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Barillot, C.

Publications and source records attributed to Barillot, C..

8 recordsLinked to original sources

Building memories on prior knowledge: behavioral and fMRI evidence of impairment in early Alzheimer's Disease

Impaired memory is a hallmark of prodromal Alzheimers Disease (AD). Prior knowledge associated with the memoranda has proved to have a powerful effect on memory in healthy subjects. Yet, barely nothing is known about its effect in early AD. We used functional MRI to ask whether prior knowledge enhanced memory encoding in early AD and whether the nature of prior knowledge mattered. Early AD patients and healthy controls underwent a task-based fMRI experiment, being scanned while learning face-scene associations. Famous faces carried Pre-Experimental Knowledge (PEK) while unknown faces repeatedly familiarized prior to learning carried Experimental Knowledge (EK). As expected, PEK increased subsequent memory in healthy elderly. However, patients did not benefit from PEK. Partly non-overlapping brain networks supported PEK vs. EK encoding in healthy controls. Patients displayed impaired activation in a right subhippocampal region where activity predicted successful associative memory formation of PEK stimuli. These findings call for a thorough consideration of how prior knowledge impacts learning and suggest a possible underestimation of the extent of associative memory impairment in early AD. HighlightsO_LILearning is impaired in prodromal AD, but we currently ignore whether prior knowledge available at encoding promotes learning in AD as it does in healthy controls. C_LIO_LIPatients with AD failed to benefit from pre-experimental prior knowledge (famous faces) by comparison with experimental knowledge (unknown but familiarized faces). C_LIO_LIfMRI responses at study revealed distinct networks underlying associative encoding for both pre-experimental and experimental knowledge. C_LIO_LIA subsequent memory effect found in control subjects for associations carrying pre-experimental knowledge in the right subhippocampal structures, including the perirhinal cortex, was absent in patients. C_LIO_LIPre-experimental knowledge-based associative encoding relies on brain regions specifically targeted by early tau pathology. C_LIO_LIUsing unfamiliar materials to probe memory in early AD might underestimate learning impairment. C_LI

neuroscience↗

Simultaneous MRI-EEG during a motor imagery neurofeedback task: an open access brain imaging dataset for multi-modal data integration.

Combining EEG and fMRI allows for integration of fine spatial and accurate temporal resolution yet presents numerous challenges, noticeably if performed in real-time to implement a Neurofeedback (NF) loop. Here we describe a multimodal dataset of EEG and fMRI acquired simultaneously during a motor imagery NF task, supplemented with MRI structural data. The study involved 30 healthy volunteers undergoing five training sessions. We showed the potential and merit of simultaneous EEG-fMRI NF in previous work. Here we illustrate the type of information that can be extracted from this dataset and show its potential use. Our group is the second in the world to have integrated EEG and fMRI for NF, therefore this dataset is unique of its kind. We believe that it will be a valuable tool to O_LIAdvance and test methodologies to integrate complementary neuroimaging techniques (design and validation of methods of multi-modal data integration at various scales) C_LIO_LIImprove the quality of Neurofeedback provided C_LIO_LIImprove methodologies for de-noising EEG acquired under MRI C_LIO_LIInvestigate the neuromarkers of motor-imagery using multi-modal information C_LI

neuroscience↗

A sparse EEG-informed fMRI model for hybrid EEG-fMRI neurofeedback prediction

Measures of brain activity through functional magnetic resonance imaging (fMRI) or Electroencephalography (EEG), two complementary modalities, are ground solutions in the context of neuro-feedback (NF) mechanisms for brain rehabilitation protocols. While NF-EEG (real-time neurofeedback scores computed from EEG signals) have been explored for a very long time, NF-fMRI (real-time neurofeedback scores computed from fMRI signals) appeared more recently and provides more robust results and more specific brain training. Using simultaneously fMRI and EEG for bi-modal neurofeedback sessions (NF-EEG-fMRI, real-time neurofeedback scores computed from fMRI and EEG) is very promising to devise brain rehabilitation protocols. However, fMRI is cumbersome and more exhausting for patients. The original contribution of this paper concerns the prediction of bi-modal NF scores from EEG recordings only, using a training phase where EEG signals as well as the NF-EEG and NF-fMRI scores are available. We propose a sparse regression model able to exploit EEG only to predict NF-fMRI or NF-EEG-fMRI in motor imagery tasks. We compared different NF-predictors steaming from the proposed model. We showed that predicting NF-fMRI scores from EEG signals adds information to NF-EEG scores and significantly improve the correlation with bi-modal NF sessions, compared to classical NF-EEG scores.

neuroscience↗

Regional brain development analysis through registration using anisotropic similarity, a constrained affine transformation

We propose a novel method to quantify brain growth in 3 arbitrary orthogonal directions of the brain or its sub-regions through linear registration. This is achieved by introducing a 9 degrees of freedom (dof) transformation called anisotropic similarity which is an affine transformation with constrained scaling directions along arbitrarily chosen orthogonal vectors. This gives the opportunity to extract scaling factors describing brain growth along those directions by registering a database of subjects onto a common reference. This information about directional growth brings insights that are not usually available in longitudinal volumetry analysis. The interest of this method is illustrated by studying the anisotropic regional and global brain development of 308 healthy subjects betwen 0 and 19 years old. A gender comparison of those scaling factors is also performed for 4 classes of age. We demonstrate through these applications the stability of the method to the chosen reference and its ability to highlight growth differences accros regions and gender.

