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1.
Encephale ; 45(3): 245-255, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30885442

ABSTRACT

The clinical efficacy of neurofeedback is still a matter of debate. This paper analyzes the factors that should be taken into account in a transdisciplinary approach to evaluate the use of EEG NFB as a therapeutic tool in psychiatry. Neurofeedback is a neurocognitive therapy based on human-computer interaction that enables subjects to train voluntarily and modify functional biomarkers that are related to a defined mental disorder. We investigate three kinds of factors related to this definition of neurofeedback. We focus this article on EEG NFB. The first part of the paper investigates neurophysiological factors underlying the brain mechanisms driving NFB training and learning to modify a functional biomarker voluntarily. Two kinds of neuroplasticity involved in neurofeedback are analyzed: Hebbian neuroplasticity, i.e. long-term modification of neural membrane excitability and/or synaptic potentiation, and homeostatic neuroplasticity, i.e. homeostasis attempts to stabilize network activity. The second part investigates psychophysiological factors related to the targeted biomarker. It is demonstrated that neurofeedback involves clearly defining which kind of relationship between EEG biomarkers and clinical dimensions (symptoms or cognitive processes) is to be targeted. A nomenclature of accurate EEG biomarkers is proposed in the form of a short EEG encyclopedia (EEGcopia). The third part investigates human-computer interaction factors for optimizing NFB training and learning during the closed loop interaction. A model is proposed to summarize the different features that should be controlled to optimize learning. The need for accurate and reliable metrics of training and learning in line with human-computer interaction is also emphasized, including targeted biomarkers and neuroplasticity. All these factors related to neurofeedback show that it can be considered as a fertile ground for innovative research in psychiatry.


Subject(s)
Electroencephalography , Neurofeedback/methods , Psychiatry/methods , Cognitive Behavioral Therapy/methods , Humans , Mental Disorders/therapy
2.
J Autism Dev Disord ; 45(6): 1603-13, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25433404

ABSTRACT

To learn to deal with the unexpected is essential to adaptation to a social, therefore often unpredictable environment. Fourteen adults with autism spectrum disorders (ASD) and 15 controls underwent a decision-making task aimed at investigating the influence of either a social or a non-social environment, and its interaction with either a stable (with constant probabilities) or an unstable (with changing probabilities) context on their performance. Participants with ASD presented with difficulties in accessing underlying statistical rules in an unstable context, a deficit especially enhanced in the social environment. These results point out that the difficulties people with ASD encounter in their social life might be caused by impaired social cues processing and by the unpredictability associated with the social world.


Subject(s)
Autism Spectrum Disorder/psychology , Decision Making , Adult , Case-Control Studies , Cues , Female , Humans , Male , Social Behavior , Uncertainty , Young Adult
3.
Brain Topogr ; 25(1): 55-63, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21744296

ABSTRACT

A challenge in designing a Brain-Computer Interface (BCI) is the choice of the channels, e.g. the most relevant sensors. Although a setup with many sensors can be more efficient for the detection of Event-Related Potential (ERP) like the P300, it is relevant to consider only a low number of sensors for a commercial or clinical BCI application. Indeed, a reduced number of sensors can naturally increase the user comfort by reducing the time required for the installation of the EEG (electroencephalogram) cap and can decrease the price of the device. In this study, the influence of spatial filtering during the process of sensor selection is addressed. Two of them maximize the Signal to Signal-plus-Noise Ratio (SSNR) for the different sensor subsets while the third one maximizes the differences between the averaged P300 waveform and the non P300 waveform. We show that the locations of the most relevant sensors subsets for the detection of the P300 are highly dependent on the use of spatial filtering. Applied on data from 20 healthy subjects, this study proves that subsets obtained where sensors are suppressed in relation to their individual SSNR are less efficient than when sensors are suppressed in relation to their contribution once the different selected sensors are combined for enhancing the signal. In other words, it highlights the difference between estimating the P300 projection on the scalp and evaluating the more efficient sensor subsets for a P300-BCI. Finally, this study explores the issue of channel commonality across subjects. The results support the conclusion that spatial filters during the sensor selection procedure allow selecting better sensors for a visual P300 Brain-Computer Interface.


