Brain Advance Access originally published online on April 7, 2005
Brain 2005 128(7):1556-1570; doi:10.1093/brain/awh491
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Electrocorticographic high gamma activity versus electrical cortical stimulation mapping of naming
Departments of 1 Neurology, 3 Otolaryngology and 4 Neurosurgery, The Johns Hopkins University School of Medicine and 2 Department of Biostatistics, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
Correspondence to: Nathan E. Crone, MD, The Johns Hopkins Hospital, 600 N. Wolfe Street, Meyer 2147, Baltimore, MD 21287, USA E-mail: ncrone{at}jhmi.edu
Subdural electrocorticographic (ECoG) recordings in patients undergoing epilepsy surgery have shown that functional activation is associated with event-related broadband gamma activity in a higher frequency range (>70 Hz) than previously studied in human scalp EEG. To investigate the utility of this high gamma activity (HGA) for mapping language cortex, we compared its neuroanatomical distribution with functional maps derived from electrical cortical stimulation (ECS), which remains the gold standard for predicting functional impairment after surgery for epilepsy, tumours or vascular malformations. Thirteen patients had undergone subdural electrode implantation for the surgical management of intractable epilepsy. Subdural ECoG signals were recorded while each patient verbally named sequentially presented line drawings of objects, and estimates of event-related HGA (80100 Hz) were made at each recording site. Routine clinical ECS mapping used a subset of the same naming stimuli at each cortical site. If ECS disrupted mouth-related motor function, i.e. if it affected the mouth, lips or tongue, naming could not be tested with ECS at the same cortical site. Because naming during ECoG involved these muscles of articulation, the sensitivity and specificity of ECoG HGA were estimated relative to both ECS-induced impairments of naming and ECS disruption of mouth-related motor function. When these estimates were made separately for 12 electrode sites per patient (the average number with significant HGA), the specificity of ECoG HGA with respect to ECS was 78% for naming and 81% for mouth-related motor function, and equivalent sensitivities were 38% and 46%, respectively. When ECS maps of naming and mouth-related motor function were combined, the specificity and sensitivity of ECoG HGA with respect to ECS were 84% and 43%, respectively. This study indicates that event-related ECoG HGA during confrontation naming predicts ECS interference with naming and mouth-related motor function with good specificity but relatively low sensitivity. Its favourable specificity suggests that ECoG HGA can be used to construct a preliminary functional map that may help identify cortical sites of lower priority for ECS mapping. Passive recordings of ECoG gamma activity may be done simultaneously at all electrode sites without the risk of after-discharges associated with ECS mapping, which must be done sequentially at pairs of electrodes. We discuss the relative merits of these two functional mapping techniques.
Key Words: electrical cortical stimulation; electrocorticography; functional mapping; gamma band; language
Abbreviations: ECoG = electrocorticography; ECS = electrical cortical stimulation; fMRI = functional MRI; HGA = high gamma activity; MEG = magnetoencephalography
Received September 23, 2004. Revised February 3, 2005. Accepted March 1, 2005.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. R. Kipke, W. Shain, G. Buzsaki, E. Fetz, J. M. Henderson, J. F. Hetke, and G. Schalk Advanced Neurotechnologies for Chronic Neural Interfaces: New Horizons and Clinical Opportunities J. Neurosci., November 12, 2008; 28(46): 11830 - 11838. [Full Text] [PDF] |
||||
![]() |
V. L. Towle, H.-A. Yoon, M. Castelle, J. C. Edgar, N. M. Biassou, D. M. Frim, J.-P. Spire, and M. H. Kohrman ECoG gamma activity during a language task: differentiating expressive and receptive speech areas Brain, August 1, 2008; 131(8): 2013 - 2027. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ray, S. S. Hsiao, N. E. Crone, P. J. Franaszczuk, and E. Niebur Effect of Stimulus Intensity on the Spike-Local Field Potential Relationship in the Secondary Somatosensory Cortex J. Neurosci., July 16, 2008; 28(29): 7334 - 7343. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Fukuda, M. Nishida, C. Juhasz, O. Muzik, S. Sood, H. T. Chugani, and E. Asano Short-latency median-nerve somatosensory-evoked potentials and induced gamma-oscillations in humans Brain, July 1, 2008; 131(7): 1793 - 1805. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Steinschneider, Y. I. Fishman, and J. C. Arezzo Spectrotemporal Analysis of Evoked and Induced Electroencephalographic Responses in Primary Auditory Cortex (A1) of the Awake Monkey Cereb Cortex, March 1, 2008; 18(3): 610 - 625. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.P. Lachaux, J. Jung, N. Mainy, J.C. Dreher, O. Bertrand, M. Baciu, L. Minotti, D. Hoffmann, and P. Kahane Silence Is Golden: Transient Neural Deactivation in the Prefrontal Cortex during Attentive Reading Cereb Cortex, February 1, 2008; 18(2): 443 - 450. [Abstract] [Full Text] [PDF] |
||||


