Brain topography
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Accumulating evidence suggests the existence of a shared neural substrate between imagined and executed movements. However, a better understanding of the mechanisms involved in the motor execution and motor imagery requires knowledge of the way the co-activated brain regions interact to each other during the particular (real or imagined) motor task. Within this general framework, the aim of the present study is to investigate the cortical activation and connectivity sub-serving real and imaginary rhythmic finger tapping, from the analysis of multi-channel electroencephalogram (EEG) scalp recordings. ⋯ Our results show a fronto-parietal co-activation during both real and imagined movements and similar connectivity patterns among contralateral brain areas. The results support the hypothesis that functional connectivity over the contralateral hemisphere during finger tapping is preserved in imagery. The approach and results can be regarded as indicative evidences of a new strategy for recognizing imagined movements in EEG-based brain computer interface research.
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Over the last 20 years, a body of techniques known as high resolution EEG has allowed precise estimation of cortical activity from non-invasive EEG measurements. The availability of cortical waveforms from non-invasive EEG recordings allows to have not only the level of activation within a single region of interest (ROI) during a particular task, but also to estimate the causal relationships among activities of several cortical regions. However, interpreting resulting connectivity patterns is still an open issue, due to the difficulty to provide an objective measure of their properties across different subjects or groups. ⋯ For both the experiments, the main question is whether the "architecture" of the functional connectivity networks obtained could show properties that are different in the two groups or in the two tasks. All the functional connectivity networks gathered in the two experiments showed ordered properties and significant differences from "random" networks having the same characteristic sizes. The proposed approach, based on the use of indexes derived from graph theory, can apply to cerebral connectivity patterns estimated not only from the EEG signals but also from different brain imaging methods.
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Static hemodynamic or neuroelectric images of brain regions activated during particular tasks do not convey the information of how these regions communicate to each other. Cortical connectivity estimation aims at describing these interactions as connectivity patterns which hold the direction and strength of the information flow between cortical areas. In this study, we attempted to estimate the causality between distributed cortical systems during a movement volition task in preparation for execution of simple movements by a group of normal healthy subjects and by a group of Spinal Cord Injured (SCI) patients. ⋯ In addition, the right parietal area and the bilateral premotor area 6 were also involved. Again, the patterns remained substantially stable across the different frequency bands analyzed. The target cortical patterns observed in the SCI population had larger extensions when compared to the normal ones, since in most cases they involved the bilateral activation of the primary foot movement areas as well as the SMA, the primary lip areas and the parietal cortical areas.