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Guillaume Flandin

Publications and source records attributed to Guillaume Flandin.

10 recordsLinked to original sources

Bayesian comparison of spatially regularised general linear models.

In previous work (Penny et al., [2005]: Neuroimage 24:350-362) we have developed a spatially regularised General Linear Model for the analysis of functional magnetic resonance imaging data that allows for the characterisation of regionally specific effects using Posterior Probability Maps (PPMs). In this paper we show how it also provides an approximation to the model evidence. This is important as it is the basis of Bayesian model comparison and provides a unified framework for Bayesian Analysis of Variance, Cluster of Interest analyses and the principled selection of signal and noise models. We also provide extensions that implement spatial and anatomical regularisation of noise process parameters.

Artifacts↗

Bayesian fMRI data analysis with sparse spatial basis function priors.

In previous work we have described a spatially regularised General Linear Model (GLM) for the analysis of brain functional Magnetic Resonance Imaging (fMRI) data where Posterior Probability Maps (PPMs) are used to characterise regionally specific effects. The spatial regularisation is defined over regression coefficients via a Laplacian kernel matrix and embodies prior knowledge that evoked responses are spatially contiguous and locally homogeneous. In this paper we propose to finesse this Bayesian framework by specifying spatial priors using Sparse Spatial Basis Functions (SSBFs). These are defined via a hierarchical probabilistic model which, when inverted, automatically selects an appropriate subset of basis functions. The method includes non-linear wavelet shrinkage as a special case. As compared to Laplacian spatial priors, SSBFs allow for spatial variations in signal smoothness, are more computationally efficient and are robust to heteroscedastic noise. Results are shown on synthetic data and on data from an event-related fMRI experiment.

Algorithms↗

Dopamine-dependent prediction errors underpin reward-seeking behaviour in humans.

Theories of instrumental learning are centred on understanding how success and failure are used to improve future decisions. These theories highlight a central role for reward prediction errors in updating the values associated with available actions. In animals, substantial evidence indicates that the neurotransmitter dopamine might have a key function in this type of learning, through its ability to modulate cortico-striatal synaptic efficacy. However, no direct evidence links dopamine, striatal activity and behavioural choice in humans. Here we show that, during instrumental learning, the magnitude of reward prediction error expressed in the striatum is modulated by the administration of drugs enhancing (3,4-dihydroxy-L-phenylalanine; L-DOPA) or reducing (haloperidol) dopaminergic function. Accordingly, subjects treated with L-DOPA have a greater propensity to choose the most rewarding action relative to subjects treated with haloperidol. Furthermore, incorporating the magnitude of the prediction errors into a standard action-value learning algorithm accurately reproduced subjects' behavioural choices under the different drug conditions. We conclude that dopamine-dependent modulation of striatal activity can account for how the human brain uses reward prediction errors to improve future decisions.

Adult↗

Dealing with the shortcomings of spatial normalization: multi-subject parcellation of fMRI datasets.

The analysis of functional magnetic resonance imaging (fMRI) data recorded on several subjects resorts to the so-called spatial normalization in a common reference space. This normalization is usually carried out on a voxel-by-voxel basis, assuming that after coregistration of the functional images with an anatomical template image in the Talairach reference system, a correct voxel-based inference can be carried out across subjects. Shortcomings of such approaches are often dealt with by spatially smoothing the data to increase the overlap between subject-specific activated regions. This procedure, however, cannot adapt to each anatomo-functional subject configuration. We introduce a novel technique for intra-subject parcellation based on spectral clustering that delineates homogeneous and connected regions. We also propose a hierarchical method to derive group parcels that are spatially coherent across subjects and functionally homogeneous. We show that we can obtain groups (or cliques) of parcels that well summarize inter-subject activations. We also show that the spatial relaxation embedded in our procedure improves the sensitivity of random-effect analysis.

Algorithms↗

Identification of degenerate neuronal systems based on intersubject variability.

Group studies implicitly assume that all subjects activate one common system to sustain a particular cognitive task. Intersubject variability is generally treated as well-behaved and uninteresting noise. However, intersubject variability might result from subjects engaging different degenerate neuronal systems that are each sufficient for task performance. This would produce a multimodal distribution of intersubject variability. We have explored this idea with the help of Gaussian Mixture Modeling and Bayesian model comparison procedures. We illustrate our approach using a crossmodal priming paradigm, in which subjects perform a semantic decision on environmental sounds or their spoken names that were preceded by a semantically congruent or incongruent picture or written name. All subjects consistently activated the superior temporal gyri bilaterally, the left fusiform gyrus and the inferior frontal sulcus. Comparing a One and Two Gaussian Mixture Model of the unexplained residuals provided very strong evidence for two groups with distinct activation patterns: 6 subjects exhibited additional activations in the superior temporal sulci bilaterally, the right superior frontal and central sulcus. 11 subjects showed increased activation in the striate and the right inferior parietal cortex. These results suggest that semantic decisions on auditory-visual compound stimuli might be accomplished by two overlapping degenerate neuronal systems.

Acoustic Stimulation↗

Retinotopic organization of visual mental images as revealed by functional magnetic resonance imaging.

