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Memory Timeline: Brain ERP C250 (not P300) is an Early Biomarker of Short-term Storage

Overview
Journal Brain Res
Specialty Neurology
Date 2015 Feb 3
PMID 25641043
Citations 2
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Abstract

Brain event-related potentials (ERPs) offer a quantitative link between neurophysiological activity and cognitive performance. ERPs were measured while young adults performed a task that required storing a relevant stimulus in short-term memory. Using principal components analysis, ERP component C250 (maximum at 250 ms post-stimulus) was extracted from a set of ERPs that were separately averaged for various task conditions, including stimulus relevancy and stimulus sequence within a trial. C250 was more positive in response to task-specific stimuli that were successfully stored in short-term memory. This relationship between C250 and short-term memory storage of a stimulus was confirmed by a memory probe recall test where the behavioral recall of a stimulus was highly correlated with its C250 amplitude. ERP component P300 (and its subcomponents of P3a and P3b, which are commonly thought to represent memory operations) did not show a pattern of activation reflective of storing task-relevant stimuli. C250 precedes the P300, indicating that initial short-term memory storage may occur earlier than previously believed. Additionally, because C250 is so strongly predictive of a stimulus being stored in short-term memory, C250 may provide a strong index of early memory operations.

Citing Articles

Temporospatial components of brain ERPs as biomarkers for Alzheimer's disease.

Chapman R, Gardner M, Klorman R, Mapstone M, Porsteinsson A, Antonsdottir I Alzheimers Dement (Amst). 2018; 10:604-614.

PMID: 30417070 PMC: 6215980. DOI: 10.1016/j.dadm.2018.08.002.


ERP C250 shows the elderly (cognitively normal, Alzheimer's disease) store more stimuli in short-term memory than Young Adults do.

Chapman R, Gardner M, Mapstone M, Klorman R, Porsteinsson A, Dupree H Clin Neurophysiol. 2016; 127(6):2423-35.

PMID: 27178862 PMC: 4959798. DOI: 10.1016/j.clinph.2016.03.006.

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