Literature DB >> 26991386

Passive language mapping combining real-time oscillation analysis with cortico-cortical evoked potentials for awake craniotomy.

Yukie Tamura1, Hiroshi Ogawa1, Christoph Kapeller2, Robert Prueckl2, Fumiya Takeuchi3, Ryogo Anei1, Anthony Ritaccio4, Christoph Guger2, Kyousuke Kamada1.   

Abstract

OBJECTIVE Electrocortical stimulation (ECS) is the gold standard for functional brain mapping; however, precise functional mapping is still difficult in patients with language deficits. High gamma activity (HGA) between 80 and 140 Hz on electrocorticography is assumed to reflect localized cortical processing, whereas the cortico-cortical evoked potential (CCEP) can reflect bidirectional responses evoked by monophasic pulse stimuli to the language cortices when there is no patient cooperation. The authors propose the use of "passive" mapping by combining HGA mapping and CCEP recording without active tasks during conscious resections of brain tumors. METHODS Five patients, each with an intraaxial tumor in their dominant hemisphere, underwent conscious resection of their lesion with passive mapping. The authors performed functional localization for the receptive language area, using real-time HGA mapping, by listening passively to linguistic sounds. Furthermore, single electrical pulses were delivered to the identified receptive temporal language area to detect CCEPs in the frontal lobe. All mapping results were validated by ECS, and the sensitivity and specificity were evaluated. RESULTS Linguistic HGA mapping quickly identified the language area in the temporal lobe. Electrical stimulation by linguistic HGA mapping to the identified temporal receptive language area evoked CCEPs on the frontal lobe. The combination of linguistic HGA and frontal CCEPs needed no patient cooperation or effort. In this small case series, the sensitivity and specificity were 93.8% and 89%, respectively. CONCLUSIONS The described technique allows for simple and quick functional brain mapping with higher sensitivity and specificity than ECS mapping. The authors believe that this could improve the reliability of functional brain mapping and facilitate rational and objective operations. Passive mapping also sheds light on the underlying physiological mechanisms of language in the human brain.

Entities:  

Keywords:  BIS = bispectral index; CCEP = cortico-cortical evoked potential; ECS = electrocortical stimulation; ECoG = electrocorticography; ERD, ERS = event-related desynchronization, event-related synchronization; HGA = high gamma activity; PN = picture naming; WR = word reading; awake craniotomy; corticocortical evoked potentials; diagnostic and operative techniques; electrocortical stimulation; electrocorticography; fMRI = functional MRI; high gamma activity; language

Mesh:

Year:  2016        PMID: 26991386     DOI: 10.3171/2015.4.JNS15193

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  15 in total

1.  Clinical impact of intraoperative CCEP monitoring in evaluating the dorsal language white matter pathway.

Authors:  Yukihiro Yamao; Kengo Suzuki; Takeharu Kunieda; Riki Matsumoto; Yoshiki Arakawa; Takuro Nakae; Sei Nishida; Rika Inano; Sumiya Shibata; Akihiro Shimotake; Takayuki Kikuchi; Nobukatsu Sawamoto; Nobuhiro Mikuni; Akio Ikeda; Hidenao Fukuyama; Susumu Miyamoto
Journal:  Hum Brain Mapp       Date:  2017-01-23       Impact factor: 5.038

2.  Workshops of the Seventh International Brain-Computer Interface Meeting: Not Getting Lost in Translation.

Authors:  Jane E Huggins; Christoph Guger; Erik Aarnoutse; Brendan Allison; Charles W Anderson; Steven Bedrick; Walter Besio; Ricardo Chavarriaga; Jennifer L Collinger; An H Do; Christian Herff; Matthias Hohmann; Michelle Kinsella; Kyuhwa Lee; Fabien Lotte; Gernot Müller-Putz; Anton Nijholt; Elmar Pels; Betts Peters; Felix Putze; Rüdiger Rupp; Gerwin Schalk; Stephanie Scott; Michael Tangermann; Paul Tubig; Thorsten Zander
Journal:  Brain Comput Interfaces (Abingdon)       Date:  2019-12-10

3.  Electrical Stimulation Mapping of the Brain: Basic Principles and Emerging Alternatives.

Authors:  Anthony L Ritaccio; Peter Brunner; Gerwin Schalk
Journal:  J Clin Neurophysiol       Date:  2018-03       Impact factor: 2.177

Review 4.  Neuromonitoring of the language pathways using cortico-cortical evoked potentials: a systematic review and meta-analysis.

Authors:  Oleg Titov; Andrey Bykanov; David Pitskhelauri; Gleb Danilov
Journal:  Neurosurg Rev       Date:  2022-01-15       Impact factor: 3.042

5.  Dynamic tractography: Integrating cortico-cortical evoked potentials and diffusion imaging.

Authors:  Brian H Silverstein; Eishi Asano; Ayaka Sugiura; Masaki Sonoda; Min-Hee Lee; Jeong-Won Jeong
Journal:  Neuroimage       Date:  2020-04-12       Impact factor: 6.556

6.  Functional differences among stimulation-identified cortical naming sites in the temporal region.

Authors:  Marla J Hamberger; Michele Miozzo; Catherine A Schevon; Chris Morrison; Chad Carlson; Ashesh D Mehta; Gad E Klein; Guy M McKhann; Alicia C Williams
Journal:  Epilepsy Behav       Date:  2016-05-17       Impact factor: 2.937

Review 7.  Single pulse electrical stimulation to probe functional and pathological connectivity in epilepsy.

Authors:  Riki Matsumoto; Takeharu Kunieda; Dileep Nair
Journal:  Seizure       Date:  2016-11-14       Impact factor: 3.184

8.  ECoG high-gamma modulation versus electrical stimulation for presurgical language mapping.

Authors:  Ravindra Arya; Paul S Horn; Nathan E Crone
Journal:  Epilepsy Behav       Date:  2017-12-13       Impact factor: 2.937

9.  A quantitative method for evaluating cortical responses to electrical stimulation.

Authors:  Lawrence J Crowther; Peter Brunner; Christoph Kapeller; Christoph Guger; Kyousuke Kamada; Marjorie E Bunch; Bridget K Frawley; Timothy M Lynch; Anthony L Ritaccio; Gerwin Schalk
Journal:  J Neurosci Methods       Date:  2018-10-04       Impact factor: 2.390

10.  MRIES: A Matlab Toolbox for Mapping the Responses to Intracranial Electrical Stimulation.

Authors:  Kaijia Sun; Haixiang Wang; Yunxian Bai; Wenjing Zhou; Liang Wang
Journal:  Front Neurosci       Date:  2021-06-14       Impact factor: 4.677

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