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The impact of the COMT genotype and cognitive demands on facets of intra-subject variability.

Authors :
Salunkhe G
Feige B
Saville CWN
Lancaster TM
Stefanou ME
Bender S
Berger A
Smyrnis N
Biscaldi M
Linden DEJ
Klein C
Source :
Brain and cognition [Brain Cogn] 2019 Jun; Vol. 132, pp. 72-79. Date of Electronic Publication: 2019 Mar 21.
Publication Year :
2019

Abstract

Intra-Subject Variability (ISV), a potential index of catecholaminergic regulation, is elevated in several disorders linked with altered dopamine function. ISV has typically been defined as reaction time standard deviation. However, the ex-Gaussian and spectral measures capture different aspects and may delineate different underlying sources of ISV; thus reflecting different facets of the construct. We examined the impact of factors associated with dopamine metabolism, namely, Catechol-O-Methyltransferase Val158Met (COMT) genotype and Working Memory (WM) and response-switching on ISV facets in young healthy adults. The Met allele was associated with overall increased variability. The rather exclusive sensitivity of ex-Gaussian tau to frequencies below 0.025 Hz and the quasi-periodic structure of particularly slow responses support the interpretation of tau as low frequency fluctuations of neuronal networks. Sigma, by contrast, may reflect neural noise. Regarding cognitive demands, a WM load-related increase in variability was present for all genotypes and all ISV facets. Contrastingly, ISV facets reacted differently to variations in response-switching as, across genotypes, sigma was elevated for rare target trials whereas tau was elevated for frequent standard trials, particularly for Met homozygotes. Our findings support the significant role of COMT in regulating behavioural ISV with its facetted structure and presumed underlying neural processes.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1090-2147
Volume :
132
Database :
MEDLINE
Journal :
Brain and cognition
Publication Type :
Academic Journal
Accession number :
30903983
Full Text :
https://doi.org/10.1016/j.bandc.2019.03.002