Subject(s)
Brain Mapping , Brain/physiology , Event-Related Potentials, P300/physiology , Signal Detection, Psychological , User-Computer Interface , Adult , Brain Waves/physiology , Electroencephalography , Female , Humans , Male , Photic Stimulation/methods , Signal Processing, Computer-Assisted , Young Adult
4.
J Neural Eng ; 8(1): 016001, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21245524

ABSTRACT

A brain-computer interface (BCI) is a specific type of human-computer interface that enables direct communication between human and computer through decoding of brain activity. As such, event-related potentials like the P300 can be obtained with an oddball paradigm whose targets are selected by the user. This paper deals with methods to reduce the needed set of EEG sensors in the P300 speller application. A reduced number of sensors yields more comfort for the user, decreases installation time duration, may substantially reduce the financial cost of the BCI setup and may reduce the power consumption for wireless EEG caps. Our new approach to select relevant sensors is based on backward elimination using a cost function based on the signal to signal-plus-noise ratio, after some spatial filtering. We show that this cost function selects sensors' subsets that provide a better accuracy in the speller recognition rate during the test sessions than selected subsets based on classification accuracy. We validate our selection strategy on data from 20 healthy subjects.


Subject(s)
Brain Mapping/instrumentation , Brain Mapping/methods , Electroencephalography/instrumentation , Electroencephalography/methods , Event-Related Potentials, P300/physiology , User-Computer Interface , Adult , Brain , Female , Humans , Male , Young Adult
5.
Neuroimage ; 46(1): 168-76, 2009 May 15.
Article in English | MEDLINE | ID: mdl-19457358

ABSTRACT

We investigated four key aspects of forward models for distributed solutions to the MEG inverse problem: 1) the nature of the cortical mesh constraining sources (derived from an individual's MRI, or inverse-normalised from a template mesh); 2) the use of single-sphere, overlapping spheres, or Boundary Element Model (BEM) head-models; 3) the density of the cortical mesh (3000 vs. 7000 vertices); and 4) whether source orientations were constrained to be normal to that mesh. These were compared within the context of two types of spatial prior on the sources: a single prior corresponding to a standard L2-minimum-norm (MNM) inversion, or multiple sparse priors (MSP). The resulting generative models were compared using a free-energy approximation to the Bayesian model-evidence after fitting multiple epochs of responses to faces or scrambled faces. Statistical tests of the free-energy, across nine participants, showed clear superiority of MSP over MNM models; with the former reconstructing deeper sources. Furthermore, there was 1) no evidence that an individually-defined cortical mesh was superior to an inverse-normalised canonical mesh, but 2) clear evidence that a BEM was superior to spherical head-models, provided individually-defined inner skull and scalp meshes were used. Finally, for MSP models, there was evidence that the combination of 3) higher density cortical meshes and 4) dipoles constrained to be normal to the mesh was superior to lower-density or freely-oriented sources (in contrast to the MNM models, in which free-orientation was optimal). These results have practical implications for MEG source reconstruction, particularly in the context of group studies.


Subject(s)
Brain/physiology , Magnetoencephalography , Models, Neurological , Signal Processing, Computer-Assisted , Bayes Theorem , Humans , Magnetoencephalography/instrumentation , Magnetoencephalography/methods
6.
Neuroimage ; 38(3): 422-38, 2007 Nov 15.
Article in English | MEDLINE | ID: mdl-17888687

ABSTRACT

We address some key issues entailed by population inference about responses evoked in distributed brain systems using magnetoencephalography (MEG). In particular, we look at model selection issues at the within-subject level and feature selection issues at the between-subject level, using responses evoked by intact and scrambled faces around 170 ms (M170). We compared the face validity of subject-specific forward models and their summary statistics in terms of how estimated responses reproduced over subjects. At the within-subject level, we focused on the use of multiple constraints, or priors, for inverting distributed source models. We used restricted maximum likelihood (ReML) estimates of prior covariance components (in both sensor and source space) and show that their relative importance is conserved over subjects. At the between-subject level, we used standard anatomical normalization methods to create posterior probability maps that furnish inference about regionally specific population responses. We used these to compare different summary statistics, namely; (i) whether to test for differences between condition-specific source estimates, or whether to test the source estimate of differences between conditions, and (ii) whether to accommodate differences in source orientation by using signed or unsigned (absolute) estimates of source activity.


