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| Research article summary (published 30 Jan 1996): |
Changes in the P300 component of the tactile event-related potential following spinal cord injury.
Full Abstract
Previous studies have demonstrated that significant changes in action or behaviour (function) and morphology occur in the deafferentated and the adjacent somatosensory cortex after amputation or experimental spinal cord injury. These studies have shown changes in somatotopic mappings and somatosensory perception as well as altered evoked responses. The purpose of the present study was to examine the potential effect of these changes on cognitive processes using the tactile P300 event-related potential (ERP) in a spinal cord injured (SCI) population. The P300 ERP has been associated with more complex cognitive functioning such as selective attention, memory, and stimulus evaluation rather than earlier sensory processing of stimuli. Three groups consisting of healthy control, paraplegic, and tetraplegic subjects participated in a transcutaneous electrical stimulation 'oddball' task. Results indicate that all groups were successful in maintaining target counts and produced significantly larger P300 amplitudes with longer latencies to target trials compared to non-target trials. The SCI groups, however, produced P300 ERPs for both targets and non-targets that were significantly reduced in amplitude compared to the control group. In the case of the tetraplegia patients, the P300 was almost abolished. No differences in latency of the P300 was observed between any of the groups.
Author information
Author/s: Cohen, M J (MJ); Ament, P A (PA); Schandler, S L (SL); Vulpe, M (M);
Affiliation: Department of Veterans Affairs Medical Center, Long Beach, California, USA.
Journal and publication information
Publication Type: Clinical Trial; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
Journal: Paraplegia (Paraplegia), published in ENGLAND. (Language: eng)
Reference: 1996-Feb; vol 34 (issue 2) : pp 107-12
Dates: Created 1996/11/27; Completed 1996/11/27; Revised 2006/11/15;
PMID: 8835036, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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