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Decomposing P300 to identify its genetic basis.

Authors :
Ford JM
Source :
Psychophysiology [Psychophysiology] 2014 Dec; Vol. 51 (12), pp. 1325-6.
Publication Year :
2014

Abstract

In this commentary, I explore reasons why it has been difficult to associate P300 amplitude with a gene or a single nucleotide polymorphism (SNP). I suggest we decompose P300 into the factors that contribute to it to get better traction on its genetic basis. Specifically, I note that we can improve the measurement of P300 to remove state-dependent contributions by including more than one measurement occasion; we can identify and extract the neural components contributing to P300 amplitude by estimating EEG power in specific bands of the P300; we can adjust P300 for single-trial variability; we can extract single-trial variability; and we can refine the tasks to isolate the separate psychological processes that P300 reflects. In the end, each of these factors that contribute to the conglomerate P300 may be a separate endophenotype mapping onto a separate SNP or gene.<br /> (Published 2014. This article is a U.S. Government work and is in the public domain in the USA.)

Details

Language :
English
ISSN :
1469-8986
Volume :
51
Issue :
12
Database :
MEDLINE
Journal :
Psychophysiology
Publication Type :
Academic Journal
Accession number :
25387713
Full Text :
https://doi.org/10.1111/psyp.12353