Subject(s)
Brain/physiology , Evoked Potentials/physiology , Face , Magnetoencephalography/methods , Analysis of Variance , Electroencephalography , Humans , Magnetic Resonance Imaging , Models, Neurological , Reference Values , Reproducibility of Results , Visual Perception
7.
Neuroimage ; 28(1): 280-6, 2005 Oct 15.
Article in English | MEDLINE | ID: mdl-16023377

ABSTRACT

In this note we describe a heuristic, starting with a dimensional analysis, which relates hemodynamic changes to the spectral profile of ongoing EEG activity. In brief, this analysis suggests that 'activation', as indexed by increases in hemodynamic signals, should be associated with a loss of power in lower EEG frequencies, relative to higher frequencies. The fact that activation is expressed in terms of frequency (i.e., per second) is consistent with a dimensional analysis in the sense that activations reflect the rate of energy dissipation (per second). In this heuristic, activation causes an acceleration of temporal dynamics leading to (i) increased energy dissipation; (ii) decreased effective membrane time constants; (iii) increased effective coupling among neuronal ensembles; and (iv) a shift in the EEG spectral profile to higher frequencies. These predictions are consistent with empirical observations of how changes in the EEG spectrum are expressed hemodynamically. Furthermore, the heuristic provides a simple measure of neuronal activation based on spectral analyses of EEG.


Subject(s)
Cerebrovascular Circulation/physiology , Electroencephalography , Hemodynamics/physiology , Algorithms , Energy Metabolism , Humans , Magnetic Resonance Imaging , Models, Neurological , Oxygen/blood
8.
Neuroimage ; 26(2): 356-73, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15907296

ABSTRACT

Spatially characterizing and quantifying the brain electromagnetic response using MEG/EEG data still remains a critical issue since it requires solving an ill-posed inverse problem that does not admit a unique solution. To overcome this lack of uniqueness, inverse methods have to introduce prior information about the solution. Most existing approaches are directly based upon extrinsic anatomical and functional priors and usually attempt at simultaneously localizing and quantifying brain activity. By contrast, this paper deals with a preprocessing tool which aims at better conditioning the source reconstruction process, by relying only upon intrinsic knowledge (a forward model and the MEG/EEG data itself) and focusing on the key issue of localization. Based on a discrete and realistic anatomical description of the cortex, we first define functionally Informed Basis Functions (fIBF) that are subject specific. We then propose a multivariate method which exploits these fIBF to calculate a probability-like coefficient of activation associated with each dipolar source of the model. This estimated distribution of activation coefficients may then be used as an intrinsic functional prior, either by taking these quantities into account in a subsequent inverse method, or by thresholding the set of probabilities in order to reduce the dimension of the solution space. These two ways of constraining the source reconstruction process may naturally be coupled. We successively describe the proposed Multivariate Source Prelocalization (MSP) approach and illustrate its performance on both simulated and real MEG data. Finally, the better conditioning induced by the MSP process in a classical regularization scheme is extensively and quantitatively evaluated.


Subject(s)
Magnetoencephalography/statistics & numerical data , Algorithms , Computer Simulation , Data Interpretation, Statistical , Evoked Potentials, Somatosensory/physiology , Functional Laterality , Humans , Models, Neurological , Models, Statistical , Multivariate Analysis , Neural Pathways/physiology , Neurons/physiology , Principal Component Analysis , Pyramidal Cells/physiology
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