Imaging the spatial-temporal neuronal dynamics using dynamic causal modelling

Oscillatory brain activity is a ubiquitous feature of neuronal dynamics and the synchronous discharge of neurons is believed to facilitate integration both within functionally segregated brain areas and between areas engaged by the same task. There is growing interest in investigating the neural oscillatory networks in vivo. The aims of this thesis are to (1) develop an advanced method, Dynamic Causal Modelling for Induced Responses (DCM for IR), for modelling the brain network functions and (2) apply it to exploit the nonlinear coupling in the motor system during hand grips and the functional asymmetries during face perception. DCM for IR models the time-varying power over a range of frequencies of coupled electromagnetic sources. The model parameters encode coupling strength among areas and allows the differentiations between linear (within frequency) and nonlinear (between-frequency) coupling. I applied DCM for IR to show that, during hand grips, the nonlinear interactions among neuronal sources in motor system are essential while intrinsic coupling (within source) is very likely to be linear. Furthermore, the normal aging process alters both the network architecture and the frequency contents in the motor network. I then use the bilinear form of DCM for IR to model the experimental manipulations as the modulatory effects. I use MEG data to demonstrate functional asymmetries between forward and backward connections during face perception: Specifically, high (gamma) frequencies in higher cortical areas suppressed low (alpha) frequencies in lower areas. This finding provides direct evidence for functional asymmetries that is consistent with anatomical and physiological evidence from animal studies. Lastly, I generalize the bilinear form of DCM for IR to dissociate the induced responses from evoked ones in terms of their functional role. The backward modulatory effect is expressed as induced, but not evoked responses

Evaluating the neurophysiological evidence for predictive processing as a model of perception

For many years, the dominant theoretical framework guiding research into the neural origins of perceptual experience has been provided by hierarchical feedforward models, in which sensory inputs are passed through a series of increasingly complex feature detectors. However, the long‐standing orthodoxy of these accounts has recently been challenged by a radically different set of theories that contend that perception arises from a purely inferential process supported by two distinct classes of neurons: those that transmit predictions about sensory states and those that signal sensory information that deviates from those predictions. Although these predictive processing (PP) models have become increasingly influential in cognitive neuroscience, they are also criticized for lacking the empirical support to justify their status. This limited evidence base partly reflects the considerable methodological challenges that are presented when trying to test the unique predictions of these models. However, a confluence of technological and theoretical advances has prompted a recent surge in human and nonhuman neurophysiological research seeking to fill this empirical gap. Here, we will review this new research and evaluate the degree to which its findings support the key claims of PP

Obsessive-Compulsive Disorder

Although Obsessive-Compulsive Disorder (OCD) has been known since the ancient times, the exact etiology and pathogenesis of OCD unfortunately still remain unknown. In addition, the therapeutic approaches elaborated for the treatment of OCD as a whole are not perfect, and this disorder as a rule is characterized by unfavorable course and lack of full therapeutic response. In the current book some modern data on pathogenesis, phenomenology and treatment of OCD are presented. Besides, the data on co-morbidity of OCD with other neurological and psychiatric disorders are also included. This book is intended for broad circle of readers, but mostly for psychiatrists, psychologists and neurologists

Cognitive and Neural Map Representations in Schizophrenia

An ability to build structured cognitive maps of the world may lie at the heart of understanding cognitive features of schizophrenia. In rodents, cognitive map representations are supported by sequential hippocampal place cell reactivations during rest (offline), known as replay. These events occur in the context of local high frequency ripple oscillations, and whole-brain default mode network (DMN) activation. Genetic mouse models of schizophrenia also report replay and ripple abnormalities. Here, I investigate the behavioural and neural signatures of structured internal representations in people with a diagnosis of schizophrenia (PScz, n = 29) and matched control participants (n = 28) using magnetoencephalography (MEG). Participants were asked to infer correct sequential relationships between task pictures by applying a pre-learned task template to visual experiences containing these pictures. In Chapter 3 I show that, during a post-task rest session, controls exhibited fast spontaneous neural reactivation of task state representations that replayed inferred relationships. Replay was coincident with increased ripple power in hippocampus, which may be related to NMDAR availability (Chapter 4). PScz showed both reduced replay and augmented ripple power, convergent with genetic mouse models. These abnormalities were linked to impairments in behavioural acquisition of task structure, and to its subsequent representation in visually evoked neural responses. In Chapter 5 I explore the temporal coupling between replay onsets and DMN activation. I show an impairment in this association in PScz, which related to subsequent mnemonic maintenance of learned task structure, complementing previous reports of DMN abnormalities in the condition. Finally, in Chapter 6, using a separate verbal fluency task, I show that PScz exhibit evidence of reduced use of (semantic) associative information when sampling concepts from memory. Together, my results provide support for a hypothesis that schizophrenia is associated with abnormalities in neural and behavioural correlates of cognitive map representation

