Localizing the epileptogenic zone.


Journal

Current opinion in neurology
ISSN: 1473-6551
Titre abrégé: Curr Opin Neurol
Pays: England
ID NLM: 9319162

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 13 2 2020
medline: 23 1 2021
entrez: 13 2 2020
Statut: ppublish

Résumé

Epilepsy surgery is the therapy of choice for 30-40% of people with focal drug-resistant epilepsy. Currently only ∼60% of well selected patients become postsurgically seizure-free underlining the need for better tools to identify the epileptogenic zone. This article reviews the latest neurophysiological advances for EZ localization with emphasis on ictal EZ identification, interictal EZ markers, and noninvasive neurophysiological mapping procedures. We will review methods for computerized EZ assessment, summarize computational network approaches for outcome prediction and individualized surgical planning. We will discuss electrical stimulation as an option to reduce the time needed for presurgical work-up. We will summarize recent research regarding high-frequency oscillations, connectivity measures, and combinations of multiple markers using machine learning. This latter was shown to outperform single markers. The role of NREM sleep for best identification of the EZ interictally will be discussed. We will summarize recent large-scale studies using electrical or magnetic source imaging for clinical decision-making. New approaches based on technical advancements paired with artificial intelligence are on the horizon for better EZ identification. They are ultimately expected to result in a more efficient, less invasive, and less time-demanding presurgical investigation.

Identifiants

pubmed: 32049743
doi: 10.1097/WCO.0000000000000790
pii: 00019052-202004000-00008
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

