Wurosenkilde3018

This technical note presents a dynamic causal modelling (DCM) procedure for evaluating different models of neurovascular coupling in the human brain - using combined electromagnetic (M/EEG) and functional magnetic resonance imaging (fMRI) data. This procedure compares the evidence for biologically informed models of neurovascular coupling using Bayesian model comparison. read more First, fMRI data are used to localise regionally specific neuronal responses. The coordinates of these responses are then used as the location priors in a DCM of electrophysiological responses elicited by the same paradigm. The ensuing estimates of model parameters are then used to generate neuronal drive functions, which model pre- or post-synaptic activity for each experimental condition. These functions form the input to a model of neurovascular coupling, whose parameters are estimated from the fMRI data. Crucially, this enables one to evaluate different models of neurovascular coupling, using Bayesian model comparison - asking, for example, whether instantaneous or delayed, pre- or post-synaptic signals mediate haemodynamic responses. We provide an illustrative application of the procedure using a single-subject auditory fMRI and MEG dataset. The code and exemplar data accompanying this technical note are available through the statistical parametric mapping (SPM) software. Global signal (GS) is an ubiquitous construct in resting state functional magnetic resonance imaging (rs-fMRI), associated to nuisance, but containing by definition most of the neuronal signal. Global signal regression (GSR) effectively removes the impact of physiological noise and other artifacts, but at the same time it alters correlational patterns in unpredicted ways. Performing GSR taking into account the underlying physiology (mainly the blood arrival time) has been proven to be beneficial. From these observations we aimed to 1) characterize the effect of GSR on network-level functional connectivity in a large dataset; 2) assess the complementary role of global signal and vessels; and 3) use the framework of partial information decomposition to further look into the joint dynamics of the global signal and vessels, and their respective influence on the dynamics of cortical areas. We observe that GSR affects intrinsic connectivity networks in the connectome in a non-uniform way. Furthermore, by estimating the predictive information of blood flow and the global signal using partial information decomposition, we observe that both signals are present in different amounts across intrinsic connectivity networks. Simulations showed that differences in blood arrival time can largely explain this phenomenon, while using hemodynamic and calcium mouse recordings we were able to confirm the presence of vascular effects, as calcium recordings lack hemodynamic information. With these results we confirm network-specific effects of GSR and the importance of taking blood flow into account for improving de-noising methods. Additionally, and beyond the mere issue of data denoising, we quantify the diverse and complementary effect of global and vessel BOLD signals on the dynamics of cortical areas. The planning and execution of an efficient motor plan is essential to everyday cognitive function, and relies on oscillatory neural responses in both the beta (14-30 ​Hz) and gamma (>30 ​Hz) bands. Such motor control requires not only the integration of salient information from the environment, but also the inhibition of irrelevant or distracting inputs that often manifest as forms of cognitive interference. While the effects of cognitive interference on motor neural dynamics has been an area of increasing interest recently, it remains unclear whether different subtypes of interference differentially impact these dynamics. We address this issue using magnetoencephalography and a novel adaptation of the Multi-Source Interference Task, wherein two common subtypes of cognitive interference are each presented in isolation, as well as simultaneously. We find evidence for the subtype-invariant indexing of cognitive interference across a widely distributed set of motor regions oscillating in the beta range, including the bilateral primary motor and posterior parietal cortices. Further, we find that superadditive effects of cognitive interference subtypes on behavior are paralleled by gamma oscillations in the contralateral premotor cortex, and determine that these gamma oscillations also predict the superadditive effects on behavior. Recent electrophysiological research highlights the significance of global scene properties (GSPs) for scene perception. However, since real-world scenes span a range of low-level stimulus properties and high-level contextual semantics, GSP effects may also reflect additional processing of such non-global factors. We examined this question by asking whether Event-Related Potentials (ERPs) to GSPs will still be observed when specific low- and high-level scene properties are absent from the scene. We presented participants with computer-based artificially-manipulated scenes varying in two GSPs (spatial expanse and naturalness) which minimized other sources of scene information (color and semantic object detail). We found that the peak amplitude of the P2 component was sensitive to the spatial expanse and naturalness of the artificially-generated scenes P2 amplitude was higher to closed than open scenes, and in response to manmade than natural scenes. A control experiment showed that the effect of Naturalness on the P2 is not driven by local texture information, while earlier effects of naturalness, expressed as a modulation of the P1 and N1 amplitudes, are sensitive to texture information. Our results demonstrate that GSPs are processed robustly around 220 ms and that P2 can be used as an index of global scene perception. Face recognition ability is often reported to be a relative strength in Williams syndrome (WS). Yet methodological issues associated with the supporting research, and evidence that atypical face processing mechanisms may drive outcomes 'in the typical range', challenge these simplistic characterisations of this important social ability. Detailed investigations of face processing abilities in WS both at a behavioural and neural level provide critical insights. Here, we behaviourally characterised face recognition ability in 18 individuals with WS comparatively to typically developing children and adult control groups. A subset of 11 participants with WS as well as chronologically age matched typical adults further took part in an EEG task where they were asked to attentively view a series of upright and inverted faces and houses. State-of-the-art multivariate pattern analysis (MVPA) was used alongside standard ERP analysis to obtain a detailed characterisation of the neural profile associated with 1) viewing faces as an overall category (by examining neural activity associated with upright faces and houses), and to 2) the canonical upright configuration of a face, critically associated with expertise in typical development and often linked with holistic processing (upright and inverted faces).