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Dunkley, B. T.

Publications and source records attributed to Dunkley, B. T..

10 recordsLinked to original sources

Quantifying Neural Stability: Validation of a New Brain Stability Index

Quantifying longitudinal changes in an individual's brain is central to the development of personalised neural biomarkers in neurology and psychiatry. However, existing approaches for characterising individual neurophysiological signatures focus on discrimination between people rather than the quantification of within-subject change. To address this, we introduce the Brain Stability Index (BSI), a whole-brain metric that quantifies the similarity between two longitudinal neurophysiological scans in a low-dimensional latent space, with reference to a normative magnetoencephalography (MEG) database. Using 276 open resting-state MEG datasets and matched synthetic data, we first characterise how finite test-retest reliability sets a noise floor on the BSI. We then demonstrate that the BSI is sensitive to graded changes in whole-brain neural change that extend beyond measurement variability. Finally, we show that Factor Analysis, by separating shared structure from feature-specific noise, makes the BSI more robust to measurement artefacts. Together, these findings establish the BSI as a robust, bounded measure of neural stability that is well suited to longitudinal monitoring in neurology and psychiatry.

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Intrinsic electrophysiological activity maps a latent dimension of poor sleep quality and reduced cognitive performance: a magnetoencephalography study using Cam-CAN data.

Sleep quality and cognition vary as functions of lifestyle, genetics, and health. However, poor sleep quality is prevalent, reportedly affecting approximately 38% of the adult population. Poor sleep quality is a significant risk factor for mood disorders, a predictive factor in cognitive decline in later life, and sleep disturbance is a putative precursor to severe cognitive impairment and is predictive of dementia onset. The direct relationship between these factors and intrinsic neural function is poorly understood. Integrating neurophysiology, cognition, and sleep quality to reveal latent factors would help understand the neurophysiology of sleep disturbances and their relation to cognitive performance. Here, we used data from the Cam-CAN dataset with a partial least squares (PLS) approach, producing a multivariate cross-decomposition model to map resting-state magnetoencephalography (MEG) data and cognitive/sleep scores of healthy controls (n = 490, age 18-86). Normative modelling was applied to MEG data, correcting for effects of age, sex, and handedness. We identify a significant relationship between poorer self-reported sleep quality and lower cognitive performance across multiple domains, characterised by excess low-frequency neural activity and reduced high-frequency activity, particularly in the alpha band. Moreover, globally increased low frequency and decreased alpha-beta functional connectivity - the dominant frequency channel in neural connectivity at rest across the brain - contribute significantly to this relationship. Our multivariate mapping approach enabled us to parse the electrophysiological signatures directly related to sleep quality and cognitive performance, independent of the confounding effects of age, and show that neural slowing and dysconnectivity are intrinsically linked to self-reported sleep quality and cognitive performance.

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Functional connectivity differences in adult's ADHD - a MEG study

The neurobiology of adult Attention-Deficit/Hyperactivity Disorder (ADHD), particularly functional brain network connectivity, remain poorly understood. Magnetoencephalography (MEG) can reveal frequency-specific network dynamics given its high temporal resolution. Here, we investigated intrinsic functional connectivity differences between adults with ADHD (n = 24) and healthy controls (n = 44) using MEG data from the Open MEG Archive (OMEGA) dataset. We employed source reconstruction (Destrieux atlas), weighted phase-lag index (wPLI) connectivity across six frequency bands, graph theory metrics (Characteristic Path Length (CPL), node strength, clustering coefficient), and network-based statistics (NBS). We observed widespread hypo-connectivity in the high-gamma band (50-150 Hz) in adults with ADHD compared to controls. NBS identified a significant high-gamma sub-network, predominantly involving dorsal and ventral attention networks (DAN/VAN) and default mode network (DMN) nodes centered around a left fusiform gyrus hub, where all constituent connections exhibited consistently lower connectivity in the ADHD group. Globally, this was reflected in reduced gamma network integration (longer CPL) within the DAN and VAN. Locally, reduced high-gamma clustering was observed in VAN nodes (e.g., insula) and reduced node strength in a DAN region (postcentral sulcus). Predictive modeling using ElasticNet regression confirmed the importance of high-gamma metrics, with CPL measures yielding moderate classification accuracy (AUC {approx} 0.70-0.73). In contrast to high-gamma findings, the alpha band showed increased integration (shorter CPL) within the DMN and between the VAN and DAN in the ADHD group, alongside differences in alpha and beta band node properties in cingulate and somatomotor regions. Our findings reveal robust, frequency-dependent functional network alterations in adult ADHD, particularly highlighting disrupted high-frequency communication within and between key cognitive networks.