198-206

Références

Chen Z, Brodie MJ, Liew D, Kwan P. Treatment outcomes in patients with newly diagnosed epilepsy treated with established and new antiepileptic drugs: a 30-year longitudinal cohort study. JAMA Neurol 2018; 75:279–286.
Vakharia VN, Duncan JS, Witt JA, et al. Getting the best outcomes from epilepsy surgery. Ann Neurol 2018; 83:676–690.
West S, Nevitt SJ, Cotton J, et al. Surgery for epilepsy. Cochrane Database Syst Rev 2019; 6:CD010541.
Jayakar P, Gotman J, Harvey AS, et al. Diagnostic utility of invasive EEG for epilepsy surgery: indications, modalities, and techniques. Epilepsia 2016; 57:1735–1747.
Cardinale F, Rizzi M, Vignati E, et al. Stereoelectroencephalography: retrospective analysis of 742 procedures in a single centre. Brain 2019; 142:2688–2704.
Tandon N, Tong BA, Friedman ER, et al. Analysis of morbidity and outcomes associated with use of subdural grids vs stereoelectroencephalography in patients with intractable epilepsy. JAMA Neurol 2019; 76:672–681.
Bartolomei F, Chauvel P, Wendling F. Epileptogenicity of brain structures in human temporal lobe epilepsy: a quantified study from intracerebral EEG. Brain 2008; 131 (Pt 7):1818–1830.
David O, Blauwblomme T, Job AS, et al. Imaging the seizure onset zone with stereo-electroencephalography. Brain 2011; 134 (Pt 10):2898–2911.
Li J, Grinenko O, Mosher JC, Gonzalez-Martinez J, et al. Learning to define an electrical biomarker of the EZ. Hum Brain Mapp 2020; 41:429–441.
Lagarde S, Buzori S, Trebuchon A, et al. The repertoire of seizure onset patterns in human focal epilepsies: determinants and prognostic values. Epilepsia 2019; 60:85–95.
Woolfe M, Prime D, Gillinder L, et al. Automatic detection of the EZ: an application of the fingerprint of epilepsy. J Neurosci Methods 2019; 325:108347.
Frauscher B, von Ellenrieder N, Zelman R, et al. Atlas of the normal human intracranial electroencephalogram: neurophysiological awake activity in different cortical areas. Brain 2018; 141:1130–1144.
Deman P, Bhattacharjee M, Tadel F, et al. IntrAnat electrodes: a free database and visualization software for intracranial electroencephalographic data processed for case and group studies. Fron Neuroinfrom 2018; 12:40.
Medina Villalon S, Paz R, Roehri N, et al. EpiTools, a software suite for presurgical brain mapping in epilepsy: intracerebral EEG. J Neurosci Methods 2018; 303:7–15.
Andrews JP, Gummadavelli A, Farooque P, et al. Association of seizure spread with surgical failure in epilepsy. JAMA Neurol 2019; 76:462–469.
Kini LG, Bernabei JM, Mikhail F, et al. Virtual resection predicts surgical outcome for drug-resistant epilepsy. Brain 2019; 142:3892–3905. [Epub ahead of print].
Amiri M, Frauscher B, Gotman J. Interictal coupling of HFOs and slow oscillations predicts the seizure-onset pattern in mesiotemporal lobe epilepsy. Epilepsia 2019; 60:1160–1170.
An S, Bartolomei F, Guye M, Jirsa V. Optimization of surgical intervention outside the EZ in the Virtual Epileptic Patient (VEP). PLoS Comput Biol 2019; 15:e1007051.
Cuello Oderiz C, von Ellenrieder N, Dubeau F, et al. Association of cortical stimulation-induced seizure with surgical outcome in patients with focal drug-resistant epilepsy. JAMA Neurol 2019; doi: 10.1001/jamaneurol.2019.1464. [Epub ahead of print].
doi: 10.1001/jamaneurol.2019.1464.
Thomschewski A, Hincapie AS, Frauscher B. Localization of the EZ using high-frequency oscillations. Front Neurol 2019; 10:94.
Jacobs J, Wu JY, Perucca P, et al. Removing high-frequency oscillations: a prospective multicenter study on seizure outcome. Neurology 2018; 91:e1040–e1052.
Frauscher B, von Ellenrieder N, Zelmann R, et al. High-frequency oscillations in the normal human brain. Ann Neurol 2018; 84:374–385.
Nariai H, Hussain SA, Bernardo D, et al. Prospective observational study: fast ripple localization delineates the EZ. Clin Neurophysiol 2019; 130:2144–2152.
Tamilia E, Park EH, Percivati S, et al. Surgical resection of ripple onset predicts outcome in pediatric epilepsy. Ann Neurol 2018; 84:331–346.
Gonzalez Otarula KA, von Ellenrieder N, Cuello-Oderiz C, et al. High-frequency oscillation networks and surgical outcome in adult focal epilepsy. Ann Neurol 2019; 85:485–494.
Boran E, Ramantani G, Krayenbühl N, et al. High-density ECoG improves the detection of high frequency oscillations that predict seizure outcome. Clin Neurphysiol 2019; 130:1882–1888.
Lagarde S, Roehri N, Lambert I, et al. Interictal stereotactic-EEG functional connectivity in refractory focal epilepsies. Brain 2018; 141:2966–2980.
Motoi H, Miyakoshi M, Abel TJ, et al. Phase-amplitude coupling between interictal high-frequency activity and slow waves in epilepsy surgery. Epilepsia 2018; 59:1954–1965.
Li A, Chennuri B, Subramanian S, et al. Using network analysis to localize the EZ from invasive EEG recordings in intractable focal epilepsy. Netw Neurosci 2018; 2:218–240.
Motoi H, Jeong JW, Juhasz C, et al. Quantitative analysis of intracranial electrocorticography signals using the concept of statistical parametric mapping. Sci Rep 2019; 9:17385.
Vila-Vidal M, Enriquez CP, Principe A, et al. Low entropy map of brain oscillatory activity identifies spatially localized events: a new method for automated epilepsy focus prediction. NeuroImage 2019; 116410[Epub ahead of print].
Zweiphenning WJEM, Keijzer HM, van Diessen E, et al. Increased gamma and decreased fast ripple Tomlinson SB, Wong JN, Conrad EC, et al. Reproducibility of interictal spike propagation in children with refractory epilepsy. Epilepsia 2019; 60:898–910.
Cimbalnik J, Klimes P, Sladky V, et al. Multifeature localization of epileptic foci from interictal intracranial EEG. Clin Neurophysiol 2019; 130:1945–1953.
Klimes P, Cimbalnik J, Brazdil M, et al. NREM sleep is the state of vigilance that best identifies the EZ in the interictal electroencephalogram. Epilepsia 2019; 60:2404–2415. [Epub ahead of print].
Gliske SV, Irwin ZT, Chestek C, et al. Variability in the location of high frequency oscillations during prolonged intracranial EEG recordings. Nat Commun 2018; 9:2155.
Abbasi B, Goldenholz DM. Machine learning applications in epilepsy. Epilespia 2019; 60:2037–2047.
Coito A, Biethahn S, Tepperberg J, et al. Interictal EZ localization with focal epilepsy using electric source imaging and directed functional connectivity from low-density EEG. Epilepsia Open 2019; 4:281–292.
Van Klink N, Mooij A, Huiskamp G, et al. Simultaneous MEG and EEG to detect ripples in people with focal epilepsy. Clin Neurophysiol 2019; 130:1175–1183.
Velmurugan J, Nagarajan SS, Mariyappa N, et al. Magnetoencephalography imaging of high frequency oscillations strenghtens presurgical localization and outcome prediction. Brain 2019; 142:3514–3529.
Alkawadri R, Burgess RC, Kakisaka Y, et al. Assessment of the utility of ictal magnetoencephalography in the localization of the epileptic seizure onset zone. JAMA Neurol 2018; 75:1264–1272.
Rampp S, Stefan H, Wu X, et al. Magnetoencephalography for epileptic focus localization in a series of 1000 cases. Brain 2019; 142:3059–3071.
Duez L, Tankisi H, Hansen PO, et al. Electromagnetic source imaging in presurgical work-up of patients with epilepsy: a prospective study. Neurology 2019; 92:e576–e586.
Foged MT, Martens T, Pinborg LH, et al. Diagnostic added value of electrical source imaging in presurgical evaluation of patients with epilepsy: a prospective study. Clin Neurophysiol 2019; 131:324–329.
Kowalczik MA, Omidvarnia A, Abbott DF, et al. Clinical benefit of presurgical EEG-fMRI in difficult-to-localize focal epilepsy: a single-institution retrospective review. Epilepsia 2020; 61:49–60.
Nissen IA, Stam CJ, van Straaten ECW, et al. Localization of the EZ using interictal MEG and machine learning in a large cohort of drug-resistant epilepsy patients. Front Neurol 2018; 9:647.
Plummer C, Vogrin SJ, Woods WP. Interictal and ictal source localization for epilepsy surgery using high-density EEG with MEG: a prospective long-term study. Brain 2019; 142:932–951.
Khoo HM, von Ellenrieder N, Zazubovits N, et al. The spike onset zone: the region where epileptic spikes start and from where they propagate. Neurology 2018; 91:e666–674.
Baroumand AG, van Mierlo P, Strobbe G, et al. Automated EEG source imaging: a retrospective, blinded clinical validation study. Clin Neurophysiol 2018; 129:2403–2410.
Pizzo F, Roehri N, Medina Villalon S, et al. Deep brain activities can be detected with magnetoencephalography. Nat Commun 2019; 10:971.
Kuhnke N, Schwind J, Duempelmann M, et al. High frequency oscillations in the ripple band (80–250 Hz) in scalp EEG: higher density of electrodes allows for better localization of the seizure onset zone. Brain Topogr 2018; 31:1059–1072.

Auteurs

Birgit Frauscher (B)

Analytical Neurophysiology Lab, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH