Literature DB >> 22782131

Recording human electrocorticographic (ECoG) signals for neuroscientific research and real-time functional cortical mapping.

N Jeremy Hill1, Disha Gupta, Peter Brunner, Aysegul Gunduz, Matthew A Adamo, Anthony Ritaccio, Gerwin Schalk.   

Abstract

Neuroimaging studies of human cognitive, sensory, and motor processes are usually based on noninvasive techniques such as electroencephalography (EEG), magnetoencephalography or functional magnetic-resonance imaging. These techniques have either inherently low temporal or low spatial resolution, and suffer from low signal-to-noise ratio and/or poor high-frequency sensitivity. Thus, they are suboptimal for exploring the short-lived spatio-temporal dynamics of many of the underlying brain processes. In contrast, the invasive technique of electrocorticography (ECoG) provides brain signals that have an exceptionally high signal-to-noise ratio, less susceptibility to artifacts than EEG, and a high spatial and temporal resolution (i.e., <1 cm/<1 millisecond, respectively). ECoG involves measurement of electrical brain signals using electrodes that are implanted subdurally on the surface of the brain. Recent studies have shown that ECoG amplitudes in certain frequency bands carry substantial information about task-related activity, such as motor execution and planning, auditory processing and visual-spatial attention. Most of this information is captured in the high gamma range (around 70-110 Hz). Thus, gamma activity has been proposed as a robust and general indicator of local cortical function. ECoG can also reveal functional connectivity and resolve finer task-related spatial-temporal dynamics, thereby advancing our understanding of large-scale cortical processes. It has especially proven useful for advancing brain-computer interfacing (BCI) technology for decoding a user's intentions to enhance or improve communication and control. Nevertheless, human ECoG data are often hard to obtain because of the risks and limitations of the invasive procedures involved, and the need to record within the constraints of clinical settings. Still, clinical monitoring to localize epileptic foci offers a unique and valuable opportunity to collect human ECoG data. We describe our methods for collecting recording ECoG, and demonstrate how to use these signals for important real-time applications such as clinical mapping and brain-computer interfacing. Our example uses the BCI2000 software platform and the SIGFRIED method, an application for real-time mapping of brain functions. This procedure yields information that clinicians can subsequently use to guide the complex and laborious process of functional mapping by electrical stimulation. PREREQUISITES AND PLANNING: Patients with drug-resistant partial epilepsy may be candidates for resective surgery of an epileptic focus to minimize the frequency of seizures. Prior to resection, the patients undergo monitoring using subdural electrodes for two purposes: first, to localize the epileptic focus, and second, to identify nearby critical brain areas (i.e., eloquent cortex) where resection could result in long-term functional deficits. To implant electrodes, a craniotomy is performed to open the skull. Then, electrode grids and/or strips are placed on the cortex, usually beneath the dura. A typical grid has a set of 8 x 8 platinum-iridium electrodes of 4 mm diameter (2.3 mm exposed surface) embedded in silicon with an inter-electrode distance of 1cm. A strip typically contains 4 or 6 such electrodes in a single line. The locations for these grids/strips are planned by a team of neurologists and neurosurgeons, and are based on previous EEG monitoring, on a structural MRI of the patient's brain, and on relevant factors of the patient's history. Continuous recording over a period of 5-12 days serves to localize epileptic foci, and electrical stimulation via the implanted electrodes allows clinicians to map eloquent cortex. At the end of the monitoring period, explantation of the electrodes and therapeutic resection are performed together in one procedure. In addition to its primary clinical purpose, invasive monitoring also provides a unique opportunity to acquire human ECoG data for neuroscientific research. The decision to include a prospective patient in the research is based on the planned location of their electrodes, on the patient's performance scores on neuropsychological assessments, and on their informed consent, which is predicated on their understanding that participation in research is optional and is not related to their treatment. As with all research involving human subjects, the research protocol must be approved by the hospital's institutional review board. The decision to perform individual experimental tasks is made day-by-day, and is contingent on the patient's endurance and willingness to participate. Some or all of the experiments may be prevented by problems with the clinical state of the patient, such as post-operative facial swelling, temporary aphasia, frequent seizures, post-ictal fatigue and confusion, and more general pain or discomfort. At the Epilepsy Monitoring Unit at Albany Medical Center in Albany, New York, clinical monitoring is implemented around the clock using a 192-channel Nihon-Kohden Neurofax monitoring system. Research recordings are made in collaboration with the Wadsworth Center of the New York State Department of Health in Albany. Signals from the ECoG electrodes are fed simultaneously to the research and the clinical systems via splitter connectors. To ensure that the clinical and research systems do not interfere with each other, the two systems typically use separate grounds. In fact, an epidural strip of electrodes is sometimes implanted to provide a ground for the clinical system. Whether research or clinical recording system, the grounding electrode is chosen to be distant from the predicted epileptic focus and from cortical areas of interest for the research. Our research system consists of eight synchronized 16-channel g.USBamp amplifier/digitizer units (g.tec, Graz, Austria). These were chosen because they are safety-rated and FDA-approved for invasive recordings, they have a very low noise-floor in the high-frequency range in which the signals of interest are found, and they come with an SDK that allows them to be integrated with custom-written research software. In order to capture the high-gamma signal accurately, we acquire signals at 1200Hz sampling rate-considerably higher than that of the typical EEG experiment or that of many clinical monitoring systems. A built-in low-pass filter automatically prevents aliasing of signals higher than the digitizer can capture. The patient's eye gaze is tracked using a monitor with a built-in Tobii T-60 eye-tracking system (Tobii Tech., Stockholm, Sweden). Additional accessories such as joystick, bluetooth Wiimote (Nintendo Co.), data-glove (5(th) Dimension Technologies), keyboard, microphone, headphones, or video camera are connected depending on the requirements of the particular experiment. Data collection, stimulus presentation, synchronization with the different input/output accessories, and real-time analysis and visualization are accomplished using our BCI2000 software. BCI2000 is a freely available general-purpose software system for real-time biosignal data acquisition, processing and feedback. It includes an array of pre-built modules that can be flexibly configured for many different purposes, and that can be extended by researchers' own code in C++, MATLAB or Python. BCI2000 consists of four modules that communicate with each other via a network-capable protocol: a Source module that handles the acquisition of brain signals from one of 19 different hardware systems from different manufacturers; a Signal Processing module that extracts relevant ECoG features and translates them into output signals; an Application module that delivers stimuli and feedback to the subject; and the Operator module that provides a graphical interface to the investigator. A number of different experiments may be conducted with any given patient. The priority of experiments will be determined by the location of the particular patient's electrodes. However, we usually begin our experimentation using the SIGFRIED (SIGnal modeling For Realtime Identification and Event Detection) mapping method, which detects and displays significant task-related activity in real time. The resulting functional map allows us to further tailor subsequent experimental protocols and may also prove as a useful starting point for traditional mapping by electrocortical stimulation (ECS). Although ECS mapping remains the gold standard for predicting the clinical outcome of resection, the process of ECS mapping is time consuming and also has other problems, such as after-discharges or seizures. Thus, a passive functional mapping technique may prove valuable in providing an initial estimate of the locus of eloquent cortex, which may then be confirmed and refined by ECS. The results from our passive SIGFRIED mapping technique have been shown to exhibit substantial concurrence with the results derived using ECS mapping. The protocol described in this paper establishes a general methodology for gathering human ECoG data, before proceeding to illustrate how experiments can be initiated using the BCI2000 software platform. Finally, as a specific example, we describe how to perform passive functional mapping using the BCI2000-based SIGFRIED system.