neuroscience↗

Learning 2-in-1: towards integrated EEG-fMRI-neurofeedback

Neurofeedback (NF) allows to exert self-regulation over specific aspects of ones own brain activity by returning information extracted in real-time from brain activity measures. These measures are usually acquired from a single modality, most commonly electroencephalography (EEG) or functional magnetic resonance imaging (fMRI). EEG-fMRI-neurofeedback (EEG-fMRI-NF) is a new approach that consists in providing a NF based simultaneously on EEG and fMRI signals. By exploiting the complementarity of these two modalities, EEG-fMRI-NF opens a new spectrum of possibilities for defining bimodal NF targets that could be more robust, flexible and effective than unimodal ones. Since EEG-fMRI-NF allows for a richer amount of information to be fed back, the question arises of how to represent the EEG and fMRI features simultaneously in order to allow the subject to achieve better self-regulation. In this work, we propose to represent EEG and fMRI features in a single bimodal feedback (integrated feedback). We introduce two integrated feedback strategies for EEG-fMRI-NF and compare their early effects on a motor imagery task with a between-group design. The BiDim group (n=10) was shown a two-dimensional (2D) feedback in which each dimension depicted the information from one modality. The UniDim group (n=10) was shown a one-dimensional (1D) feedback that integrated both types of information even further by merging them into one. Online fMRI activations were significantly higher in the UniDim group than in the BiDim group, which suggests that the 1D feedback is easier to control than the 2D feedback. However subjects from the BiDim group produced more specific BOLD activations with a notably stronger activation in the right superior parietal lobe (BiDim > UniDim, p < 0.001, uncorrected). These results suggest that the 2D feedback encourages subjects to explore their strategies to recruit more specific brain patterns. To summarize, our study shows that 1D and 2D integrated feedbacks are effective but also appear to be complementary and could therefore be used in a bimodal NF training program. Altogether, our study paves the way to novel integrated feedback strategies for the development of flexible and effective bimodal NF paradigms that fully exploits bimodal information and are adapted to clinical applications.

bioengineering↗

Automated Electrodes Detection during simultaneous EEG/fMRI

1The coupling of Electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) enables the measure of brain activity at high spatial and temporal resolution. The localisation of EEG sources depends on several parameters including the knowledge of the position of the electrodes on the scalp. An accurate knowledge about this information is important for source reconstruction. Currently, when acquiring EEG and fMRI together, the position of the electrodes is generally estimated according to fiducial points by using a template. In the context of simultaneous EEG/fMRI acquisition, a natural idea is to use magnetic resonance (MR) images to localise EEG electrodes. However, most MR compatible electrodes are built to be almost invisible on MR Images. Taking advantage of a recently proposed Ultra short Echo Time (UTE) sequence, we introduce a fully automatic method to detect and label those electrodes in MR images. Our method was tested on 8 subjects wearing a 64-channel EEG cap. This automated method showed an average detection accuracy of 94% and the average position error was 3.1 mm. These results suggest that the proposed method has potential for determining the position of the electrodes during simultaneous EEG/fMRI acquisition with a very light cost procedure.

neuroscience↗

Objective Evaluation of Multiple Sclerosis Lesion Segmentation using a Data Management and Processing Infrastructure

We present a study of multiple sclerosis segmentation algorithms conducted at the international MICCAI 2016 challenge. This challenge was operated using a new open-science computing infrastructure. This allowed for the automatic and independent evaluation of a large range of algorithms in a fair and completely automatic manner. This computing infrastructure was used to evaluate thirteen methods of MS lesions segmentation, exploring a broad range of state-of-the-art algorithms, against a high-quality database of 53 MS cases coming from four centers following a common definition of the acquisition protocol. Each case was annotated manually by an unprecedented number of seven different experts. Results of the challenge highlighted that automatic algorithms, including the recent machine learning methods (random forests, deep learning, ...), are still trailing human expertise on both detection and delineation criteria. In addition, we demonstrate that computing a statistically robust consensus of the algorithms performs closer to human expertise on one score (segmentation) although still trailing on detection scores.

neuroscience↗

A three year follow-up study of gadolinium enhanced and non-enhanced regions in multiple sclerosis lesions using a multi-compartment T2 relaxometry model

Demyelination, axonal damage and inflammation are critical indicators of the onset and progress of neurodegenerative diseases such as multiple sclerosis (MS) in patients. Due to physical limitations of imaging such as acquisition time and imaging resolution, a voxel in a MR image is heterogeneous in terms of tissue microstructure such as myelin, axons, intra and extra cellular fluids and free water. We present a multi-compartment tissue model which estimates the water fraction (WF) of tissues with short, medium and high T2 relaxation times in a T2 relaxometry MRI voxel. The proposed method is validated on test-retest data of healthy controls. This model was then used to study longitudinal trends of the tissue microstructures for two sub-regions of the lesions: gadolinium enhanced (E+) and non-enhanced (L-) regions of MS lesions in 10 MS patients over a period of three years. The water fraction values in E+ and L- regions were found to be significantly different (p < 0.05) over the period of first three months. The results of this study also showed that the estimates of the proposed T2 relaxometry model on brain tissue microstructures have potential to distinguish between regions undergoing active blood brain barrier breakdown from the other regions of the lesion.

neuroscience↗