Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (51)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Parra, J.
Right arrow Articles by Lopes da Silva, F. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Parra, J.
Right arrow Articles by Lopes da Silva, F. H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 126, No. 5, 1164-1172, May 2003
© 2003 Guarantors of Brain
doi: 10.1093/brain/awg109

Gamma-band phase clustering and photosensitivity: is there an underlying mechanism common to photosensitive epilepsy and visual perception?

J. Parra1, S. N. Kalitzin1, J. Iriarte2, W. Blanes1, D. N. Velis1 and F. H. Lopes da Silva1

1 Dutch Epilepsy Clinics Foundation, ‘Meer en Bosch’, Heemstede, The Netherlands, 2 Department of Neurology, Clínica Universitaria de Navarra, Pamplona, Spain

Correspondence to: Jaime Parra, MD, PhD, Department of Clinical Neurophysiology, Stichting Epilepsie Instellingen Nederland (SEIN), ‘Meer en Bosch’, Achterweg 5, 2103 SW Heemstede, The Netherlands E-mail: jparra{at}sein.nl

Photosensitive epilepsy (PSE) is the most common form of human reflex epilepsy, appearing in up to 10% of epileptic children. It also offers a highly reproducible model to investigate whether changes in neuronal activity preceding the transition to an epileptic photoparoxysmal response (PPR) may be detected. We studied 10 patients with idiopathic PSE (eight female, mean age 26 years, range 9–51 years) using magnetoencephalography. In addition, we also studied the responses of five normal controls (mean age 24 years, age range 9–35 years) and three non-photosensitive epileptic patients (mean age 10 years, range 8–11 years). Spectral analysis of the MEG signals recorded during intermittent photic stimulation revealed relevant information in the phase spectrum. To quantify this effect, we introduced a second order response feature of the stimulus-triggered visual response preceding the PPR: the phase clustering index, which measures how close the phases of successive periods are grouped for each frequency component for all periods of the stimuli applied. We recorded a total of 86 PPRs, including several absence seizures, in nine of the 10 patients. We found that an enhancement of phase synchrony in the gamma-band (30–120 Hz), harmonically related to the frequency of stimulation, preceded the stimulation trials that evolved into PPRs, and differed significantly from that encountered in trials not followed by PPR or in control subjects. This novel finding leads us to postulate that a pathological deviation of normally occurring synchronization of gamma oscillations, underlying perceptional processes, mediates the epileptic transition in PSE.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
J. B. Swettenham, S. D. Muthukumaraswamy, and K. D. Singh
Spectral Properties of Induced and Evoked Gamma Oscillations in Human Early Visual Cortex to Moving and Stationary Stimuli
J Neurophysiol, August 1, 2009; 102(2): 1241 - 1253.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. D. Muthukumaraswamy, R. A.E. Edden, D. K. Jones, J. B. Swettenham, and K. D. Singh
Resting GABA concentration predicts peak gamma frequency and fMRI amplitude in response to visual stimulation in humans
PNAS, May 19, 2009; 106(20): 8356 - 8361.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
S. Monto, S. Vanhatalo, M. D. Holmes, and J. M. Palva
Epileptogenic Neocortical Networks Are Revealed by Abnormal Temporal Dynamics in Seizure-Free Subdural EEG
Cereb Cortex, June 1, 2007; 17(6): 1386 - 1393.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
F. Mormann, R. G. Andrzejak, C. E. Elger, and K. Lehnertz
Seizure prediction: the long and winding road
Brain, February 1, 2007; 130(2): 314 - 333.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
M. Siniatchkin, S. Groppa, B. Jerosch, H. Muhle, C. Kurth, A. J. Shepherd, H. Siebner, and U. Stephani
Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability pattern
Brain, January 1, 2007; 130(1): 78 - 87.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
E. Ferlazzo, B. G. Zifkin, E. Andermann, and F. Andermann
Cortical triggers in generalized reflex seizures and epilepsies
Brain, April 1, 2005; 128(4): 700 - 710.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
D. Pinto, B. Westland, G.-J. de Haan, G. Rudolf, B. M. da Silva, E. Hirsch, D. Lindhout, D. G.A. K.-N. Trenite, and B. P.C. Koeleman
Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13
Hum. Mol. Genet., January 1, 2005; 14(1): 171 - 178.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.