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Mesh:

Year:  2012        PMID: 22782131      PMCID: PMC3471287          DOI: 10.3791/3993

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  9 in total

1.  BCI2000: a general-purpose brain-computer interface (BCI) system.

Authors:  Gerwin Schalk; Dennis J McFarland; Thilo Hinterberger; Niels Birbaumer; Jonathan R Wolpaw
Journal:  IEEE Trans Biomed Eng       Date:  2004-06       Impact factor: 4.538

2.  Spectral changes in cortical surface potentials during motor movement.

Authors:  Kai J Miller; Eric C Leuthardt; Gerwin Schalk; Rajesh P N Rao; Nicholas R Anderson; Daniel W Moran; John W Miller; Jeffrey G Ojemann
Journal:  J Neurosci       Date:  2007-02-28       Impact factor: 6.167

3.  A brain-computer interface using electrocorticographic signals in humans.

Authors:  Eric C Leuthardt; Gerwin Schalk; Jonathan R Wolpaw; Jeffrey G Ojemann; Daniel W Moran
Journal:  J Neural Eng       Date:  2004-06-14       Impact factor: 5.379

Review 4.  High-frequency gamma oscillations and human brain mapping with electrocorticography.

Authors:  Nathan E Crone; Alon Sinai; Anna Korzeniewska
Journal:  Prog Brain Res       Date:  2006       Impact factor: 2.453

5.  Spatiotemporal dynamics of electrocorticographic high gamma activity during overt and covert word repetition.

Authors:  Xiaomei Pei; Eric C Leuthardt; Charles M Gaona; Peter Brunner; Jonathan R Wolpaw; Gerwin Schalk
Journal:  Neuroimage       Date:  2010-10-26       Impact factor: 6.556

6.  A practical procedure for real-time functional mapping of eloquent cortex using electrocorticographic signals in humans.

