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Mullier, E.

Publications and source records attributed to Mullier, E..

4 recordsLinked to original sources

Non-invasive prediction of conduction velocities in the human brain from MRI-derived microstructure features at 7 Tesla

The conduction velocity of neuronal signals along axons is a key neurophysiological property that can be altered in various disease processes. While cortico-cortical evoked potentials (CCEPs) can be measured in presurgical assessment to provide information about conduction delay between a subset of brain regions, it is currently not possible to efficiently and systematically estimate conduction velocity in vivo across the whole brain. Given the established link between conduction velocity and axon morphology (most notably axon diameter but also myelination), mapping a reliable and quantitative metric linked to axon properties could fill the gap of inferring conduction velocity across the entire human brain. By integrating multiple MRI-derived microstructural measures - including axon radius, axonal water fraction, extra-axonal perpendicular diffusivity, and longitudinal relaxation time - and conduction velocity estimates obtained from a large database of CCEPs, we developed a whole-brain prediction model of conduction velocity. Our multivariate MRI-based model explained 29% of variance in neurophysiological conduction velocity, making it possible to partially predict whole-brain conduction velocity and delay matrices along connections for which no direct measurement is commonly available from epilepsy surgery investigations. This integrative MRI-based approach could provide a non-invasive framework for comprehensively characterising conduction delays in vivo across the human brain white matter.

neuroscience↗

Defacing biases visual quality assessments of structural MRI

A critical step before data-sharing of human neuroimaging is removing facial features to protect individuals privacy. However, not only does this process redact identifiable information about individuals, but it also removes non-identifiable information. This introduces undesired variability into downstream analysis and interpretation. This registered report investigated the degree to which the so-called defacing altered the quality assessment of T1-weighted images of the human brain from the openly available "IXI dataset". The effect of defacing on manual quality assessment was investigated on a single-site subset of the dataset (N=185). By comparing two linear mixed-effects models, we determined that four trained human raters perception of quality was significantly influenced by defacing by modeling their ratings on the same set of images in two conditions: "nondefaced" (i.e., preserving facial features) and "defaced". In addition, we investigated these biases on automated quality assessments by applying repeated-measures, multivariate ANOVA (rm-MANOVA) on the image quality metrics extracted with MRIQC on the full IXI dataset (N=581; three acquisition sites). This study found that defacing altered the quality assessments by humans and showed that MRIQCs quality metrics were mostly insensitive to defacing.

bioinformatics↗

Distinct profiles of spatio-temporal brain dynamics along symptoms dimensions in autism

Autism Spectrum Disorders are accompanied by atypical brain activity and impairments in brain connectivity. In particular, dynamic functional connectivity approaches highlighted aberrant brain fluctuations at rest in individuals with autism compared to a group composed of typically developed individuals, matched in age and gender. However, the characterization of these variations remains unclear. Here, we quantified the spatio-temporal network dynamics using two novel dynamic group-based measures, namely system diversity and spatio-temporal diversity. Using the public database ABIDE 1, we explored the differences between individuals with autism and typically developed individuals. Our results show evidence that individuals with autism have atypical connectivity patterns over time characterized by a lower integration of heterogeneous cognitive processes and unstable functional activity, except for the default mode network presenting its own specific dynamic pattern. Within the autism group, we find this pattern of results to be stronger in more severely affected patients with a predominance of symptoms in the social affect domain. However, patients with prominently restricted and repetitive behaviours demonstrate a more conservative profile of brain dynamics characterized by a lower spatio-temporal diversity of the default mode network.

neuroscience↗

Using structural connectivity to augment community structure in EEG functional connectivity

Recently, EEG recording techniques and source analysis have improved, making it feasible to tap into fast network dynamics. Yet, analyzing whole-cortex EEG signals in source space is not standard, partly because EEG suffers from volume conduction: Functional connectivity (FC) reflecting genuine functional relationships is impossible to disentangle from spurious FC introduced by volume conduction. Here, we investigate the relationship between white matter structural connectivity (SC) and large scale network structure encoded in EEG-FC. We start by confirming that FC (power envelope correlations) is predicted by SC beyond the impact of Euclidean distance, in line with the assumption that SC mediates genuine FC. We then use information from white matter structural connectivity (SC) in order to smooth the EEG signal in the space spanned by graphs derived from SC. Thereby, FC between nearby, structurally connected brain regions increases while FC between non-connected regions remains unchanged, resulting in an increase in genuine, SC-mediated FC. We analyze the induced changes in FC, assessing the resemblance between EEG- and volume-conduction-free fMRI-FC, and find that smoothing increases resemblance in terms of overall correlation and community structure. This result suggests that our method boosts genuine FC, an outcome that is of interest for many EEG network neuroscience questions. Author summaryIn this study, we combine high-density EEG recorded during resting state with white matter connectivity obtained from diffusion MRI and fiber tracking. We leverage the additional information contained in the structural connectome towards augmenting the source level EEG functional connectivity. In particular, it is known - and confirmed in this study - that the activity of brain regions that possess a direct anatomical connection is, on average, more strongly correlated than that of regions that have no such direct link. We use the structural connectome to define a graph and smooth the source reconstructed EEG signal in the space spanned by this graph. We compare the resulting "filtered" signal correlation matrices to those obtained from fMRI and find that such "graph filtering" improves the agreement between EEG and fMRI functional connectivity structure. This suggests that structural connectivity can be used to attenuate some of the limitations imposed by volume conduction.

neuroscience↗