Spatial Updating in Human Cortex

Single neurons in several cortical areas in monkeys update visual information in conjunction with eye movements. This remapping of stimulus representations is thought to contribute to spatial constancy. The central hypothesis here is that spatial updating also occurs in humans and that it can be visualized with functional MRI.In Chapter 2, we describe experiments in which we tested the role of human parietal cortex in spatial updating. We scanned subjects during a task that involved remapping of visual signals across hemifields. This task is directly analogous to the single-step saccade task used to test spatial updating in monkeys. We observed an initial response in the hemisphere contralateral to the visual stimulus, followed by a remapped response in the hemisphere ipsilateral to the stimulus. Our results demonstrate that updating of visual information occurs in human parietal cortex and can be visualized with fMRI.The experiments in Chapter 2 show that updated visual responses have a characteristic latency and response shape. Chapter 3 describes a statistical model for estimating these parameters. The method is based on a nonlinear, fully Bayesian, hierarchical model that decomposes the fMRI time series data into baseline, smooth drift, activation signal, and noise. This chapter shows that this model performs well relative to commonly-used general linear models. In Chapter 4, we use the statistical method described in Chapter 3 to test for the presence of spatial updating activity in human extrastriate visual cortex. We identified the borders of several retinotopically defined visual areas in the occipital lobe. We then tested for spatial updating using the single step saccade task. We found a roughly monotonic relationship between the strength of updating activity and position in the visual area hierarchy. We observed the strongest responses in area V4, and the weakest response in V1. We conclude that updating is not restricted to brain regions involved primarily in attention and the generation of eye movements, but rather, is present in occipital lobe visual areas as well

Change blindness: eradication of gestalt strategies

Arrays of eight, texture-defined rectangles were used as stimuli in a one-shot change blindness (CB) task where there was a 50% chance that one rectangle would change orientation between two successive presentations separated by an interval. CB was eliminated by cueing the target rectangle in the first stimulus, reduced by cueing in the interval and unaffected by cueing in the second presentation. This supports the idea that a representation was formed that persisted through the interval before being 'overwritten' by the second presentation (Landman et al, 2003 Vision Research 43149–164]. Another possibility is that participants used some kind of grouping or Gestalt strategy. To test this we changed the spatial position of the rectangles in the second presentation by shifting them along imaginary spokes (by ±1 degree) emanating from the central fixation point. There was no significant difference seen in performance between this and the standard task [F(1,4)=2.565, p=0.185]. This may suggest two things: (i) Gestalt grouping is not used as a strategy in these tasks, and (ii) it gives further weight to the argument that objects may be stored and retrieved from a pre-attentional store during this task

A Role for Hippocampal Sharp-wave Ripples in Active Visual Search

Sharp-wave ripples (SWRs) in the hippocampus are thought to contribute to memory formation, though this effect has only been demonstrated in rodents. The SWR, a large deflection in the hippocampal LFP (local field potential), is known to occur primarily during slow wave sleep and during immobility and consummator behaviors. SWRs have widespread effects throughout the cortex, and are directly implicated in memory formation their occurrence correlates with correct performance, and their ablation impairs memory in spatial memory tasks. Though SWRs have been reported in primates, their role is poorly understood. Whether or not SWRs play a role in memory formation, as they do in rodents, has yet to be confirmed. This work encompasses three separate studies with the goal of determining whether there is a link between SWR occurrence and memory formation in the macaque. Chapter 2 establishes the validity of the modified Change Blindness task as a memory task which is sensitive to normal hippocampal function in monkeys. Chapter 3 establishes that SWR events occur during waking (and stationary) activity, during visual search, in the macaque. Until this work, the prevalence of SWRs in macaques during waking exploration was unknown. Chapter 4 shows that gaze during SWRs was more likely to be near the target object on repeated than on novel presentations, even after accounting for overall differences in gaze location with scene repetition. The increase in ripple likelihood near remembered visual objects suggests a link between ripples and memory in primates; specifically, SWRs may reflect part of a mechanism supporting the guidance of search based on experience. The amalgamation of this work reveals several novel findings and establishes an important step towards understanding the role that SWRs play in memory formation in predominantly-visual primate brains