Authors:  Peter Brunner; Anthony L Ritaccio; Timothy M Lynch; Joseph F Emrich; J Adam Wilson; Justin C Williams; Erik J Aarnoutse; Nick F Ramsey; Eric C Leuthardt; Horst Bischof; Gerwin Schalk
Journal:  Epilepsy Behav       Date:  2009-06-17       Impact factor: 2.937

7.  Rapid Communication with a "P300" Matrix Speller Using Electrocorticographic Signals (ECoG).

Authors:  Peter Brunner; Anthony L Ritaccio; Joseph F Emrich; Horst Bischof; Gerwin Schalk
Journal:  Front Neurosci       Date:  2011-02-07       Impact factor: 4.677

8.  Categorical speech representation in human superior temporal gyrus.

Authors:  Edward F Chang; Jochem W Rieger; Keith Johnson; Mitchel S Berger; Nicholas M Barbaro; Robert T Knight
Journal:  Nat Neurosci       Date:  2010-10-03       Impact factor: 24.884

9.  Neural correlates of visual-spatial attention in electrocorticographic signals in humans.

Authors:  Aysegul Gunduz; Peter Brunner; Amy Daitch; Eric C Leuthardt; Anthony L Ritaccio; Bijan Pesaran; Gerwin Schalk
Journal:  Front Hum Neurosci       Date:  2011-09-24       Impact factor: 3.169

  9 in total
  19 in total

1.  Chronic embedded cortico-thalamic closed-loop deep brain stimulation for the treatment of essential tremor.

Authors:  Enrico Opri; Stephanie Cernera; Rene Molina; Robert S Eisinger; Jackson N Cagle; Leonardo Almeida; Timothy Denison; Michael S Okun; Kelly D Foote; Aysegul Gunduz
Journal:  Sci Transl Med       Date:  2020-12-02       Impact factor: 17.956

2.  A modular, closed-loop platform for intracranial stimulation in people with neurological disorders.

Authors:  Anish A Sarma; Britni Crocker; Sydney S Cash; Wilson Truccolo
Journal:  Conf Proc IEEE Eng Med Biol Soc       Date:  2016-08

3.  Differentiating tic electrophysiology from voluntary movement in the human thalamocortical circuit.

Authors:  Jackson N Cagle; Michael S Okun; Enrico Opri; Stephanie Cernera; Rene Molina; Kelly D Foote; Aysegul Gunduz
Journal:  J Neurol Neurosurg Psychiatry       Date:  2020-03-05       Impact factor: 10.154

4.  Performing behavioral tasks in subjects with intracranial electrodes.

Authors:  Matthew A Johnson; Susan Thompson; Jorge Gonzalez-Martinez; Hyun-Joo Park; Juan Bulacio; Imad Najm; Kevin Kahn; Matthew Kerr; Sridevi V Sarma; John T Gale
Journal:  J Vis Exp       Date:  2014-10-02       Impact factor: 1.355

5.  The Functional Role of Thalamocortical Coupling in the Human Motor Network.

Authors:  Enrico Opri; Stephanie Cernera; Michael S Okun; Kelly D Foote; Aysegul Gunduz
Journal:  J Neurosci       Date:  2019-08-30       Impact factor: 6.167

6.  Multiphasic modification of intrinsic functional connectivity of the rat brain during increasing levels of propofol.

Authors:  Xiping Liu; Siveshigan Pillay; Rupeng Li; Jeannette A Vizuete; Kimberly R Pechman; Kathleen M Schmainda; Anthony G Hudetz
Journal:  Neuroimage       Date:  2013-07-10       Impact factor: 6.556

7.  Chronic ambulatory electrocorticography from human speech cortex.

Authors:  Vikram R Rao; Matthew K Leonard; Jonathan K Kleen; Ben A Lucas; Emily A Mirro; Edward F Chang
Journal:  Neuroimage       Date:  2017-04-07       Impact factor: 6.556

8.  Collaborative approach in the development of high-performance brain-computer interfaces for a neuroprosthetic arm: translation from animal models to human control.

Authors:  Jennifer L Collinger; Michael A Kryger; Richard Barbara; Timothy Betler; Kristen Bowsher; Elke H P Brown; Samuel T Clanton; Alan D Degenhart; Stephen T Foldes; Robert A Gaunt; Ferenc E Gyulai; Elizabeth A Harchick; Deborah Harrington; John B Helder; Timothy Hemmes; Matthew S Johannes; Kapil D Katyal; Geoffrey S F Ling; Angus J C McMorland; Karina Palko; Matthew P Para; Janet Scheuermann; Andrew B Schwartz; Elizabeth R Skidmore; Florian Solzbacher; Anita V Srikameswaran; Dennis P Swanson; Scott Swetz; Elizabeth C Tyler-Kabara; Meel Velliste; Wei Wang; Douglas J Weber; Brian Wodlinger; Michael L Boninger
Journal:  Clin Transl Sci       Date:  2013-08-27       Impact factor: 4.689

Review 9.  The Evolution of Neuroprosthetic Interfaces.

Authors:  Dayo O Adewole; Mijail D Serruya; James P Harris; Justin C Burrell; Dmitriy Petrov; H Isaac Chen; John A Wolf; D Kacy Cullen
Journal:  Crit Rev Biomed Eng       Date:  2016

10.  Simultaneous real-time monitoring of multiple cortical systems.

Authors:  Disha Gupta; N Jeremy Hill; Peter Brunner; Aysegul Gunduz; Anthony L Ritaccio; Gerwin Schalk
Journal:  J Neural Eng       Date:  2014-07-31       Impact factor: 5.379

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