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


Journal

Brain and cognition
ISSN: 1090-2147
Titre abrégé: Brain Cogn
Pays: United States
ID NLM: 8218014

Informations de publication

Date de publication:
06 2019
Historique:
received: 02 01 2019
revised: 16 03 2019
accepted: 16 03 2019
pubmed: 25 3 2019
medline: 11 9 2019
entrez: 24 3 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30903983
pii: S0278-2626(18)30488-3
doi: 10.1016/j.bandc.2019.03.002
pii:
doi:

Substances chimiques

COMT protein, human EC 2.1.1.6
Catechol O-Methyltransferase EC 2.1.1.6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-79

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

G Salunkhe (G)

Department of Child and Adolescent Psychiatry, Psychotherapy, and Psychosomatics, Medical Faculty, University of Freiburg, Germany.

B Feige (B)

Department of Psychiatry and Psychotherapy, Medical Faculty, University of Freiburg, Germany.

C W N Saville (CWN)

School of Psychology, Bangor University, United Kingdom.

T M Lancaster (TM)

Neuroscience and Mental Health Research Institute, Cardiff University, United Kingdom.

M E Stefanou (ME)

Department of Child and Adolescent Psychiatry, Psychotherapy, and Psychosomatics, Medical Faculty, University of Freiburg, Germany.

S Bender (S)

Department of Child and Adolescent Psychiatry, Medical Faculty, University of Cologne, Germany.

A Berger (A)

Department of Psychology and Zlotowski Center of Neuroscience, Ben-Gurion University of the Negev, Beer Sheva, Israel.

N Smyrnis (N)

Department of Psychiatry, National and Kapodistrian University of Athens, Athens, Greece.

M Biscaldi (M)

Department of Child and Adolescent Psychiatry, Psychotherapy, and Psychosomatics, Medical Faculty, University of Freiburg, Germany.

D E J Linden (DEJ)

School for Mental Health and Neuroscience, Maastricht University, Netherlands.

C Klein (C)

Department of Child and Adolescent Psychiatry, Psychotherapy, and Psychosomatics, Medical Faculty, University of Freiburg, Germany; Department of Child and Adolescent Psychiatry, Medical Faculty, University of Cologne, Germany; Department of Psychiatry, National and Kapodistrian University of Athens, Athens, Greece. Electronic address: christoph.klein.kjp@uniklinik-freiburg.de.

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