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The brain selectively allocates energy to functional brain networks under cognitive control

Network energy has been conceptualized based on structural balance theory in the physics of complex networks. We utilized this framework to assess the energy of functional brain networks under cognitive control and to understand how energy is allocated across canonical functional networks during various cognitive control tasks. We extracted network energy from functional connectivity patterns of subjects who underwent fMRI scans during cognitive tasks involving working memory, inhibitory control, and cognitive flexibility, in addition to task-free scans. We found that the energy of the whole-brain network increases when exposed to cognitive control tasks compared to the task-free resting state, which serves as a reference point. The brain selectively allocates this elevated energy to canonical functional networks; sensory networks receive more energy to support flexibility for processing sensory stimuli, while cognitive networks relevant to the task, functioning efficiently, require less energy. Furthermore, employing network energy, as a global network measure, improves the performance of predictive modeling, particularly in classifying cognitive control tasks and predicting chronological age. Our results highlight the robustness of this framework and the utility of network energy in understanding brain and cognitive mechanisms, including its promising potential as a biomarker for mental conditions and neurological disorders.

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Elevated body mass index in youth is associated with dysregulated surrogate markers of neural inhibition & excitation, and internetwork functional dysconnectivity

The developing child and adolescent brain is thought to have an increased vulnerability to the negative impact of obesity and excessive consumption of hyperpalatable and energy-rich foods. In this study, we investigated the neurophysiological effects of overweight and obesity in 30 participants spanning childhood and adolescence (8-19 years), using a naturalistic viewing paradigm with Inscapes, in a pseudo-resting-state protocol scan with magnetoencephalography (MEG). Subjects were median split on body mass indices (BMI), categorised into two groups comprising: lower <25 kg/m2 (n=15) and higher [&ge;]25 kg/m2 (n=15). We assessed spontaneous, regional neural function indexed by oscillatory activity, and functional connectivity within and between intrinsic resting brain networks, including the default mode network, dorsal and ventral attention, somatomotor, visual, language, central executive and salience networks. Elevated BMI was associated with significant reductions in activity of the posterior dominant rhythm, and gamma hyperactivity across widespread cortical areas, suggesting intrinsic neuronal hyperexcitability and disinhibition in children and adolescents. Additionally, we observed low-frequency theta hypoconnectivity between resting state networks including the salience, visual, and default mode networks, and overall reduced global efficiency in brain network structure, suggesting reduced effectiveness in neural communication. These findings underscore the neural impact of body composition on the developing brain, suggesting deleterious alterations in excitation and inhibition from surrogate neural markers associated with neurochemistry and brain networks linked with cognitive and behavioural functioning. These alterations may contribute to the persistent behavioural rigidity and difficulties in adopting healthier eating behaviours into adulthood.

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Predicting brain age across the adult lifespan with spontaneous oscillations and functional coupling in resting brain networks captured with magnetoencephalography

The functional repertoire of the human brain changes dramatically throughout the developmental trajectories of early life and even all the way throughout the adult lifespan into older age. Capturing this arc is important to understand healthy brain ageing, and conversely, how injury and diseased states can lead to accelerated brain ageing. Regression modelling using lifespan imaging data can reliably predict an individuals brain age based on expected arcs of ageing. One feature of brain function that is important in this respect, and understudied to date, is neural oscillations - the rhythmic fluctuations of brain activity that index neural cell assemblies and their functioning, as well as coordinating information flow around networks. Here, we analysed resting-state magnetoencephalography (MEG) recordings from 367 healthy participants aged 18 to 83, using two distinct statistical approaches to link neural oscillations & functional coupling with that of healthy ageing. Spectral power and leakage-corrected amplitude envelope correlations were calculated for each canonical frequency band from delta through gamma ranges. Spatially and spectrally consistent associations between healthy ageing and neurophysiological features were found across the applied methods, showing differential effects on neural oscillations, with decreasing amplitude of low frequencies throughout the adult lifespan, and increasing high frequency amplitude. Functional connectivity within and between resting-state brain networks mediated by alpha coupling generally decreased throughout adulthood and increased in the beta band. Predictive modelling of brain age via regression showed an age dependent prediction bias resulting in overestimating the age of younger people (<40 years old) and underestimating the age of older individuals. These findings evidence strong age-related neurophysiological changes in oscillatory activity and functional networks of the brain as measured by resting-state MEG and that cortical oscillations are moderately reliable markers for predictive modelling. For researchers in the field of predictive brain age modelling with neurophysiological data, we recommend attention is paid to predictive biases for younger and older age ranges and consider using specific models for different age brackets. Nevertheless, these results suggest brain age prediction from MEG data can be used to model arcs of ageing throughout the adult lifespan and predict accelerated ageing in pathological brain states.

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Parietal Mechanisms for Transsaccadic Spatial Frequency Perception: An fMRI Study

Posterior parietal cortex (PPC), specifically right supramarginal gyrus, is involved in transsaccadic memory of object orientation for both perception and action. Here, we investigated whether PPC is involved in transsaccadic memory of other features, namely spatial frequency. We employed a functional magnetic resonance imaging paradigm where participants briefly viewed a grating stimulus with a specific spatial frequency that later reappeared with the same or different frequency, after a saccade or continuous fixation. Post-saccadic frequency modulation activated a region in the right hemisphere spanning medial PPC (ventral precuneus) and posterior cingulate cortex. Importantly, the site of peak precuneus activation showed saccade-specific feature modulation (compared to fixation) and task-specific saccade modulation (compared to a saccade localizer task). Psychophysiological interaction analysis revealed functional connectivity between this precuneus site and the precentral gyrus (M1), lingual gyrus (V1/V2), and medial occipitotemporal sulcus. This differed from the transsaccadic orientation network, perhaps because spatial frequency signaled changes in object identity. Overall, this experiment supports a general role for PPC in transsaccadic vision, but suggests that different networks are employed for specific features.

