Pathological and physiological high-frequency oscillations in focal human epilepsy (original) (raw)

High-frequency oscillations as a new biomarker in epilepsy

Annals of Neurology, 2012

The discovery that electroencephalography (EEG) contains useful information at frequencies above the traditional 80Hz limit has had a profound impact on our understanding of brain function. In epilepsy, high-frequency oscillations (HFOs, >80Hz) have proven particularly important and useful. This literature review describes the morphology, clinical meaning, and pathophysiology of epileptic HFOs. To record HFOs, the intracranial EEG needs to be sampled at least at 2,000Hz. The oscillatory events can be visualized by applying a high-pass filter and increasing the time and amplitude scales, or EEG time-frequency maps can show the amount of high-frequency activity. HFOs appear excellent markers for the epileptogenic zone. In patients with focal epilepsy who can benefit from surgery, invasive EEG is often required to identify the epileptic cortex, but current information is sometimes inadequate. Removal of brain tissue generating HFOs has been related to better postsurgical outcome than removing the seizure onset zone, indicating that HFOs may mark cortex that needs to be removed to achieve seizure control. The pathophysiology of epileptic HFOs is challenging, probably involving populations of neurons firing asynchronously. They differ from physiological HFOs in not being paced by rhythmic inhibitory activity and in their possible origin from population spikes. Their link to the epileptogenic zone argues that their study will teach us much about the pathophysiology of epileptogenesis and ictogenesis. HFOs show promise for improving surgical outcome and accelerating intracranial EEG investigations. Their potential needs to be assessed by future research.

High-Frequency Oscillations in the Normal Human Brain

Annals of neurology, 2018

High-frequency oscillations (HFOs) are a promising biomarker for the epileptogenic zone. It has not been possible, however, to differentiate physiological from pathological HFOs, and baseline rates of HFO occurrence vary substantially across brain regions. This project establishes region-specific normative values for physiological HFOs and high-frequency activity (HFA). Intracerebral stereo-encephalographic recordings with channels displaying normal physiological activity from nonlesional tissue were selected from 2 tertiary epilepsy centers. Twenty-minute sections from N2/N3 sleep were selected for automatic detection of ripples (80-250Hz), fast ripples (>250Hz), and HFA defined as long-lasting activity > 80Hz. Normative values are provided for 17 brain regions. A total of 1,171 bipolar channels with normal physiological activity from 71 patients were analyzed. The highest rates of ripples were recorded in the occipital cortex, medial and basal temporal region, transverse tem...

Localizing epileptogenic regions using high-frequency oscillations and machine learning

Biomarkers in Medicine, 2019

Pathological high frequency oscillations (HFOs) are putative neurophysiological biomarkers of epileptogenic brain tissue. Utilizing HFOs for epilepsy surgery planning offers the promise of improved seizure outcomes for patients with medically refractory epilepsy. This review discusses possible machine learning strategies that can be applied to HFO biomarkers to better identify epileptogenic regions. We discuss the role of HFO rate, and utilizing features such as explicit HFO properties (spectral content, duration, and power) and phase-amplitude coupling for distinguishing pathological HFO (pHFO) events from physiological HFO events. In addition, the review highlights the importance of neuroanatomical localization in machine learning strategies.

Stereotyped high-frequency oscillations discriminate seizure onset zones and critical functional cortex in focal epilepsy

Brain : a journal of neurology, 2018

High-frequency oscillations in local field potentials recorded with intracranial EEG are putative biomarkers of seizure onset zones in epileptic brain. However, localized 80-500 Hz oscillations can also be recorded from normal and non-epileptic cerebral structures. When defined only by rate or frequency, physiological high-frequency oscillations are indistinguishable from pathological ones, which limit their application in epilepsy presurgical planning. We hypothesized that pathological high-frequency oscillations occur in a repetitive fashion with a similar waveform morphology that specifically indicates seizure onset zones. We investigated the waveform patterns of automatically detected high-frequency oscillations in 13 epilepsy patients and five control subjects, with an average of 73 subdural and intracerebral electrodes recorded per patient. The repetitive oscillatory waveforms were identified by using a pipeline of unsupervised machine learning techniques and were then correla...

