» Articles » PMID: 19034898

Attention Impairment in Temporal Lobe Epilepsy: a Neurophysiological Approach Via Analysis of the P300 Wave

Overview
Journal Hum Brain Mapp
Publisher Wiley
Specialty Neurology
Date 2008 Nov 27
PMID 19034898
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Attention is often impaired in temporal lobe epilepsy (TLE). The P300 wave (an endogenous, event-related potential) is a correlate of attention which is usually recorded during an "oddball paradigm," where the subject is instructed to detect an infrequent target stimulus presented amongst frequent, standard stimuli. Modifications of the P300 wave's latency and amplitude in TLE have been suggested, but it is still not known whether the source regions also differ. Our hypothesis was that temporal lobe dysfunction would modify the P3 source regions in TLE patients.

Methods: A comparative, high density, 128-channel electroencephalographic analysis of the characteristics of P300 (P3b latency and amplitude) was performed in 10 TLE patients and 10 healthy controls during auditory and visual oddball paradigms. The P3b sources were localized on individual 3D MR images using the LORETA method and intergroup statistical comparisons were performed using SPM2(R) software.

Results: Our main results (in both individual analyses and intergroup comparisons) revealed a reduction in temporal (and more particularly mesiotemporal) sources and, to a lesser extent, frontal sources in TLE patients, compared with controls.

Discussion: This reduction may reflect direct, local cortical dysfunction caused by the epileptic focus or more complex interference between epileptic networks and normal attentional pathways.

Citing Articles

Resting state EEG microstate profiling and a machine-learning based classifier model in epilepsy.

Sa A, C S, P D, Ps S, Ml A, Kumar D Cogn Neurodyn. 2024; 18(5):2419-2432.

PMID: 39555277 PMC: 11564422. DOI: 10.1007/s11571-024-10095-z.


Inhibitory control deficits in patients with mesial temporal lobe epilepsy: an event-related potential analysis based on Go/NoGo task.

Shao C, Li D, Zhang X, Xiang F, Zhang X, Wang X Front Neurol. 2024; 14:1326841.

PMID: 38264090 PMC: 10804952. DOI: 10.3389/fneur.2023.1326841.


Current development of biosensing technologies towards diagnosis of mental diseases.

Zheng Y, Liu C, Lai N, Wang Q, Xia Q, Sun X Front Bioeng Biotechnol. 2023; 11:1190211.

PMID: 37456720 PMC: 10342212. DOI: 10.3389/fbioe.2023.1190211.


Abnormal directed connectivity of resting state networks in focal epilepsy.

Carboni M, De Stefano P, Vorderwulbecke B, Tourbier S, Mullier E, Rubega M Neuroimage Clin. 2020; 27:102336.

PMID: 32679553 PMC: 7363703. DOI: 10.1016/j.nicl.2020.102336.


Application of the P300 Event-Related Potential in the Diagnosis of Epilepsy Disorder: A Review.

Sowndhararajan K, Kim M, Deepa P, Park S, Kim S Sci Pharm. 2018; 86(2).

PMID: 29587468 PMC: 6027667. DOI: 10.3390/scipharm86020010.


References
1.
Oddo S, Silvia O, Solis P, Patricia S, Consalvo D, Damian C . Mesial temporal lobe epilepsy and hippocampal sclerosis: cognitive function assessment in Hispanic patients. Epilepsy Behav. 2003; 4(6):717-22. DOI: 10.1016/j.yebeh.2003.09.008. View

2.
Grunwald T, Beck H, Lehnertz K, Blumcke I, Pezer N, Kutas M . Limbic P300s in temporal lobe epilepsy with and without Ammon's horn sclerosis. Eur J Neurosci. 1999; 11(6):1899-906. DOI: 10.1046/j.1460-9568.1999.00613.x. View

3.
Tarkka I, Stokic D . Source localization of P300 from oddball, single stimulus, and omitted-stimulus paradigms. Brain Topogr. 1999; 11(2):141-51. DOI: 10.1023/a:1022258606418. View

4.
Menon V, Ford J, Lim K, Glover G, Pfefferbaum A . Combined event-related fMRI and EEG evidence for temporal-parietal cortex activation during target detection. Neuroreport. 1997; 8(14):3029-37. DOI: 10.1097/00001756-199709290-00007. View

5.
Pascual-Marqui R, Michel C, Lehmann D . Low resolution electromagnetic tomography: a new method for localizing electrical activity in the brain. Int J Psychophysiol. 1994; 18(1):49-65. DOI: 10.1016/0167-8760(84)90014-x. View