52 research outputs found
Integrating EEG and MEG signals to improve motor imagery classification in brain-computer interfaces
We propose a fusion approach that combines features from simultaneously
recorded electroencephalographic (EEG) and magnetoencephalographic (MEG)
signals to improve classification performances in motor imagery-based
brain-computer interfaces (BCIs). We applied our approach to a group of 15
healthy subjects and found a significant classification performance enhancement
as compared to standard single-modality approaches in the alpha and beta bands.
Taken together, our findings demonstrate the advantage of considering
multimodal approaches as complementary tools for improving the impact of
non-invasive BCIs
Evidence of state-dependence in the effectiveness of responsive neurostimulation for seizure modulation
An implanted device for brain-responsive neurostimulation (RNS System) is
approved as an effective treatment to reduce seizures in adults with
medically-refractory focal epilepsy. Clinical trials of the RNS System
demonstrate population-level reduction in average seizure frequency, but
therapeutic response is highly variable. Recent evidence links seizures to
cyclical fluctuations in underlying risk. We tested the hypothesis that
effectiveness of responsive neurostimulation varies based on current state
within cyclical risk fluctuations. We analyzed retrospective data from 25
adults with medically-refractory focal epilepsy implanted with the RNS System.
Chronic electrocorticography was used to record electrographic seizures, and
hidden Markov models decoded seizures into fluctuations in underlying risk.
State-dependent associations of RNS System stimulation parameters with changes
in risk were estimated. Higher charge density was associated with improved
outcomes, both for remaining in a low seizure risk state and for transitioning
from a high to a low seizure risk state. The effect of stimulation frequency
depended on initial seizure risk state: when starting in a low risk state,
higher stimulation frequencies were associated with remaining in a low risk
state, but when starting in a high risk state, lower stimulation frequencies
were associated with transition to a low risk state. Findings were consistent
across bipolar and monopolar stimulation configurations. The impact of RNS on
seizure frequency exhibits state-dependence, such that stimulation parameters
which are effective in one seizure risk state may not be effective in another.
These findings represent conceptual advances in understanding the therapeutic
mechanism of RNS, and directly inform current practices of RNS tuning and the
development of next-generation neurostimulation systems
Genetic and Neuroanatomical Support for Functional Brain Network Dynamics in Epilepsy
Focal epilepsy is a devastating neurological disorder that affects an
overwhelming number of patients worldwide, many of whom prove resistant to
medication. The efficacy of current innovative technologies for the treatment
of these patients has been stalled by the lack of accurate and effective
methods to fuse multimodal neuroimaging data to map anatomical targets driving
seizure dynamics. Here we propose a parsimonious model that explains how
large-scale anatomical networks and shared genetic constraints shape
inter-regional communication in focal epilepsy. In extensive ECoG recordings
acquired from a group of patients with medically refractory focal-onset
epilepsy, we find that ictal and preictal functional brain network dynamics can
be accurately predicted from features of brain anatomy and geometry, patterns
of white matter connectivity, and constraints complicit in patterns of gene
coexpression, all of which are conserved across healthy adult populations.
Moreover, we uncover evidence that markers of non-conserved architecture,
potentially driven by idiosyncratic pathology of single subjects, are most
prevalent in high frequency ictal dynamics and low frequency preictal dynamics.
Finally, we find that ictal dynamics are better predicted by white matter
features and more poorly predicted by geometry and genetic constraints than
preictal dynamics, suggesting that the functional brain network dynamics
manifest in seizures rely on - and may directly propagate along - underlying
white matter structure that is largely conserved across humans. Broadly, our
work offers insights into the generic architectural principles of the human
brain that impact seizure dynamics, and could be extended to further our
understanding, models, and predictions of subject-level pathology and response
to intervention
Distributed Subnetworks of Depression Defined by Direct Intracranial Neurophysiology
Major depressive disorder is a common and disabling disorder with high rates of treatment resistance. Evidence suggests it is characterized by distributed network dysfunction that may be variable across patients, challenging the identification of quantitative biological substrates. We carried out this study to determine whether application of a novel computational approach to a large sample of high spatiotemporal resolution direct neural recordings in humans could unlock the functional organization and coordinated activity patterns of depression networks. This group level analysis of depression networks from heterogenous intracranial recordings was possible due to application of a correlational model-based method for inferring whole-brain neural activity. We then applied a network framework to discover brain dynamics across this model that could classify depression. We found a highly distributed pattern of neural activity and connectivity across cortical and subcortical structures that was present in the majority of depressed subjects. Furthermore, we found that this depression signature consisted of two subnetworks across individuals. The first was characterized by left temporal lobe hypoconnectivity and pathological beta activity. The second was characterized by a hypoactive, but hyperconnected left frontal cortex. These findings have applications toward personalization of therapy
White Matter Network Architecture Guides Direct Electrical Stimulation Through Optimal State Transitions
Electrical brain stimulation is currently being investigated as a therapy for
neurological disease. However, opportunities to optimize such therapies are
challenged by the fact that the beneficial impact of focal stimulation on both
neighboring and distant regions is not well understood. Here, we use network
control theory to build a model of brain network function that makes
predictions about how stimulation spreads through the brain's white matter
network and influences large-scale dynamics. We test these predictions using
combined electrocorticography (ECoG) and diffusion weighted imaging (DWI) data
who volunteered to participate in an extensive stimulation regimen. We posit a
specific model-based manner in which white matter tracts constrain stimulation,
defining its capacity to drive the brain to new states, including states
associated with successful memory encoding. In a first validation of our model,
we find that the true pattern of white matter tracts can be used to more
accurately predict the state transitions induced by direct electrical
stimulation than the artificial patterns of null models. We then use a targeted
optimal control framework to solve for the optimal energy required to drive the
brain to a given state. We show that, intuitively, our model predicts larger
energy requirements when starting from states that are farther away from a
target memory state. We then suggest testable hypotheses about which structural
properties will lead to efficient stimulation for improving memory based on
energy requirements. Our work demonstrates that individual white matter
architecture plays a vital role in guiding the dynamics of direct electrical
stimulation, more generally offering empirical support for the utility of
network control theoretic models of brain response to stimulation
Hippocampal network activity forecasts epileptic seizures.
Seizures in people with epilepsy were long thought to occur at random, but recent methods for seizure forecasting enable estimation of the likelihood of seizure occurrence over short horizons. These methods rely on days-long cyclical patterns of brain electrical activity and other physiological variables that determine seizure likelihood and that require measurement through long-term, multimodal recordings. In this retrospective cohort study of 15 adults with bitemporal epilepsy who had a device that provides chronic intracranial recordings, functional connectivity of hippocampal networks fluctuated in multiday cycles with patterns that mirrored cycles of seizure likelihood. A functional connectivity biomarker of seizure likelihood derived from 90-s recordings of background hippocampal activity generalized across individuals and forecasted 24-h seizure likelihood as accurately as cycle-based models requiring months-long baseline recordings. Larger, prospective studies are needed to validate this approach, but our results have the potential to make reliable seizure forecasts accessible to more people with epilepsy
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