Understanding mechanisms related to psychosis in Motor Neurone Disease

Psychosis is a challenging feature of the syndromes of motor neurone disease (MND), frontotemporal dementia (FTD) and their overlap (FTD-MND). Clinically evident psychosis is not common, except in those with C9orf72+ expansions. However, subthreshold psychosis or pre-psychosis processes are common and provide the opportunity to study the mechanisms of psychosis in MND and FTD-MND. My aim was to identify the prevalence and the cognitive and neural correlates of psychosis, and related processes, in MND. I used a tiered cohort study approach. Tier 1 introduced screening as standard in a regional MND clinic (N=111) using the Edinburgh Cognitive and Behavioural ALS Screen and Cambridge Behavioural Inventory-Revised (CBI-R). In Tier 2, 60 patients and 30 controls underwent neuropsychological assessment, including (i) evidence-based decision-making, to quantify jumping to conclusions (JTC), (ii) attentional control and associative learning, (iii) perceptual inference, and (iv) psychiatric screening with Neuropsychiatric Inventory (NPI), Brief Psychiatric Rating Scale (BRPS), and the Comprehensive Assessment of At-Risk Mental States (CAARMS). Tier 3 included magnetic resonance imaging of 30 patients and 20 controls. Carer reports in Tier 1 indicated that 10% of patients exhibited features suggestive of psychosis and 40% exhibited behavioural change. In Tier 2, many patients manifested abnormal behaviours (CBI-R 41%; NPI showed 19%; BPRS 24%), with 12-16% showing psychosis-specific symptoms (CBI-R and NPI psychosis index scores). In the jumping to conclusions task, patients made decisions based on less evidence than controls and were insensitive to negative feedback. Carer ratings of patient behaviour correlated with performance on the jumping to conclusions task when decisions were rewarded or costs fixed. Attentional shifting and perceptual inference were normal in MND. A principal component analysis (PCA) of questionnaires revealed two component scores, reflecting distinct patients’ and carers’ perspectives. The imaging analyses focused on the correlates of jumping to conclusions and insensitivity to negative feedback, as a potential risk profile for psychosis, with exploratory analyses of the correlates of the CBI-R psychosis index, and carers’ ratings of behaviour from the PCA. Using a Freesurfer regions-of-interest approach, grey matter volume correlated inversely with CBI-R psychosis index in the caudate, amygdala, cingulate and hippocampus. Using tract-based spatial statistics, increased mean diffusivity (MD) of diffusion weighted imaging correlated with the CBI-R psychosis responses in inferior longitudinal and uncinate fasciculi. Cost sensitivity in the JTC task correlated with cingulate and cerebellar grey matter volumes. White matter correlates of cost sensitivity included reduced FA with increasing cost sensitivity in white matter connecting the inferior frontal lobe in controls and patients. Although overt psychosis is uncommon in MND, many patients displayed abnormal behaviour or cognitive symptoms, including suboptimal reasoning biases and inferential impulsivity. Degeneration of cerebellar, cingulate and striatal grey matter, and adjacent major white matter tracts, may underlie these cognitive impairments and together represent a vulnerability to develop psychosis. Compromised reasoning and inference have implications for clinical management, including decisions around treatment options and management of well-being in MND.This research was funded by Alzheimer’s Research UK Studentship (PhD2017-26); Medical Research Council (SUAG 051/ G101400); and the NIHR Cambridge Biomedical Research Centre (BRC-1215-20014). The views expressed are those of the authors and not necessarily those of the NIHR or the Department of Health and Social Care

Psychology Is a Property of Persons, Not Averages or Distributions: Confronting the Group-to-Person Generalizability Problem in Experimental Psychology

This is the final version. Available on open access from SAGE Publications via the DOI in this recordWhen experimental psychologists make a claim (e.g., “Participants judged X as morally worse than Y”), how many participants are represented? Such claims are often based exclusively on group-level analyses; here, psychologists often fail to report or perhaps even investigate how many participants judged X as morally worse than Y. More troubling, group-level analyses do not necessarily generalize to the person level: “the group-to-person generalizability problem.” We first argue for the necessity of designing experiments that allow investigation of whether claims represent most participants. Second, we report findings that in a survey of researchers (and laypeople), most interpret claims based on group-level effects as being intended to represent most participants in a study. Most believe this ought to be the case if a claim is used to support a general, person-level psychological theory. Third, building on prior approaches, we document claims in the experimental-psychology literature, derived from sets of typical group-level analyses, that describe only a (sometimes tiny) minority of participants. Fourth, we reason through an example from our own research to illustrate this group-to-person generalizability problem. In addition, we demonstrate how claims from sets of simulated group-level effects can emerge without a single participant’s responses matching these patterns. Fifth, we conduct four experiments that rule out several methodology-based noise explanations of the problem. Finally, we propose a set of simple and flexible options to help researchers confront the group-to-person generalizability problem in their own work