Temporal changes of neocortical high-frequency oscillations in epilepsy

Journal of Neurophysiology, 2013

High-frequency (100–500 Hz) oscillations (HFOs) recorded from intracranial electrodes are a potential biomarker for epileptogenic brain. HFOs are commonly categorized as ripples (100–250 Hz) or fast ripples (250–500 Hz), and a third class of mixed frequency events has also been identified. We hypothesize that temporal changes in HFOs may identify periods of increased the likelihood of seizure onset. HFOs (86,151) from five patients with neocortical epilepsy implanted with hybrid (micro + macro) intracranial electrodes were detected using a previously validated automated algorithm run over all channels of each patient's entire recording. HFOs were characterized by extracting quantitative morphologic features and divided into four time epochs (interictal, preictal, ictal, and postictal) and three HFO clusters (ripples, fast ripples, and mixed events). We used supervised classification and nonparametric statistical tests to explore quantitative changes in HFO features before, durin...

Developement of Matlab-based Graphical User Interface (GUI) for detection of high frequency oscillations (HFOs) in epileptic patients

2012

High-Frequency Oscillations (HFOs) in the 80-500 Hz band are important biomarkers of epileptogenic brain areas and could have a central role in theprocess of epileptogenesis and seizure genesis. Visual marking of HFOs is highly time consuming and tedious especially for long electroencephalographic (EEG) recordings. Automated HFO detection methods are potentially more efficient, repeatable and objective.Therefore,numerous automatic HFOs detection methodshave been developed. Toevaluate and compare theperformance of thesealgorithms in an intuitive and userfriendly framework accessible to researchers, neurologists and students,it is useful to implement the various methodsusing adedicated Graphical User Interfaces (GUI). In this paper we describe a GUI-based tool thatcontains three HFOs detectionmethods. It allowsthe user to test and runthree different methods based respectively on FIR filter, Complex MORLET Wavelet andmatching pursuit (MP). We also show how the GUI can be used to measure the performanceof each method. Generally,high sensitivity entrains high false-positive detection rates. For that, the developed GUI contains a supplementary module that allowsan expert(e.g. neurologist) to reject false detected events and only save the clinically relevant (true) events. In addition, the GUI presented here can be used to perform classification, as well as estimation of duration, frequency and position of different events. The presented software is easy to use and can easily be extended to include further methods. We thus expect it to become a valuable clinical tool for diagnosis of epilepsy and research purposes.

High-Frequency Oscillations and Their Importance in Epilepsy

Journal of Neurological Disorders, 2014

High-frequency oscillations are changes in electrical potentials in the EEG in frequencies above 80 Hz. In recent years it was discovered that these oscillations have great importance both in physiologic processes and as an expression of epileptogenic areas in the cerebral cortex. The measurement of these oscillations via depth-electrodes during pre-surgical evaluation of epilepsy patients has been proven to be an important tool in improving the ability to delineate exactly the area which should be resected, in case such an operation is feasible. New technical developments enable the acquisition of high-frequency oscillations from scalp electrodes as well, which could have great importance in brain research and care of epilepsy patients in the future.

Data mining neocortical high-frequency oscillations in epilepsy and controls

Brain, 2011

Transient high-frequency (100-500 Hz) oscillations of the local field potential have been studied extensively in human mesial temporal lobe. Previous studies report that both ripple (100-250 Hz) and fast ripple (250-500 Hz) oscillations are increased in the seizure-onset zone of patients with mesial temporal lobe epilepsy. Comparatively little is known, however, about their spatial distribution with respect to seizure-onset zone in neocortical epilepsy, or their prevalence in normal brain. We present a quantitative analysis of high-frequency oscillations and their rates of occurrence in a group of nine patients with neocortical epilepsy and two control patients with no history of seizures. Oscillations were automatically detected and classified using an unsupervised approach in a data set of unprecedented volume in epilepsy research, over 12 terabytes of continuous long-term micro-and macro-electrode intracranial recordings, without human preprocessing, enabling selection-bias-free estimates of oscillation rates. There are three main results: (i) a cluster of ripple frequency oscillations with median spectral centroid = 137 Hz is increased in the seizure-onset zone more frequently than a cluster of fast ripple frequency oscillations (median spectral centroid = 305 Hz); (ii) we found no difference in the rates of high frequency oscillations in control neocortex and the non-seizure-onset zone neocortex of patients with epilepsy, despite the possibility of different underlying mechanisms of generation; and (iii) while previous studies have demonstrated that oscillations recorded by parenchyma-penetrating micro-electrodes have higher peak 100-500 Hz frequencies than penetrating macro-electrodes, this was not found for the epipial electrodes used here to record from the neocortical surface. We conclude that the relative rate of ripple frequency oscillations is a potential biomarker for epileptic neocortex, but that larger prospective studies correlating high-frequency oscillations rates with seizure-onset zone, resected tissue and surgical outcome are required to determine the true predictive value.