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Early life maturation of human visual system white matter is altered by monocular enucleation

Monocular enucleation early in life and the resultant lack of binocular visual input during visual development results in functional and structural brain changes in adulthood, including alterations in white matter microstructure. However, the time courses of these neurodevelopmental changes are unknown. Here, we investigated whether structural brain changes were present at 8 to 12 years of age in a group of children with a history of monocular enucleation prior to 3 years of age (the ME group) relative to control participants with normal binocular vision (the BC group). Structural connectivity was measured using diffusion tensor imaging (DTI). Relative to the BC group, the ME group exhibited significantly increased radial and mean diffusivity in the optic radiation contralateral to the enucleated eye, the bidirectional interhemispheric V1 to V1 tracts and the V1 to MT tract ipsilateral to the enucleated eye. These changes indicate abnormal myelinization and reduced axonal density in subcortical and cortical visual pathway white matter structures following unilateral enucleation and loss of binocular vision. Our findings are broadly consistent with those recently reported for older uniocular individuals suggesting that these effects are present in childhood and persist into adulthood.

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Transsaccadic feature interactions in multiple reference frames: an fMRIa study

Transsaccadic integration of visual features can operate in various frames of reference, but the corresponding neural mechanisms have not been differentiated. A recent fMRIa (adaptation) study identified two cortical regions in supramarginal gyrus (SMG) and extrastriate cortex that were sensitive to transsaccadic changes in stimulus orientation (Dunkley et al., 2016). Here, we modified this paradigm to identify the neural correlates for transsaccadic comparison of object orientations in: 1) Spatially Congruent (SC), 2) Retinally Congruent (RC) or 3) Spatially Incongruent (SI)) coordinates. Functional data were recorded from 12 human participants while they observed a grating (oriented 45{degrees} or 135{degrees}) before a saccade, and then judged whether a post-saccadic grating (in SC, RC, or SI configuration) had the same or different orientation. Our analysis focused on areas that showed a significant repetition suppression (Different > Same) or repetition enhancement (Same > Different) BOLD responses. Several cortical areas were significantly modulated in all three conditions: premotor/motor cortex (likely related to the manual response), and posterior-middle intraparietal sulcus. In the SC condition, uniquely activated areas included left SMG and left lateral occipitotemporal gyrus (LOtG). In the RC condition, unique areas included inferior frontal gyrus and the left lateral BA 7. In the SI condition, uniquely activated areas included the frontal eye field, medial BA 7, and right LOtG. Overall, the SC results were significantly different from both RC and SI. These data suggest that different cortical networks are used to compare pre- and post-saccadic orientation information, depending on the spatial nature of the task.\n\nSignificance StatementEvery time one makes a saccade, the brain must compare and integrate stored visual information with new information. It has recently been shown that transsaccadic integration of visual object orientation involves specific areas within parietal and occipital cortex (Dunkley et al., 2016). Here, we show that this pattern of cortical activation also depends on the spatial nature of the task: when the visual object is fixed relative to space, the eye, or relative to neither space nor the eye, different frontal, parietal, and occipital regions are engaged. More generally, these findings suggest that different aspects of trans-saccadic integration flexibly employ different cortical networks.

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Oscillatory Default Mode Network Coupling In Concussion

BackgroundConcussion is a common form of mild traumatic brain injury (mTBI). Despite the descriptor mild, a single injury can leave long-lasting and sustained alterations to brain function, including changes to localised activity and large-scale interregional communication. Cognitive complaints are thought to arise from such functional deficits. We investigated the impact of injury on neurophysiological and functionally-specialised resting networks, known as intrinsic connectivity networks (ICNs), using MEG.\n\nMethodsWe assessed neurophysiological connectivity in 40 males, 20 with concussion, 20 without, using MEG. Regions-of-interest that comprise nodes of ICNs were defined, and their time courses derived using a beamformer approach. Pairwise fluctuations and covariations in band-limited amplitude envelopes were computed reflecting measures of functional connectivity. Intra-network connectivity was compared between groups using permutation testing, and correlated with symptoms.\n\nResultsWe observed increased resting spectral connectivity in the default mode and motor networks in our concussion group when compared with controls, across alpha through gamma ranges. Moreover, these differences were not explained by power spectrum density (absolute changes in the spectral profiles within the ICNs). Furthermore, this increased coupling was significantly associated with symptoms in the DMN and MOT networks - but once accounting for comorbid symptoms (including, depression, anxiety, and ADHD) only the DMN continued to be associated with symptoms.\n\nConclusionThe DMN network plays a critical role in shifting between cognitive tasks. These data suggest even a single concussion can perturb the intrinsic coupling of functionally-specialised networks in the brain and may explain persistent and wide-ranging symptomatology.

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