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Litt, Brian

https://orcid.org/0000-0003-2732-6927

Mayo Clinic

University of Pennsylvania

Citations 7

Artificial intelligence in epilepsy phenotyping
Knight, Andrew , Gschwind, Tilo , Galer, Peter D. , Litt, Brian , Soltész, Iván , Galer, Peter , Beniczky, Sándor , Knight, Andrew , Worrell, Gregory A.

Epilepsia | November 21, 2023 | Volume: 66 | Issue: S3 | Pages: 39-52

10.1111/epi.17833 Get It

AbstractArtificial intelligence (AI) allows data analysis and integration at an unprecedented granularity and scale. Here we review the technological advances, challenges, and future perspectives of using AI for electro‐clinical phenotyping of animal models and patients with epilepsy. In translational research, AI models accurately identify behavioral states in animal models of epilepsy, allowing identification of correlations between neural activity and interictal and ictal behavior. Clinical applications of AI‐based automated and semi‐automated analysis of audio and video recordings of people with epilepsy, allow significant data reduction and reliable detection and classification of major motor seizures. AI models can accurately identify electrographic biomarkers of epilepsy, such as spikes, high‐frequency oscillations, and seizure patterns. Integrating AI analysis of electroencephalographic, clinical, and behavioral data will contribute to optimizing therapy for patients with epilepsy.
Towards network-guided neuromodulation for epilepsy
Piper, Rory J. , Carmichael, David W. , Litt, Brian , Tisdall, Martin , Tisdall, Martin M , Richardson, Robert Mark , Worrell, Gregory A. , Baldeweg, Torsten , Denison, Timothy

Brain | June 30, 2022 | Volume: 145 | Issue: 10 | Pages: 3347-3362

10.1093/brain/awac234 Get It

Abstract Epilepsy is well-recognized as a disorder of brain networks. There is a growing body of research to identify critical nodes within dynamic epileptic networks with the aim to target therapies that halt the onset and propagation of seizures. In parallel, intracranial neuromodulation, including deep brain stimulation and responsive neurostimulation, are well-established and expanding as therapies to reduce seizures in adults with focal-onset epilepsy; and there is emerging evidence for their efficacy in children and generalized-onset seizure disorders. The convergence of these advancing fields is driving an era of ‘network-guided neuromodulation’ for epilepsy. In this review, we distil the current literature on network mechanisms underlying neurostimulation for epilepsy. We discuss the modulation of key ‘propagation points’ in the epileptogenic network, focusing primarily on thalamic nuclei targeted in current clinical practice. These include (i) the anterior nucleus of thalamus, now a clinically approved and targeted site for open loop stimulation, and increasingly targeted for responsive neurostimulation; and (ii) the centromedian nucleus of the thalamus, a target for both deep brain stimulation and responsive neurostimulation in generalized-onset epilepsies. We discuss briefly the networks associated with other emerging neuromodulation targets, such as the pulvinar of the thalamus, piriform cortex, septal area, subthalamic nucleus, cerebellum and others. We report synergistic findings garnered from multiple modalities of investigation that have revealed structural and functional networks associated with these propagation points — including scalp and invasive EEG, and diffusion and functional MRI. We also report on intracranial recordings from implanted devices which provide us data on the dynamic networks we are aiming to modulate. Finally, we review the continuing evolution of network-guided neuromodulation for epilepsy to accelerate progress towards two translational goals: (i) to use pre-surgical network analyses to determine patient candidacy for neurostimulation for epilepsy by providing network biomarkers that predict efficacy; and (ii) to deliver precise, personalized and effective antiepileptic stimulation to prevent and arrest seizure propagation through mapping and modulation of each patients’ individual epileptogenic networks.
Crowdsourcing seizure detection: algorithm development and validation on human implanted device recordings
Baldassano, Steven N. , Brinkmann, Benjamin H. , Ung, Hoameng , Blevins, Tyler, Conrad, Erin C. , Leyde, Kent, Cook, Mark , Khambhati, Ankit N. , Wagenaar, Joost , Litt, Brian , Worrell, Gregory A. , Brinkmann, Benjamin H , Cook, Mark J

Brain | April 5, 2017 | Volume: 140 | Issue: 6 | Pages: 1680-1691

10.1093/brain/awx098 Get It

Temporal behavior of seizures and interictal bursts in prolonged intracranial recordings from epileptic canines
Ung, Hoameng , Wulsin, Drausin, Wagenaar, Joost , Fox, Emily B. , McDonnell, John, Patterson, Ned, Vite, Charles H. , Litt, Brian , Davis, Kathryn A. , Worrell, Gregory A.

