitzalis, S., & Martinez, A. (2001), ‘Mapping of contralateral space in retinotopic coordinates by a parietal cortical area in humans’, Science, vol. 294, pp. 1350-1354.

Human Brain Mapping 2009, San Francisco, USA

(3) Direction decoding

Left Center

(4) Effector decoding

Left Parietal IC Right Parietal IC

As shown in the ERP envelops of the lateralized parietal ICs, effector-specific information involved distinct changes in ERP amplitude and latency (reach vs. saccade), while movement direction information was reflected by hemispheric asymmetry.

For 4-class classification, we obtained an average accuracy of 49.8% (44.8%-55.0% across all subjects; chance level, 25%). Considered separately, direction classification accuracy was 80.3%, effectorclassification 69.1%. Binary condition classification was performed for all 6 pairwise condition combinations for each subject; the most distinguishable pair (mean, 84.9%; range, 80.0%-90.5%) differed across subjects.

MethodWe recorded 128-channel EEG from four healthy subjects. The task comprised nine conditions differing by movement type (saccade, reach to touch without eye movement, and visually guided reach to touch) and movement direction (left, center, and right). Each task was indicated to the subject by an effector cue, followed by a direction cue and then an action (go) cue. EEG data between the direction and action cues were extracted for further analysis.

Independent component analysis (ICA) was applied to decompose the scalp EEG into functionally specific component processes using the EEGLAB toolbox (Delorme and Makeig, 2004). Parietal ICs were selected and then back projected ontothe scalp. Normalized single-trial amplitudes of these ICs were concatenated and input into a support vector machine (SVM) classifier. Cross validation was run to estimate classification performance. For simplicity, we included four tasks: saccade left, saccade right, reach left, and reach right.

Time-frequency parameters and classification performance (left vs. right)

Two lateralized temporal-parietal and one medial parietal components were identified in each subject’s decomposition based on their spatial distributions and prominent contributions to the average event-related potential (ERP) waveforms. Equivalent dipole localization fitting two symmetric bilateral model dipoles to each IC scalp map indicated that these lateralized IC processes originated from the bilateral PPC (Brodmann Area 39/40).

1. The PPC (BA 7,39,40) plays an important role in intended movement planning.

2. Two lateral tempo-parietal components (BA 39,40) and a medial parietal component (BA 7), which contribute most to scalp ERPs, can be easily identified after ICA.

3. Direction and effector information during intended movement planning can be decoded using features derived from two lateral tempo-parietal (BA 39,40) ICs.

Conclusion: Here we have shown that brain activity in the PPC is modulated by movement planning. We obtained classification accuracy well above chance level for direction and effector estimation. Based on these findings, we find that intended movements can be predicted using EEG recordings, providing a new basis for design of a noninvasive brain-machine interface (BMI).

Motor planning

Independent component analysis (ICA) has been widely used in EEG analysis. It can decompose the overlapping source activitiesconstituting the scalp EEG into functionally specific component processes. Here, we used ICA as an unsupervised spatial filtering technique to extract parietal EEG independent component (IC) activities that excluded noise from eye and muscle components as well as brain activities from other functional processes (e.g., in motor, visual, and frontal areas). For each subject, all trials were band-pass filtered (1-30 Hz), concatenated, and then decomposed using the extended infomax ICA algorithm.

80.25±2.22Mean

81.9±0.810-35210-510S4

77.2±0.860-20180-450S3

81.9±0.940-25150-480S2

79.9±0.450-25180-500S1

Accuracy (%)Frequency Window (Hz)Time Window (ms)Subject Binary classification of “left” versus “right” trials was performed using standard machine learning techniques. Because this study focused on EEG modulation in the parietal cortex, only the parietal IC components were used for feature extraction. After low-pass filtering, normalized amplitudes in the selected time window, normalized at each time point to have a range of [-1 1] across trials, were employed as features. Feature vectors from both parietal components were concatenated and then input to a support vector machine (SVM) classifier using an RBF kernel.

Reach Left Reach Right

Saccade Left Saccade Right

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left parietal 3 (4 Ss, 4 ICs) gil/ic8

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right parietal 2 (4 Ss, 4 ICs)gil/ic11

michael/ic9

yijun/ic5 zeynep/ic4

medial parietal 4 (4 Ss, 4 ICs)

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Fixate Effector Cue Delay Period Direction cue Delay Period Go Cue Saccade or Reach