In this study, we used event-related functional magnetic resonance imaging to investigate whether visual mental images retinotopically activate early visual cortex. Six participants were instructed to visualize or view horizontally or vertically oriented flashing bow-tie shaped stimuli. When compared to baseline, imagery globally activated Area V1. When the activation evoked by the stimuli at the different orientations was directly compared, distinct spatial activation patterns were obtained for each orientation in most participants. Not only was the topography of the activation patterns from imagery similar to the topography obtained with a corresponding visual perception task, but it closely matched the individual cortical representation of either the horizontal or the vertical visual field meridians. These findings strongly support that visual imagery and perception share low-level anatomical substrate and functional processes. Binding of spatial features is suggested as one possible mechanism.

Acoustic Stimulation↗

Automatized clustering and functional geometry of human parietofrontal networks for language, space, and number.

Human functional MRI studies frequently reveal the joint activation of parietal and of lateral and mesial frontal areas during various cognitive tasks. To analyze the geometrical organization of those networks, we used an automatized clustering algorithm that parcels out sets of areas based on their similar profile of task-related activations or deactivations. This algorithm allowed us to reanalyze published fMRI data (Simon, O., Mangin, J.F., Cohen, L., Le Bihan, D., Dehaene, S., 2002. Topographical layout of hand, eye, calculation, and language-related areas in the human parietal lobe. Neuron 33, 475-487) and to reproduce the previously observed geometrical organization of activations for saccades, attention, grasping, pointing, calculation, and language processing in the parietal lobe. Further, we show that this organization extends to lateral and mesial prefrontal regions. Relative to the parietal lobe, the prefrontal functional geometry is characterized by a partially symmetrical anteroposterior ordering of activations, a decreased representation of effector-specific tasks, and a greater emphasis on higher cognitive functions of attention, higher-order spatial representation, calculation, and language. Anatomically, our results in humans are closely homologous to the known connectivity of parietal and frontal regions in the macaque monkey.

Animals↗

Group analysis in functional neuroimaging: selecting subjects using similarity measures.

Standard group analyses of fMRI data rely on spatial and temporal averaging of individuals. This averaging operation is only sensible when the mean is a good representation of the group. This is not the case if subjects are not homogeneous, and it is therefore a major concern in fMRI studies to assess this group homogeneity. We present a method that provides relevant distances or similarity measures between temporal series of brain functional images belonging to different subjects. The method allows a multivariate comparison between data sets of several subjects in the time or in the space domain. These analyses assess the global intersubject variability before averaging subjects and drawing conclusions across subjects, at the population level. We adapt the RV coefficient to measure meaningful spatial or temporal similarities and use multidimensional scaling to give a visual representation of each subject's position with respect to other subjects in the group. We also provide a measure for detecting subjects that may be outliers. Results show that the method is a powerful tool to detect subjects with specific temporal or spatial patterns, and that, despite the apparent loss of information, restricting the analysis to a homogeneous subgroup of subjects does not reduce the statistical sensitivity of standard group fMRI analyses.

Algorithms↗

Functional connectivity: studying nonlinear, delayed interactions between BOLD signals.

Correlation analysis has been widely used in the study of functional connectivity based on fMRI data. It assumes that the relevant information about the interactions of brain regions is reflected by a linear relationship between the values of two signals at the same time. However, this hypothesis has not been thoroughly investigated yet. In this work, we study in depth the information shared by BOLD signals of pairs of brain regions. In particular, we assess the amount of nonlinear and/or nonsynchronous interactions present in data. This is achieved by testing models reflecting linear, synchronous interactions against more general models, encompassing nonlinear, nonsynchronous interactions. Many factors influencing measured BOLD signals are critical for the study of connectivity, such as paradigm-induced BOLD responses, preprocessing, motion artifacts, and geometrical distortions. Interactions are also influenced by the proximity of brain regions. The influence of all these factors is taken into account and the nature of the interactions is studied using various experimental conditions such that the conclusions reached are robust with respect to variation of these factors. After defining nonlinear and/or nonsynchronous interaction models in the framework of general linear models, statistical tests are performed on different fMRI data sets to infer the nature of the interactions. Finally, a new connectivity metric is proposed which takes these inferences into account. We find that BOLD signal interactions are statistically more significant when taking into account the history of the distant signal, i.e., the signal from the interacting region, than when using a model of linear instantaneous interaction. Moreover, about 75% of the interactions are symmetric, as assessed with the proposed connectivity metric. The history-dependent part of the coupling between brain regions can explain a high percentage of the variance in the data sets studied. As these results are robust with respect to various confounding factors, this work suggests that models used to study the functional connectivity between brain areas should in general take the BOLD signal history into account.

Algorithms↗

Multivariate model specification for fMRI data.

We present a general method-denoted MoDef-to help specify (or define) the model used to analyze brain imaging data. This method is based on the use of the multivariate linear model on a training data set. We show that when the a priori knowledge about the expected brain response is not too precise, the method allows for the specification of a model that yields a better sensitivity in the statistical results. This obviously relies on the validity of the a priori information, in our case the representativity of the training set, an issue addressed using a cross-validation technique. We propose a fast implementation that allows the use of the method on large data sets as found with functional Magnetic Resonance Images. An example of application is given on an experimental fMRI data set that includes nine subjects who performed a mental computation task. Results show that the method increases the statistical sensitivity of fMRI analyses.

Brain↗