Epilepsia | November 3, 2016 | Volume: 57 | Issue: 12 | Pages: 1949-1957

10.1111/epi.13591 Get It

SummaryObjectiveEpilepsy is a chronic disorder, but seizure recordings are usually obtained in the acute setting. The chronic behavior of seizures and the interictal bursts that sometimes initiate them is unknown. We investigate the variability of these electrographic patterns over an extended period of time using chronic intracranial recordings in canine epilepsy.MethodsContinuous, yearlong intracranial electroencephalography (iEEG) recordings from four dogs with naturally occurring epilepsy were analyzed for seizures and interictal bursts. Following automated detection and clinician verification of interictal bursts and seizures, temporal trends of seizures, burst count, and burst–burst similarities were determined. One dog developed status epilepticus, the recordings of which were also investigated.ResultsMultiple seizure types, determined by onset channels, were observed in each dog, with significant temporal variation between types. The first 14 days of invasive recording, analogous to the average duration of clinical invasive recordings in humans, did not capture the entirety of seizure types. Seizures typically occurred in clusters, and isolated seizures were rare. The count and dynamics of interictal bursts form distinct groups and do not stabilize until several weeks after implantation.SignificanceThere is significant temporal variability in seizures and interictal bursts after electrode implantation that requires several weeks to reach steady state. These findings, comparable to those reported in humans implanted with the NeuroPace Responsive Neurostimulator System (RNS) device, suggest that transient network changes following electrode implantation may need to be taken into account when interpreting or analyzing iEEG during evaluation for epilepsy surgery. Chronic, ambulatory iEEG may be better suited to accurately map epileptic networks in appropriate individuals.
Mining continuous intracranial EEG in focal canine epilepsy: Relating interictal bursts to seizure onsets
Ung, Hoameng , Wulsin, Drausin, Wagenaar, Joost , Fox, Emily B. , Patterson, Ned, Vite, Charles H. , Litt, Brian , Davis, Kathryn A. , Worrell, Gregory A.

Epilepsia | November 26, 2015 | Volume: 57 | Issue: 1 | Pages: 89-98

10.1111/epi.13249 Get It

SummaryObjectiveBrain regions are localized for resection during epilepsy surgery based on rare seizures observed during a short period of intracranial electroencephalography (iEEG) monitoring. Interictal epileptiform bursts, which are more prevalent than seizures, may provide complementary information to aid in epilepsy evaluation. In this study, we leverage a long‐term iEEG dataset from canines with naturally occurring epilepsy to investigate interictal bursts and their electrographic relationship to seizures.MethodsFour dogs were included in this study, each monitored previously with continuous iEEG for periods of 475.7, 329.9, 45.8, and 451.8 days, respectively, for a total of >11,000 h. Seizures and bursts were detected and validated by two board‐certified epileptologists. A published Bayesian model was applied to analyze the dynamics of interictal epileptic bursts on EEG and compare them to seizures.ResultsIn three dogs, bursts were stereotyped and found to be statistically similar to periods before or near seizure onsets. Seizures from one dog during status epilepticus were markedly different from other seizures in terms of burst similarity.SignificanceShorter epileptic bursts explored in this work have the potential to yield significant information about the distribution of epileptic events. In our data, bursts are at least an order of magnitude more prevalent than seizures and occur much more regularly. Our finding that bursts often display pronounced similarity to seizure onsets suggests that they contain relevant information about the epileptic networks from which they arise and may aide in the clinical evaluation of epilepsy in patients.
Unsupervised Classification of High-Frequency Oscillations in Human Neocortical Epilepsy and Control Patients
Blanco, Justin A. , Stead, Matt, Krieger, Abba Μ. , Viventi, Jonathan , Marsh, W. Richard , Lee, Kendall H. , Litt, Brian , Worrell, Gregory A.

Journal of Neurophysiology | September 2, 2010 | Volume: 104 | Issue: 5 | Pages: 2900-2912

10.1152/jn.01082.2009 Get It

High-frequency oscillations (HFOs) have been observed in animal and human intracranial recordings during both normal and aberrant brain states. It has been proposed that the relationship between subclasses of these oscillations can be used to identify epileptic brain. Studies of HFOs in epilepsy have been hampered by selection bias arising primarily out of the need to reduce the volume of data so that clinicians can manually review it. In this study, we introduce an algorithm for detecting and classifying these signals automatically and demonstrate the tractability of analyzing a data set of unprecedented size, over 31,000 channel-hours of intracranial electroencephalographic (iEEG) recordings from micro- and macroelectrodes in humans. Using an unsupervised approach that does not presuppose a specific number of clusters in the data, we show direct evidence for the existence of distinct classes of transient oscillations within the 100- to 500-Hz frequency range in a population of nine neocortical epilepsy patients and two controls. The number of classes we find, four (three plus one putative artifact class), is consistent with prior studies that identify “ripple” and “fast ripple” oscillations using human-intensive methods and, additionally, identifies a less examined class of mixed-frequency events.